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The association between familial risk and brain abnormalities is disease specific: an ENIGMA-relatives study of schizophrenia and bipolar disorder
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2019 (English)In: Biological Psychiatry, ISSN 0006-3223, E-ISSN 1873-2402, Vol. 86, no 7, p. 545-556Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Schizophrenia and bipolar disorder share genetic liability, and some structural brain abnormalities are common to both conditions. First-degree relatives of patients with schizophrenia (FDRs-SZ) show similar brain abnormalities to patients, albeit with smaller effect sizes. Imaging findings in first-degree relatives of patients with bipolar disorder (FDRs-BD) have been inconsistent in the past, but recent studies report regionally greater volumes compared with control subjects.

METHODS: We performed a meta-analysis of global and subcortical brain measures of 6008 individuals (1228 FDRs-SZ, 852 FDRs-BD, 2246 control subjects, 1016 patients with schizophrenia, 666 patients with bipolar disorder) from 34 schizophrenia and/or bipolar disorder family cohorts with standardized methods. Analyses were repeated with a correction for intracranial volume (ICV) and for the presence of any psychopathology in the relatives and control subjects.

RESULTS: FDRs-BD had significantly larger ICV (d = +0.16, q < .05 corrected), whereas FDRs-SZ showed smaller thalamic volumes than control subjects (d = -0.12, q < .05 corrected). ICV explained the enlargements in the brain measures in FDRs-BD. In FDRs-SZ, after correction for ICV, total brain, cortical gray matter, cerebral white matter, cerebellar gray and white matter, and thalamus volumes were significantly smaller; the cortex was thinner (d < -0.09, q < .05 corrected); and third ventricle was larger (d = +0.15, q < .05 corrected). The findings were not explained by psychopathology in the relatives or control subjects.

CONCLUSIONS: Despite shared genetic liability, FDRs-SZ and FDRs-BD show a differential pattern of structural brain abnormalities, specifically a divergent effect in ICV. This may imply that the neurodevelopmental trajectories leading to brain anomalies in schizophrenia or bipolar disorder are distinct.

Place, publisher, year, edition, pages
Elsevier, 2019. Vol. 86, no 7, p. 545-556
Keywords [en]
Bipolar disorder, Familial risk, Imaging, Meta-analysis, Neurodevelopment, Schizophrenia
National Category
Psychiatry Neurosciences Neurology
Identifiers
URN: urn:nbn:se:umu:diva-206300DOI: 10.1016/j.biopsych.2019.03.985ISI: 000485217300010PubMedID: 31443932Scopus ID: 2-s2.0-85071651930OAI: oai:DiVA.org:umu-206300DiVA, id: diva2:1748808
Funder
The Research Council of Norway, 223273NIH (National Institutes of Health), R01 MH117601NIH (National Institutes of Health), R01 MH116147NIH (National Institutes of Health), R01 MH111671NIH (National Institutes of Health), P41 EB015922NIH (National Institutes of Health), 5T32MH073526NIH (National Institutes of Health), U54EB020403NIH (National Institutes of Health), R03 MH105808Swedish Research Council, K2007-62X-15077-04-1Swedish Research Council, K2008-62P-20597-01-3Swedish Research Council, K2010-62X-15078-07-2Swedish Research Council, K2012-61X-15078-09-3European Regional Development Fund (ERDF)European CommissionWellcome trust, 064971Wellcome trust, 085475/B/08/ZWellcome trust, 085475/Z/08/ZGerman Research Foundation (DFG), 1617Available from: 2023-04-04 Created: 2023-04-04 Last updated: 2023-05-12Bibliographically approved

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Johansson, Viktoria

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