Abnormal brain activation and connectivity to standardized disorder-related visual scenes in social anxiety disorder
Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated imme...
Saved in:
Published in | Human brain mapping Vol. 37; no. 4; pp. 1559 - 1572 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.04.2016
John Wiley & Sons, Inc John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder‐related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder‐related complex visual scenes. SAD patients rated disorder‐related as compared with neutral scenes as more unpleasant, arousing and anxiety‐inducing than HC. On the neural level, disorder‐related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para‐)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder‐related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder‐related stimuli for the investigation of altered emotion processing in SAD. Disorder‐related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self‐referential processing reported in previous studies. Hum Brain Mapp 37:1559‐1572, 2016. © 2016 Wiley Periodicals, Inc. |
---|---|
AbstractList | Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder-related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder-related complex visual scenes. SAD patients rated disorder-related as compared with neutral scenes as more unpleasant, arousing and anxiety-inducing than HC. On the neural level, disorder-related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para-)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder-related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder-related stimuli for the investigation of altered emotion processing in SAD. Disorder-related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self-referential processing reported in previous studies. Hum Brain Mapp 37:1559-1572, 2016. © 2016 Wiley Periodicals, Inc. Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder‐related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder‐related complex visual scenes. SAD patients rated disorder‐related as compared with neutral scenes as more unpleasant, arousing and anxiety‐inducing than HC. On the neural level, disorder‐related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para‐)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder‐related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder‐related stimuli for the investigation of altered emotion processing in SAD. Disorder‐related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self‐referential processing reported in previous studies. Hum Brain Mapp 37:1559‐1572, 2016 . © 2016 Wiley Periodicals, Inc. Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder-related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder-related complex visual scenes. SAD patients rated disorder-related as compared with neutral scenes as more unpleasant, arousing and anxiety-inducing than HC. On the neural level, disorder-related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para-)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder-related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder-related stimuli for the investigation of altered emotion processing in SAD. Disorder-related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self-referential processing reported in previous studies. Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder-related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder-related complex visual scenes. SAD patients rated disorder-related as compared with neutral scenes as more unpleasant, arousing and anxiety-inducing than HC. On the neural level, disorder-related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para-)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder-related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder-related stimuli for the investigation of altered emotion processing in SAD. Disorder-related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self-referential processing reported in previous studies. Hum Brain Mapp 37:1559-1572, 2016. Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder-related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder-related complex visual scenes. SAD patients rated disorder-related as compared with neutral scenes as more unpleasant, arousing and anxiety-inducing than HC. On the neural level, disorder-related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para-)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder-related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder-related stimuli for the investigation of altered emotion processing in SAD. Disorder-related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self-referential processing reported in previous studies.Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the vastly different methods and materials used so far. This is why the present functional magnetic resonance imaging (fMRI) study investigated immediate disorder-related threat processing in 30 SAD patients and 30 healthy controls (HC) with a novel, standardized set of highly ecologically valid, disorder-related complex visual scenes. SAD patients rated disorder-related as compared with neutral scenes as more unpleasant, arousing and anxiety-inducing than HC. On the neural level, disorder-related as compared with neutral scenes evoked differential responses in SAD patients in a widespread emotion processing network including (para-)limbic structures (e.g. amygdala, insula, thalamus, globus pallidus) and cortical regions (e.g. dorsomedial prefrontal cortex (dmPFC), posterior cingulate cortex (PCC), and precuneus). Functional connectivity analysis yielded an altered interplay between PCC/precuneus and paralimbic (insula) as well as cortical regions (dmPFC, precuneus) in SAD patients, which emphasizes a central role for PCC/precuneus in disorder-related scene processing. Hyperconnectivity of globus pallidus with amygdala, anterior cingulate cortex (ACC) and medial prefrontal cortex (mPFC) additionally underlines the relevance of this region in socially anxious threat processing. Our findings stress the importance of specific disorder-related stimuli for the investigation of altered emotion processing in SAD. Disorder-related threat processing in SAD reveals anomalies at multiple stages of emotion processing which may be linked to increased anxiety and to dysfunctionally elevated levels of self-referential processing reported in previous studies. |
Author | Zepp, Britta Maria Heitmann, Carina Yvonne Peterburs, Jutta Feldker, Katharina Neumeister, Paula Zwitserlood, Pienie Straube, Thomas |
AuthorAffiliation | 1 Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster Germany 2 Institute of Psychology, University of Muenster, Muenster Germany |
AuthorAffiliation_xml | – name: 1 Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster Germany – name: 2 Institute of Psychology, University of Muenster, Muenster Germany |
Author_xml | – sequence: 1 givenname: Carina Yvonne surname: Heitmann fullname: Heitmann, Carina Yvonne email: carina.heitmann@uni-muenster.de organization: Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster, Germany – sequence: 2 givenname: Katharina surname: Feldker fullname: Feldker, Katharina organization: Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster, Germany – sequence: 3 givenname: Paula surname: Neumeister fullname: Neumeister, Paula organization: Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster, Germany – sequence: 4 givenname: Britta Maria surname: Zepp fullname: Zepp, Britta Maria organization: Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster, Germany – sequence: 5 givenname: Jutta surname: Peterburs fullname: Peterburs, Jutta organization: Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster, Germany – sequence: 6 givenname: Pienie surname: Zwitserlood fullname: Zwitserlood, Pienie organization: Institute of Psychology, University of Muenster, Muenster, Germany – sequence: 7 givenname: Thomas surname: Straube fullname: Straube, Thomas organization: Institute of Medical Psychology and Systems Neuroscience, University of Muenster, Muenster, Germany |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26806013$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkk1v1DAQhi1URD_gwB9AkbjAIa0_EntzQWor2gUVEBKoR2viTKhL1m5tZ-n219fb3a2gAomTx-PnfTXjmV2y5bxDQl4yus8o5QcX7WyfC8bpE7LDaKNKyhqxtYxlXTaVYttkN8ZLShmrKXtGtrmcUEmZ2CHpsHU-zGAo2gDWFWCSnUOyPoeuK4x3DpcpmxZF8kVMOQuhs7fYFZ2NPnQYyoADpJyY2zhmp2jQYSyyW_TG5gS4G4vZYCN4Tp72MER8sT73yPeT99-Op-XZl9MPx4dnpalZRcsWq76X2APl_UQa2SGKFoBxqFoKqq_BtBUIA7KlStYtzRfoe6MmAinyWuyRdyvfq7GdYZfLSgEGfRXsDMJCe7D6zxdnL_QPP9dyIhVvqmzwZm0Q_PWIMemZzd0NAzj0Y9RMKSmlqPl_oZxVqmYqo68foZd-DC7_xJJinDdK8Ey9-r34h6o3s8vAwQowwccYsNfGpvvR5V7soBnVy-3QeTv0_XZkxdtHio3p39i1-y874OLfoJ4efdooypXCxoQ3DwoIP7VUQtX6_POp_khPps3X8yMtxB0aJttc |
CitedBy_id | crossref_primary_10_1097_MD_0000000000005358 crossref_primary_10_1016_j_biopsycho_2018_09_010 crossref_primary_10_1016_j_jad_2022_02_023 crossref_primary_10_1016_j_ebiom_2021_103445 crossref_primary_10_1177_10738584211030497 crossref_primary_10_1002_acn3_570 crossref_primary_10_3389_fnagi_2024_1375435 crossref_primary_10_1016_j_neubiorev_2018_06_007 crossref_primary_10_1111_psyp_14643 crossref_primary_10_1016_j_nicl_2017_08_001 crossref_primary_10_1007_s00330_022_08908_y crossref_primary_10_1111_psyp_70006 crossref_primary_10_9758_cpn_2022_20_2_279 crossref_primary_10_1007_s11920_021_01249_5 crossref_primary_10_7554_eLife_23608 crossref_primary_10_1097_WCO_0000000000001233 crossref_primary_10_1017_S0033291716002634 crossref_primary_10_1027_2151_2604_a000240 crossref_primary_10_3389_fpsyt_2018_00449 crossref_primary_10_1002_hbm_25100 crossref_primary_10_1016_j_neubiorev_2023_105475 crossref_primary_10_12688_f1000research_21214_1 crossref_primary_10_1007_s40653_023_00549_7 crossref_primary_10_1017_S0033291722003439 crossref_primary_10_1016_j_bbr_2020_112589 crossref_primary_10_1093_scan_nsaf012 crossref_primary_10_1080_13554794_2022_2160262 crossref_primary_10_1016_j_ebiom_2018_08_048 crossref_primary_10_1016_j_ynstr_2023_100578 crossref_primary_10_1016_j_nicl_2021_102615 crossref_primary_10_1016_j_bbr_2020_112808 crossref_primary_10_3390_ijerph18115556 crossref_primary_10_1002_wcs_1692 crossref_primary_10_1016_j_jad_2018_04_046 crossref_primary_10_1038_s41398_024_02844_9 crossref_primary_10_9758_cpn_2019_17_1_12 crossref_primary_10_1016_j_nicl_2017_01_020 crossref_primary_10_1016_j_biopsycho_2025_108998 crossref_primary_10_1016_j_jad_2017_12_075 |
Cites_doi | 10.1016/j.biopsych.2005.01.044 10.1016/j.neuroscience.2008.08.014 10.2741/1074 10.1016/0028-3932(71)90067-4 10.1016/S1053-8119(03)00230-1 10.1162/0898929042568578 10.1016/j.cortex.2012.08.003 10.1002/hbm.20345 10.1002/da.20347 10.1001/archpsyc.59.11.1027 10.1007/s00429-013-0580-0 10.1016/j.tics.2005.03.010 10.1016/j.biopsycho.2008.01.014 10.1006/nimg.2001.0978 10.1097/00001756-199712220-00024 10.1016/j.neures.2010.09.008 10.1111/ejn.12094 10.3389/fpsyg.2013.00282 10.1186/2045-5380-4-6 10.1016/j.neuroimage.2011.02.021 10.1016/S0166-2236(97)01125-9 10.1016/S0005-7967(97)00022-3 10.1016/0166-2236(90)90107-L 10.1038/nrn2555 10.1016/S0887-6185(02)00134-2 10.1016/j.pscychresns.2010.12.016 10.1016/j.neuroimage.2013.11.001 10.1207/S15327078IN0204_02 10.1098/rstb.2007.2092 10.1073/pnas.98.2.676 10.1016/j.tics.2010.11.004 10.1016/j.neulet.2004.09.050 10.1093/brain/awl004 10.1038/79871 10.1016/j.brainresbull.2009.02.002 10.1016/j.neubiorev.2011.08.002 10.1001/archpsyc.65.10.1176 10.1176/appi.ajp.2007.07030504 10.1159/000087987 10.1016/j.pscychresns.2010.05.001 10.1016/j.biopsych.2004.09.024 10.1002/hbm.22602 10.1006/nimg.2002.1087 10.1016/j.neuroimage.2011.05.073 10.1006/nimg.2001.0789 10.1097/00001756-200303030-00006 10.1016/j.mri.2011.02.013 10.1016/S1053-8119(03)00169-1 10.1176/appi.books.9780890423349 10.1002/hbm.10075 10.1026//0084-5345.28.1.28 10.1016/j.brainres.2010.12.084 10.1016/j.biopsych.2005.08.012 10.1016/j.neubiorev.2014.08.003 10.1016/j.pnpbp.2010.02.028 10.1371/journal.pone.0015238 10.1016/S0925-4927(97)00018-8 10.1002/mrm.1910330508 10.1007/s00429-010-0262-0 10.1038/nn1176 10.1089/brain.2011.0030 10.1038/2245 10.1080/17470910802250519 10.3389/fnhum.2012.00347 10.1016/S1364-6613(98)01271-6 10.1002/hbm.20249 10.1098/rstb.2002.1218 10.1002/da.22014 10.1002/(SICI)1097-0193(1999)8:2/3<109::AID-HBM7>3.0.CO;2-W 10.1093/cercor/bhq268 10.1023/A:1025048802629 10.1016/j.tics.2007.11.010 10.1016/j.neuropsychologia.2014.08.027 10.1007/s00429-005-0025-5 10.1016/j.biopsycho.2010.03.005 10.1016/j.pscychresns.2015.03.005 10.1093/cercor/bhl017 10.1523/JNEUROSCI.3087-11.2011 |
ContentType | Journal Article |
Copyright | 2016 Wiley Periodicals, Inc. |
Copyright_xml | – notice: 2016 Wiley Periodicals, Inc. |
DBID | BSCLL AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QR 7TK 7U7 8FD C1K FR3 K9. P64 7X8 5PM |
DOI | 10.1002/hbm.23120 |
DatabaseName | Istex CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Chemoreception Abstracts Neurosciences Abstracts Toxicology Abstracts Technology Research Database Environmental Sciences and Pollution Management Engineering Research Database ProQuest Health & Medical Complete (Alumni) Biotechnology and BioEngineering Abstracts MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Technology Research Database Toxicology Abstracts ProQuest Health & Medical Complete (Alumni) Chemoreception Abstracts Engineering Research Database Neurosciences Abstracts Biotechnology and BioEngineering Abstracts Environmental Sciences and Pollution Management MEDLINE - Academic |
DatabaseTitleList | Technology Research Database CrossRef MEDLINE Neurosciences Abstracts MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Anatomy & Physiology |
DocumentTitleAlternate | Processing of Disorder‐Related Scenes in SAD |
EISSN | 1097-0193 |
EndPage | 1572 |
ExternalDocumentID | PMC6867294 3973769761 26806013 10_1002_hbm_23120 HBM23120 ark_67375_WNG_J0FH9QWB_3 |
Genre | article Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: German Research Society (Deutsche Forschungsgemeinschaft, DFG) funderid: SFB/TRR 58: C06, C07 – fundername: German Research Society (Deutsche Forschungsgemeinschaft, DFG) grantid: SFB/TRR 58: C06, C07 |
GroupedDBID | --- .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 24P 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5VS 66C 702 7PT 7X7 8-0 8-1 8-3 8-4 8-5 8FI 8FJ 8UM 930 A03 AAESR AAEVG AAHHS AAONW AAZKR ABCQN ABCUV ABEML ABIJN ABIVO ABJNI ABPVW ABUWG ACBWZ ACCFJ ACGFS ACIWK ACPOU ACPRK ACSCC ACXQS ADBBV ADEOM ADIZJ ADMGS ADPDF ADXAS ADZOD AEEZP AEIMD AENEX AEQDE AEUQT AFBPY AFGKR AFKRA AFPWT AFRAH AFZJQ AHMBA AIURR AIWBW AJBDE AJXKR ALAGY ALIPV ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR ASPBG ATUGU AUFTA AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BENPR BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BY8 C45 CCPQU CS3 D-E D-F DCZOG DPXWK DR1 DR2 DU5 EBD EBS EJD EMOBN F00 F01 F04 F5P FEDTE FYUFA G-S G.N GAKWD GNP GODZA GROUPED_DOAJ H.T H.X HBH HF~ HHY HHZ HMCUK HVGLF HZ~ IAO IHR ITC IX1 J0M JPC KQQ L7B LAW LC2 LC3 LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M6M MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG OK1 OVD OVEED P2P P2W P2X P4D PALCI PIMPY PQQKQ Q.N Q11 QB0 QRW R.K RIWAO RJQFR ROL RPM RWD RWI RX1 RYL SAMSI SUPJJ SV3 TEORI UB1 UKHRP V2E W8V W99 WBKPD WIB WIH WIK WIN WJL WNSPC WOHZO WQJ WRC WUP WXSBR WYISQ XG1 XSW XV2 ZZTAW ~IA ~WT AANHP AAYCA ACCMX ACRPL ACYXJ ADNMO AAFWJ AAYXX AFPKN AGQPQ CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NPM 7QR 7TK 7U7 8FD AAMMB AEFGJ AGXDD AIDQK AIDYY C1K FR3 K9. P64 7X8 5PM |
ID | FETCH-LOGICAL-c5140-be4ff6efa02f86c6dee3baa12a4b0a7f5acb4a3ca6b0765b04a3affc783e0e253 |
IEDL.DBID | DR2 |
ISSN | 1065-9471 1097-0193 |
IngestDate | Thu Aug 21 18:18:23 EDT 2025 Fri Jul 11 04:36:15 EDT 2025 Fri Jul 11 08:59:54 EDT 2025 Sat Jul 26 02:17:31 EDT 2025 Thu Apr 03 07:01:18 EDT 2025 Tue Jul 01 04:26:04 EDT 2025 Thu Apr 24 23:07:11 EDT 2025 Wed Jan 22 16:42:32 EST 2025 Wed Oct 30 09:53:00 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Keywords | amygdala default-mode-network precuneus social phobia self-referential processing psychophysiological interaction globus pallidus |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor 2016 Wiley Periodicals, Inc. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c5140-be4ff6efa02f86c6dee3baa12a4b0a7f5acb4a3ca6b0765b04a3affc783e0e253 |
Notes | ark:/67375/WNG-J0FH9QWB-3 istex:7C72DDFB611D157C75102AD53A6DA5BDAE0F12CC ArticleID:HBM23120 German Research Society (Deutsche Forschungsgemeinschaft, DFG) - No. SFB/TRR 58: C06, C07 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
OpenAccessLink | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/hbm.23120 |
PMID | 26806013 |
PQID | 1771229732 |
PQPubID | 996345 |
PageCount | 14 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_6867294 proquest_miscellaneous_1776663524 proquest_miscellaneous_1772147517 proquest_journals_1771229732 pubmed_primary_26806013 crossref_citationtrail_10_1002_hbm_23120 crossref_primary_10_1002_hbm_23120 wiley_primary_10_1002_hbm_23120_HBM23120 istex_primary_ark_67375_WNG_J0FH9QWB_3 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | April 2016 |
PublicationDateYYYYMMDD | 2016-04-01 |
PublicationDate_xml | – month: 04 year: 2016 text: April 2016 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: San Antonio – name: Hoboken |
PublicationTitle | Human brain mapping |
PublicationTitleAlternate | Hum. Brain Mapp |
PublicationYear | 2016 |
Publisher | Blackwell Publishing Ltd John Wiley & Sons, Inc John Wiley and Sons Inc |
Publisher_xml | – name: Blackwell Publishing Ltd – name: John Wiley & Sons, Inc – name: John Wiley and Sons Inc |
References | Nakao T, Sanematsu H, Yoshiura T, Togao O, Murayama K, Tomita M, Masuda Y, Kanba S (2011): fMRI of patients with social anxiety disorder during a social situation task. Neurosci Res 69:67-72. Klumpp H, Angstadt M, Nathan PJ, Phan KL (2010): Amygdala reactivity to faces at varying intensities of threat in generalized social phobia: An event-related functional MRI study. Psychiatry Res Neuroimaging 183:167-169. Boll S, Gamer M, Kalisch R, Büchel C (2011): Processing of facial expressions and their significance for the observer in subregions of the human amygda. Neuroimage 56:299-306. Ochsner KN, Gross JJ (2005): The cognitive control of emotion. Trends Cogn Sci 9:242-249. Etkin A, Wager TD (2007): Functional neuroimaging of anxiety: A meta-analysis of emotional processing in PTSD, social anxiety disorder, and specific phobia. Am J Psychiatry 164:1476-1488. Etkin A, Egner T, Kalisch R (2011): Emotional processing in anterior cingulate and medial prefrontal cortex. Trends Cogn Sci 15:85-93. Quadflieg S, Mohr A, Mentzel H-J, Miltner WHR, Straube T (2008): Modulation of the neural network involved in the processing of anger prosody: The role of task-relevance and social phobia. Biol Psychol 78:129-137. Maddock RJ, Buonocore MH (1997): Activation of left posterior cingulate gyrus by the auditory presentation ofthreat-related words: An fMRI study. Psychiatry Res Neuroimaging 75:1-14. Pitkänen A, Savander V, LeDoux JE (1997): Organization of intra-amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala. Trends Neurosci 20:517-523. Sabatinelli D, Lang PJ, Keil A, Bradley MM (2007): Emotional perception: Correlation of functional MRI and event-related potentials. Cereb Cortex 17:1085-1091. Amir N, Klumpp H, Elias J, Bedwell JS, Yanasak N, Miller LS (2005): Increased activation of the anterior cingulate cortex during processing of disgust faces in individuals with social phobia. Biol Psychiatry 57:975-981. Boll S, Gamer M, Gluth S, Finsterbusch J, Büchel C (2013): Separate amygdala subregions signal surprise and predictiveness during associative fear learning in humans. Eur J Neurosci 37:758-767. American Psychiatric Association (2000): Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition: DSM-IV-TR. Washington, DC: American Psychiatric Publications. Brühl AB, Rufer M, Delsignore A, Kaffenberger T, Jäncke L, Herwig U (2011): Neural correlates of altered general emotion processing in social anxiety disorder. Brain Res 1378:72-83. Heitmann CY, Peterburs J, Mothes-Lasch M, Hallfarth MC, Böhme S, Miltner WHR, Straube T (2014): Neural correlates of anticipation and processing of performance feedback in social anxiety. Hum Brain Mapp 35:6023-6031. Cabeza R, Prince S, Daselaar S, Greenberg D, Budde M, Dolcos F, LaBar K, Rubin D (2004): Brain activity during episodic retrieval of autobiographical and laboratory events: An fMRI study using a novel photo paradigm. J Cogn Neurosci 16:1583-1594. Oldfield R (1971): The assessment and analysis of handedness: The Edinburgh inventory. Neuropsychologia 9:97-113. Schmidt S, Mohr A, Miltner WHR, Straube T (2010): Task-dependent neural correlates of the processing of verbal threat-related stimuli in social phobia. Biol Psychol 84:304-312. Gentili C, Cristea IA, Angstadt M, Klumpp H, Tozzi L, Phan KL, Pietrini P (2015a): Beyond emotions: A meta-analysis of neural response within face processing system in social anxiety. Exp Biol Med 0:1-13. Sztainberg Y, Kuperman Y, Justice N, Chen A (2011): An anxiolytic role for CRF receptor type 1 in the Globus pallidus. J Neurosci 31:17416-17424. Stangier U, Fydrich T (2002): Soziale Phobie und Soziale Angststörung: Psychologische Grundlagen, Diagnostik und Therapie. Göttingen: Hogrefe Verlag. Damasio AR, Grabowski TJ, Bechara A, Damasio H, Ponto LLB, Parvizi J, Hichwa RD (2000): Subcortical and cortical brain activity during the feeling of self-generated emotions. Nat Neurosci 3:1049-1056. Hattingh CJ, Ipser J, Tromp SA, Syal S, Lochner C, Brooks SJ, Stein DJ (2013): Functional magnetic resonance imaging during emotion recognition in social anxiety disorder: an activation likelihood meta-analysis. Front Hum Neurosci 6:347. Schulz C, Mothes-Lasch M, Straube T (2013): Automatic neural processing of disorder-related stimuli in social anxiety disorder: faces and more. Front Psychol 4:282 Boehme S, Mohr A, Becker MP, Miltner WH, Straube T (2014): Area-dependent time courses of brain activation during video-induced symptom provocation in social anxiety disorder. Biol Mood Anxiety Disord 4:6. Holland PC, Gallagher M (1999): Amygdala circuitry in attentional and representational processes. Trends Cogn Sci 3:65-73. Schneider F, Bermpohl F, Heinzel A, Rotte M, Walter M, Tempelmann C, Wiebking C, Dobrowolny H, Heinze HJ, Northoff G (2008): The resting brain and our self: self-relatedness modulates resting state neural activity in cortical midline structures. Neuroscience 157:120-131. Tomasi D, Volkow ND (2011): Association between functional connectivity hubs and brain networks. Cereb Cortex 21:2003-2013. Evans KC, Wright CI, Wedig MM, Gold AL, Pollack MH, Rauch SL (2008): A functional MRI study of amygdala responses to angry schematic faces in social anxiety disorder. Depress Anxiety 25:496-505. Freitas-Ferrari MC, Hallak JEC, Trzesniak C, Filho AS, Machado-de-Sousa JP, Chagas MHN, Nardi AE, Crippa JAS (2010): Neuroimaging in social anxiety disorder: A systematic review of the literature. Prog Neuropsychopharmacol Biol Psychiatry 34:565-580. Wittchen H-U, Zaudig M, Fydrich T (1997): SKID Strukturiertes Klinisches Interview für DSM-IV. Achse I und II. Göttingen: Hogrefe. Z Für Klin Psychol Psychother 28:68-70. Phan KL, Fitzgerald DA, Nathan PJ, Tancer ME (2006): Association between amygdala hyperactivity to harsh faces and severity of social anxiety in generalized social phobia. Biol Psychiatry 59:424-429. Critchley HD, Wiens S, Rotshtein P, Öhman A, Dolan RJ (2004): Neural systems supporting interoceptive awareness. Nat Neurosci 7:189-195. Reiman EM (1997): The application of positron emission tomography to the study of normal and pathologic emotions. J Clin Psychiatry 58:4-12. Miskovic V, Schmidt LA (2012): Social fearfulness in the human brain. Neurosci Biobehav Rev 36:459-478. Schmuckler MA (2001): What is ecological validity? A dimensional analysis. Infancy 2:419-436. Mennin DS, Fresco DM, Heimberg RG, Schneier FR, Davies SO, Liebowitz MR (2002): Screening for social anxiety disorder in the clinical setting: Using the Liebowitz social anxiety scale. J Anxiety Disord 16:661-673. Boehme S, Ritter V, Tefikow S, Stangier U, Strauss B, Miltner WHR, Straube T (2013): Brain activation during anticipatory anxiety in social anxiety disorder. Soc Cogn Affect Neurosci nst129. Binelli C, Subirà S, Batalla A, Muñiz A, Sugranyés G, Crippa JA, Farré M, Pérez-Jurado L, Martín-Santos R (2014): Common and distinct neural correlates of facial emotion processing in social anxiety disorder and Williams syndrome: A systematic review and voxel-based meta-analysis of functional resonance imaging studies. Neuropsychologia 64:205-217. Blair K, Geraci M, Devido J, McCaffrey D, Chen G, Vythilingam M, Ng P, Hollon N, Jones M, Blair RJR, Pine DS (2008): Neural response to self- and other referential praise and criticism in generalized social phobia. Arch Gen Psychiatry 65:1176-1184. Frühholz S, Grandjean D (2013): Amygdala subregions differentially respond and rapidly adapt to threatening voices. Cortex 49:1394-1403. Saxe R, Kanwisher N (2003): People thinking about thinking people. The role of the temporo-parietal junction in "theory of mind.". Neuroimage 19:1835-1842. Frith U, Frith CD (2003): Development and neurophysiology of mentalizing. Philos Trans R Soc Lond B Biol Sci 358:459-473. Olsson A, Ochsner KN (2008): The role of social cognition in emotion. Trends Cogn Sci 12:65-71. LeDoux JE (2003): The emotional brain, fear, and the amygdala. Cell Mol Neurobiol 23:727-738. Dennis EL, Gotlib IH, Thompson PM, Thomason ME (2011): Anxiety modulates insula recruitment in resting-state functional magnetic resonance imaging in youth and adults. Brain Connect 1:245-254. Moran JM, Heatherton TF, Kelley WM (2009): Modulation of cortical midline structures by implicit and explicit self-relevance evaluation. Soc Neurosci 4:197-211. Gentili C, Vanello N, Cristea I, David D, Ricciardi E, Pietrini P (2015b): Proneness to social anxiety modulates neural complexity in the absence of exposure: A resting state fMRI study using Hurst exponent. Psychiatry Res 232:135-144. Lane RD, Fink GR, Chau PM, Dolan RJ (1997): Neural activation during selective attention to subjective emotional responses. Neuroreport 8:3969-3972. Maldjian JA, Laurienti PJ, Kraft RA, Burdette JH (2003): An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets. Neuroimage 19:1233-1239. Alexander GE, Crutcher MD (1990): Functional architecture of basal ganglia circuits: Neural substrates of parallel processing. Trends Neurosci 13:266-271. Amunts K, Kedo O, Kindler M, Pieperhoff P, Mohlberg H, Shah NJ, Habel U, Schneider F, Zilles K (2005): Cytoarchitectonic mapping of the human amygdala, hippocampal region and entorhinal cortex: Intersubject variability and probability maps. Anat Embryol (Berl) 210:343-352. Brühl AB, Delsignore A, Komossa K, Weidt S (2014): Neuroimaging in social anxiety disorder-A meta-analytic review resulting in a new neurofunctional model. Neurosci Biobehav Rev 47:260-280. Wessa M, Kanske P, Neumeister P, Bode K, Heissler J, Schönfelder S (2010): EmoPics: Subjektive und psychophysiologische Evaluation neuen Bildmaterials für die klinisch-bio-psychologische Forschung. Z Für Klin Psychol Psychother 39:77. Gentili C, Ricciardi E, Gobbini MI, Santarelli MF, Haxby JV, Pietrini P, Guazzelli M (2009): Beyond amygdala: Default mode network activity differs between patients with Social Phobia and healthy controls. Brain Res Bull 79:409-413. Talairach J, Tournoux P (1988): 2002; 16 2002; 59 2002; 15 2013; 4 1990; 13 2002; 18 2014; 219 2003; 358 2005; 210 2000; 3 2004; 7 1995; 33 2003; 14 2008; 78 2010; 183 2011; 56 2011; 15 2015b; 232 2003; 19 2011; 58 2011; 193 2013; 6 2014; 64 1997; 8 2007; 28 1971; 9 2014; 4 2009; 10 2000 2006; 27 1997; 58 2003; 8 2008; 25 2011; 21 2008; 65 2015a; 0 2011; 69 2008; 157 2006; 129 2010; 5 2004b; 372 2011; 29 2001; 14 2001; 98 1988 2010; 34 2007; 17 2011; 1 2013; 49 1997; 20 2010; 39 1999; 28 2015; 11 2007; 164 2006; 59 2007; 362 2011; 31 2008 2014; 47 2008; 12 1997; 28 1995 1999; 3 2004 2002 1999; 8 2012; 36 2010; 84 2014; 87 2009; 79 2013; 37 2004; 16 1997; 75 2004a; 56 2005; 9 2004; 15 2010; 214 1997; 35 2013; 30 2005; 52 2014; 35 2001; 2 1998; 1 2013 2009; 4 2011; 1378 2005; 57 2003; 23 e_1_2_6_51_1 e_1_2_6_74_1 e_1_2_6_76_1 e_1_2_6_32_1 e_1_2_6_70_1 e_1_2_6_93_1 e_1_2_6_30_1 e_1_2_6_72_1 Duval ER (e_1_2_6_25_1) 2015; 11 e_1_2_6_19_1 e_1_2_6_13_1 e_1_2_6_36_1 e_1_2_6_59_1 e_1_2_6_11_1 e_1_2_6_55_1 e_1_2_6_78_1 e_1_2_6_15_1 e_1_2_6_57_1 e_1_2_6_62_1 e_1_2_6_85_1 e_1_2_6_64_1 e_1_2_6_87_1 e_1_2_6_43_1 Boehme S (e_1_2_6_9_1) 2013 e_1_2_6_81_1 e_1_2_6_20_1 e_1_2_6_41_1 e_1_2_6_60_1 e_1_2_6_83_1 Talairach J (e_1_2_6_86_1) 1988 Hautzinger M (e_1_2_6_38_1) 1995 e_1_2_6_5_1 e_1_2_6_7_1 e_1_2_6_24_1 e_1_2_6_3_1 e_1_2_6_22_1 e_1_2_6_66_1 e_1_2_6_89_1 e_1_2_6_28_1 e_1_2_6_45_1 Gentili C (e_1_2_6_34_1) 2015; 0 e_1_2_6_26_1 e_1_2_6_47_1 e_1_2_6_68_1 Wessa M (e_1_2_6_91_1) 2010; 39 e_1_2_6_52_1 e_1_2_6_73_1 e_1_2_6_54_1 e_1_2_6_75_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_50_1 e_1_2_6_90_1 Stangier U (e_1_2_6_79_1) 2002 e_1_2_6_14_1 e_1_2_6_35_1 e_1_2_6_12_1 e_1_2_6_33_1 e_1_2_6_18_1 e_1_2_6_39_1 e_1_2_6_56_1 e_1_2_6_77_1 e_1_2_6_16_1 e_1_2_6_37_1 e_1_2_6_58_1 e_1_2_6_63_1 e_1_2_6_84_1 e_1_2_6_42_1 e_1_2_6_65_1 e_1_2_6_21_1 e_1_2_6_80_1 e_1_2_6_40_1 e_1_2_6_61_1 Reiman EM (e_1_2_6_71_1) 1997; 58 e_1_2_6_82_1 Mai JK (e_1_2_6_53_1) 2004 Lorberbaum JP (e_1_2_6_49_1) 2004; 15 Wittchen H‐U (e_1_2_6_92_1) 1997; 28 e_1_2_6_8_1 e_1_2_6_4_1 e_1_2_6_6_1 Clark DM (e_1_2_6_17_1) 1995 e_1_2_6_48_1 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_29_1 e_1_2_6_44_1 e_1_2_6_67_1 e_1_2_6_88_1 e_1_2_6_27_1 e_1_2_6_46_1 e_1_2_6_69_1 |
References_xml | – reference: Gentili C, Cristea IA, Angstadt M, Klumpp H, Tozzi L, Phan KL, Pietrini P (2015a): Beyond emotions: A meta-analysis of neural response within face processing system in social anxiety. Exp Biol Med 0:1-13. – reference: Maddock RJ, Garrett AS, Buonocore MH (2002): Posterior cingulate cortex activation by emotional words: fMRI evidence from a valence decision task. Hum Brain Mapp 18:30-41. – reference: Boehme S, Mohr A, Becker MP, Miltner WH, Straube T (2014): Area-dependent time courses of brain activation during video-induced symptom provocation in social anxiety disorder. Biol Mood Anxiety Disord 4:6. – reference: Schmidt S, Mohr A, Miltner WHR, Straube T (2010): Task-dependent neural correlates of the processing of verbal threat-related stimuli in social phobia. Biol Psychol 84:304-312. – reference: Liao W, Qiu C, Gentili C, Walter M, Pan Z, Ding J, Zhang W, Gong Q, Chen H (2010): Altered effective connectivity network of the amygdala in social anxiety disorder: A resting-state fMRI study. PLoS One 5:e15238. – reference: Phan KL, Wager T, Taylor SF, Liberzon I (2002): Functional neuroanatomy of emotion: A meta-analysis of emotion activation studies in PET and fMRI. Neuroimage 16:331-348. – reference: Etkin A, Egner T, Kalisch R (2011): Emotional processing in anterior cingulate and medial prefrontal cortex. Trends Cogn Sci 15:85-93. – reference: Moran JM, Heatherton TF, Kelley WM (2009): Modulation of cortical midline structures by implicit and explicit self-relevance evaluation. Soc Neurosci 4:197-211. – reference: Brühl AB, Delsignore A, Komossa K, Weidt S (2014): Neuroimaging in social anxiety disorder-A meta-analytic review resulting in a new neurofunctional model. Neurosci Biobehav Rev 47:260-280. – reference: Frith U, Frith CD (2003): Development and neurophysiology of mentalizing. Philos Trans R Soc Lond B Biol Sci 358:459-473. – reference: Oldfield R (1971): The assessment and analysis of handedness: The Edinburgh inventory. Neuropsychologia 9:97-113. – reference: Jones BE (2003): Arousal systems. Front Biosci J Virtual Libr 8:s438-s451. – reference: Boehme S, Ritter V, Tefikow S, Stangier U, Strauss B, Miltner WHR, Straube T (2013): Brain activation during anticipatory anxiety in social anxiety disorder. Soc Cogn Affect Neurosci nst129. – reference: Diekhof EK, Geier K, Falkai P, Gruber O (2011): Fear is only as deep as the mind allows: A coordinate-based meta-analysis of neuroimaging studies on the regulation of negative effect. Neuroimage 58:275-285. – reference: Wessa M, Kanske P, Neumeister P, Bode K, Heissler J, Schönfelder S (2010): EmoPics: Subjektive und psychophysiologische Evaluation neuen Bildmaterials für die klinisch-bio-psychologische Forschung. Z Für Klin Psychol Psychother 39:77. – reference: Dennis EL, Gotlib IH, Thompson PM, Thomason ME (2011): Anxiety modulates insula recruitment in resting-state functional magnetic resonance imaging in youth and adults. Brain Connect 1:245-254. – reference: Maddock RJ, Buonocore MH, Kile SJ, Garrett AS (2003): Brain regions showing increased activation by threat-related words in panic disorder. Neuroreport 14:325-328. – reference: Blair KS, Geraci M, Otero M, Majestic C, Odenheimer S, Jacobs M, Blair RJR, Pine DS (2011): Atypical modulation of medial prefrontal cortex to self-referential comments in generalized social phobia. Psychiatry Res 193:38-45. – reference: Blair K, Geraci M, Devido J, McCaffrey D, Chen G, Vythilingam M, Ng P, Hollon N, Jones M, Blair RJR, Pine DS (2008): Neural response to self- and other referential praise and criticism in generalized social phobia. Arch Gen Psychiatry 65:1176-1184. – reference: Critchley HD, Wiens S, Rotshtein P, Öhman A, Dolan RJ (2004): Neural systems supporting interoceptive awareness. Nat Neurosci 7:189-195. – reference: Damasio AR, Grabowski TJ, Bechara A, Damasio H, Ponto LLB, Parvizi J, Hichwa RD (2000): Subcortical and cortical brain activity during the feeling of self-generated emotions. Nat Neurosci 3:1049-1056. – reference: Prater KE, Hosanagar A, Klumpp H, Angstadt M, Phan KL (2013): Aberrant amygdala-frontal cortex connectivity during perception of fearful faces and at rest in generalized social anxiety disorder. Depress Anxiety 30:234-241. – reference: Sztainberg Y, Kuperman Y, Justice N, Chen A (2011): An anxiolytic role for CRF receptor type 1 in the Globus pallidus. J Neurosci 31:17416-17424. – reference: Kohn N, Eickhoff SB, Scheller M, Laird AR, Fox PT, Habel U (2014): Neural network of cognitive emotion regulation-An ALE meta-analysis and MACM analysis. Neuroimage 87:345-355. – reference: Menon V, Uddin LQ (2010): Saliency, switching, attention and control: A network model of insula function. Brain Struct Funct 214:655-667. – reference: Vogeley K, Bussfeld P, Newen A, Herrmann S, Happé F, Falkai P, Maier W, Shah NJ, Fink GR, Zilles K (2001): Mind reading: neural mechanisms of theory of mind and self-perspective. Neuroimage 14:170-181. – reference: Binelli C, Subirà S, Batalla A, Muñiz A, Sugranyés G, Crippa JA, Farré M, Pérez-Jurado L, Martín-Santos R (2014): Common and distinct neural correlates of facial emotion processing in social anxiety disorder and Williams syndrome: A systematic review and voxel-based meta-analysis of functional resonance imaging studies. Neuropsychologia 64:205-217. – reference: Wittchen H-U, Zaudig M, Fydrich T (1997): SKID Strukturiertes Klinisches Interview für DSM-IV. Achse I und II. Göttingen: Hogrefe. Z Für Klin Psychol Psychother 28:68-70. – reference: Hautzinger M, Bailer M, Worall H, Keller F (1995): Beck-Depressions-Inventar (BDI). Testhandbuch der deutschen Ausgabe. Bern: Huber. – reference: Rapee RM, Heimberg RG (1997): A cognitive-behavioral model of anxiety in social phobia. Beh Res Ther 35:741-756. – reference: Schmuckler MA (2001): What is ecological validity? A dimensional analysis. Infancy 2:419-436. – reference: Brühl AB, Rufer M, Delsignore A, Kaffenberger T, Jäncke L, Herwig U (2011): Neural correlates of altered general emotion processing in social anxiety disorder. Brain Res 1378:72-83. – reference: Lancaster JL, Tordesillas-Gutiérrez D, Martinez M, Salinas F, Evans A, Zilles K, Mazziotta JC, Fox PT (2007): Bias between MNI and Talairach coordinates analyzed using the ICBM-152 brain template. Hum Brain Mapp 28:1194-1205. – reference: Duval ER, Javanbakht A, Liberzon I (2015): Neural circuits in anxiety and stress disorders: a focused review. Ther Clin Risk Manage 11:115-126. – reference: Gentili C, Ricciardi E, Gobbini MI, Santarelli MF, Haxby JV, Pietrini P, Guazzelli M (2009): Beyond amygdala: Default mode network activity differs between patients with Social Phobia and healthy controls. Brain Res Bull 79:409-413. – reference: LeDoux JE (2003): The emotional brain, fear, and the amygdala. Cell Mol Neurobiol 23:727-738. – reference: Nakao T, Sanematsu H, Yoshiura T, Togao O, Murayama K, Tomita M, Masuda Y, Kanba S (2011): fMRI of patients with social anxiety disorder during a social situation task. Neurosci Res 69:67-72. – reference: Holland PC, Gallagher M (1999): Amygdala circuitry in attentional and representational processes. Trends Cogn Sci 3:65-73. – reference: American Psychiatric Association (2000): Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition: DSM-IV-TR. Washington, DC: American Psychiatric Publications. – reference: Tomasi D, Volkow ND (2011): Association between functional connectivity hubs and brain networks. Cereb Cortex 21:2003-2013. – reference: Straube T, Mentzel HJ, Glauer M, Miltner WHR (2004b): Brain activation to phobia-related words in phobic subjects. Neurosci Lett 372:204-208. – reference: Ochsner KN, Gross JJ (2005): The cognitive control of emotion. Trends Cogn Sci 9:242-249. – reference: Reiman EM (1997): The application of positron emission tomography to the study of normal and pathologic emotions. J Clin Psychiatry 58:4-12. – reference: Cabeza R, Prince S, Daselaar S, Greenberg D, Budde M, Dolcos F, LaBar K, Rubin D (2004): Brain activity during episodic retrieval of autobiographical and laboratory events: An fMRI study using a novel photo paradigm. J Cogn Neurosci 16:1583-1594. – reference: Olsson A, Ochsner KN (2008): The role of social cognition in emotion. Trends Cogn Sci 12:65-71. – reference: Amunts K, Kedo O, Kindler M, Pieperhoff P, Mohlberg H, Shah NJ, Habel U, Schneider F, Zilles K (2005): Cytoarchitectonic mapping of the human amygdala, hippocampal region and entorhinal cortex: Intersubject variability and probability maps. Anat Embryol (Berl) 210:343-352. – reference: Evans KC, Wright CI, Wedig MM, Gold AL, Pollack MH, Rauch SL (2008): A functional MRI study of amygdala responses to angry schematic faces in social anxiety disorder. Depress Anxiety 25:496-505. – reference: Miskovic V, Schmidt LA (2012): Social fearfulness in the human brain. Neurosci Biobehav Rev 36:459-478. – reference: Radua J, Sarró S, Vigo T, Alonso-Lana S, Bonnín CM, Ortiz-Gil J, Canales-Rodríguez EJ, Maristany T, Vieta E, Mckenna PJ, Salvador R, Pomarol-Clotet E (2014): Common and specific brain responses to scenic emotional stimuli. Brain Struct Funct 219:1463-1472. – reference: Talairach J, Tournoux P (1988): Co-Planar Stereotaxic Atlas of the Human Brain. 3-Dimensional Proportional System: An Approach to Cerebral Imaging. New York: Thieme Medical Publishers. – reference: Alexander GE, Crutcher MD (1990): Functional architecture of basal ganglia circuits: Neural substrates of parallel processing. Trends Neurosci 13:266-271. – reference: Straube T, Kolassa I-T, Glauer M, Mentzel H-J, Miltner WHR (2004a): Effect of task conditions on brain responses to threatening faces in social phobics: An event-related functional magnetic resonance imaging study. Biol Psychiatry 56:921-930. – reference: Amir N, Klumpp H, Elias J, Bedwell JS, Yanasak N, Miller LS (2005): Increased activation of the anterior cingulate cortex during processing of disgust faces in individuals with social phobia. Biol Psychiatry 57:975-981. – reference: Stein MB, Goldin PR, Sareen J, Zorrilla LTE, Brown GG (2002): Increased amygdala activation to angry and contemptuous faces in generalized social phobia. Arch Gen Psychiatry 59:1027-1034. – reference: Schneider F, Bermpohl F, Heinzel A, Rotte M, Walter M, Tempelmann C, Wiebking C, Dobrowolny H, Heinze HJ, Northoff G (2008): The resting brain and our self: self-relatedness modulates resting state neural activity in cortical midline structures. Neuroscience 157:120-131. – reference: Saxe R, Kanwisher N (2003): People thinking about thinking people. The role of the temporo-parietal junction in "theory of mind.". Neuroimage 19:1835-1842. – reference: Pitkänen A, Savander V, LeDoux JE (1997): Organization of intra-amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala. Trends Neurosci 20:517-523. – reference: Tzourio-Mazoyer N, Landeau B, Papathanassiou D, Crivello F, Etard O, Delcroix N, Mazoyer B, Joliot M (2002): Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. Neuroimage 15:273-289. – reference: Craig ADB (2009): How do you feel-now? The anterior insula and human awareness. Nat Rev Neurosci 10:59-70. – reference: Ding J, Chen H, Qiu C, Liao W, Warwick JM, Duan X, Zhang W, Gong Q (2011): Disrupted functional connectivity in social anxiety disorder: A resting-state fMRI study. Magn Reson Imaging 29:701-711. – reference: Mai JK, Assheuer J, Paxinos G (2004): Atlas of the Human Brain, 2nd Edition. Amsterdam: Elsevier Academic Press. – reference: Quadflieg S, Mohr A, Mentzel H-J, Miltner WHR, Straube T (2008): Modulation of the neural network involved in the processing of anger prosody: The role of task-relevance and social phobia. Biol Psychol 78:129-137. – reference: Raichle ME, MacLeod AM, Snyder AZ, Powers WJ, Gusnard DA, Shulman GL (2001): A default mode of brain function. Proc Natl Acad Sci USA 98:676-682. – reference: Boll S, Gamer M, Kalisch R, Büchel C (2011): Processing of facial expressions and their significance for the observer in subregions of the human amygda. Neuroimage 56:299-306. – reference: Forman SD, Cohen JD, Fitzgerald M, Eddy WF, Mintun MA, Noll DC (1995): Improved assessment of significant activation in functional magnetic resonance imaging (fMRI): Use of a cluster-size threshold. Magn Reson Med 33:636-647. – reference: Heitmann CY, Peterburs J, Mothes-Lasch M, Hallfarth MC, Böhme S, Miltner WHR, Straube T (2014): Neural correlates of anticipation and processing of performance feedback in social anxiety. Hum Brain Mapp 35:6023-6031. – reference: Lorberbaum JP, Kose S, Johnson MR, Arana GW, Sullivan LK, Hamner MB, Ballenger JC, Lydiard RB, Brodrick PS, Bohning DE, George MS (2004): Neural correlates of speech anticipatory anxiety in generalized social phobia. Neuroreport 15:2701-2705. – reference: Schulz C, Mothes-Lasch M, Straube T (2013): Automatic neural processing of disorder-related stimuli in social anxiety disorder: faces and more. Front Psychol 4:282 – reference: Maddock RJ, Buonocore MH (1997): Activation of left posterior cingulate gyrus by the auditory presentation ofthreat-related words: An fMRI study. Psychiatry Res Neuroimaging 75:1-14. – reference: Wolpert DM, Goodbody SJ, Husain M (1998): Maintaining internal representations: The role of the human superior parietal lobe. Nat Neurosci 1:529-533. – reference: Cavanna AE, Trimble MR (2006): The precuneus: A review of its functional anatomy and behavioural correlates. Brain J Neurol 129:564-583. – reference: Frühholz S, Grandjean D (2013): Amygdala subregions differentially respond and rapidly adapt to threatening voices. Cortex 49:1394-1403. – reference: Stangier U, Fydrich T (2002): Soziale Phobie und Soziale Angststörung: Psychologische Grundlagen, Diagnostik und Therapie. Göttingen: Hogrefe Verlag. – reference: Vuilleumier P, Driver J (2007): Modulation of visual processing by attention and emotion: windows on causal interactions between human brain regions. Philos Trans R Soc Lond B Biol Sci 362:837-855. – reference: Boll S, Gamer M, Gluth S, Finsterbusch J, Büchel C (2013): Separate amygdala subregions signal surprise and predictiveness during associative fear learning in humans. Eur J Neurosci 37:758-767. – reference: Hattingh CJ, Ipser J, Tromp SA, Syal S, Lochner C, Brooks SJ, Stein DJ (2013): Functional magnetic resonance imaging during emotion recognition in social anxiety disorder: an activation likelihood meta-analysis. Front Hum Neurosci 6:347. – reference: Straube T, Mentzel H-J, Miltner WHR (2005): Common and distinct brain activation to threat and safety signals in social phobia. Neuropsychobiology 52:163-168. – reference: Etkin A, Wager TD (2007): Functional neuroimaging of anxiety: A meta-analysis of emotional processing in PTSD, social anxiety disorder, and specific phobia. Am J Psychiatry 164:1476-1488. – reference: Freitas-Ferrari MC, Hallak JEC, Trzesniak C, Filho AS, Machado-de-Sousa JP, Chagas MHN, Nardi AE, Crippa JAS (2010): Neuroimaging in social anxiety disorder: A systematic review of the literature. Prog Neuropsychopharmacol Biol Psychiatry 34:565-580. – reference: Maldjian JA, Laurienti PJ, Kraft RA, Burdette JH (2003): An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets. Neuroimage 19:1233-1239. – reference: Goebel R, Esposito F, Formisano E (2006): Analysis of functional image analysis contest (FIAC) data with brainvoyager QX: From single-subject to cortically aligned group general linear model analysis and self-organizing group independent component analysis. Hum Brain Mapp 27:392-401. – reference: Sabatinelli D, Lang PJ, Keil A, Bradley MM (2007): Emotional perception: Correlation of functional MRI and event-related potentials. Cereb Cortex 17:1085-1091. – reference: Stangier U, Heidenreich T, Berardi A, Golbs U, Hoyer J (1999): Die Erfassung sozialer Phobie durch die Social Interaction Anxiety Scale (SIAS) und die Social Phobia Scale (SPS). Z Für Klin Psychol Psychother 28:28-36. – reference: Gentili C, Vanello N, Cristea I, David D, Ricciardi E, Pietrini P (2015b): Proneness to social anxiety modulates neural complexity in the absence of exposure: A resting state fMRI study using Hurst exponent. Psychiatry Res 232:135-144. – reference: Klumpp H, Angstadt M, Nathan PJ, Phan KL (2010): Amygdala reactivity to faces at varying intensities of threat in generalized social phobia: An event-related functional MRI study. Psychiatry Res Neuroimaging 183:167-169. – reference: Dale AM (1999): Optimal experimental design for event-related fMRI. Hum Brain Mapp 8:109-114. – reference: Mennin DS, Fresco DM, Heimberg RG, Schneier FR, Davies SO, Liebowitz MR (2002): Screening for social anxiety disorder in the clinical setting: Using the Liebowitz social anxiety scale. J Anxiety Disord 16:661-673. – reference: Lane RD, Fink GR, Chau PM, Dolan RJ (1997): Neural activation during selective attention to subjective emotional responses. Neuroreport 8:3969-3972. – reference: Phan KL, Fitzgerald DA, Nathan PJ, Tancer ME (2006): Association between amygdala hyperactivity to harsh faces and severity of social anxiety in generalized social phobia. Biol Psychiatry 59:424-429. – volume: 28 start-page: 68 year: 1997 end-page: 70 article-title: SKID Strukturiertes Klinisches Interview für DSM‐IV. Achse I und II. Göttingen: Hogrefe publication-title: Z Für Klin Psychol Psychother – volume: 219 start-page: 1463 year: 2014 end-page: 1472 article-title: Common and specific brain responses to scenic emotional stimuli publication-title: Brain Struct Funct – volume: 14 start-page: 170 year: 2001 end-page: 181 article-title: Mind reading: neural mechanisms of theory of mind and self‐perspective publication-title: Neuroimage – volume: 25 start-page: 496 year: 2008 end-page: 505 article-title: A functional MRI study of amygdala responses to angry schematic faces in social anxiety disorder publication-title: Depress Anxiety – volume: 372 start-page: 204 year: 2004b end-page: 208 article-title: Brain activation to phobia‐related words in phobic subjects publication-title: Neurosci Lett – volume: 2 start-page: 419 year: 2001 end-page: 436 article-title: What is ecological validity? A dimensional analysis publication-title: Infancy – volume: 362 start-page: 837 year: 2007 end-page: 855 article-title: Modulation of visual processing by attention and emotion: windows on causal interactions between human brain regions publication-title: Philos Trans R Soc Lond B Biol Sci – volume: 18 start-page: 30 year: 2002 end-page: 41 article-title: Posterior cingulate cortex activation by emotional words: fMRI evidence from a valence decision task publication-title: Hum Brain Mapp – volume: 47 start-page: 260 year: 2014 end-page: 280 article-title: Neuroimaging in social anxiety disorder—A meta‐analytic review resulting in a new neurofunctional model publication-title: Neurosci Biobehav Rev – start-page: 69 year: 1995 end-page: 93 – volume: 157 start-page: 120 year: 2008 end-page: 131 article-title: The resting brain and our self: self‐relatedness modulates resting state neural activity in cortical midline structures publication-title: Neuroscience – volume: 65 start-page: 1176 year: 2008 end-page: 1184 article-title: Neural response to self‐ and other referential praise and criticism in generalized social phobia publication-title: Arch Gen Psychiatry – volume: 4 start-page: 6 year: 2014 article-title: Area‐dependent time courses of brain activation during video‐induced symptom provocation in social anxiety disorder publication-title: Biol Mood Anxiety Disord – volume: 19 start-page: 1835 year: 2003 end-page: 1842 article-title: People thinking about thinking people. The role of the temporo‐parietal junction in “theory of mind publication-title: Neuroimage – volume: 4 start-page: 282 year: 2013 article-title: Automatic neural processing of disorder‐related stimuli in social anxiety disorder: faces and more publication-title: Front Psychol – volume: 19 start-page: 1233 year: 2003 end-page: 1239 article-title: An automated method for neuroanatomic and cytoarchitectonic atlas‐based interrogation of fMRI data sets publication-title: Neuroimage – volume: 183 start-page: 167 year: 2010 end-page: 169 article-title: Amygdala reactivity to faces at varying intensities of threat in generalized social phobia: An event‐related functional MRI study publication-title: Psychiatry Res Neuroimaging – volume: 58 start-page: 275 year: 2011 end-page: 285 article-title: Fear is only as deep as the mind allows: A coordinate‐based meta‐analysis of neuroimaging studies on the regulation of negative effect publication-title: Neuroimage – volume: 27 start-page: 392 year: 2006 end-page: 401 article-title: Analysis of functional image analysis contest (FIAC) data with brainvoyager QX: From single‐subject to cortically aligned group general linear model analysis and self‐organizing group independent component analysis publication-title: Hum Brain Mapp – volume: 52 start-page: 163 year: 2005 end-page: 168 article-title: Common and distinct brain activation to threat and safety signals in social phobia publication-title: Neuropsychobiology – volume: 56 start-page: 921 year: 2004a end-page: 930 article-title: Effect of task conditions on brain responses to threatening faces in social phobics: An event‐related functional magnetic resonance imaging study publication-title: Biol Psychiatry – volume: 9 start-page: 242 year: 2005 end-page: 249 article-title: The cognitive control of emotion publication-title: Trends Cogn Sci – volume: 33 start-page: 636 year: 1995 end-page: 647 article-title: Improved assessment of significant activation in functional magnetic resonance imaging (fMRI): Use of a cluster‐size threshold publication-title: Magn Reson Med – volume: 49 start-page: 1394 year: 2013 end-page: 1403 article-title: Amygdala subregions differentially respond and rapidly adapt to threatening voices publication-title: Cortex – volume: 29 start-page: 701 year: 2011 end-page: 711 article-title: Disrupted functional connectivity in social anxiety disorder: A resting‐state fMRI study publication-title: Magn Reson Imaging – volume: 1 start-page: 529 year: 1998 end-page: 533 article-title: Maintaining internal representations: The role of the human superior parietal lobe publication-title: Nat Neurosci – volume: 59 start-page: 424 year: 2006 end-page: 429 article-title: Association between amygdala hyperactivity to harsh faces and severity of social anxiety in generalized social phobia publication-title: Biol Psychiatry – volume: 30 start-page: 234 year: 2013 end-page: 241 article-title: Aberrant amygdala‐frontal cortex connectivity during perception of fearful faces and at rest in generalized social anxiety disorder publication-title: Depress Anxiety – year: 2008 – volume: 232 start-page: 135 year: 2015b end-page: 144 article-title: Proneness to social anxiety modulates neural complexity in the absence of exposure: A resting state fMRI study using Hurst exponent publication-title: Psychiatry Res – year: 2004 – volume: 78 start-page: 129 year: 2008 end-page: 137 article-title: Modulation of the neural network involved in the processing of anger prosody: The role of task‐relevance and social phobia publication-title: Biol Psychol – volume: 214 start-page: 655 year: 2010 end-page: 667 article-title: Saliency, switching, attention and control: A network model of insula function publication-title: Brain Struct Funct – volume: 36 start-page: 459 year: 2012 end-page: 478 article-title: Social fearfulness in the human brain publication-title: Neurosci Biobehav Rev – volume: 35 start-page: 6023 year: 2014 end-page: 6031 article-title: Neural correlates of anticipation and processing of performance feedback in social anxiety publication-title: Hum Brain Mapp – volume: 8 start-page: s438 year: 2003 end-page: s451 article-title: Arousal systems publication-title: Front Biosci J Virtual Libr – volume: 15 start-page: 85 year: 2011 end-page: 93 article-title: Emotional processing in anterior cingulate and medial prefrontal cortex publication-title: Trends Cogn Sci – volume: 21 start-page: 2003 year: 2011 end-page: 2013 article-title: Association between functional connectivity hubs and brain networks publication-title: Cereb Cortex – volume: 3 start-page: 1049 year: 2000 end-page: 1056 article-title: Subcortical and cortical brain activity during the feeling of self‐generated emotions publication-title: Nat Neurosci – volume: 79 start-page: 409 year: 2009 end-page: 413 article-title: Beyond amygdala: Default mode network activity differs between patients with Social Phobia and healthy controls publication-title: Brain Res Bull – volume: 0 start-page: 1 year: 2015a end-page: 13 article-title: Beyond emotions: A meta‐analysis of neural response within face processing system in social anxiety publication-title: Exp Biol Med – volume: 11 start-page: 115 year: 2015 end-page: 126 article-title: Neural circuits in anxiety and stress disorders: a focused review publication-title: Ther Clin Risk Manage – volume: 15 start-page: 2701 year: 2004 end-page: 2705 article-title: Neural correlates of speech anticipatory anxiety in generalized social phobia publication-title: Neuroreport – volume: 193 start-page: 38 year: 2011 end-page: 45 article-title: Atypical modulation of medial prefrontal cortex to self‐referential comments in generalized social phobia publication-title: Psychiatry Res – volume: 35 start-page: 741 year: 1997 end-page: 756 article-title: A cognitive‐behavioral model of anxiety in social phobia publication-title: Beh Res Ther – volume: 6 start-page: 347 year: 2013 article-title: Functional magnetic resonance imaging during emotion recognition in social anxiety disorder: an activation likelihood meta‐analysis publication-title: Front Hum Neurosci – volume: 69 start-page: 67 year: 2011 end-page: 72 article-title: fMRI of patients with social anxiety disorder during a social situation task publication-title: Neurosci Res – volume: 16 start-page: 661 year: 2002 end-page: 673 article-title: Screening for social anxiety disorder in the clinical setting: Using the Liebowitz social anxiety scale publication-title: J Anxiety Disord – volume: 8 start-page: 109 year: 1999 end-page: 114 article-title: Optimal experimental design for event‐related fMRI publication-title: Hum Brain Mapp – volume: 28 start-page: 1194 year: 2007 end-page: 1205 article-title: Bias between MNI and Talairach coordinates analyzed using the ICBM‐152 brain template publication-title: Hum Brain Mapp – year: 2000 – volume: 64 start-page: 205 year: 2014 end-page: 217 article-title: Common and distinct neural correlates of facial emotion processing in social anxiety disorder and Williams syndrome: A systematic review and voxel‐based meta‐analysis of functional resonance imaging studies publication-title: Neuropsychologia – volume: 75 start-page: 1 year: 1997 end-page: 14 article-title: Activation of left posterior cingulate gyrus by the auditory presentation ofthreat‐related words: An fMRI study publication-title: Psychiatry Res Neuroimaging – volume: 16 start-page: 331 year: 2002 end-page: 348 article-title: Functional neuroanatomy of emotion: A meta‐analysis of emotion activation studies in PET and fMRI publication-title: Neuroimage – volume: 98 start-page: 676 year: 2001 end-page: 682 article-title: A default mode of brain function publication-title: Proc Natl Acad Sci USA – volume: 57 start-page: 975 year: 2005 end-page: 981 article-title: Increased activation of the anterior cingulate cortex during processing of disgust faces in individuals with social phobia publication-title: Biol Psychiatry – volume: 1378 start-page: 72 year: 2011 end-page: 83 article-title: Neural correlates of altered general emotion processing in social anxiety disorder publication-title: Brain Res – volume: 58 start-page: 4 year: 1997 end-page: 12 article-title: The application of positron emission tomography to the study of normal and pathologic emotions publication-title: J Clin Psychiatry – volume: 358 start-page: 459 year: 2003 end-page: 473 article-title: Development and neurophysiology of mentalizing publication-title: Philos Trans R Soc Lond B Biol Sci – volume: 17 start-page: 1085 year: 2007 end-page: 1091 article-title: Emotional perception: Correlation of functional MRI and event‐related potentials publication-title: Cereb Cortex – volume: 59 start-page: 1027 year: 2002 end-page: 1034 article-title: Increased amygdala activation to angry and contemptuous faces in generalized social phobia publication-title: Arch Gen Psychiatry – volume: 129 start-page: 564 year: 2006 end-page: 583 article-title: The precuneus: A review of its functional anatomy and behavioural correlates publication-title: Brain J Neurol – volume: 34 start-page: 565 year: 2010 end-page: 580 article-title: Neuroimaging in social anxiety disorder: A systematic review of the literature publication-title: Prog Neuropsychopharmacol Biol Psychiatry – volume: 3 start-page: 65 year: 1999 end-page: 73 article-title: Amygdala circuitry in attentional and representational processes publication-title: Trends Cogn Sci – volume: 210 start-page: 343 year: 2005 end-page: 352 article-title: Cytoarchitectonic mapping of the human amygdala, hippocampal region and entorhinal cortex: Intersubject variability and probability maps publication-title: Anat Embryol (Berl) – volume: 10 start-page: 59 year: 2009 end-page: 70 article-title: How do you feel–now? The anterior insula and human awareness publication-title: Nat Rev Neurosci – volume: 13 start-page: 266 year: 1990 end-page: 271 article-title: Functional architecture of basal ganglia circuits: Neural substrates of parallel processing publication-title: Trends Neurosci – volume: 31 start-page: 17416 year: 2011 end-page: 17424 article-title: An anxiolytic role for CRF receptor type 1 in the publication-title: J Neurosci – volume: 15 start-page: 273 year: 2002 end-page: 289 article-title: Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single‐subject brain publication-title: Neuroimage – volume: 4 start-page: 197 year: 2009 end-page: 211 article-title: Modulation of cortical midline structures by implicit and explicit self‐relevance evaluation publication-title: Soc Neurosci – year: 2013 article-title: Brain activation during anticipatory anxiety in social anxiety disorder publication-title: Soc Cogn Affect Neurosci – volume: 164 start-page: 1476 year: 2007 end-page: 1488 article-title: Functional neuroimaging of anxiety: A meta‐analysis of emotional processing in PTSD, social anxiety disorder, and specific phobia publication-title: Am J Psychiatry – volume: 1 start-page: 245 year: 2011 end-page: 254 article-title: Anxiety modulates insula recruitment in resting‐state functional magnetic resonance imaging in youth and adults publication-title: Brain Connect – volume: 84 start-page: 304 year: 2010 end-page: 312 article-title: Task‐dependent neural correlates of the processing of verbal threat‐related stimuli in social phobia publication-title: Biol Psychol – year: 2002 – volume: 28 start-page: 28 year: 1999 end-page: 36 article-title: Die Erfassung sozialer Phobie durch die Social Interaction Anxiety Scale (SIAS) und die Social Phobia Scale (SPS) publication-title: Z Für Klin Psychol Psychother – year: 1988 – volume: 16 start-page: 1583 year: 2004 end-page: 1594 article-title: Brain activity during episodic retrieval of autobiographical and laboratory events: An fMRI study using a novel photo paradigm publication-title: J Cogn Neurosci – year: 1995 – volume: 8 start-page: 3969 year: 1997 end-page: 3972 article-title: Neural activation during selective attention to subjective emotional responses publication-title: Neuroreport – volume: 56 start-page: 299 year: 2011 end-page: 306 article-title: Processing of facial expressions and their significance for the observer in subregions of the human amygda publication-title: Neuroimage – volume: 7 start-page: 189 year: 2004 end-page: 195 article-title: Neural systems supporting interoceptive awareness publication-title: Nat Neurosci – volume: 12 start-page: 65 year: 2008 end-page: 71 article-title: The role of social cognition in emotion publication-title: Trends Cogn Sci – volume: 39 start-page: 77 year: 2010 article-title: EmoPics: Subjektive und psychophysiologische Evaluation neuen Bildmaterials für die klinisch‐bio‐psychologische Forschung publication-title: Z Für Klin Psychol Psychother – volume: 5 start-page: e15238 year: 2010 article-title: Altered effective connectivity network of the amygdala in social anxiety disorder: A resting‐state fMRI study publication-title: PLoS One – volume: 37 start-page: 758 year: 2013 end-page: 767 article-title: Separate amygdala subregions signal surprise and predictiveness during associative fear learning in humans publication-title: Eur J Neurosci – volume: 9 start-page: 97 year: 1971 end-page: 113 article-title: The assessment and analysis of handedness: The Edinburgh inventory publication-title: Neuropsychologia – volume: 14 start-page: 325 year: 2003 end-page: 328 article-title: Brain regions showing increased activation by threat‐related words in panic disorder publication-title: Neuroreport – volume: 87 start-page: 345 year: 2014 end-page: 355 article-title: Neural network of cognitive emotion regulation–An ALE meta‐analysis and MACM analysis publication-title: Neuroimage – volume: 20 start-page: 517 year: 1997 end-page: 523 article-title: Organization of intra‐amygdaloid circuitries in the rat: an emerging framework for understanding functions of the amygdala publication-title: Trends Neurosci – volume: 23 start-page: 727 year: 2003 end-page: 738 article-title: The emotional brain, fear, and the amygdala publication-title: Cell Mol Neurobiol – ident: e_1_2_6_4_1 doi: 10.1016/j.biopsych.2005.01.044 – ident: e_1_2_6_76_1 doi: 10.1016/j.neuroscience.2008.08.014 – ident: e_1_2_6_41_1 doi: 10.2741/1074 – ident: e_1_2_6_61_1 doi: 10.1016/0028-3932(71)90067-4 – ident: e_1_2_6_73_1 doi: 10.1016/S1053-8119(03)00230-1 – volume: 39 start-page: 77 year: 2010 ident: e_1_2_6_91_1 article-title: EmoPics: Subjektive und psychophysiologische Evaluation neuen Bildmaterials für die klinisch‐bio‐psychologische Forschung publication-title: Z Für Klin Psychol Psychother – ident: e_1_2_6_15_1 doi: 10.1162/0898929042568578 – ident: e_1_2_6_32_1 doi: 10.1016/j.cortex.2012.08.003 – ident: e_1_2_6_44_1 doi: 10.1002/hbm.20345 – volume: 15 start-page: 2701 year: 2004 ident: e_1_2_6_49_1 article-title: Neural correlates of speech anticipatory anxiety in generalized social phobia publication-title: Neuroreport – ident: e_1_2_6_28_1 doi: 10.1002/da.20347 – ident: e_1_2_6_81_1 doi: 10.1001/archpsyc.59.11.1027 – ident: e_1_2_6_68_1 doi: 10.1007/s00429-013-0580-0 – ident: e_1_2_6_60_1 doi: 10.1016/j.tics.2005.03.010 – ident: e_1_2_6_67_1 doi: 10.1016/j.biopsycho.2008.01.014 – ident: e_1_2_6_88_1 doi: 10.1006/nimg.2001.0978 – ident: e_1_2_6_45_1 doi: 10.1097/00001756-199712220-00024 – ident: e_1_2_6_59_1 doi: 10.1016/j.neures.2010.09.008 – ident: e_1_2_6_12_1 doi: 10.1111/ejn.12094 – ident: e_1_2_6_77_1 doi: 10.3389/fpsyg.2013.00282 – ident: e_1_2_6_10_1 doi: 10.1186/2045-5380-4-6 – ident: e_1_2_6_11_1 doi: 10.1016/j.neuroimage.2011.02.021 – ident: e_1_2_6_65_1 doi: 10.1016/S0166-2236(97)01125-9 – volume: 58 start-page: 4 year: 1997 ident: e_1_2_6_71_1 article-title: The application of positron emission tomography to the study of normal and pathologic emotions publication-title: J Clin Psychiatry – ident: e_1_2_6_70_1 doi: 10.1016/S0005-7967(97)00022-3 – ident: e_1_2_6_2_1 doi: 10.1016/0166-2236(90)90107-L – ident: e_1_2_6_18_1 doi: 10.1038/nrn2555 – ident: e_1_2_6_55_1 doi: 10.1016/S0887-6185(02)00134-2 – ident: e_1_2_6_80_1 – volume: 11 start-page: 115 year: 2015 ident: e_1_2_6_25_1 article-title: Neural circuits in anxiety and stress disorders: a focused review publication-title: Ther Clin Risk Manage – ident: e_1_2_6_8_1 doi: 10.1016/j.pscychresns.2010.12.016 – ident: e_1_2_6_43_1 doi: 10.1016/j.neuroimage.2013.11.001 – ident: e_1_2_6_75_1 doi: 10.1207/S15327078IN0204_02 – ident: e_1_2_6_90_1 doi: 10.1098/rstb.2007.2092 – ident: e_1_2_6_69_1 doi: 10.1073/pnas.98.2.676 – ident: e_1_2_6_27_1 doi: 10.1016/j.tics.2010.11.004 – ident: e_1_2_6_83_1 doi: 10.1016/j.neulet.2004.09.050 – ident: e_1_2_6_16_1 doi: 10.1093/brain/awl004 – ident: e_1_2_6_21_1 doi: 10.1038/79871 – ident: e_1_2_6_33_1 doi: 10.1016/j.brainresbull.2009.02.002 – ident: e_1_2_6_57_1 doi: 10.1016/j.neubiorev.2011.08.002 – ident: e_1_2_6_7_1 doi: 10.1001/archpsyc.65.10.1176 – ident: e_1_2_6_26_1 doi: 10.1176/appi.ajp.2007.07030504 – ident: e_1_2_6_84_1 doi: 10.1159/000087987 – ident: e_1_2_6_42_1 doi: 10.1016/j.pscychresns.2010.05.001 – ident: e_1_2_6_82_1 doi: 10.1016/j.biopsych.2004.09.024 – ident: e_1_2_6_39_1 doi: 10.1002/hbm.22602 – ident: e_1_2_6_63_1 doi: 10.1006/nimg.2002.1087 – ident: e_1_2_6_23_1 doi: 10.1016/j.neuroimage.2011.05.073 – ident: e_1_2_6_89_1 doi: 10.1006/nimg.2001.0789 – ident: e_1_2_6_52_1 doi: 10.1097/00001756-200303030-00006 – ident: e_1_2_6_24_1 doi: 10.1016/j.mri.2011.02.013 – ident: e_1_2_6_54_1 doi: 10.1016/S1053-8119(03)00169-1 – year: 2013 ident: e_1_2_6_9_1 article-title: Brain activation during anticipatory anxiety in social anxiety disorder publication-title: Soc Cogn Affect Neurosci – ident: e_1_2_6_3_1 doi: 10.1176/appi.books.9780890423349 – ident: e_1_2_6_51_1 doi: 10.1002/hbm.10075 – ident: e_1_2_6_78_1 doi: 10.1026//0084-5345.28.1.28 – ident: e_1_2_6_13_1 doi: 10.1016/j.brainres.2010.12.084 – ident: e_1_2_6_64_1 doi: 10.1016/j.biopsych.2005.08.012 – ident: e_1_2_6_14_1 doi: 10.1016/j.neubiorev.2014.08.003 – ident: e_1_2_6_30_1 doi: 10.1016/j.pnpbp.2010.02.028 – ident: e_1_2_6_48_1 doi: 10.1371/journal.pone.0015238 – ident: e_1_2_6_50_1 doi: 10.1016/S0925-4927(97)00018-8 – volume-title: Soziale Phobie und Soziale Angststörung: Psychologische Grundlagen, Diagnostik und Therapie year: 2002 ident: e_1_2_6_79_1 – ident: e_1_2_6_29_1 doi: 10.1002/mrm.1910330508 – ident: e_1_2_6_56_1 doi: 10.1007/s00429-010-0262-0 – ident: e_1_2_6_19_1 doi: 10.1038/nn1176 – ident: e_1_2_6_22_1 doi: 10.1089/brain.2011.0030 – ident: e_1_2_6_93_1 doi: 10.1038/2245 – ident: e_1_2_6_58_1 doi: 10.1080/17470910802250519 – volume: 0 start-page: 1 year: 2015 ident: e_1_2_6_34_1 article-title: Beyond emotions: A meta‐analysis of neural response within face processing system in social anxiety publication-title: Exp Biol Med – ident: e_1_2_6_37_1 doi: 10.3389/fnhum.2012.00347 – ident: e_1_2_6_40_1 doi: 10.1016/S1364-6613(98)01271-6 – volume: 28 start-page: 68 year: 1997 ident: e_1_2_6_92_1 article-title: SKID Strukturiertes Klinisches Interview für DSM‐IV. Achse I und II. Göttingen: Hogrefe publication-title: Z Für Klin Psychol Psychother – ident: e_1_2_6_36_1 doi: 10.1002/hbm.20249 – ident: e_1_2_6_31_1 doi: 10.1098/rstb.2002.1218 – ident: e_1_2_6_66_1 doi: 10.1002/da.22014 – ident: e_1_2_6_20_1 doi: 10.1002/(SICI)1097-0193(1999)8:2/3<109::AID-HBM7>3.0.CO;2-W – start-page: 69 volume-title: Social Phobia: Diagnosis, Assessment, and Treatment year: 1995 ident: e_1_2_6_17_1 – ident: e_1_2_6_87_1 doi: 10.1093/cercor/bhq268 – volume-title: Atlas of the Human Brain year: 2004 ident: e_1_2_6_53_1 – ident: e_1_2_6_47_1 doi: 10.1023/A:1025048802629 – ident: e_1_2_6_62_1 doi: 10.1016/j.tics.2007.11.010 – ident: e_1_2_6_46_1 – ident: e_1_2_6_6_1 doi: 10.1016/j.neuropsychologia.2014.08.027 – ident: e_1_2_6_5_1 doi: 10.1007/s00429-005-0025-5 – volume-title: Beck‐Depressions‐Inventar (BDI). Testhandbuch der deutschen Ausgabe year: 1995 ident: e_1_2_6_38_1 – ident: e_1_2_6_74_1 doi: 10.1016/j.biopsycho.2010.03.005 – volume-title: Co‐Planar Stereotaxic Atlas of the Human Brain. 3‐Dimensional Proportional System: An Approach to Cerebral Imaging year: 1988 ident: e_1_2_6_86_1 – ident: e_1_2_6_35_1 doi: 10.1016/j.pscychresns.2015.03.005 – ident: e_1_2_6_72_1 doi: 10.1093/cercor/bhl017 – ident: e_1_2_6_85_1 doi: 10.1523/JNEUROSCI.3087-11.2011 |
SSID | ssj0011501 |
Score | 2.3891766 |
Snippet | Our understanding of altered emotional processing in social anxiety disorder (SAD) is hampered by a heterogeneity of findings, which is probably due to the... |
SourceID | pubmedcentral proquest pubmed crossref wiley istex |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1559 |
SubjectTerms | Adult amygdala Anxiety Disorders - diagnostic imaging Anxiety Disorders - physiopathology default-mode-network Female globus pallidus Humans Magnetic Resonance Imaging - methods Male Nerve Net - diagnostic imaging Nerve Net - physiopathology Phobia, Social - diagnostic imaging Phobia, Social - physiopathology Photic Stimulation - methods Pilot Projects precuneus psychophysiological interaction Random Allocation self-referential processing social phobia Young Adult |
Title | Abnormal brain activation and connectivity to standardized disorder-related visual scenes in social anxiety disorder |
URI | https://api.istex.fr/ark:/67375/WNG-J0FH9QWB-3/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.23120 https://www.ncbi.nlm.nih.gov/pubmed/26806013 https://www.proquest.com/docview/1771229732 https://www.proquest.com/docview/1772147517 https://www.proquest.com/docview/1776663524 https://pubmed.ncbi.nlm.nih.gov/PMC6867294 |
Volume | 37 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqIiEuUFoeoQUZhKpess06iZOI0xaxrCptJRBVe0Cy_FRXbbOou1uVnvgJ_EZ-CTN2ElgoCHHLY2LZztj-Zjz-hpCX_nSkM1ms8xIMFONsXGmnYikLZ0pcMA3u6I4P-Ogw2z_Oj1fIq_YsTOCH6BxuODL8fI0DXKrZ7g_S0BN13gNwwtBex1gtBETvO-ooBDre2IIlNq5gBm5ZhRK22325tBbdwm69uglo_h4v-TOO9QvR8B752DYhxJ-c9hZz1dPXv7A7_mcb18jdBqDSQdCo-2TF1utkY1CDcX7-mW5THzLqffHr5Pa42ZnfIJcDVSP8PaMKk05QPC8RvL1U1oZqjKfRIVMFnU9p68GYXFtDTcMA-u3LV3-0Bh5dTmYLKAuppuyMQnnBtw9lXWGQaffJA3I4fPPh9ShucjqAMmAkqbKZc9w6mTBXcs2NtamSss9kphLQj1xqlclUS66SgucqgRvpnC7K1CaW5elDslpPa_uYULDseCItAwmVFWDG2ZS5ilfWKJVn_SIiO-3fFbohPMe8G2ciUDUzAd0rfPdG5EUn-imwfNwktO1VpJOQF6cYFlfk4ujgrdhPhqPq3dGeSCOy1eqQaGaEmegXRZ9hojAWkefdaxjLuEEjaztdeBlMG5Vj3f8iwxElsiwij4JadhVivER6HahAsaSwnQByiS-_qScnnlOclxzMLChzx-vjn3tBjPbG_uLJv4tukjuAM3kIeNoiq_OLhX0KWG6unvlB-x1gKkmh |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqVgIuPFoegQIGoaqXbLNO4mQlLlvEEkp3JVCr9oIs27HVVdss6u5WpSd-Ar-RX8KMnQQWCkLc8phYtjO2vxmPvyHkhTsdacsk1GkOBkppTdjTVoVSZrbMccEscUd3OOLFfrJzmB4ukZfNWRjPD9E63HBkuPkaBzg6pLd-sIYeqdMOoBMGBvsKZvR2BtWHljwKoY4zt2CRDXswBze8QhHbaj9dWI1WsGMvroKav0dM_oxk3VI0uEU-No3wESjHnflMdfTlL_yO_9vK2-RmjVFp3yvVHbJkqlWy1q_APj_9TDeoixp17vhVcm1Yb86vkfO-qhABn1CFeScoHpnwDl8qq5JqDKnRPlkFnU1o48QYX5qSljUJ6LcvX93pGnh0Pp7OoSxkmzJTCuV59z6UdYFxpu0nd8n-4PXeqyKs0zqAPmAwqTKJtdxYGTGbc81LY2IlZZfJREWgIqnUKpGxllxFGU9VBDfSWp3lsYkMS-N7ZLmaVOYBoWDc8UgaBhIqycCSMzGzPd4zpVJp0s0Cstn8XqFrznNMvXEiPFszE9C9wnVvQJ63op880cdVQhtOR1oJeXaMkXFZKg5Gb8RONCh67w-2RRyQ9UaJRD0pTEU3y7oMc4WxgDxrX8Nwxj0aWZnJ3Mlg5qgU6_4XGY5AkSUBue_1sq0Q4zky7EAFsgWNbQWQTnzxTTU-crTiPOdgaUGZm04h_9wLotgeuouH_y76lFwv9oa7Yvft6N0jcgNgJ_fxT-tkeXY2N48B2s3UEzeCvwO7tk28 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxELaqVqq4QGl5LC1gEKp62XTj3fVuxCmlhFBIBIiqPSBZfqpR203VJFXpiZ_Ab-SXMON9QKAgxG0fs5btHdvfjMffEPLMn450Jgl1moOBYpwNO9qpUMrMmRwXTIM7uoMh7-8ne4fp4QJ5Xp-FKfkhGocbjgw_X-MAPzNu-wdp6JE6bQE4YWCvLyU8ylGldz803FGIdLy1BWts2IEpuKYVith28-ncYrSE_Xp5HdL8PWDyZyDrV6LeLfKpbkMZgHLcmk1VS1_9Qu_4n41cITcrhEq7pUrdJgu2WCVr3QKs89PPdJP6mFHvjF8ly4Nqa36NXHRVgfj3hCrMOkHxwETp7qWyMFRjQI0uU1XQ6ZjWLozRlTXUVBSg37589Wdr4NHFaDKDspBryk4olFc696GsS4wybT65Q_Z7Lz--6IdVUgfQBgwlVTZxjlsnI-ZyrrmxNlZStplMVAQKkkqtEhlryVWU8VRFcCOd01ke28iyNL5LFotxYe8TCqYdj6RlIKGSDOw4GzPX4R1rlEqTdhaQrfrvCl0xnmPijRNRcjUzAd0rfPcG5GkjelbSfFwntOlVpJGQ58cYF5el4mD4SuxFvX7n_cGOiAOyUeuQqKaEiWhnWZthpjAWkCfNaxjMuEMjCzueeRnMG5Vi3f8iwxEmsiQg90q1bCrEeI78OlCBbE5hGwEkE59_U4yOPKk4zznYWVDmltfHP_eC6O8M_MWDfxd9TJbf7fbE29fDN-vkBmBOXgY_bZDF6fnMPgRcN1WP_Pj9DsdGTHQ |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Abnormal+brain+activation+and+connectivity+to+standardized+disorder%E2%80%90related+visual+scenes+in+social+anxiety+disorder&rft.jtitle=Human+brain+mapping&rft.au=Heitmann%2C+Carina+Yvonne&rft.au=Feldker%2C+Katharina&rft.au=Neumeister%2C+Paula&rft.au=Zepp%2C+Britta+Maria&rft.date=2016-04-01&rft.issn=1065-9471&rft.eissn=1097-0193&rft.volume=37&rft.issue=4&rft.spage=1559&rft.epage=1572&rft_id=info:doi/10.1002%2Fhbm.23120&rft.externalDBID=10.1002%252Fhbm.23120&rft.externalDocID=HBM23120 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1065-9471&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1065-9471&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1065-9471&client=summon |