The possible role of NF‐κB1 Rs28362491 polymorphism in male fertility of Egyptian population
Male reproductive impairment is responsible for at least 50% of cases of couple infertility. Nuclear factor‐kappa B (NF‐κB) has been functionally linked to germ cell apoptosis, which may affect human fertility. The aim of this study was to determine the association between the rs28362491 SNP of the...
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Published in | Andrologia Vol. 52; no. 7; pp. e13659 - n/a |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
01.08.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Male reproductive impairment is responsible for at least 50% of cases of couple infertility. Nuclear factor‐kappa B (NF‐κB) has been functionally linked to germ cell apoptosis, which may affect human fertility. The aim of this study was to determine the association between the rs28362491 SNP of the NF‐κB1 gene and infertility in Egyptian men. In this case–control study, semen and blood samples of 247 infertile men, constituting the case group, and of 113 fertile healthy men as the control group were analysed. All study participants were genotyped for polymorphism of the NF‐κB1 gene (rs28362491) by the polymerase chain reaction—restriction fragment length polymorphism (PCR‐RFLP) technique. Heterozygous I/D genotype of the NF‐κB1 rs28362491 polymorphism was associated with a significantly lower risk of poor semen quality, including asthenozoospermia, astheno–teratozoospermia, and oligo–astheno–teratozoospermia, when compared to I/I genotype (odds ratio = 0.25, 0.26, 0.18, p < .0005, <.0005, <.0005) respectively. Overall, the presence of the D allele was associated with a significantly decreased risk of poor sperm quality as compared to the I allele (odds ratio = 0.56, 0.64, 0.49, p = .050, .038, .001). In conclusion, these results suggest that heterozygosity of the NF‐κB1 gene may play a protecting role against male infertility in Egyptians. |
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ISSN: | 0303-4569 1439-0272 |
DOI: | 10.1111/and.13659 |