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March 29, 2026Ankara Üniversitesi Tıp Fakültesi Mecmuası0 citationsOpen Access

rs1800734: a risk allele for nonobstructive azoospermia related to maturation arrest

YÜYasemin ÜlgerSağlık Bilimleri ÜniversitesiKAKaan AYDOSTTTimur TunçalıAnkara University

Key Points

  • The study aims to identify risk alleles in the MLH1 gene related to nonobstructive azoospermia and maturation arrest in males.
  • Genotyping of MLH1 variants in 42 patients with maturation arrest
  • Comparison of allele frequencies with GnomAD v.3.1.2 male population database
  • Utilization of exome data from a national genetic disease evaluation center for validation
  • Higher frequencies of rs1800734 allele were observed in the patient group than in the GnomAD database
  • Findings suggest a significant association between rs1800734 and nonobstructive azoospermia

Abstract

Background: Male infertility is increasingly being conceived as a biomarker of general male health status other than being a significant reproductive health issue. Nonobstructive azoospermia (NOA) patients have the worst health status impairment as well as highest risk of developing cancer. It’s well known that cancer susceptibility gene, MLH1 have roles in homologous recombination during meiosis. Mlh1 mutant mice have azoospermia with meiotic arrest. Aim: We aimed to identify risk alleles in MLH1 gene in males with nonobstructive azoospermia related maturation arrest (MA) to investigate further whether this cancer susceptibility gene is also related to male infertility. Patients and Methods: MLH1 variants were genotyped in 42 patients with MA. The variants of interest then compared to GnomAD v.3.1.2 (non-cancer) male population database and to the repository exome data of a national genetic disease evaluation center (NGDEC). Results: rs1800734 allele frequencies were significantly higher in the patient group compared to GnomAD (p

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Cite This Study

Ülger et al. (2026) studied this question.

synapsesocial.com/papers/69c8c3cede0f0f753b39ed27https://doi.org/10.65092/autfm.1767777
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over1996 · 840 citations
  2. 2A Core Promoter and a Frequent Single-Nucleotide Polymorphism of the Mismatch Repair GenehMLH11999 · 97 citations
  3. 3Infertility as a proxy of general male health: results of a cross-sectional survey2015 · 136 citations
  4. 4Evidence for heritable predisposition to epigenetic silencing of MLH12007 · 79 citations
  5. 5Haplotype defined by the MLH1-93G/A polymorphism is associated with MLH1 promoter hypermethylation in sporadic colorectal cancers2014 · 24 citations