| Abstrakt: |
Background Steroidogenic Factor 1/Nuclear Receptor Subfamily 5 Group A Member 1 (SF-1/ NR5A1) is critical for the development and function of sex organs, influencing steroidogenesis and reproduction. While rare deleterious NR5A1 /SF-1 variants have been identified in individuals with various differences of sex development (DSD), primary ovarian insufficiency, and infertility, their impact on the general population remains unclear. Methods We analyzed health records and exome sequencing data from up to 420 162 individuals (227 858 women) from the UK Biobank study to assess the impact of rare (frequency < 0.1%) predicted deleterious NR5A1 /SF-1 variants on age at menopause and 26 other traits. Results No carriers of rare protein truncating variants in NR5A1 /SF-1 were identified. We found that the previously reported association of rare deleterious missense NR5A1 /SF-1 variants with earlier age at menopause is driven by variants in the DNA binding domain (DBD) and ligand binding domain (LBD) (combined test: beta = −2.36 years/allele, [95% CI: 3.21, −1.51], N = 107 carriers, P = 4.6 × 10−8). Carriers also had a higher risk of adult obesity (OR = 1.061, [95% CI: 1.003, 1.104], N = 344, P =.015), particularly among women (OR = 1.095 [95% CI: 1.034, 1.163, P = 3.87 × 10−3], N = 176), but not men (OR = 1.019, [95% CI: 0.955, 1.088], P =.57, N = 168). Conclusion Deleterious missense variants in the DBD and LBD likely disrupt NR5A1 /SF-1 function. This study broadens the relevance of deleterious NR5A1 /SF-1 variants beyond rare DSDs, suggesting the need for extended phenotyping and monitoring of affected individuals. [ABSTRACT FROM AUTHOR] |
