Back to Search Start Over

The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder.

Authors :
de Zwarte SMC
Brouwer RM
Agartz I
Alda M
Aleman A
Alpert KI
Bearden CE
Bertolino A
Bois C
Bonvino A
Bramon E
Buimer EEL
Cahn W
Cannon DM
Cannon TD
Caseras X
Castro-Fornieles J
Chen Q
Chung Y
De la Serna E
Di Giorgio A
Doucet GE
Eker MC
Erk S
Fears SC
Foley SF
Frangou S
Frankland A
Fullerton JM
Glahn DC
Goghari VM
Goldman AL
Gonul AS
Gruber O
de Haan L
Hajek T
Hawkins EL
Heinz A
Hillegers MHJ
Hulshoff Pol HE
Hultman CM
Ingvar M
Johansson V
Jönsson EG
Kane F
Kempton MJ
Koenis MMG
Kopecek M
Krabbendam L
Krämer B
Lawrie SM
Lenroot RK
Marcelis M
Marsman JC
Mattay VS
McDonald C
Meyer-Lindenberg A
Michielse S
Mitchell PB
Moreno D
Murray RM
Mwangi B
Najt P
Neilson E
Newport J
van Os J
Overs B
Ozerdem A
Picchioni MM
Richter A
Roberts G
Aydogan AS
Schofield PR
Simsek F
Soares JC
Sugranyes G
Toulopoulou T
Tronchin G
Walter H
Wang L
Weinberger DR
Whalley HC
Yalin N
Andreassen OA
Ching CRK
van Erp TGM
Turner JA
Jahanshad N
Thompson PM
Kahn RS
van Haren NEM
Source :
Biological psychiatry [Biol Psychiatry] 2019 Oct 01; Vol. 86 (7), pp. 545-556. Date of Electronic Publication: 2019 Jun 13.
Publication Year :
2019

Abstract

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.<br />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.<br />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.<br />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.<br /> (Copyright © 2019 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-2402
Volume :
86
Issue :
7
Database :
MEDLINE
Journal :
Biological psychiatry
Publication Type :
Academic Journal
Accession number :
31443932
Full Text :
https://doi.org/10.1016/j.biopsych.2019.03.985