Literature DB >> 23864160

Gray matter abnormalities as brain structural vulnerability factors for bipolar disorder: A review of neuroimaging studies of individuals at high genetic risk for bipolar disorder.

Fabiano G Nery1, E Serap Monkul, Beny Lafer.   

Abstract

OBJECTIVE: Cortical and subcortical gray matter abnormalities have been reported in individuals at high genetic risk for bipolar disorder, but the findings are inconsistent. The aim of this study was to review the available literature to identify common findings that could represent brain structural vulnerability factors for bipolar disorder and to discuss challenges for the advancement of the field.
METHOD: A systematic search was conducted using the PubMed database to identify all original articles investigating cortical or subcortical gray matter abnormalities in first-degree relatives of bipolar disorder patients.
RESULTS: Very few findings were replicated, with the exception of larger insular cortex volumes in adult first-degree relatives and larger right inferior frontal gyrus in offspring of probands with bipolar disorder, both when compared with healthy controls. Isolated findings included decreased gray matter density in the left thalamus, decreased gray matter volumes in the left hippocampus and parahippocampal gyrus, and thicker right hippocampus in unaffected first-degree relatives. Genetic liability for bipolar disorder was associated with gray matter volumes in regions of the anterior cingulate cortex, ventral striatum, medial frontal gyrus, right precentral gyrus, right insular cortex, and medial orbital gyrus. Some studies found no evidence for gray matter abnormalities in first-degree relatives of bipolar disorder patients.
CONCLUSIONS: Possible reasons for the discrepancies of findings across studies include small samples sizes, small effect size of susceptibility genes, the phenotypic heterogeneity of bipolar disorder, and the possible confounding effect of other Axis I psychopathologies among the relatives of patients. Future multisite, prospective, large studies with more homogeneous samples would be a key strategy to advance the field. The ultimate benefit would be an understanding of how to use brain imaging tools to identify individuals at increased risk for bipolar disorder and develop preventive strategies for that population.

Entities:  

Keywords:  Bipolar disorder; cerebral cortex; endophenotypes; insular cortex; magnetic resonance imaging; review

Mesh:

Year:  2013        PMID: 23864160     DOI: 10.1177/0004867413496482

Source DB:  PubMed          Journal:  Aust N Z J Psychiatry        ISSN: 0004-8674            Impact factor:   5.744


  16 in total

Review 1.  Baby brain atlases.

Authors:  Kenichi Oishi; Linda Chang; Hao Huang
Journal:  Neuroimage       Date:  2018-04-03       Impact factor: 6.556

2.  The Lausanne-Geneva cohort study of offspring of parents with mood disorders: methodology, findings, current sample characteristics, and perspectives.

Authors:  Caroline L Vandeleur; Marie-Pierre F Strippoli; Enrique Castelao; Mehdi Gholam-Rezaee; François Ferrero; Pierre Marquet; Jean-Michel Aubry; Martin Preisig
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2017-04-10       Impact factor: 4.328

3.  Brain structural correlates of familial risk for mental illness: a meta-analysis of voxel-based morphometry studies in relatives of patients with psychotic or mood disorders.

Authors:  Wenjing Zhang; John A Sweeney; Li Yao; Siyi Li; Jiaxin Zeng; Mengyuan Xu; Maxwell J Tallman; Qiyong Gong; Melissa P DelBello; Su Lui; Fabiano G Nery
Journal:  Neuropsychopharmacology       Date:  2020-04-30       Impact factor: 7.853

4.  Differences in gray matter volume corresponding to delusion and hallucination in patients with schizophrenia compared with patients who have bipolar disorder.

Authors:  Jinuk Song; Doug Hyun Han; Sun Mi Kim; Ji Sun Hong; Kyung Joon Min; Jae Hoon Cheong; Bung Nyun Kim
Journal:  Neuropsychiatr Dis Treat       Date:  2015-05-18       Impact factor: 2.570

Review 5.  Neurobiology of Risk for Bipolar Disorder.

Authors:  Ayşegül Özerdem; Deniz Ceylan; Güneş Can
Journal:  Curr Treat Options Psychiatry       Date:  2016-10-20

6.  Shared and Specific Intrinsic Functional Connectivity Patterns in Unmedicated Bipolar Disorder and Major Depressive Disorder.

Authors:  Ying Wang; Junjing Wang; Yanbin Jia; Shuming Zhong; Meiqi Niu; Yao Sun; Zhangzhang Qi; Ling Zhao; Li Huang; Ruiwang Huang
Journal:  Sci Rep       Date:  2017-06-15       Impact factor: 4.379

7.  Commentary: Microstructure, length, and connection of limbic tracts in normal human brain development.

Authors:  Kenichi Oishi
Journal:  Front Neurosci       Date:  2017-03-13       Impact factor: 4.677

8.  Prospective longitudinal study of subcortical brain volumes in individuals at high familial risk of mood disorders with or without subsequent onset of depression.

Authors:  Martina Papmeyer; Jessika E Sussmann; Tiffany Stewart; Stephen Giles; John G Centola; Vasileios Zannias; Stephen M Lawrie; Heather C Whalley; Andrew M McIntosh
Journal:  Psychiatry Res Neuroimaging       Date:  2015-12-31       Impact factor: 2.376

Review 9.  Brain Structural Effects of Psychopharmacological Treatment in Bipolar Disorder.

Authors:  Colm McDonald
Journal:  Curr Neuropharmacol       Date:  2015       Impact factor: 7.363

10.  Evidence for association between familial bipolar risk and ventral striatal volume.

Authors:  T M Lancaster
Journal:  J Affect Disord       Date:  2018-02-17       Impact factor: 4.839

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