Association of PRMT6, PEX10 and SOX5 genetic variants with idiopathic male infertility: Evidence from North Macedonian population and an updated meta-analysis
نویسندگان
چکیده
PRMT6, PEX10 and SOX5 genetic variants were identified as male infertility-associated loci in a genome-wide association study further validated various populations. Still, the results of previous case-control studies varied, which could be due to differences participants? ethnic backgrounds. The main purpose present was evaluate supposed these with idiopathic infertility North Macedonian population. Furthermore, we aimed conduct systematic quantitative data synthesis includes on same issue other European non-European A total 137 men from Macedonia diagnosed 130 age-matched fertile controls included study. PCR-RFLP method used for genotyping. Meta-analysis performed by OpenMeta-analyst statistical software. Variants rs10842262 SOX5, rs2477686 rs12097821 PRMT6 showed lack statistically significant genotype distributions between control group. allele G frequency significantly increased poor sperm concentration (P= 0.024, OR = 2.10, 95%CI 1.08-4.06). risk infertility. Our obtained population supported reports involvement basis meta-analysis confirmed occurrence. additional are needed support findings.
منابع مشابه
AB186. Association study between polymorphisms of PRMT6, PEX10, SOX5, and non-obstructive azoospermia in the Han Chinese population
A previous genomewide association study of nonobstructive azoospermia (NOA) in the Han Chinese population identified three risk loci (rs12097821, rs2477686, and rs10842262) and provided strong evidence for a genetic influence in male infertility. However, recently, a follow-up study of these single nucleotide polymorphism (SNP) loci in the Japanese population showed that none of them were signi...
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ژورنال
عنوان ژورنال: Genetika
سال: 2023
ISSN: ['0016-6758']
DOI: https://doi.org/10.2298/gensr2301355r