ABSTRACT Hirsutism is a condition characterized by excessive hair growth in women, with a prevalence of 5-10 %. The diagnostic criteria usually include hair appearing in male-pattern areas, such as the face, abdomen, and chest. The contributing factors for hirsutism symptoms are heterogeneous and vary from genetic and ethnic background to diverse endocrinological causes, most commonly polycystic ovary syndrome (PCOS). In this cross-ancestry genome-wide association study (GWAS) including 4,834 cases and 352,966 controls, we explored the genetic background of hirsutism and identified seven loci associated with hirsutism, four of which have not been previously reported in GWAS. To capture low-frequency variants, we analyzed the Finnish FinnGen cohort separately, leveraging its bottleneck history that enriches for rare variants with larger effects. A missense variant rs199649605 (MAF = 0.005) enriched in the Finnish population near FGF5, a gene regulating the hair follicle cycle, showed a particularly strong effect (p = 1.39e-10, OR=5.02, 95 % CI=3.06-8.21). Genetic correlation analyses revealed shared genetic architecture between hirsutism, PCOS, and metabolic traits such as obesity and type 2 diabetes. These findings uncover genetic contributors to hirsutism beyond PCOS, suggesting that both androgen-dependent and independent mechanisms underlie excessive hair growth in women.
Takala et al. (Fri,) studied this question.