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04 August 2019 : Clinical Research  

Targeted Next-Generation Sequencing Identifies Novel Sequence Variations of Genes Associated with Nonobstructive Azoospermia in the Han Population of Northeast China

Xiangyin Liu1BCE, Qi Xi1BDF, Leilei Li1BF, Qiyuan Wang2CF, Yuting Jiang1BD, Hongguo Zhang1EF, Ruizhi Liu1CFG, Ruixue Wang3AG*

DOI: 10.12659/MSM.915375

Med Sci Monit 2019; 25:5801-5812


BACKGROUND: This study aimed to screen common and low-frequency variants of nonobstructive azoospermia (NOA)-associated genes, and to construct a database for NOA-associated single nucleotide variants (SNVs).

MATERIAL AND METHODS: Next-generation sequencing of 466 NOA-associated genes was performed in 34 patients with NOA (mean age, 29.06±4.49 years) and 40 sperm donors (mean age, 25.08±5.75 years) from the Han population of northeast China. The SNV database was constructed by summarizing NOA non-negatively-associated SNVs showing statistical differences between NOA cases and controls, and then selecting low-frequency variants using Baylor’s pipeline, to identify statistically valid SNVs.

RESULTS: There were 65 SNVs identified that were significantly different between both groups (p<0.05). Five genetic variants showed positive correlations with NOA: MTRR c.537T>C (rs161870), odds ratios (OR), 3.686, 95% confidence interval (CI), 1.228–11.066; MTRR, c.1049A>G (rs162036), OR, 3.686, 95% CI, 1.228–11.066; PIWIL1, c.1580G>A (rs1106042), OR, 4.737, 95% CI, 1.314–17.072; TAF4B, c.1815T>C (rs1677016), OR, 3.599, 95% CI, 1.255–10.327; and SOX10 c.927T>C (rs139884), OR, 3.192, 95% CI, 1.220–8.353. Also, 52 NOA non-negatively associated SNVs and 39 SNVs were identified by Baylor’s pipeline and selected for the SNV database.

CONCLUSIONS: Five genetic variants were shown to have positive correlations with NOA. The SNV database constructed contained NOA non-negatively associated SNVs and low-frequency variants. This study showed that this approach was an effective strategy to identify risk alleles of NOA.

Keywords: azoospermia, Gene Library, High-Throughput Nucleotide Sequencing, Polymorphism, Single Nucleotide, Alleles, Argonaute Proteins, Asians, ethnicity, Ferredoxin-NADP Reductase, Gene Frequency, Genetic Predisposition to Disease, genetic variation, Genotype, Infertility, Male, Odds Ratio, SOXE Transcription Factors, Sequence Analysis, DNA, Spermatogenesis, TATA-Binding Protein Associated Factors, Transcription Factor TFIID

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DOI: 10.12659/MSM.943911

Med Sci Monit 2024; 30:e943911


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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750