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Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression
Bolun Cheng1, Xin Qi2, Peilin Meng1
1Key Laboratory of Trace Elements and Endemic Diseases, Collaborative Innovation Center of Endemic Disease and Health Promotion for Silk Road Region, School of Public Health, Health Science Center, Xi'an Jiaotong University, Xi'an710061, China.
Background:
Depression is a debilitating mental disorder that often coexists with anxiety. The genetic mechanisms of depression and anxiety have considerable overlap, and studying depression in non-anxiety samples could help to discover novel gene. We assess the genetic variation of depression in non-anxiety samples, using genome-wide association studies (GWAS) and linkage disequilibrium score regression (LDSC).
Methods:
The GWAS of depression score and self-reported depression were conducted using the UK Biobank samples, comprising 99,178 non-anxiety participants with anxiety score <5 and 86,503 non-anxiety participants without self-reported anxiety, respectively. Replication analysis was then performed using two large-scale GWAS summary data of depression from Psychiatric Genomics Consortium (PGC). LDSC was finally used to evaluate genetic correlations with 855 health-related traits based on the primary GWAS.
Results:
Two genome-wide significant loci for non-anxiety depression were identified: rs139702470 (p = 1.54 × 10-8, OR = 0.29) locate in PIEZO2, and rs6046722 (p = 2.52 × 10-8, OR = 1.09) locate in CFAP61. These associated genes were replicated in two GWAS of depression from PGC, such as rs1040582 (preplication GWAS1 = 0.02, preplication GWAS2 = 2.71 × 10-3) in CFAP61, and rs11661122 (preplication GWAS1 = 8.16 × 10-3, preplication GWAS2 = 8.08 × 10-3) in PIEZO2. LDSC identified 19 traits genetically associated with non-anxiety depression (p < 0.001), such as marital separation/divorce (rg = 0.45, SE = 0.15).
Conclusions:
Our findings provide novel clues for understanding of the complex genetic architecture of depression.
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