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Cortical abnormalities in bipolar disorder: An MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group

  • D. P. Hibar
  • , L. T. Westlye
  • , N. T. Doan
  • , N. Jahanshad
  • , J. W. Cheung
  • , C. R.K. Ching
  • , A. Versace
  • , A. C. Bilderbeck
  • , A. Uhlmann
  • , B. Mwangi
  • , B. Krämer
  • , B. Overs
  • , C. B. Hartberg
  • , C. Abe
  • , D. Dima
  • , D. Grotegerd
  • , E. Sprooten
  • , E. Ben
  • , E. Jimenez
  • , F. M. Howells
  • G. Delvecchio, H. Temmingh, J. Starke, J. R.C. Almeida, J. M. Goikolea, J. Houenou, L. M. Beard, L. Rauer, L. Abramovic, M. Bonnin, M. F. Ponteduro, M. Keil, M. M. Rive, N. Yao, N. Yalin, P. Najt, P. G. Rosa, R. Redlich, S. Trost, S. Hagenaars, S. C. Fears, S. Alonso-Lana, T. G.M. Van Erp, T. Nickson, T. M. Chaim-Avancini, T. B. Meier, T. Elvsashagen, U. K. Haukvik, W. H. Lee, A. H. Schene, A. J. Lloyd, A. H. Young, A. Nugent, A. M. Dale, A. Pfennig, A. M. McIntosh, B. Lafer, B. T. Baune, C. J. Ekman, C. A. Zarate, C. E. Bearden, C. Henry, C. Simhandl, C. McDonald, C. Bourne, D. J. Stein, D. H. Wolf, D. M. Cannon, D. C. Glahn, D. J. Veltman, E. Pomarol-Clotet, E. Vieta, E. J. Canales-Rodriguez, F. G. Nery, F. L.S. Duran, G. F. Busatto, G. Roberts, G. D. Pearlson, G. M. Goodwin, H. Kugel, H. C. Whalley, H. G. Ruhe, J. C. Soares, J. M. Fullerton, J. K. Rybakowski, J. Savitz, K. T. Chaim, M. Fatjó-Vilas, M. G. Soeiro-De-Souza, M. P. Boks, M. V. Zanetti, M. C.G. Otaduy, M. S. Schaufelberger, M. Alda, M. Ingvar, M. L. Phillips, M. J. Kempton, M. Bauer, M. Landén, N. S. Lawrence, N. E.M. Van Haren, N. R. Horn, N. B. Freimer, O. Gruber, P. R. Schofield, P. B. Mitchell, R. S. Kahn, R. Lenroot, R. Machado-Vieira, R. A. Ophoff, S. Sarró, S. Frangou, T. D. Satterthwaite, T. Hajek, U. Dannlowski, U. F. Malt, V. Arolt, W. F. Gattaz, W. C. Drevets, X. Caseras, I. Agartz, P. M. Thompson, O. A. Andreassen
  • University of Southern California
  • Johnson & Johnson
  • University of Oslo
  • University of California at Los Angeles
  • University of Pittsburgh
  • University of Oxford
  • University of Cape Town
  • University of Texas Health Science Center at Houston
  • Heidelberg University 
  • Neuroscience Research Australia
  • Karolinska Institutet
  • City, University of London
  • King's College London
  • University of Münster
  • Icahn School of Medicine at Mount Sinai
  • Diakonhjemmet Hospital
  • University of Barcelona
  • IRCCS E. Medea Scientific Institute
  • Brown University
  • Hôpital Henri Mondor
  • DBJC/SBFM CEA-Saclay
  • University of Pennsylvania
  • Utrecht University
  • University of Göttingen
  • University of Amsterdam
  • Yale University
  • Institute of Living
  • University of Galway
  • Universidade de São Paulo
  • University of Edinburgh
  • VA Medical Center
  • Sisters Hospitallers Research Foundation
  • CIBERSAM
  • University of California
  • Froedtert & Medical College of Wisconsin
  • Laureate Institute for Brain Research
  • Radboud University Nijmegen
  • Newcastle University
  • National Institutes of Health
  • University of California at San Diego
  • Technische Universität Dresden
  • University of Adelaide
  • Institut Pasteur Paris
  • Bipolar Center Wiener Neustadt
  • Newman University
  • VUMC
  • University of Cincinnati
  • University of New South Wales
  • University of Groningen
  • University of Medical Sciences Poznan
  • University of Tulsa
  • Dalhousie University
  • University of Gothenburg
  • University of Exeter
  • National Institute of Mental Health
  • Cardiff University

Research output: Contribution to journalArticlepeer-review

Abstract

Despite decades of research, the pathophysiology of bipolar disorder (BD) is still not well understood. Structural brain differences have been associated with BD, but results from neuroimaging studies have been inconsistent. To address this, we performed the largest study to date of cortical gray matter thickness and surface area measures from brain magnetic resonance imaging scans of 6503 individuals including 1837 unrelated adults with BD and 2582 unrelated healthy controls for group differences while also examining the effects of commonly prescribed medications, age of illness onset, history of psychosis, mood state, age and sex differences on cortical regions. In BD, cortical gray matter was thinner in frontal, temporal and parietal regions of both brain hemispheres. BD had the strongest effects on left pars opercularis (Cohen's d='0.293; P=1.71 × 10 '21), left fusiform gyrus (d='0.288; P=8.25 × 10 '21) and left rostral middle frontal cortex (d='0.276; P=2.99 × 10 '19). Longer duration of illness (after accounting for age at the time of scanning) was associated with reduced cortical thickness in frontal, medial parietal and occipital regions. We found that several commonly prescribed medications, including lithium, antiepileptic and antipsychotic treatment showed significant associations with cortical thickness and surface area, even after accounting for patients who received multiple medications. We found evidence of reduced cortical surface area associated with a history of psychosis but no associations with mood state at the time of scanning. Our analysis revealed previously undetected associations and provides an extensive analysis of potential confounding variables in neuroimaging studies of BD.

Original languageEnglish
Pages (from-to)932-942
Number of pages11
JournalMolecular Psychiatry
Volume23
Issue number4
DOIs
Publication statusPublished - 1 Apr 2018
Externally publishedYes

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