Structural magnetic resonance imaging in bipolar disorder: an international collaborative mega-analysis of individual adult patient data.

Published

Journal Article

BACKGROUND: There is substantial inconsistency in results of brain structural magnetic resonance imaging studies in adult bipolar disorder. This is likely consequent upon limited statistical power of studies together with their clinical and methodological heterogeneity. The current study was undertaken to perform an international collaborative mega-analysis of regional volumetric measurements of individual patient and healthy subject data, to optimize statistical power, detect case-control differences, assess the association of psychotropic medication usage with brain structural variation, and detect other possible sources of heterogeneity. METHODS: Eleven international research groups contributed published and unpublished data on 321 individuals with bipolar disorder I and 442 healthy subjects. We used linear mixed effects regression models to evaluate differences in brain structure between patient groups. RESULTS: Individuals with bipolar disorder had increased right lateral ventricular, left temporal lobe, and right putamen volumes. Bipolar patients taking lithium displayed significantly increased hippocampal and amygdala volume compared with patients not treated with lithium and healthy comparison subjects. Cerebral volume reduction was significantly associated with illness duration in bipolar individuals. CONCLUSIONS: The application of mega-analysis to bipolar disorder imaging identified lithium use and illness duration as substantial and consistent sources of heterogeneity, with lithium use associated with regionally specific increased brain volume.

Full Text

Duke Authors

Cited Authors

  • Hallahan, B; Newell, J; Soares, JC; Brambilla, P; Strakowski, SM; Fleck, DE; Kieseppä, T; Altshuler, LL; Fornito, A; Malhi, GS; McIntosh, AM; Yurgelun-Todd, DA; Labar, KS; Sharma, V; MacQueen, GM; Murray, RM; McDonald, C

Published Date

  • February 2011

Published In

Volume / Issue

  • 69 / 4

Start / End Page

  • 326 - 335

PubMed ID

  • 21030008

Pubmed Central ID

  • 21030008

Electronic International Standard Serial Number (EISSN)

  • 1873-2402

International Standard Serial Number (ISSN)

  • 0006-3223

Digital Object Identifier (DOI)

  • 10.1016/j.biopsych.2010.08.029

Language

  • eng