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The association between familial risk and brain abnormalities is disease specific: an ENIGMA-Relatives study of schizophrenia and Bipolar disorder

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023752%3A_____%2F19%3A43919959" target="_blank" >RIV/00023752:_____/19:43919959 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11120/19:43918607

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0006322319314374?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0006322319314374?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.biopsych.2019.03.985" target="_blank" >10.1016/j.biopsych.2019.03.985</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The association between familial risk and brain abnormalities is disease specific: an ENIGMA-Relatives study of schizophrenia and Bipolar disorder

  • Original language description

    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 &lt; .05 corrected), whereas FDRs-SZ showed smaller thalamic volumes than control subjects (d = -0.12, q &lt; .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 &lt; -0.09, q &lt; .05 corrected); and third ventricle was larger (d = +0.15, q &lt; .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.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30215 - Psychiatry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Biological Psychiatry

  • ISSN

    0006-3223

  • e-ISSN

  • Volume of the periodical

    86

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    545-556

  • UT code for WoS article

    000485217300010

  • EID of the result in the Scopus database

    2-s2.0-85071651930