Incapacity to control emotion in major depression may arise from disrupted white matter integrity and OFC‐amygdala inhibition
Summary Background Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital...
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Published in | CNS neuroscience & therapeutics Vol. 24; no. 11; pp. 1053 - 1062 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
John Wiley & Sons, Inc
01.11.2018
John Wiley and Sons Inc |
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Abstract | Summary
Background
Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.
Methods
This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.
Key Results
The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere.
Conclusions & Inferences
Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity? |
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AbstractList | Summary
Background
Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.
Methods
This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.
Key Results
The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere.
Conclusions & Inferences
Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity? Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.BACKGROUNDDisturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting-state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.METHODSThis study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting-state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through "top-down" influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC-amygdala structural and effective connectivity in the left hemisphere.KEY RESULTSThe results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through "top-down" influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC-amygdala structural and effective connectivity in the left hemisphere.Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity-dependent myelination following a therapeutic restoration of effective connectivity?CONCLUSIONS & INFERENCESOur findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity-dependent myelination following a therapeutic restoration of effective connectivity? Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems. This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting-state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD. The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through "top-down" influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC-amygdala structural and effective connectivity in the left hemisphere. Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity-dependent myelination following a therapeutic restoration of effective connectivity? BackgroundDisturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems.MethodsThis study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD.Key ResultsThe results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere.Conclusions & InferencesOur findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity? |
Author | Wang, Hua‐Ning Li, Liang Lu, Hong‐Bing Liu, Jian Tan, Qing‐Rong Li, Bao‐Juan Xi, Yi‐Bin Zheng, Kai‐Zhong Zhang, Xi Yin, Hong Li, Jia‐Ming |
AuthorAffiliation | 1 School of Biomedical Engineering Fourth Military Medical University Xi'an China 2 Xijing Hospital Fourth Military Medical University Xi'an China 3 Network Center Fourth Military Medical University Xi'an China |
AuthorAffiliation_xml | – name: 2 Xijing Hospital Fourth Military Medical University Xi'an China – name: 3 Network Center Fourth Military Medical University Xi'an China – name: 1 School of Biomedical Engineering Fourth Military Medical University Xi'an China |
Author_xml | – sequence: 1 givenname: Kai‐Zhong orcidid: 0000-0002-9723-3227 surname: Zheng fullname: Zheng, Kai‐Zhong organization: Fourth Military Medical University – sequence: 2 givenname: Hua‐Ning surname: Wang fullname: Wang, Hua‐Ning organization: Fourth Military Medical University – sequence: 3 givenname: Jian surname: Liu fullname: Liu, Jian organization: Fourth Military Medical University – sequence: 4 givenname: Yi‐Bin surname: Xi fullname: Xi, Yi‐Bin organization: Fourth Military Medical University – sequence: 5 givenname: Liang surname: Li fullname: Li, Liang organization: Fourth Military Medical University – sequence: 6 givenname: Xi surname: Zhang fullname: Zhang, Xi organization: Fourth Military Medical University – sequence: 7 givenname: Jia‐Ming surname: Li fullname: Li, Jia‐Ming organization: Fourth Military Medical University – sequence: 8 givenname: Hong surname: Yin fullname: Yin, Hong organization: Fourth Military Medical University – sequence: 9 givenname: Qing‐Rong surname: Tan fullname: Tan, Qing‐Rong organization: Fourth Military Medical University – sequence: 10 givenname: Hong‐Bing surname: Lu fullname: Lu, Hong‐Bing email: luhb@fmmu.edu.cn organization: Fourth Military Medical University – sequence: 11 givenname: Bao‐Juan orcidid: 0000-0002-2916-9948 surname: Li fullname: Li, Bao‐Juan email: libjuan@163.com organization: Fourth Military Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29368421$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.jaac.2014.04.021 10.1016/j.pscychresns.2010.06.008 10.1038/tp.2016.81 10.1001/jamapsychiatry.2015.1376 10.1016/S0006-3223(02)01817-6 10.1016/j.biopsych.2009.11.025 10.1007/s00406-015-0614-0 10.1016/j.brat.2016.07.007 10.1016/j.cortex.2008.02.002 10.1001/archpsyc.1965.01730060026004 10.1016/j.jaac.2009.11.005 10.1016/j.cortex.2008.03.005 10.1037/a0019010 10.1159/000165381 10.1001/archpsyc.1965.01720310065008 10.1016/S1053-8119(03)00202-7 10.1038/npp.2011.279 10.1016/j.pscychresns.2016.06.005 10.1016/S0006-3223(03)00168-9 10.1371/journal.pone.0022697 10.1093/brain/awt094 10.1016/j.jpsychires.2016.10.001 10.1002/jmri.21053 10.1136/jnnp.23.1.56 10.1016/j.nicl.2016.09.001 10.1016/j.yebeh.2015.02.022 10.1080/02699930903407948 10.1093/cercor/bht279 10.1001/jamapsychiatry.2015.0161 10.1017/S0033291712000918 10.1016/j.jad.2008.04.027 10.1002/hbm.460020107 10.1016/j.cortex.2008.05.004 10.1016/S0924-9338(13)76335-1 10.1038/mp.2008.82 10.1192/bjp.bp.113.140376 |
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Keywords | uncinate fasciculus white matter integrity major depressive disorder dynamic causal modeling effective connectivity |
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References | 2017; 84 2010; 10 1965; 12 2013; 28 1965; 13 2013; 43 2015; 72 2016; 266 2009; 112 2008; 13 2010; 184 2011; 37 2003; 19 2011; 6 1993; 2 2003; 53 2003; 54 2016; 12 2010; 67 2015; 45 2016; 6 2015; 25 2014; 205 2010; 49 2010; 24 1960; 23 2016; 86 2008; 26 2013; 136 2016; 254 2008; 44 2013 2007; 26 2014; 53 e_1_2_7_6_1 e_1_2_7_5_1 e_1_2_7_4_1 e_1_2_7_3_1 e_1_2_7_8_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_18_1 e_1_2_7_17_1 e_1_2_7_16_1 e_1_2_7_2_1 e_1_2_7_15_1 e_1_2_7_14_1 e_1_2_7_13_1 e_1_2_7_12_1 e_1_2_7_11_1 e_1_2_7_10_1 e_1_2_7_26_1 e_1_2_7_27_1 e_1_2_7_28_1 e_1_2_7_29_1 e_1_2_7_30_1 Konduru N (e_1_2_7_9_1) 2013 e_1_2_7_25_1 e_1_2_7_31_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_23_1 e_1_2_7_33_1 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_20_1 e_1_2_7_36_1 e_1_2_7_37_1 e_1_2_7_38_1 |
References_xml | – volume: 6 start-page: e819 year: 2016 article-title: Aberrant emotion networks in early major depressive disorder patients: an eigenvector centrality mapping study[J] publication-title: Transl Psychiat – volume: 112 start-page: 206 year: 2009 article-title: Antidepressant treatment normalizes hypoactivity in dorsolateral prefrontal cortex during emotional interference processing in major depression.[J] publication-title: J Affect Disorders – volume: 13 start-page: 508 year: 1965 article-title: Self‐rating depression scale in an outpatient clinic. Further validation of the SDS[J] publication-title: Arch Gen Psychiatry – volume: 25 start-page: 895 year: 2015 article-title: Disrupted effective connectivity between the amygdala and orbitofrontal cortex in social anxiety disorder during emotion discrimination revealed by dynamic causal modeling for fMRI[J] publication-title: Cereb Cortex – volume: 53 start-page: 899 year: 2014 end-page: 909 article-title: White matter correlates of adolescent depression: structural evidence for frontolimbic disconnectivity.[J] publication-title: J Am Acad Child Adolesc Psychiatry – volume: 12 start-page: 1022 year: 2016 end-page: 1034 article-title: Shared white matter alterations across emotional disorders: a voxel‐based meta‐analysis of fractional anisotropy:[J] publication-title: Neuroimage Clin – volume: 45 start-page: 68 year: 2015 end-page: 73 article-title: Uncinate fasciculus connectivity in patients with psychogenic nonepileptic seizures: a preliminary diffusion tensor tractography study[J] publication-title: Epilepsy Behav – volume: 72 start-page: 1045 year: 2015 article-title: Meta‐analysis of functional neuroimaging of major depressive disorder in youth[J] publication-title: Jama Psychiat – volume: 44 start-page: 1010 year: 2008 end-page: 1022 article-title: Sensory‐specific amnesia and hypoemotionality in humans and monkeys: gateway for developing a hodology of memory[J] publication-title: Cortex – volume: 72 start-page: 687 year: 2015 article-title: State‐dependent differences in emotion regulation between unmedicated bipolar disorder and major depressive disorder[J] publication-title: Jama Psychiat – volume: 67 start-page: 422 year: 2010 end-page: 431 article-title: Abnormal left and right amygdala‐orbitofrontal cortical functional connectivity to emotional faces: state versus trait vulnerability markers of depression in bipolar disorder.[J] publication-title: Biol Psychiatry – volume: 205 start-page: 321 year: 2014 article-title: Diffusion tensor imaging predictors of treatment outcomes in major depressive disorder[J] publication-title: Br J Psychiatry – volume: 24 start-page: 281 year: 2010 article-title: Emotion regulation in depression: relation to cognitive inhibition[J] publication-title: Cogn Emot – volume: 26 start-page: 432 year: 2008 end-page: 439 article-title: The Role of the uncinate fasciculus in memory and emotional recognition in amnestic mild cognitive impairment[J] publication-title: Dement Geriatr Cogn Disord – volume: 86 start-page: 35 year: 2016 end-page: 49 article-title: Examining emotion regulation in depression: a review and future directions[J] publication-title: Behav Res Ther – year: 2013 article-title: Resting‐State Functional Connections of the Amygdala in Patients with Major Depressive Disorder[J] publication-title: Neuroscience – volume: 136 start-page: 1692 year: 2013 article-title: Dissecting the uncinate fasciculus: disorders, controversies and a hypothesis.[J] publication-title: Brain – volume: 254 start-page: 67 year: 2016 end-page: 73 article-title: Amygdala response to explicit sad face stimuli at baseline predicts antidepressant treatment response to scopolamine in major depressive disorder[J] publication-title: Psychiat Res – volume: 13 start-page: 829 year: 2008 article-title: A neural model of voluntary and automatic emotion regulation: implications for understanding the pathophysiology and neurodevelopment of bipolar disorder[J] publication-title: Mol Psychiatr – volume: 10 start-page: 563 year: 2010 end-page: 572 article-title: Emotion regulation and vulnerability to depression: spontaneous versus instructed use of emotion suppression and reappraisal.[J] publication-title: Emotion – volume: 43 start-page: 293 year: 2013 article-title: Heterogeneity of amygdala response in major depressive disorder: the impact of lifetime subthreshold mania.[J] publication-title: Psychol Med – volume: 54 start-page: 504 year: 2003 article-title: Neurobiology of emotion perception I: the neural basis of normal emotion perception.[J] publication-title: Biol Psychiat – volume: 53 start-page: 502 year: 2003 end-page: 510 article-title: Neural circuitry underlying voluntary suppression of sadness.[J] publication-title: Biol Psychiat – volume: 44 start-page: 1105 year: 2008 end-page: 1132 article-title: A diffusion tensor imaging tractography atlas for virtual in vivo dissections[J] publication-title: Cortex – volume: 23 start-page: 56 year: 1960 article-title: A rating scale for depression[J] publication-title: J Neurol Neurosurg Psychiatry – volume: 84 start-page: 237 year: 2017 article-title: Abnormalities in the structural covariance of emotion regulation networks in major depressive disorder.[J] publication-title: J Psychiatr Res – volume: 44 start-page: 928 year: 2008 end-page: 935 article-title: Medial temporal and prefrontal function: recent behavioural disconnection studies in the macaque monkey.[J] publication-title: Cortex – volume: 2 start-page: 56 year: 1993 end-page: 78 article-title: Functional and effective connectivity in neuroimaging: a[J] publication-title: Hum Brain Mapp – volume: 19 start-page: 1273 year: 2003 end-page: 1302 article-title: Dynamic causal modelling[J] publication-title: NeuroImage – volume: 28 start-page: 1 year: 2013 article-title: Reduced fractional anisotropy in the uncinate fasciculus in patients with major depression carrying the met‐allele of the Val66Met brain‐derived neurotrophic factor genotype[J] publication-title: Eur Psychiat – volume: 49 start-page: 173 year: 2010 end-page: 183 article-title: Altered white matter microstructure in adolescents with major depression: a preliminary study.[J] publication-title: J Am Acad Child Adolesc Psychiatry – volume: 6 start-page: e22697 year: 2011 article-title: Structural integrity of the uncinate fasciculus and resting state functional connectivity of the ventral prefrontal cortex in late life depression[J] publication-title: PLoS ONE – volume: 266 start-page: 239 year: 2016 article-title: Altered functional connectivity density in major depressive disorder at rest.[J] publication-title: Eur Arch Psychiatry Clin Neurosci – volume: 26 start-page: 756 year: 2007 article-title: Effects of SNR on the accuracy and reproducibility of DTI‐derived fractional anisotropy, mean diffusivity, and principal eigenvector measurements at 1.5T[J] publication-title: J Magn Reson Imaging JMRI – volume: 184 start-page: 38 year: 2010 end-page: 48 article-title: Depression severity is correlated to the integrity of white matter fiber tracts in late‐onset major depression[J] publication-title: Psychiat Res – volume: 12 start-page: 63 year: 1965 article-title: A self‐rating depression scale.[J] publication-title: Arch Gen Psychiatry – volume: 37 start-page: 959 year: 2011 end-page: 967 article-title: Quantitative tract‐specific measures of uncinate and cingulum in major depression using diffusion tensor imaging[J] publication-title: Neuropsychopharmacology – year: 2013 ident: e_1_2_7_9_1 article-title: Resting‐State Functional Connections of the Amygdala in Patients with Major Depressive Disorder[J] publication-title: Neuroscience – ident: e_1_2_7_26_1 doi: 10.1016/j.jaac.2014.04.021 – ident: e_1_2_7_29_1 doi: 10.1016/j.pscychresns.2010.06.008 – ident: e_1_2_7_2_1 doi: 10.1038/tp.2016.81 – ident: e_1_2_7_11_1 doi: 10.1001/jamapsychiatry.2015.1376 – ident: e_1_2_7_33_1 doi: 10.1016/S0006-3223(02)01817-6 – ident: e_1_2_7_14_1 doi: 10.1016/j.biopsych.2009.11.025 – ident: e_1_2_7_3_1 doi: 10.1007/s00406-015-0614-0 – ident: e_1_2_7_4_1 doi: 10.1016/j.brat.2016.07.007 – ident: e_1_2_7_18_1 doi: 10.1016/j.cortex.2008.02.002 – ident: e_1_2_7_37_1 doi: 10.1001/archpsyc.1965.01730060026004 – ident: e_1_2_7_19_1 doi: 10.1016/j.jaac.2009.11.005 – ident: e_1_2_7_17_1 doi: 10.1016/j.cortex.2008.03.005 – ident: e_1_2_7_6_1 doi: 10.1037/a0019010 – ident: e_1_2_7_30_1 doi: 10.1159/000165381 – ident: e_1_2_7_36_1 doi: 10.1001/archpsyc.1965.01720310065008 – ident: e_1_2_7_22_1 doi: 10.1016/S1053-8119(03)00202-7 – ident: e_1_2_7_20_1 doi: 10.1038/npp.2011.279 – ident: e_1_2_7_23_1 doi: 10.1016/j.pscychresns.2016.06.005 – ident: e_1_2_7_32_1 doi: 10.1016/S0006-3223(03)00168-9 – ident: e_1_2_7_34_1 doi: 10.1371/journal.pone.0022697 – ident: e_1_2_7_16_1 doi: 10.1093/brain/awt094 – ident: e_1_2_7_5_1 doi: 10.1016/j.jpsychires.2016.10.001 – ident: e_1_2_7_25_1 doi: 10.1002/jmri.21053 – ident: e_1_2_7_35_1 doi: 10.1136/jnnp.23.1.56 – ident: e_1_2_7_27_1 doi: 10.1016/j.nicl.2016.09.001 – ident: e_1_2_7_31_1 doi: 10.1016/j.yebeh.2015.02.022 – ident: e_1_2_7_7_1 doi: 10.1080/02699930903407948 – ident: e_1_2_7_13_1 doi: 10.1093/cercor/bht279 – ident: e_1_2_7_10_1 doi: 10.1001/jamapsychiatry.2015.0161 – ident: e_1_2_7_8_1 doi: 10.1017/S0033291712000918 – ident: e_1_2_7_24_1 doi: 10.1016/j.jad.2008.04.027 – ident: e_1_2_7_21_1 doi: 10.1002/hbm.460020107 – ident: e_1_2_7_15_1 doi: 10.1016/j.cortex.2008.05.004 – ident: e_1_2_7_28_1 doi: 10.1016/S0924-9338(13)76335-1 – ident: e_1_2_7_12_1 doi: 10.1038/mp.2008.82 – ident: e_1_2_7_38_1 doi: 10.1192/bjp.bp.113.140376 |
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Background
Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in... Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been... BackgroundDisturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has... |
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SubjectTerms | Adult Amygdala Amygdala - diagnostic imaging Amygdala - drug effects Amygdala - physiopathology Antidepressive Agents - therapeutic use Brain Mapping Cortex (frontal) Depressive Disorder, Major - diagnostic imaging Depressive Disorder, Major - drug therapy dynamic causal modeling effective connectivity Emotions - drug effects Emotions - physiology Female Frontal Lobe - diagnostic imaging Frontal Lobe - drug effects Frontal Lobe - physiopathology Functional magnetic resonance imaging Hemispheric laterality Humans Image Processing, Computer-Assisted Limbic system Magnetic Resonance Imaging major depressive disorder Male Mental depression Middle Aged Myelination Neural Pathways - diagnostic imaging Neural Pathways - drug effects Original Patients Psychiatric Status Rating Scales Substantia alba uncinate fasciculus White Matter - diagnostic imaging White Matter - drug effects white matter integrity |
Title | Incapacity to control emotion in major depression may arise from disrupted white matter integrity and OFC‐amygdala inhibition |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcns.12800 https://www.ncbi.nlm.nih.gov/pubmed/29368421 https://www.proquest.com/docview/2118680849 https://www.proquest.com/docview/1991182761 https://pubmed.ncbi.nlm.nih.gov/PMC6489955 |
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