Publication | Open Access
Combined effect of GSTM1 gene deletion, GSTT1 gene deletion and MTHFR C677T mutation in male infertility
16
Citations
21
References
2010
Year
FertilityGstt1 Gene DeletionGeneticsGenetic EpidemiologyReproductive HealthGynecologyHuman PolymorphismMolecular GeneticsReproductive BiologyReproductive MedicineMale InfertilityPublic HealthGstt1 Gene DeletionsGenetic PredispositionInfertilityAndrologyGenetic VariationHuman ReproductionDouble Gstm1/gstt1 DeletionGenetic DisorderMedicineGstm1 Gene Deletion
The aim of the study was to investigate the association between the GSTM1 and GSTT1 gene deletion and MTHFR C677T mutation and male infertility. The study has encompassed 52 infertile and 56 fertile males. Genotype distributions of GSTM1 and GSTT1 gene deletions and the MTHFR C677T mutation did not differ significantly among the analyzed groups, however, a difference in distribution of certain genotype combinations was observed. The obtained results indicate that carriers of double GSTM1/GSTT1 deletion and the MTHFR 677CC genotype are at higher risk of infertility than carriers of any other combination of genotypes (OR 3.5, 95%CI 0.68-18.30). .
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