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Updated: Mar 1, 2026

Flow Cytometric Analysis of Biomarkers for Detecting Human Sperm Functional Defects
Published on: April 21, 2022
Aberrations in sperm DNA methylation patterns are associated with abnormalities in semen parameters of subfertile
Mohammed Laqqan1, Erich-Franz Solomayer1, Mohamed Hammadeh1
1Department of Obstetrics, Gynecology & Assisted Reproduction Laboratory, Saarland University, Homburg, Germany.
Abstract:
Infertility affects about 15% of couples worldwide, with approximately 7% of males suffering from infertility problems. This study was designed to assess the relationship between alterations in sperm DNA methylation patterns and semen parameters in subfertile males. Of a total of 108 males, 30 samples were subjected to 450K BeadChip arrays to evaluate the variation in DNA methylation level between cases and controls. Three CpG sites showed the highest difference in methylation levels (cg09737095, cg14271023, and cg17662493), which are located in the KCNJ5, MLPH, and SMC1β genes, respectively; these were selected for further analysis using deep bisulfite sequencing in 78 independent samples (21 proven fertile "controls", and 57 subfertile "cases"). The results of a validation study showed that variation in methylation levels was found in more than one CpG site: there was a significant decrease in methylation levels at six CpGs (CpG1, CpG3, CpG4, CpG6, CpG7, and CpG8) in the KCNJ5 gene-related amplicon (p≤0.001, p≤0.009, p≤0.007, p≤0.007, p≤0.020, and p≤0.016, respectively), and at (CpG1, CpG2, and CpG4) in the MLPH gene-related amplicon (p≤0.003, p≤0.005, and p≤0.0001, respectively), while there was a significant increase in the methylation level at six out of eight CpGs in the SMC1β gene-related amplicon in cases compared to controls. Our results show that three CpGs have a significant difference in sperm DNA methylation levels in subfertile males compared to proven fertile males.
Insights
Sperm DNA methylation patterns are altered in subfertile males. Specific changes in KCNJ5, MLPH, and SMC1β genes were identified, offering potential biomarkers for male infertility.
Area of Science:
- Epigenetics
- Reproductive Biology
- Genetics
Background:
- Infertility affects 15% of couples globally, with male factors contributing significantly.
- Approximately 7% of males experience infertility issues.
- Sperm DNA methylation is crucial for male fertility.
Purpose of the Study:
- To investigate the relationship between sperm DNA methylation patterns and semen parameters in subfertile males.
- To identify specific DNA methylation alterations associated with male infertility.
Main Methods:
- Utilized 450K BeadChip arrays to assess DNA methylation variations in 30 males (cases vs. controls).
- Selected three key CpG sites (in KCNJ5, MLPH, SMC1β genes) for validation.
- Employed deep bisulfite sequencing for validation in 78 independent samples (57 subfertile, 21 fertile).
Main Results:
- Identified significant differences in DNA methylation levels at specific CpG sites in subfertile males.
- Observed decreased methylation in KCNJ5 and MLPH gene regions and increased methylation in the SMC1β gene region.
- Three CpG sites (cg09737095, cg14271023, cg17662493) showed the highest methylation level differences.
Conclusions:
- Sperm DNA methylation patterns are significantly altered in subfertile males compared to fertile controls.
- Specific gene methylation changes (KCNJ5, MLPH, SMC1β) may serve as potential biomarkers for male infertility.
- Further research is warranted to explore the functional implications of these epigenetic alterations.
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