Impact of region of interest definition on visual stimulation‐based cerebral vascular reactivity functional MRI with a special focus on applications in cerebral amyloid angiopathy
Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of...
Saved in:
Published in | NMR in biomedicine Vol. 36; no. 7; pp. e4916 - n/a |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.07.2023
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm3 most responding voxels). Evaluation is performed both in a test–retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch‐type cerebral amyloid angiopathy patients and 33 age‐ and sex‐matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or “double dipping” by defining a subject‐specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method.
In cerebral amyloid angiopathy several postprocessing methods exist to quantify vascular reactivity from visually stimulated BOLD fMRI. In this work three commonly applied methods are investigated. |
---|---|
AbstractList | Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm3 most responding voxels). Evaluation is performed both in a test–retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch‐type cerebral amyloid angiopathy patients and 33 age‐ and sex‐matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or “double dipping” by defining a subject‐specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method. Cerebral vascular reactivity quantified using blood oxygen level-dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm3 most responding voxels). Evaluation is performed both in a test-retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch-type cerebral amyloid angiopathy patients and 33 age- and sex-matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or "double dipping" by defining a subject-specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method.Cerebral vascular reactivity quantified using blood oxygen level-dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm3 most responding voxels). Evaluation is performed both in a test-retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch-type cerebral amyloid angiopathy patients and 33 age- and sex-matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or "double dipping" by defining a subject-specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method. Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm 3 most responding voxels). Evaluation is performed both in a test–retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch‐type cerebral amyloid angiopathy patients and 33 age‐ and sex‐matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or “double dipping” by defining a subject‐specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method. Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm3 most responding voxels). Evaluation is performed both in a test–retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch‐type cerebral amyloid angiopathy patients and 33 age‐ and sex‐matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or “double dipping” by defining a subject‐specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method. In cerebral amyloid angiopathy several postprocessing methods exist to quantify vascular reactivity from visually stimulated BOLD fMRI. In this work three commonly applied methods are investigated. Cerebral vascular reactivity quantified using blood oxygen level-dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent and early marker for cerebral amyloid angiopathy. This work investigates the influence of different postprocessing methods on the outcome of such vascular reactivity measurements. Three methods for defining the region of interest (ROI) over which the reactivity is measured are investigated: structural (transformed V1), functional (template based on the activation of a subset of subjects), and percentile (11.5 cm most responding voxels). Evaluation is performed both in a test-retest experiment in healthy volunteers (N = 12), as well as in 27 Dutch-type cerebral amyloid angiopathy patients and 33 age- and sex-matched control subjects. The results show that the three methods select a different subset of voxels, although all three lead to similar outcome measures in healthy subjects. However, in (severe) pathology, the percentile method leads to higher reactivity measures than the other two, due to circular analysis or "double dipping" by defining a subject-specific ROI based on the strongest responses within each subject. Furthermore, while different voxels are included in the presence of lesions, this does not necessarily result in different outcome measures. In conclusion, to avoid bias created by the method, either a structural or a functional method is recommended. Both of these methods provide similar reactivity measures, although the functional ROI appears to be less reproducible between studies, because slightly different subsets of voxels were found to be included. On the other hand, the functional method did include fewer lesion voxels than the structural method. |
Author | Grond, Jeroen Osch, Matthias J. P. Harten, Thijs W. Rooden, Sanneke Opstal, Anna M. Koemans, Emma A. Greenberg, Steven M. Wermer, Marieke J. H. |
Author_xml | – sequence: 1 givenname: Thijs W. orcidid: 0000-0002-3408-9379 surname: Harten fullname: Harten, Thijs W. email: t.w.van_harten@lumc.nl organization: Leiden University Medical Center – sequence: 2 givenname: Sanneke surname: Rooden fullname: Rooden, Sanneke organization: Leiden University Medical Center – sequence: 3 givenname: Emma A. surname: Koemans fullname: Koemans, Emma A. organization: Leiden University Medical Center – sequence: 4 givenname: Anna M. surname: Opstal fullname: Opstal, Anna M. organization: Leiden University Medical Center – sequence: 5 givenname: Steven M. surname: Greenberg fullname: Greenberg, Steven M. organization: Massachusetts General Hospital – sequence: 6 givenname: Jeroen surname: Grond fullname: Grond, Jeroen organization: Leiden University Medical Center – sequence: 7 givenname: Marieke J. H. surname: Wermer fullname: Wermer, Marieke J. H. organization: Leiden University Medical Center – sequence: 8 givenname: Matthias J. P. surname: Osch fullname: Osch, Matthias J. P. organization: Leiden University Medical Center |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36908068$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kctu1DAUhi3Uik5LJZ4AWWLDJlNfcrGXUHEZqQUJ0bV14jjUVeIE25kqOx6hL9MX4klwZloqIVjZOufzp-PzH6MDNziD0EtK1pQQdubqfp1LWj5DK0qkzGgu2QFaEVmwjOeCHKHjEG4IISLn7Dk64qUkgpRihe43_Qg64qHF3ny3g1tu1kXjTYi4Ma11Nu7KDm9tmKDDIdp-6mCp_vp5V0MwDdaJr31qbiHo1PTJlrR2a-OM28nphU7ty68bfGvjNQYcRqNtKrWDnsKih3HsrN55QxrhyQn93A22weDSgCPE6_kFOmyhC-b04TxBVx_efzv_lF18-bg5f3uRaS54mdUF6LKmWtaMFUYIoIIwXZWyaXLDaSVaIaFuWCVLWUiecyhawuqihSo3DeT8BL3Ze0c__JjSRlRvgzZdB84MU1CsEmVBKZMyoa__Qm-Gyac_J0qwgpWVKHiiXj1QU92bRo3e9uBn9RhIAtZ7QPshBG9apW3c7SR6sJ2iRC2Jq5S4WhJ_GvHPg0fnP9Bsj97azsz_5dTnd5c7_jfzbr5n |
CitedBy_id | crossref_primary_10_1177_0271678X231200425 |
Cites_doi | 10.1002/jmri.28194 10.1006/nimg.2002.1132 10.1126/science.aav9518 10.1016/j.nicl.2016.02.020 10.1177/0271678X17691056 10.1109/42.906424 10.1002/ana.22516 10.1097/WCO.0000000000000510 10.1016/j.neuroimage.2009.06.060 10.1006/nimg.2001.0931 10.1016/S1474‐4422(14)70003‐1 10.1002/hbm.23629 10.3389/fphys.2021.643468 10.1002/jmri.28362 10.1002/hbm.10062 10.1016/j.neuroimage.2007.11.059 10.3233/JAD‐210138 10.1161/STROKEAHA.109.554378 10.1097/00004728‐199305000‐00024 10.1016/j.jcm.2016.02.012 10.1002/acn3.574 10.1016/j.neuroimage.2012.01.021 10.1016/S1474‐4422(16)30030‐8 10.1016/j.neuroimage.2003.12.024 10.1093/brain/awx047 10.1016/S1474‐4422(16)30346‐5 10.1016/S1361‐8415(01)00036‐6 10.1212/01.wnl.0000435291.49598.54 10.1111/j.1750‐3639.1996.tb00794.x 10.1177/1747493017730740 10.1161/STROKEAHA.121.035826 10.1212/01.wnl.0000327887.64299.a4 10.1002/hbm.24322 10.17219/acem/114762 10.1109/TMI.2003.822821 10.1212/WNL.56.4.537 10.1002/ana.23566 10.1212/WNL.0000000000200136 10.1111/j.1750‐3639.1996.tb00793.x 10.1212/WNL.0000000000010201 10.1055/s‐0036‐1581993 10.1006/nimg.1999.0516 10.1016/j.neuroimage.2008.09.029 |
ContentType | Journal Article |
Copyright | 2023 The Authors. published by John Wiley & Sons Ltd. 2023 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd. 2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
Copyright_xml | – notice: 2023 The Authors. published by John Wiley & Sons Ltd. – notice: 2023 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd. – notice: 2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
DBID | 24P AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QO 8FD FR3 K9. P64 7X8 |
DOI | 10.1002/nbm.4916 |
DatabaseName | Wiley Online Library Open Access (WRLC) CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Biotechnology Research Abstracts Technology Research Database Engineering Research Database ProQuest Health & Medical Complete (Alumni) Biotechnology and BioEngineering Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Health & Medical Complete (Alumni) Engineering Research Database Biotechnology Research Abstracts Technology Research Database Biotechnology and BioEngineering Abstracts MEDLINE - Academic |
DatabaseTitleList | ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic CrossRef MEDLINE |
Database_xml | – sequence: 1 dbid: 24P name: Wiley Online Library Open Access url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html sourceTypes: Publisher – sequence: 2 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: 3 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 Chemistry Physics |
EISSN | 1099-1492 |
EndPage | n/a |
ExternalDocumentID | 36908068 10_1002_nbm_4916 NBM4916 |
Genre | article Journal Article |
GrantInformation_xml | – fundername: Dutch Research Council (NWO) funderid: 14729 – fundername: Dutch Heart Foundation to M.J.H. Wermer funderid: 2016T86 – fundername: Dutch Heart Foundation to M.J.H. Wermer grantid: 2016T86 – fundername: Dutch Research Council (NWO) grantid: 14729 |
GroupedDBID | --- .3N .GA .Y3 05W 0R~ 10A 123 1L6 1OB 1OC 1ZS 24P 31~ 33P 3SF 3WU 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52V 52W 52X 53G 5RE 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHHS AAHQN AAIPD AAMNL AANHP AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABIJN ABPVW ABQWH ABXGK ACAHQ ACBWZ ACCFJ ACCZN ACFBH ACGFS ACGOF ACIWK ACMXC ACPOU ACPRK ACRPL ACSCC ACXBN ACXQS ACYXJ ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADNMO ADOZA ADXAS ADZMN AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFPM AFGKR AFPWT AFRAH AFWVQ AFZJQ AHBTC AIACR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB ASPBG ATUGU AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMXJE BROTX BRXPI BY8 CS3 D-6 D-7 D-E D-F DCZOG DPXWK DR2 DRFUL DRMAN DRSTM DU5 DUUFO EBD EBS EJD EMOBN F00 F01 F04 F5P FEDTE FUBAC G-S G.N GNP GODZA H.X HBH HF~ HGLYW HHY HHZ HVGLF HZ~ IX1 J0M JPC KBYEO LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M65 MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P2Z P4D PALCI Q.N Q11 QB0 QRW R.K RGB RIWAO RJQFR ROL RWI RX1 SAMSI SUPJJ SV3 UB1 V2E W8V W99 WBKPD WHWMO WIB WIH WIJ WIK WJL WOHZO WQJ WRC WUP WVDHM WXSBR XG1 XPP XV2 ZZTAW ~IA ~WT AAYXX AEYWJ AGHNM AGQPQ AGYGG CITATION AAMMB AEFGJ AGXDD AIDQK AIDYY CGR CUY CVF ECM EIF NPM 7QO 8FD FR3 K9. P64 7X8 |
ID | FETCH-LOGICAL-c3836-b5ac6b1c9b225e88a1802c769dd4e3178f89abd2796959343a5f02b5fa74eda43 |
IEDL.DBID | DR2 |
ISSN | 0952-3480 1099-1492 |
IngestDate | Fri Jul 11 08:42:58 EDT 2025 Fri Jul 25 10:01:18 EDT 2025 Mon Jul 21 06:06:17 EDT 2025 Tue Jul 01 02:45:47 EDT 2025 Thu Apr 24 23:05:05 EDT 2025 Wed Jan 22 16:20:25 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 7 |
Keywords | functional MRI postprocessing cerebral amyloid angiopathy cerebral vascular reactivity |
Language | English |
License | Attribution 2023 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3836-b5ac6b1c9b225e88a1802c769dd4e3178f89abd2796959343a5f02b5fa74eda43 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-3408-9379 |
OpenAccessLink | https://proxy.k.utb.cz/login?url=https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fnbm.4916 |
PMID | 36908068 |
PQID | 2825267853 |
PQPubID | 2029982 |
PageCount | 11 |
ParticipantIDs | proquest_miscellaneous_2786511299 proquest_journals_2825267853 pubmed_primary_36908068 crossref_citationtrail_10_1002_nbm_4916 crossref_primary_10_1002_nbm_4916 wiley_primary_10_1002_nbm_4916_NBM4916 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | July 2023 2023-07-00 2023-Jul 20230701 |
PublicationDateYYYYMMDD | 2023-07-01 |
PublicationDate_xml | – month: 07 year: 2023 text: July 2023 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: Oxford |
PublicationTitle | NMR in biomedicine |
PublicationTitleAlternate | NMR Biomed |
PublicationYear | 2023 |
Publisher | Wiley Subscription Services, Inc |
Publisher_xml | – name: Wiley Subscription Services, Inc |
References | 2004; 21 2002; 17 2009; 44 2023; 57 2009; 40 2010 2004; 23 2016; 15 2008; 71 2016; 36 2019; 365 2009; 48 2001; 20 2016; 11 2012; 72 2018; 39 2021; 12 1993; 17 2018; 5 2017; 37 2001; 5 2020; 95 2017; 38 2017; 16 2011; 70 2000; 11 2022; 56 2013; 81 2014; 13 2017; 140 2022; 53 2022; 98 2001; 56 2008; 40 2018; 31 2001; 14 2021; 81 1996; 6 2020; 29 2018; 13 2012; 62 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_9_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_40_1 e_1_2_7_2_1 e_1_2_7_15_1 e_1_2_7_41_1 e_1_2_7_14_1 e_1_2_7_42_1 e_1_2_7_13_1 e_1_2_7_43_1 e_1_2_7_12_1 e_1_2_7_44_1 e_1_2_7_11_1 e_1_2_7_45_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 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 e_1_2_7_39_1 |
References_xml | – volume: 95 start-page: e1333 issue: 10 year: 2020 end-page: e1340 article-title: Cerebrovascular reactivity in cerebral amyloid angiopathy, Alzheimer disease, and mild cognitive impairment publication-title: Neurology – volume: 40 start-page: 644 issue: 2 year: 2008 end-page: 654 article-title: The respiration response function: the temporal dynamics of fMRI signal fluctuations related to changes in respiration publication-title: Neuroimage – volume: 62 start-page: 774 issue: 2 year: 2012 end-page: 781 article-title: FreeSurfer publication-title: Neuroimage – volume: 56 start-page: 1863 issue: 6 year: 2022 end-page: 1871 article-title: Cerebrovascular reactivity mapping using resting‐state functional MRI in patients with gliomas publication-title: J Magn Reson Imaging – volume: 31 start-page: 28 issue: 1 year: 2018 end-page: 35 article-title: The growing clinical spectrum of cerebral amyloid angiopathy publication-title: Curr Opin Neurol – volume: 15 start-page: 155 issue: 2 year: 2016 end-page: 163 article-title: A guideline of selecting and reporting intraclass correlation coefficients for reliability research publication-title: J Chiropr Med – volume: 29 start-page: 183 issue: 2 year: 2020 end-page: 188 article-title: Cerebrovascular reactivity and disease activity in relapsing‐remitting multiple sclerosis publication-title: Adv Clin Exp Med – volume: 98 start-page: e1716 issue: 17 year: 2022 end-page: e1728 article-title: Cerebrovascular reactivity across the entire brain in cerebral amyloid angiopathy publication-title: Neurology – volume: 365 issue: 6450 year: 2019 article-title: Amyloid β oligomers constrict human capillaries in Alzheimer's disease via signaling to pericytes publication-title: Science – volume: 38 start-page: 3723 issue: 7 year: 2017 end-page: 3731 article-title: Relationship between white matter connectivity loss and cortical thinning in cerebral amyloid angiopathy publication-title: Hum Brain Mapp – volume: 13 start-page: 195 issue: 2 year: 2018 end-page: 206 article-title: Cerebrovascular reactivity measurement in cerebral small vessel disease: Rationale and reproducibility of a protocol for MRI acquisition and image processing publication-title: Int J Stroke – volume: 5 start-page: 143 issue: 2 year: 2001 end-page: 156 article-title: A global optimisation method for robust affine registration of brain images publication-title: Med Image Anal – volume: 81 start-page: 1659 issue: 19 year: 2013 end-page: 1665 article-title: Neurovascular decoupling is associated with severity of cerebral amyloid angiopathy publication-title: Neurology – volume: 72 start-page: 76 issue: 1 year: 2012 end-page: 81 article-title: Functional MRI detection of vascular reactivity in cerebral amyloid angiopathy publication-title: Ann Neurol – volume: 13 start-page: 419 issue: 4 year: 2014 end-page: 428 article-title: Outcome markers for clinical trials in cerebral amyloid angiopathy publication-title: Lancet Neurol – volume: 17 start-page: 143 issue: 3 year: 2002 end-page: 155 article-title: Fast robust automated brain extraction publication-title: Hum Brain Mapp – volume: 14 start-page: 1370 issue: 6 year: 2001 end-page: 1386 article-title: Temporal autocorrelation in univariate linear modeling of FMRI data publication-title: Neuroimage – volume: 11 start-page: 66 issue: 1 year: 2000 end-page: 84 article-title: Brodmann's areas 17 and 18 brought into stereotaxic space‐where and how variable? publication-title: Neuroimage – volume: 37 start-page: 3433 issue: 10 year: 2017 end-page: 3445 article-title: Identification of neurovascular changes associated with cerebral amyloid angiopathy from subject‐specific hemodynamic response functions publication-title: J Cereb Blood Flow Metab – volume: 70 start-page: 871 issue: 6 year: 2011 end-page: 880 article-title: Cerebral amyloid angiopathy in the elderly publication-title: Ann Neurol – volume: 6 start-page: 111 issue: 2 year: 1996 end-page: 114 article-title: Hereditary cerebral hemorrhage with amyloidosis‐Dutch type (HCHWA‐D): I ‐ a review of clinical, radiologic and genetic aspects publication-title: Brain Pathol – volume: 5 start-page: 788 issue: 7 year: 2018 end-page: 802 article-title: Altered dynamics of neurovascular coupling in CADASIL publication-title: Ann Clin Transl Neurol – volume: 17 start-page: 825 issue: 2 year: 2002 end-page: 841 article-title: Improved optimization for the robust and accurate linear registration and motion correction of brain images publication-title: Neuroimage – volume: 48 start-page: 63 issue: 1 year: 2009 end-page: 72 article-title: Accurate and robust brain image alignment using boundary‐based registration publication-title: Neuroimage – volume: 81 start-page: 1663 issue: 4 year: 2021 end-page: 1671 article-title: Cortical thickness and its association with clinical cognitive and neuroimaging markers in cerebral amyloid angiopathy publication-title: J Alzheimers Dis – year: 2010 – volume: 21 start-page: 1748 issue: 4 year: 2004 end-page: 1761 article-title: Constrained linear basis sets for HRF modelling using variational Bayes publication-title: Neuroimage – volume: 11 start-page: 461 year: 2016 end-page: 467 article-title: Longitudinal decrease in blood oxygenation level dependent response in cerebral amyloid angiopathy publication-title: NeuroImage Clin – volume: 16 start-page: 115 issue: 2 year: 2017 end-page: 122 article-title: Cerebrovascular function in pre‐symptomatic and symptomatic individuals with hereditary cerebral amyloid angiopathy: a case‐control study publication-title: Lancet Neurol – volume: 56 start-page: 537 issue: 4 year: 2001 end-page: 539 article-title: Clinical diagnosis of cerebral amyloid angiopathy: validation of the Boston criteria publication-title: Neurology – volume: 23 start-page: 137 issue: 2 year: 2004 end-page: 152 article-title: Probabilistic independent component analysis for functional magnetic resonance imaging publication-title: IEEE Trans Med Imaging – volume: 57 start-page: 909 issue: 3 year: 2023 end-page: 915 article-title: Aging effect, reproducibility, and test‐retest reliability of a new cerebral amyloid angiopathy MRI severity marker‐cerebrovascular reactivity to visual stimulation publication-title: J Magn Reson Imaging – volume: 6 start-page: 115 issue: 2 year: 1996 end-page: 120 article-title: Hereditary cerebral hemorrhage with amyloidosis‐Dutch type (HCHWA‐D): II ‐ a review of histopathological aspects publication-title: Brain Pathol – volume: 71 start-page: 1424 issue: 18 year: 2008 end-page: 1430 article-title: Impaired visual evoked flow velocity response in cerebral amyloid angiopathy publication-title: Neurology – volume: 44 start-page: 857 issue: 3 year: 2009 end-page: 869 article-title: Influence of heart rate on the BOLD signal: the cardiac response function publication-title: Neuroimage – volume: 12 year: 2021 article-title: Cerebrovascular reactivity measurement using magnetic resonance imaging: a systematic review publication-title: Front Physiol – volume: 15 start-page: 811 issue: 8 year: 2016 end-page: 819 article-title: Alzheimer's Disease Neuroimaging Initiative (ADNI)Cortical atrophy in patients with cerebral amyloid angiopathy: a case‐control study publication-title: Lancet Neurol – volume: 36 start-page: 233 issue: 3 year: 2016 end-page: 243 article-title: Sporadic cerebral amyloid angiopathy: pathophysiology, neuroimaging features, and clinical implications publication-title: Semin Neurol – volume: 17 start-page: 461 issue: 3 year: 1993 end-page: 470 article-title: Graphical analysis of MR feature space for measurement of CSF, gray‐matter, and white‐matter volumes publication-title: J Comput Assist Tomogr – volume: 140 start-page: 1829 issue: 7 year: 2017 end-page: 1850 article-title: Emerging concepts in sporadic cerebral amyloid angiopathy publication-title: Brain – volume: 53 start-page: 2006 issue: 6 year: 2022 end-page: 2015 article-title: Longitudinal progression of magnetic resonance imaging markers and cognition in Dutch‐type hereditary cerebral amyloid angiopathy publication-title: Stroke – volume: 40 start-page: 3022 issue: 9 year: 2009 end-page: 3027 article-title: Descriptive analysis of the Boston criteria applied to a Dutch‐type cerebral amyloid angiopathy population publication-title: Stroke – volume: 39 start-page: 4776 issue: 12 year: 2018 end-page: 4786 article-title: Structural and functional changes of the visual cortex in early Huntington's disease publication-title: Hum Brain Mapp – volume: 20 start-page: 45 issue: 1 year: 2001 end-page: 57 article-title: Segmentation of brain MR images through a hidden Markov random field model and the expectation‐maximization algorithm publication-title: IEEE Trans Med Imaging – ident: e_1_2_7_3_1 doi: 10.1002/jmri.28194 – ident: e_1_2_7_28_1 doi: 10.1006/nimg.2002.1132 – ident: e_1_2_7_17_1 doi: 10.1126/science.aav9518 – ident: e_1_2_7_14_1 doi: 10.1016/j.nicl.2016.02.020 – ident: e_1_2_7_24_1 doi: 10.1177/0271678X17691056 – ident: e_1_2_7_26_1 doi: 10.1109/42.906424 – ident: e_1_2_7_5_1 doi: 10.1002/ana.22516 – ident: e_1_2_7_12_1 doi: 10.1097/WCO.0000000000000510 – ident: e_1_2_7_27_1 doi: 10.1016/j.neuroimage.2009.06.060 – ident: e_1_2_7_33_1 doi: 10.1006/nimg.2001.0931 – ident: e_1_2_7_25_1 doi: 10.1016/S1474‐4422(14)70003‐1 – ident: e_1_2_7_13_1 doi: 10.1002/hbm.23629 – ident: e_1_2_7_21_1 doi: 10.3389/fphys.2021.643468 – ident: e_1_2_7_19_1 doi: 10.1002/jmri.28362 – ident: e_1_2_7_31_1 doi: 10.1002/hbm.10062 – ident: e_1_2_7_40_1 doi: 10.1016/j.neuroimage.2007.11.059 – ident: e_1_2_7_11_1 doi: 10.3233/JAD‐210138 – ident: e_1_2_7_9_1 doi: 10.1161/STROKEAHA.109.554378 – ident: e_1_2_7_38_1 doi: 10.1097/00004728‐199305000‐00024 – ident: e_1_2_7_39_1 doi: 10.1016/j.jcm.2016.02.012 – ident: e_1_2_7_45_1 doi: 10.1002/acn3.574 – ident: e_1_2_7_35_1 doi: 10.1016/j.neuroimage.2012.01.021 – ident: e_1_2_7_10_1 doi: 10.1016/S1474‐4422(16)30030‐8 – ident: e_1_2_7_37_1 doi: 10.1016/j.neuroimage.2003.12.024 – ident: e_1_2_7_7_1 doi: 10.1093/brain/awx047 – ident: e_1_2_7_18_1 doi: 10.1016/S1474‐4422(16)30346‐5 – ident: e_1_2_7_29_1 doi: 10.1016/S1361‐8415(01)00036‐6 – ident: e_1_2_7_23_1 doi: 10.1212/01.wnl.0000435291.49598.54 – ident: e_1_2_7_43_1 doi: 10.1111/j.1750‐3639.1996.tb00794.x – ident: e_1_2_7_30_1 – ident: e_1_2_7_4_1 doi: 10.1177/1747493017730740 – ident: e_1_2_7_20_1 doi: 10.1161/STROKEAHA.121.035826 – ident: e_1_2_7_16_1 doi: 10.1212/01.wnl.0000327887.64299.a4 – ident: e_1_2_7_36_1 doi: 10.1002/hbm.24322 – ident: e_1_2_7_2_1 doi: 10.17219/acem/114762 – ident: e_1_2_7_32_1 doi: 10.1109/TMI.2003.822821 – ident: e_1_2_7_8_1 doi: 10.1212/WNL.56.4.537 – ident: e_1_2_7_15_1 doi: 10.1002/ana.23566 – ident: e_1_2_7_22_1 doi: 10.1212/WNL.0000000000200136 – ident: e_1_2_7_42_1 doi: 10.1111/j.1750‐3639.1996.tb00793.x – ident: e_1_2_7_44_1 doi: 10.1212/WNL.0000000000010201 – ident: e_1_2_7_6_1 doi: 10.1055/s‐0036‐1581993 – ident: e_1_2_7_34_1 doi: 10.1006/nimg.1999.0516 – ident: e_1_2_7_41_1 doi: 10.1016/j.neuroimage.2008.09.029 |
SSID | ssj0008432 |
Score | 2.3916142 |
Snippet | Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent... Cerebral vascular reactivity quantified using blood oxygen level-dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent... Cerebral vascular reactivity quantified using blood oxygen level‐dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent... Cerebral vascular reactivity quantified using blood oxygen level-dependent functional MRI in conjuncture with a visual stimulus has been proven to be a potent... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | e4916 |
SubjectTerms | Amyloid Biological products Cardiovascular System - pathology Cerebral amyloid angiopathy Cerebral Amyloid Angiopathy - diagnostic imaging Cerebral Amyloid Angiopathy - pathology cerebral vascular reactivity Functional magnetic resonance imaging functional MRI Humans Lesions Magnetic Resonance Imaging - methods Methods Photic Stimulation postprocessing Reactive oxygen species Structure-function relationships Visual stimuli |
Title | Impact of region of interest definition on visual stimulation‐based cerebral vascular reactivity functional MRI with a special focus on applications in cerebral amyloid angiopathy |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fnbm.4916 https://www.ncbi.nlm.nih.gov/pubmed/36908068 https://www.proquest.com/docview/2825267853 https://www.proquest.com/docview/2786511299 |
Volume | 36 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1fa9UwFD_MwXQvul3_XZ0jA9Gn3l3TNGkedTg24Y4xNhj4UJI0hYv3tsPeCvPJj-CX8Qv5STwnbe82nSBCoYWeJik5OfklOed3AF5K7-i0TEZoHPNIaI520HgVSW29kp6WZBScPDmSB2fiw3ly3nlVUixMyw-x3HCjkRHsNQ1wY-vda6Shdj4SCG7Q_JKrFuGhkyvmqFSE3GQIIHgUi3Tc886O-W7_4c2Z6A94eROthulm_wF87Bvaepl8GjULO3Jff-Nw_L8_2YD7HQplb1u12YQVXw7g3l6f_G0AdyfdmfsA1oKTqKsfwo_DEFLJqoJRPoeqpCfim6D8Hiz3xbQMDmAMry_TusEa0IDMuwRhP799pykzZw7lsbkz1nvBYmkUXkFZLBjNs-32JJucHDLaJmaGUTwoDhRWVK6pqfjr5-7YhKsyzfxyVk1zZkpsIKVbvnwEZ_vvT_cOoi7tQ-RwuSwjmxgn7RunLdoan6aGSOqckjrPhUe4kxapNjbnSktiVRaxSYoxt0lhlPC5EfFjWC2r0j8FpnRhCkQkiILGIrYUhuyVkc7jss0qLobwuleBzHWc6JSaY5a1bM48w77JqG-GsLOUvGh5QG6R2eq1KOssQZ1RbDBHRJDEWMTyNfYmHcyY0lcNyqhUBuCrh_Ck1b5lJbHUCOplOoRXQYf-Wnt29G5C92f_Kvgc1jkittb3eAtWF58b_wIR1sJuwx0ujrfDiPoFY6smxw |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3dbtMwFD4aQzBu-CkDCgOMhOAqXUkcO9auYGJqYenFtEm7QIpsx5Eq2gTRBmlc8Qi8zF5oT7JznKTb-JEQUqVU6ontysfHn3_O9wG8FM7SaZkIMDjmAVchxkHtZCCUcVI4WpJRcnI6EaMj_uE4Pl6DnS4XpuGHWG240cjw8ZoGOG1Ib19iDTXzAUd0cw2uk6C3X08dXHBHJdyrkyGECIOIJ8OOeXYYbndvXp2LfgOYV_Gqn3D27sCnrqnNPZPPg3ppBvb7LyyO__lf7sLtFoiyt43n3IM1V_ZgY7fTf-vBzbQ9du_BDX9P1C7uw-nYZ1WyqmAk6VCV9I0oJ0jig-WumJb-DhjDz7fposYaMIbMW42wsx8_adbMmUV7bO-MdRdhsTTKsCAhC0ZTbbNDydKDMaOdYqYZpYTiWGFFZesFFX_56B2bcFGmnp_MqmnOdIkNJMXlk0042nt_uDsKWuWHwOKKWQQm1laYN1YZDDcuSTTx1FkpVJ5zh4gnKRKlTR5KJYhYmUc6LoahiQstucs1jx7AelmV7hEwqQpdIChBIDTkkaFMZCe1sA5XbkaGvA-vOx_IbEuLTuocs6whdA4z7JuM-qYPL1aWXxoqkD_YbHVulLXBYJFRenCIoCCOsIjVz9ibdDajS1fVaCMT4bGv6sPDxv1WlURCIa4XSR9eeSf6a-3Z5F1Kz8f_avgcNkaH6X62P558fAK3QgRwzVXkLVhffq3dUwRcS_PMD6xzsTIqCw |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NbtQwEB5BEYVLgaXAlgJGQnDKNjiO7RyhZdUFdoUqKlXiENmOI63YTSp2g1ROPAIv0xfqkzCTn23Lj4SQIiVSJrYjj8ef7ZlvAJ5J7-i0TAZoHLNAJBztoPEqkIn1SnpaklFw8ngi9w_F26P4qPWqpFiYhh9iteFGI6O21zTAj7N85wJpqJ0PBIKbq3BNyFCTRu8dnFNHaVEnJ0MEwYNI6LAjng35Tvfl5anoN3x5Ga7W883wFnzqWtq4mXweVEs7cN9-IXH8v1-5DRstDGWvGr25A1d80YMbu132tx6sj9tD9x5cr71E3eIunI7qmEpW5owSOpQFPRHhBCX4YJnPp0XtAcbw-jpdVFgDWpB5myHs7PsPmjMz5lAemztjnRsslkbxFZTGgtFE2-xPsvHBiNE-MTOMAkJxpLC8dNWCir948I5NOC_TzE9m5TRjpsAGUr7lk004HL75uLsftHkfAofrZRnY2DhpX7rEorHxWhtiqXNKJlkmPOIdnevE2IyrRBKtsohMnIfcxrlRwmdGRPdgrSgL_wCYSnKTIyRBGBSKyFIcsldGOo_rNqu46MOLTgVS15KiU26OWdrQOfMU-yalvunD05XkcUME8geZ7U6L0tYULFIKDuYICeIIi1i9xt6kkxlT-LJCGaVljXyTPtxvtG9VSSQTRPVS9-F5rUN_rT2dvB7TfetfBZ_A-oe9Yfp-NHn3EG5yRG-NH_I2rC2_VP4Roq2lfVwPq58_vyjD |
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=Impact+of+region+of+interest+definition+on+visual+stimulation%E2%80%90based+cerebral+vascular+reactivity+functional+MRI+with+a+special+focus+on+applications+in+cerebral+amyloid+angiopathy&rft.jtitle=NMR+in+biomedicine&rft.au=Harten%2C+Thijs+W.&rft.au=Rooden%2C+Sanneke&rft.au=Koemans%2C+Emma+A.&rft.au=Opstal%2C+Anna+M.&rft.date=2023-07-01&rft.issn=0952-3480&rft.eissn=1099-1492&rft.volume=36&rft.issue=7&rft.epage=n%2Fa&rft_id=info:doi/10.1002%2Fnbm.4916&rft.externalDBID=10.1002%252Fnbm.4916&rft.externalDocID=NBM4916 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0952-3480&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0952-3480&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0952-3480&client=summon |