Evidence map›Paper›PMID 40531769›Full record

ArticleRevista da Associacao Medica Brasileira (1992)2025

Genotyping of the gene polymorphisms FASL 844C/T and FAS 670A/G in patients with idiopathic infertility in Iraq.

Abbas Ali Manshd, Mohammed Ali Alaboudi, Abbas Abdulameer Al-Raad

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Article in Revista da Associacao Medica Brasileira (1992), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Abbas Ali ManshdSawa University, College of Health and Medical Technology, Department of Medical Laboratories - Al-Muthanna, Iraq.ORCID http://orcid.org/0000-0002-0991-5077
Mohammed Ali AlaboudiSawa University, College of Health and Medical Technology, Department of Medical Laboratories - Al-Muthanna, Iraq.ORCID http://orcid.org/0009-0005-4719-0889
Abbas Abdulameer Al-RaadSawa University, College of Health and Medical Technology, Department of Medical Laboratories - Al-Muthanna, Iraq.ORCID http://orcid.org/0000-0001-6893-860X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe failure to conceive following 12 months of unprotected intercourse is referred to as infertility. About 35% of the instances include women and 30% involve men.

aimThe aim of this study was to investigate the gene polymorphisms FASL-844C/T and FAS-670A/G in the promoter region to evaluate susceptibility to male infertility.

methodsWe have investigated single-nucleotide polymorphisms of FAS-670A/G gene and FASL-844C/T gene in 100 subjects. A total of 50 male patients with infertility constituted the infertility group and another group consisting of 50 apparently healthy individuals comprised the control group.

resultsThe prevalence rate of FAS-670A/G gene polymorphism was statistically significant among both azoospermia and oligospermia subgroups, the homozygous mutant genotype GG (p=0.014 and p=0.043), and mutant allele G (p=0.001 and p=0.004), respectively. Also, FASL-844C/T gene polymorphism was statistically significant among both azoospermia and oligospermia subgroups, the homozygous mutant genotype TT (p=0.032 and p=0.032), and mutant allele T (p=0.007 and p=0.002), respectively.

conclusionsFAS homozygous mutant genotype (GG) and FASL homozygous mutant genotype (TT) act as etiologic factors in male infertility.

Indexed as

Fas Ligand Proteinfas ReceptorInfertility, MalePolymorphism, Single NucleotideAdultAzoospermiaCase-Control StudiesGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansIraqMaleOligospermiaFASLG protein, humanFas Ligand Proteinfas Receptor

Identifiers

PMID40531769
PMCPMC12172534

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