BRCA1/2 Polymorphisms and the Risk of Recurrent Implantation Failure in Korean Women
Recurrent implantation failure (RIF) is a major cause of unsuccessful assisted reproduction, yet its genetic basis remains poorly defined. Because BRCA1 and BRCA2 are central to homologous recombination-mediated repair of DNA double-strand breaks, we examined whether common variants in these genes are associated with RIF. Seven BRCA1/2 single-nucleotide polymorphisms, prioritized from whole-exome sequencing data, were genotyped in 128 women with RIF and 330 controls with proven natural fertility, and associations were estimated by age-adjusted logistic regression with false discovery rate (FDR) correction. The BRCA2 rs1799943 A allele was associated with lower odds of RIF under the heterozygous (adjusted odds ratio [AOR] 0.445, FDR q = 0.006) and dominant (AOR 0.443, q = 0.004) models; no other variant remained associated after correction. In exploratory analyses of the same participants, this inverse association was largely confined to carriers of the BRCA1 rs12516 A allele (interaction q = 0.003), the BRCA2 haplotype carrying the rs1799943 A allele was associated with lower odds of RIF (AOR 0.551, q = 0.012), and nominal associations of genotype combinations involving rs15869 were not supported by formal interaction testing. These findings identify rs1799943 as a candidate variant associated with RIF that warrants replication and functional investigation.
Authors
- So Yeon Shin (ORCID: https://orcid.org/0000-0002-5248-6300)
- Nam Keun Kim (ORCID: https://orcid.org/0000-0003-0541-3528)
- D. Kim (ORCID: https://orcid.org/0009-0004-5305-101X)
- Hyeon Woo Park
- Ji Hyang Kim (ORCID: https://orcid.org/0000-0002-0514-5132)
- Ji Eun Ko
Institutions
- CHA University Bundang Medical Center (KR)
- CHA University (KR)
Publication Details
- Journal
- International Journal of Molecular Sciences
- Published
- 2026-11-09
- DOI
- https://doi.org/10.3390/ijms272110032
- Primary Topic
- Reproductive System and Pregnancy
- Type
- article
- Field-Weighted Citation Impact
- 0.00