Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression

Eur Psychiatry. 2022 Jun 22;65(1):e38. doi: 10.1192/j.eurpsy.2022.32.

Abstract

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.

Keywords: Depression; genome-wide association study; linkage disequilibrium score regression; non-anxiety.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anxiety Disorders
  • Depression* / genetics
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study*
  • Humans
  • Linkage Disequilibrium
  • Phenotype
  • Polymorphism, Single Nucleotide