Evidence map›Paper›PMID 29935069›Full record

ArticleInternational journal of fertility & sterility2018

IL-1ɑ C376A Transversion Variant and Risk of Idiopathic Male Infertility in Iranian Men: A Genetic Association Study.

Tayyebeh Zamani-Badi, Mohammad Karimian, Abolfazl Azami Tameh, Hossein Nikzad

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Article in International journal of fertility & sterility, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
1.2field-weighted citation impact, top 18% of its field
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3 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Tayyebeh Zamani-BadiGametogenesis Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Mohammad KarimianAnatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Abolfazl Azami TamehAnatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Hossein NikzadAnatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, Iran. eLECTRONIC ADDRESS: hnikzad10@gmail.com.
Kashan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

bachgroundIL-1α produced by Sertoli cells is considered to act as a growth factor for spermatogonia. In this study, we investigated the association of the C376A polymorphism in IL-1α with male infertility in men referring to the Kashan IVF Center. MATERIALS AND

methodsIn this case-control study, 2 ml of blood was collected from 230 fertile and 230 infertile men. After DNA extraction, the C376A variant was genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). In addition, the molecular effects of the C376A transversion were analysed using bioinformatics tools.

resultsA significant association was observed between the homozygous genotype CC with male infertility [odds ratio (OR)=1.97, 95% confidence interval (CI)=1.14-3.41, P=0.016)]. Carriers of C (AC+CC) showed a similar risk for male infertility (OR=1.78, 95% CI=1.06-2.99, P=0.030). Also, allelic analysis showed that the C allele is associated with male infertility (OR=1.43, 95% CI=1.09-1.88, P=0.011). In sub-group analysis, we found that the AC genotype is associated with asthenozoospermia (OR=2.38, 95% CI=1.03-5.53, P=0.043). In addition, carriers of C were at high risk for asthenozoospermia (OR=2.25, 95% CI=1.01-4.10, P=0.047). Also, C allele was significantly associated with oligozoospermia (OR=1.44, 95% CI=1.01-2.06, P=0.049) and non-obstructive azoospermia (OR=1.67, 95% CI =1.04-2.68, P=0.034). Finally, in silico analysis showed that the C376A polymorphism could alter splicing especially in the acceptor site.

conclusionThis is the preliminary report on the association of IL-1α C376A polymorphism with male infertility in the Kashan population. This association shows that the IL-1α gene may be a biomarker for male infertility, and therefore needs additional investigations in future studies to validate this.

Indexed as

Genetic PolymorphismInterleukin-1αMale InfertilitySpermatogenesis

Identifiers

PMID29935069
PMCPMC6018182
OpenAlexW2943014206

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