Sex differences in brain structure among adolescents with bipolar disorder

Objectives Bipolar disorder (BD) is twice as prevalent amongst female as amongst male adolescents. Thus far, little is known regarding the neurostructural substrates underlying this disparity. We therefore examined sex differences in neurostructural magnetic resonane imaging (MRI) phenotypes amongst...

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Veröffentlicht in:Bipolar disorders 2018-08, Vol.20 (5), p.448-458
Hauptverfasser: Mitchell, Rachel HB, Metcalfe, Arron WS, Islam, Alvi H, Toma, Simina, Patel, Ronak, Fiksenbaum, Lisa, Korczak, Daphne, MacIntosh, Bradley J, Goldstein, Benjamin I
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container_end_page 458
container_issue 5
container_start_page 448
container_title Bipolar disorders
container_volume 20
creator Mitchell, Rachel HB
Metcalfe, Arron WS
Islam, Alvi H
Toma, Simina
Patel, Ronak
Fiksenbaum, Lisa
Korczak, Daphne
MacIntosh, Bradley J
Goldstein, Benjamin I
description Objectives Bipolar disorder (BD) is twice as prevalent amongst female as amongst male adolescents. Thus far, little is known regarding the neurostructural substrates underlying this disparity. We therefore examined sex differences in neurostructural magnetic resonane imaging (MRI) phenotypes amongst adolescents with BD. Methods T1‐weighted structural MRI was acquired from 44 BD (25 female [F] and 19 male [M]) and 58 (28 F and 30 M) healthy control (HC) adolescents (13‐21 years old). Whole‐brain and region‐of‐interest (ROI) analyses examined structural volume and cortical thickness using FreeSurfer. ROIs included the ventrolateral prefrontal cortex (vlPFC), anterior cingulate cortex (ACC), amygdala and hippocampus. General linear models evaluated sex‐by‐diagnosis interactions, controlling for age and intracranial volume. Results Whole‐brain analysis revealed sex‐by‐diagnosis interactions in the left supramarginal gyrus (SMG) (P = .02, η2 = 0.02) and right inferior parietal lobule (IPL) volumes (P = .04, η2 = 0.01). Sex differences in HCs were found in the SMG (M > F) and IPL (F > M). In BD, sex differences were reversed and of smaller magnitude in the SMG (M  M), driven by trends towards smaller SMG and IPL in BD vs HC male participants (P = .05 and .14). Whole‐brain analyses for cortical thickness, and ROI analyses for volume and cortical thickness, were not significant. Conclusions Normative sex differences may be disrupted in adolescent BD in the SMG and IPL, heteromodal association network hubs responsible for higher order integration of cognitive and emotional processing. Unexpectedly, these findings may inform our understanding of aberrant brain structure in adolescent BD male patients, rather than female patients. Future work should focus on replication, as well as the impact of puberty status and sex hormones on measures of brain structure and function.
doi_str_mv 10.1111/bdi.12663
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Thus far, little is known regarding the neurostructural substrates underlying this disparity. We therefore examined sex differences in neurostructural magnetic resonane imaging (MRI) phenotypes amongst adolescents with BD. Methods T1‐weighted structural MRI was acquired from 44 BD (25 female [F] and 19 male [M]) and 58 (28 F and 30 M) healthy control (HC) adolescents (13‐21 years old). Whole‐brain and region‐of‐interest (ROI) analyses examined structural volume and cortical thickness using FreeSurfer. ROIs included the ventrolateral prefrontal cortex (vlPFC), anterior cingulate cortex (ACC), amygdala and hippocampus. General linear models evaluated sex‐by‐diagnosis interactions, controlling for age and intracranial volume. Results Whole‐brain analysis revealed sex‐by‐diagnosis interactions in the left supramarginal gyrus (SMG) (P = .02, η2 = 0.02) and right inferior parietal lobule (IPL) volumes (P = .04, η2 = 0.01). Sex differences in HCs were found in the SMG (M &gt; F) and IPL (F &gt; M). In BD, sex differences were reversed and of smaller magnitude in the SMG (M &lt; F) and of greater magnitude in the IPL (F &gt; M), driven by trends towards smaller SMG and IPL in BD vs HC male participants (P = .05 and .14). Whole‐brain analyses for cortical thickness, and ROI analyses for volume and cortical thickness, were not significant. Conclusions Normative sex differences may be disrupted in adolescent BD in the SMG and IPL, heteromodal association network hubs responsible for higher order integration of cognitive and emotional processing. Unexpectedly, these findings may inform our understanding of aberrant brain structure in adolescent BD male patients, rather than female patients. Future work should focus on replication, as well as the impact of puberty status and sex hormones on measures of brain structure and function.</description><identifier>ISSN: 1398-5647</identifier><identifier>EISSN: 1399-5618</identifier><identifier>DOI: 10.1111/bdi.12663</identifier><identifier>PMID: 29956452</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>adolescent ; Adolescents ; Amygdala ; Bipolar disorder ; brain structure ; Cognitive ability ; Cortex (cingulate) ; Diagnosis ; Functional anatomy ; Gender differences ; Information processing ; Neuroimaging ; Phenotypes ; Prefrontal cortex ; Puberty ; Sex differences ; Sex hormones ; Structure-function relationships ; Teenagers</subject><ispartof>Bipolar disorders, 2018-08, Vol.20 (5), p.448-458</ispartof><rights>2018 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2018 John Wiley &amp; Sons A/S. 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Thus far, little is known regarding the neurostructural substrates underlying this disparity. We therefore examined sex differences in neurostructural magnetic resonane imaging (MRI) phenotypes amongst adolescents with BD. Methods T1‐weighted structural MRI was acquired from 44 BD (25 female [F] and 19 male [M]) and 58 (28 F and 30 M) healthy control (HC) adolescents (13‐21 years old). Whole‐brain and region‐of‐interest (ROI) analyses examined structural volume and cortical thickness using FreeSurfer. ROIs included the ventrolateral prefrontal cortex (vlPFC), anterior cingulate cortex (ACC), amygdala and hippocampus. General linear models evaluated sex‐by‐diagnosis interactions, controlling for age and intracranial volume. Results Whole‐brain analysis revealed sex‐by‐diagnosis interactions in the left supramarginal gyrus (SMG) (P = .02, η2 = 0.02) and right inferior parietal lobule (IPL) volumes (P = .04, η2 = 0.01). Sex differences in HCs were found in the SMG (M &gt; F) and IPL (F &gt; M). In BD, sex differences were reversed and of smaller magnitude in the SMG (M &lt; F) and of greater magnitude in the IPL (F &gt; M), driven by trends towards smaller SMG and IPL in BD vs HC male participants (P = .05 and .14). Whole‐brain analyses for cortical thickness, and ROI analyses for volume and cortical thickness, were not significant. Conclusions Normative sex differences may be disrupted in adolescent BD in the SMG and IPL, heteromodal association network hubs responsible for higher order integration of cognitive and emotional processing. Unexpectedly, these findings may inform our understanding of aberrant brain structure in adolescent BD male patients, rather than female patients. Future work should focus on replication, as well as the impact of puberty status and sex hormones on measures of brain structure and function.</description><subject>adolescent</subject><subject>Adolescents</subject><subject>Amygdala</subject><subject>Bipolar disorder</subject><subject>brain structure</subject><subject>Cognitive ability</subject><subject>Cortex (cingulate)</subject><subject>Diagnosis</subject><subject>Functional anatomy</subject><subject>Gender differences</subject><subject>Information processing</subject><subject>Neuroimaging</subject><subject>Phenotypes</subject><subject>Prefrontal cortex</subject><subject>Puberty</subject><subject>Sex differences</subject><subject>Sex hormones</subject><subject>Structure-function relationships</subject><subject>Teenagers</subject><issn>1398-5647</issn><issn>1399-5618</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kMtOwzAQRS0EoqWw4AdQJDawSBvbcR5LKK-iSizo3vJjDKnSuNiJSv8e0xQWSMxi5mp05mp0ETrHyRiHmkhdjTHJMnqAhpiWZcwyXBzudBF0mg_QiffLJMEZSdgxGpCyDGtGhuj5FT4jXRkDDhoFPqqaSDoRum9dp9rOQSRWtnmLhLY1eAVN66NN1b5HslrbWrhw7a3T4E7RkRG1h7P9HKHFw_1i-hTPXx5n05t5rCijNKYFUGJynFImpCjzVGZQZiURWKVAdJFLJhOjCaGSCV0olhORSUKNYVqlhI7QVW-7dvajA9_yVRXeqmvRgO08J0lGCpoSTAN6-Qdd2s414blAFYQWSR7QEbruKeWs9w4MX7tqJdyW44R_58tDvnyXb2Av9o6dXIH-JX8CDcCkBzZVDdv_nfjt3ay3_AIfBYOd</recordid><startdate>201808</startdate><enddate>201808</enddate><creator>Mitchell, Rachel HB</creator><creator>Metcalfe, Arron WS</creator><creator>Islam, Alvi H</creator><creator>Toma, Simina</creator><creator>Patel, Ronak</creator><creator>Fiksenbaum, Lisa</creator><creator>Korczak, Daphne</creator><creator>MacIntosh, Bradley J</creator><creator>Goldstein, Benjamin I</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0340-349X</orcidid><orcidid>https://orcid.org/0000-0002-6361-0469</orcidid></search><sort><creationdate>201808</creationdate><title>Sex differences in brain structure among adolescents with bipolar disorder</title><author>Mitchell, Rachel HB ; Metcalfe, Arron WS ; Islam, Alvi H ; Toma, Simina ; Patel, Ronak ; Fiksenbaum, Lisa ; Korczak, Daphne ; MacIntosh, Bradley J ; Goldstein, Benjamin I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3533-38e32f71435aba974b6e9692a1c4e2d87b5b0fd223b5ad8c572a6b23ff5dc423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>adolescent</topic><topic>Adolescents</topic><topic>Amygdala</topic><topic>Bipolar disorder</topic><topic>brain structure</topic><topic>Cognitive ability</topic><topic>Cortex (cingulate)</topic><topic>Diagnosis</topic><topic>Functional anatomy</topic><topic>Gender differences</topic><topic>Information processing</topic><topic>Neuroimaging</topic><topic>Phenotypes</topic><topic>Prefrontal cortex</topic><topic>Puberty</topic><topic>Sex differences</topic><topic>Sex hormones</topic><topic>Structure-function relationships</topic><topic>Teenagers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitchell, Rachel HB</creatorcontrib><creatorcontrib>Metcalfe, Arron WS</creatorcontrib><creatorcontrib>Islam, Alvi H</creatorcontrib><creatorcontrib>Toma, Simina</creatorcontrib><creatorcontrib>Patel, Ronak</creatorcontrib><creatorcontrib>Fiksenbaum, Lisa</creatorcontrib><creatorcontrib>Korczak, Daphne</creatorcontrib><creatorcontrib>MacIntosh, Bradley J</creatorcontrib><creatorcontrib>Goldstein, Benjamin I</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bipolar disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitchell, Rachel HB</au><au>Metcalfe, Arron WS</au><au>Islam, Alvi H</au><au>Toma, Simina</au><au>Patel, Ronak</au><au>Fiksenbaum, Lisa</au><au>Korczak, Daphne</au><au>MacIntosh, Bradley J</au><au>Goldstein, Benjamin I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex differences in brain structure among adolescents with bipolar disorder</atitle><jtitle>Bipolar disorders</jtitle><addtitle>Bipolar Disord</addtitle><date>2018-08</date><risdate>2018</risdate><volume>20</volume><issue>5</issue><spage>448</spage><epage>458</epage><pages>448-458</pages><issn>1398-5647</issn><eissn>1399-5618</eissn><abstract>Objectives Bipolar disorder (BD) is twice as prevalent amongst female as amongst male adolescents. Thus far, little is known regarding the neurostructural substrates underlying this disparity. We therefore examined sex differences in neurostructural magnetic resonane imaging (MRI) phenotypes amongst adolescents with BD. Methods T1‐weighted structural MRI was acquired from 44 BD (25 female [F] and 19 male [M]) and 58 (28 F and 30 M) healthy control (HC) adolescents (13‐21 years old). Whole‐brain and region‐of‐interest (ROI) analyses examined structural volume and cortical thickness using FreeSurfer. ROIs included the ventrolateral prefrontal cortex (vlPFC), anterior cingulate cortex (ACC), amygdala and hippocampus. General linear models evaluated sex‐by‐diagnosis interactions, controlling for age and intracranial volume. Results Whole‐brain analysis revealed sex‐by‐diagnosis interactions in the left supramarginal gyrus (SMG) (P = .02, η2 = 0.02) and right inferior parietal lobule (IPL) volumes (P = .04, η2 = 0.01). Sex differences in HCs were found in the SMG (M &gt; F) and IPL (F &gt; M). In BD, sex differences were reversed and of smaller magnitude in the SMG (M &lt; F) and of greater magnitude in the IPL (F &gt; M), driven by trends towards smaller SMG and IPL in BD vs HC male participants (P = .05 and .14). Whole‐brain analyses for cortical thickness, and ROI analyses for volume and cortical thickness, were not significant. Conclusions Normative sex differences may be disrupted in adolescent BD in the SMG and IPL, heteromodal association network hubs responsible for higher order integration of cognitive and emotional processing. Unexpectedly, these findings may inform our understanding of aberrant brain structure in adolescent BD male patients, rather than female patients. Future work should focus on replication, as well as the impact of puberty status and sex hormones on measures of brain structure and function.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29956452</pmid><doi>10.1111/bdi.12663</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0340-349X</orcidid><orcidid>https://orcid.org/0000-0002-6361-0469</orcidid></addata></record>
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subjects adolescent
Adolescents
Amygdala
Bipolar disorder
brain structure
Cognitive ability
Cortex (cingulate)
Diagnosis
Functional anatomy
Gender differences
Information processing
Neuroimaging
Phenotypes
Prefrontal cortex
Puberty
Sex differences
Sex hormones
Structure-function relationships
Teenagers
title Sex differences in brain structure among adolescents with bipolar disorder
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