期刊
BRITISH JOURNAL OF PSYCHIATRY
卷 213, 期 1, 页码 430-436出版社
CAMBRIDGE UNIV PRESS
DOI: 10.1192/bjp.2018.62
关键词
Genetic overlap; neuroimaging; obsessive-compulsive disorder
类别
资金
- Institutes of the National Institutes of Health [U54 EB020403]
- National Institute of Biomedical Imaging and Bioengineering
- National Cancer Institute
- NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [U54EB020403] Funding Source: NIH RePORTER
Background Many studies have identified changes in the brain associated with obsessive-compulsive disorder (OCD), but few have examined the relationship between genetic determinants of OCD and brain variation. Aims We present the first genome-wide investigation of overlapping genetic risk for OCD and genetic influences on subcortical brain structures. Method Using single nucleotide polymorphism effect concordance analysis, we measured genetic overlap between the first genome-wide association study (GWAS) of OCD (1465 participants with OCD, 5557 controls) and recent GWASs of eight subcortical brain volumes (13 171 participants). Results We found evidence of significant positive concordance between OCD risk variants and variants associated with greater nucleus accumbens and putamen volumes. When conditioning OCD risk variants on brain volume, variants influencing putamen, amygdala and thalamus volumes were associated with risk for OCD. Conclusions These results are consistent with current OCD neurocircuitry models. Further evidence will clarify the relationship between putamen volume and OCD risk, and the roles of the detected variants in this disorder.
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