Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Samvida S. Venkatesh*, Laura B.L. Wittemans, Duncan S. Palmer, Nikki Hubers, Dorret I. Boomsma, Yee Ming Chan, Triin Laisk, Cecilia M. Lindgren*, Genes & Health Research Team, Estonian Biobank Research Team, Estonian Health Informatics Research Team, DBDS Genomic Consortium, FinnGen

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Genome-wide association studies (GWASs) may help inform the etiology of infertility. Here, we perform GWAS meta-analyses across seven cohorts in up to 42,629 cases and 740,619 controls and identify 25 genetic risk loci for male and female infertility. We additionally identify up to 269 genetic loci associated with follicle-stimulating hormone, luteinizing hormone, estradiol and testosterone through sex-specific GWAS meta-analyses (n = 6,095–246,862). Exome sequencing analyses reveal that women carrying testosterone-lowering rare variants in some genes are at risk of infertility. However, we find no local or genome-wide genetic correlation between female infertility and reproductive hormones. While infertility is genetically correlated with endometriosis and polycystic ovary syndrome, we find limited genetic overlap between infertility and obesity. Finally, we show that the evolutionary persistence of infertility-risk alleles may be explained by directional selection. Taken together, we provide a comprehensive view of the genetic determinants of infertility across multiple diagnostic criteria.

Original languageEnglish
Article number22
Pages (from-to)1107-1118
Number of pages12
JournalNature genetics
Volume57
Issue number5
DOIs
Publication statusPublished - May 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

Funding

FundersFunder number
Medical Research CouncilMR/V028766/1

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