Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group

for the ENIGMA-Major Depressive Disorder Working Group(Amsterdam Neuroscience), Lianne Schmaal(Amsterdam Neuroscience), Dick J. Veltman(University of California, Irvine), Theo G.M. van Erp(University of California, Irvine), Philipp G. Sämann(Max Planck Institute of Psychiatry), Thomas Frodl(University of Southern California), Neda Jahanshad(University of Southern California), Elizabeth Loehrer(Erasmus MC), Henning Tiemeier(Erasmus MC), Albert Hofman(Erasmus MC), Wiro J. Niessen(Erasmus MC), Meike W. Vernooij(Erasmus MC), M. Arfan Ikram(German Center for Neurodegenerative Diseases), Katrin Wittfeld(German Center for Neurodegenerative Diseases), Hans J. Grabe(Universitätsmedizin Greifswald), Andrea Block(Universitätsmedizin Greifswald), Katrin Hegenscheid(Universitätsmedizin Greifswald), Henry Völzke(Universitätsmedizin Greifswald), David Hoehn(Max Planck Institute of Psychiatry), M Czisch(The University of Sydney), Jim Lagopoulos(The University of Sydney), Sean N. Hatton(The University of Sydney), Ian B. Hickie(The University of Sydney), Roberto Goya‐Maldonado(Social Neuroscience Lab), Bernd Krämer(Social Neuroscience Lab), Oliver Gruber(QIMR Berghofer Medical Research Institute), Baptiste Couvy‐Duchesne(The University of Queensland), Miguel E. Rentería(QIMR Berghofer Medical Research Institute), Lachlan T. Strike(The University of Queensland), Natalie Mills(The University of Queensland), Greig I. de Zubicaray(The University of Queensland), Katie L. McMahon(The University of Queensland), Sarah E. Medland(QIMR Berghofer Medical Research Institute), Nicholas G. Martin(Virginia Commonwealth University), Nathan A. Gillespie(Virginia Commonwealth University), Margaret J. Wright(QIMR Berghofer Medical Research Institute), Geoffrey B. Hall(University of Calgary), Glenda MacQueen(University of Calgary), Eva-Maria Frey(Trinity College Dublin), Angela Carballedo(Trinity College Dublin), Laura S. van Velzen(University Medical Center Groningen), Marie‐José van Tol(University Medical Center Groningen), Nic J. van der Wee(Leiden University Medical Center), Ilya M. Veer(Charité - Universitätsmedizin Berlin), Henrik Walter(Heidelberg University), Knut Schnell(Heidelberg University), Elisabeth Schramm(University Medical Center Freiburg), Claus Normann(University of Bonn), Dieter Schoepf(University of Bonn), Carsten Konrad(Philipps University of Marburg), Bartosz Zurowski(University of Lübeck), Thomas E. Nickson(University of Edinburgh), Andrew M. McIntosh(University of Edinburgh), Martina Papmeyer(University of Edinburgh), Heather C. Whalley(University of Edinburgh), J. E. Sussmann(Warneford Hospital), Beata R. Godlewska(Warneford Hospital), Philip J. Cowen(Warneford Hospital), Felix Fischer(Charité - Universitätsmedizin Berlin), Matthias Rose(University of Massachusetts Chan Medical School), Brenda W.J.H. Penninx(University of Southern California), Paul M. Thompson(University of Southern California), Derrek P. Hibar(University of Southern California)
Molecular Psychiatry
June 30, 2015
Cited by 1,183Open Access
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Abstract

Alterations in regional subcortical brain volumes have been investigated as part of the efforts of an international consortium, ENIGMA, to identify reliable neural correlates of major depressive disorder (MDD). Given that subcortical structures are comprised of distinct subfields, we sought to build significantly from prior work by precisely mapping localized MDD-related differences in subcortical regions using shape analysis. In this meta-analysis of subcortical shape from the ENIGMA-MDD working group, we compared 1,781 patients with MDD and 2,953 healthy controls (CTL) on individual measures of shape metrics (thickness and surface area) on the surface of seven bilateral subcortical structures: nucleus accumbens, amygdala, caudate, hippocampus, pallidum, putamen, and thalamus. Harmonized data processing and statistical analyses were conducted locally at each site, and findings were aggregated by meta-analysis. Relative to CTL, patients with adolescent-onset MDD (≤ 21 years) had lower thickness and surface area of the subiculum, cornu ammonis (CA) 1 of the hippocampus and basolateral amygdala (Cohen's d = -0.164 to -0.180). Relative to first-episode MDD, recurrent MDD patients had lower thickness and surface area in the CA1 of the hippocampus and the basolateral amygdala (Cohen's d = -0.173 to -0.184). Our results suggest that previously reported MDD-associated volumetric differences may be localized to specific subfields of these structures that have been shown to be sensitive to the effects of stress, with important implications for mapping treatments to patients based on specific neural targets and key clinical features.


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