New structural brain imaging endophenotype in bipolar disorder
Neuroimaging studies suggest anterior-limbic structural brain abnormalities in patients with bipolar disorder (BD), but few studies have shown these abnormalities in unaffected but genetically liable family members. In this study, we report morphometric correlates of genetic risk for BD using voxel-...
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Veröffentlicht in: | Molecular psychiatry 2012-04, Vol.17 (4), p.412-420 |
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description | Neuroimaging studies suggest anterior-limbic structural brain abnormalities in patients with bipolar disorder (BD), but few studies have shown these abnormalities in unaffected but genetically liable family members. In this study, we report morphometric correlates of genetic risk for BD using voxel-based morphometry. In 35 BD type I (BD-I) patients, 20 unaffected first-degree relatives (UAR) of BD patients and 40 healthy control subjects underwent 3 T magnetic resonance scanner imaging. Preprocessing of images used DARTEL (diffeomorphic anatomical registration through exponentiated lie algebra) for voxel-based morphometry in SPM8 (Wellcome Department of Imaging Neuroscience, London, UK). The whole-brain analysis revealed that the gray matter (GM) volumes of the left anterior insula and right inferior frontal gyrus showed a significant main effect of diagnosis. Multiple comparison analysis showed that the BD-I patients and the UAR subjects had smaller left anterior insular GM volumes compared with the healthy subjects, the BD-I patients had smaller right inferior frontal gyrus compared with the healthy subjects. For white matter (WM) volumes, there was a significant main effect of diagnosis for medial frontal gyrus. The UAR subjects had smaller right medial frontal WM volumes compared with the healthy subjects. These findings suggest that morphometric brain abnormalities of the anterior-limbic neural substrate are associated with family history of BD, which may give insight into the pathophysiology of BD, and be a potential candidate as a morphological endophenotype of BD. |
doi_str_mv | 10.1038/mp.2011.3 |
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In this study, we report morphometric correlates of genetic risk for BD using voxel-based morphometry. In 35 BD type I (BD-I) patients, 20 unaffected first-degree relatives (UAR) of BD patients and 40 healthy control subjects underwent 3 T magnetic resonance scanner imaging. Preprocessing of images used DARTEL (diffeomorphic anatomical registration through exponentiated lie algebra) for voxel-based morphometry in SPM8 (Wellcome Department of Imaging Neuroscience, London, UK). The whole-brain analysis revealed that the gray matter (GM) volumes of the left anterior insula and right inferior frontal gyrus showed a significant main effect of diagnosis. Multiple comparison analysis showed that the BD-I patients and the UAR subjects had smaller left anterior insular GM volumes compared with the healthy subjects, the BD-I patients had smaller right inferior frontal gyrus compared with the healthy subjects. For white matter (WM) volumes, there was a significant main effect of diagnosis for medial frontal gyrus. The UAR subjects had smaller right medial frontal WM volumes compared with the healthy subjects. These findings suggest that morphometric brain abnormalities of the anterior-limbic neural substrate are associated with family history of BD, which may give insight into the pathophysiology of BD, and be a potential candidate as a morphological endophenotype of BD.</description><identifier>ISSN: 1359-4184</identifier><identifier>EISSN: 1476-5578</identifier><identifier>DOI: 10.1038/mp.2011.3</identifier><identifier>PMID: 21321565</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Adult ; Adult and adolescent clinical studies ; Atrophy - psychology ; Behavioral Sciences ; Biological and medical sciences ; Biological Psychology ; Bipolar disorder ; Bipolar Disorder - pathology ; Bipolar disorders ; Brain Mapping - methods ; Brain Mapping - psychology ; Brain research ; Case-Control Studies ; Diagnosis ; Endophenotypes ; Family - psychology ; Family medical history ; Female ; Frontal gyrus ; Frontal Lobe - pathology ; Health risk assessment ; Humans ; Image Processing, Computer-Assisted - methods ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Magnetic Resonance Imaging - psychology ; Male ; Medical imaging ; Medical sciences ; Medicine ; Medicine & Public Health ; Mental disorders ; Middle Aged ; Mood disorders ; Morphometry ; Nerve Fibers, Myelinated - pathology ; Nerve Fibers, Unmyelinated - pathology ; Nervous system ; Neuroimaging ; Neurosciences ; original-article ; Pharmacotherapy ; Phenotype ; Psychiatric Status Rating Scales ; Psychiatry ; Psychology. 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Psychiatry ; Substantia alba ; Substantia grisea</subject><ispartof>Molecular psychiatry, 2012-04, Vol.17 (4), p.412-420</ispartof><rights>Macmillan Publishers Limited 2012</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2012 Nature Publishing Group</rights><rights>Macmillan Publishers Limited 2012.</rights><rights>Copyright Nature Publishing Group Apr 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c605t-d26ab42ae52e7bff7e156e9928c1816df93f4275fb94a9906709a2268ea7a7463</citedby><cites>FETCH-LOGICAL-c605t-d26ab42ae52e7bff7e156e9928c1816df93f4275fb94a9906709a2268ea7a7463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/mp.2011.3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/mp.2011.3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25772906$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21321565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsuo, K</creatorcontrib><creatorcontrib>Kopecek, M</creatorcontrib><creatorcontrib>Nicoletti, M A</creatorcontrib><creatorcontrib>Hatch, J P</creatorcontrib><creatorcontrib>Watanabe, Y</creatorcontrib><creatorcontrib>Nery, F G</creatorcontrib><creatorcontrib>Zunta-Soares, G</creatorcontrib><creatorcontrib>Soares, J C</creatorcontrib><title>New structural brain imaging endophenotype in bipolar disorder</title><title>Molecular psychiatry</title><addtitle>Mol Psychiatry</addtitle><addtitle>Mol Psychiatry</addtitle><description>Neuroimaging studies suggest anterior-limbic structural brain abnormalities in patients with bipolar disorder (BD), but few studies have shown these abnormalities in unaffected but genetically liable family members. In this study, we report morphometric correlates of genetic risk for BD using voxel-based morphometry. In 35 BD type I (BD-I) patients, 20 unaffected first-degree relatives (UAR) of BD patients and 40 healthy control subjects underwent 3 T magnetic resonance scanner imaging. Preprocessing of images used DARTEL (diffeomorphic anatomical registration through exponentiated lie algebra) for voxel-based morphometry in SPM8 (Wellcome Department of Imaging Neuroscience, London, UK). The whole-brain analysis revealed that the gray matter (GM) volumes of the left anterior insula and right inferior frontal gyrus showed a significant main effect of diagnosis. Multiple comparison analysis showed that the BD-I patients and the UAR subjects had smaller left anterior insular GM volumes compared with the healthy subjects, the BD-I patients had smaller right inferior frontal gyrus compared with the healthy subjects. For white matter (WM) volumes, there was a significant main effect of diagnosis for medial frontal gyrus. The UAR subjects had smaller right medial frontal WM volumes compared with the healthy subjects. These findings suggest that morphometric brain abnormalities of the anterior-limbic neural substrate are associated with family history of BD, which may give insight into the pathophysiology of BD, and be a potential candidate as a morphological endophenotype of BD.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Atrophy - psychology</subject><subject>Behavioral Sciences</subject><subject>Biological and medical sciences</subject><subject>Biological Psychology</subject><subject>Bipolar disorder</subject><subject>Bipolar Disorder - pathology</subject><subject>Bipolar disorders</subject><subject>Brain Mapping - methods</subject><subject>Brain Mapping - psychology</subject><subject>Brain research</subject><subject>Case-Control Studies</subject><subject>Diagnosis</subject><subject>Endophenotypes</subject><subject>Family - psychology</subject><subject>Family medical history</subject><subject>Female</subject><subject>Frontal gyrus</subject><subject>Frontal Lobe - pathology</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Magnetic Resonance Imaging - psychology</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mental disorders</subject><subject>Middle Aged</subject><subject>Mood disorders</subject><subject>Morphometry</subject><subject>Nerve Fibers, Myelinated - pathology</subject><subject>Nerve Fibers, Unmyelinated - pathology</subject><subject>Nervous system</subject><subject>Neuroimaging</subject><subject>Neurosciences</subject><subject>original-article</subject><subject>Pharmacotherapy</subject><subject>Phenotype</subject><subject>Psychiatric Status Rating Scales</subject><subject>Psychiatry</subject><subject>Psychology. 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Psychiatry</topic><topic>Substantia alba</topic><topic>Substantia grisea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsuo, K</creatorcontrib><creatorcontrib>Kopecek, M</creatorcontrib><creatorcontrib>Nicoletti, M A</creatorcontrib><creatorcontrib>Hatch, J P</creatorcontrib><creatorcontrib>Watanabe, Y</creatorcontrib><creatorcontrib>Nery, F G</creatorcontrib><creatorcontrib>Zunta-Soares, G</creatorcontrib><creatorcontrib>Soares, J C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsuo, K</au><au>Kopecek, M</au><au>Nicoletti, M A</au><au>Hatch, J P</au><au>Watanabe, Y</au><au>Nery, F G</au><au>Zunta-Soares, G</au><au>Soares, J C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New structural brain imaging endophenotype in bipolar disorder</atitle><jtitle>Molecular psychiatry</jtitle><stitle>Mol Psychiatry</stitle><addtitle>Mol Psychiatry</addtitle><date>2012-04-01</date><risdate>2012</risdate><volume>17</volume><issue>4</issue><spage>412</spage><epage>420</epage><pages>412-420</pages><issn>1359-4184</issn><eissn>1476-5578</eissn><abstract>Neuroimaging studies suggest anterior-limbic structural brain abnormalities in patients with bipolar disorder (BD), but few studies have shown these abnormalities in unaffected but genetically liable family members. In this study, we report morphometric correlates of genetic risk for BD using voxel-based morphometry. In 35 BD type I (BD-I) patients, 20 unaffected first-degree relatives (UAR) of BD patients and 40 healthy control subjects underwent 3 T magnetic resonance scanner imaging. Preprocessing of images used DARTEL (diffeomorphic anatomical registration through exponentiated lie algebra) for voxel-based morphometry in SPM8 (Wellcome Department of Imaging Neuroscience, London, UK). The whole-brain analysis revealed that the gray matter (GM) volumes of the left anterior insula and right inferior frontal gyrus showed a significant main effect of diagnosis. Multiple comparison analysis showed that the BD-I patients and the UAR subjects had smaller left anterior insular GM volumes compared with the healthy subjects, the BD-I patients had smaller right inferior frontal gyrus compared with the healthy subjects. For white matter (WM) volumes, there was a significant main effect of diagnosis for medial frontal gyrus. The UAR subjects had smaller right medial frontal WM volumes compared with the healthy subjects. These findings suggest that morphometric brain abnormalities of the anterior-limbic neural substrate are associated with family history of BD, which may give insight into the pathophysiology of BD, and be a potential candidate as a morphological endophenotype of BD.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>21321565</pmid><doi>10.1038/mp.2011.3</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Atrophy - psychology Behavioral Sciences Biological and medical sciences Biological Psychology Bipolar disorder Bipolar Disorder - pathology Bipolar disorders Brain Mapping - methods Brain Mapping - psychology Brain research Case-Control Studies Diagnosis Endophenotypes Family - psychology Family medical history Female Frontal gyrus Frontal Lobe - pathology Health risk assessment Humans Image Processing, Computer-Assisted - methods Magnetic resonance imaging Magnetic Resonance Imaging - methods Magnetic Resonance Imaging - psychology Male Medical imaging Medical sciences Medicine Medicine & Public Health Mental disorders Middle Aged Mood disorders Morphometry Nerve Fibers, Myelinated - pathology Nerve Fibers, Unmyelinated - pathology Nervous system Neuroimaging Neurosciences original-article Pharmacotherapy Phenotype Psychiatric Status Rating Scales Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Substantia alba Substantia grisea |
title | New structural brain imaging endophenotype in bipolar disorder |
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