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Phenotype-specific association of LHCGR rs13405728 polymorphism with anovulatory infertility in Malay women with polycystic ovary syndrome: a case-control study


Citation

Elbadie, Mariam and Abdul Hamid, Habibah and Ahmad, Zalinah and Ling, King Hwa (2026) Phenotype-specific association of LHCGR rs13405728 polymorphism with anovulatory infertility in Malay women with polycystic ovary syndrome: a case-control study. International Journal of Fertility and Sterility, 20 (3). pp. 268-277. ISSN 2008-076X; eISSN: 2008-0778

Abstract

Background: Polycystic ovary syndrome (PCOS) is a multifactorial, polygenic endocrinopathy with an incompletely understood aetiology that accounts for approximately 80% of female anovulatory infertility. Both genetic and environmental factors contribute significantly to its pathogenesis. This study is the first to investigate the association of DENN/MADD domain-containing 1A (DENND1A rs2479106 and rs10986105), luteinising hormone/choriogon-adotropin receptor (LHCGR rs13405728), follicle-stimulating hormone receptor (FSHR rs6166), thyroid adenoma-associated protein I (THADA rs13429458), and cytochrome P450 17A1 (CYP17A1 rs743572) gene polymorphisms with PCOS-related anovulatory infertility in Malay women. Materials and Methods: In this case-control study, 96 participants were recruited-48 anovulatory infertile-PCOS patients and 48 infertile non-PCOS controls. Single nucleotide polymorphisms (SNPs) were detected using high-resolution melting (HRM) analysis, with sequencing performed for validation. Results: The LHCGR rs13405728 polymorphism was strongly associated with an increased risk of PCOS-related anovulatory infertility, with each minor G allele conferring an odds ratio (OR) of 2.63 and 95% confidence interval (95% CI) of 1.11-6.27, P= 0.020). Conversely, the THADA rs7568365 T allele exhibited a protective effect, reducing the risk by 72% (OR=0.28; 95% CI: 0.08-0.90; P=0.020). No significant associations were observed for DENND1A rs2479106 and rs10986105, FSHR rs6166, THADA rs13429458, or CYP17A1 rs743572. Haplotype analysis revealed that the A-T (rs13429458-rs1317772225-rs7568365) and ATA and ACA (rs13405728-rs6166-rs13429458) haplotypes were protective, with ORs of 0.13, 0.19, and 0.30, respectively (P<0.05). Conclusion: The LHCGR rs13405728 polymorphism is significantly associated with the risk of PCOS-related anovulatory infertility in Malay women and may serve as a potential early prognostic biomarker for the development of PCOS-related infertility.


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Additional Metadata

Item Type: Article
Subject: Reproductive Medicine
Subject: Obstetrics and Gynecology
Divisions: Faculty of Medicine and Health Science
Institute of Bioscience
DOI Number: https://doi.org/10.22074/ijfs.2025.2065767.1908
Publisher: Royan Institute (ACECR)
Keywords: Anovulation; Haplotypes; Polycystic Ovary Syndrome; Polymorphism; Receptors
Sustainable Development Goals (SDGs): SDG 3: Good Health and Well-being, SDG 5: Gender Equality, SDG 10: Reduced Inequalities
Depositing User: Ms. Siti Radziah Mohamed@mahmod
Date Deposited: 26 Aug 2026 07:40
Last Modified: 26 Aug 2026 07:40
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.22074/ijfs.2025.2065767.1908
URI: http://psasir.upm.edu.my/id/eprint/128038
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