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Investigación Clínica

versión impresa ISSN 0535-5133versión On-line ISSN 2477-9393

Resumen

MORALES-MACHIN, Alisandra et al. C677T polymorphism of the methylentetrahydrofolate reductase gene as risk factor in women with recurrent abortion. Invest. clín [online]. 2009, vol.50, n.3, pp.327-333. ISSN 0535-5133.

The pathogenesis of recurrent spontaneous abortion is multifactorial, presumably involving the interaction of several genetic and environmental factors. The methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism has been implicated as risk factor for recurrent spontaneous abortion (RA). The main objective of this research was to investigate the association between the C677T polymorphism of the MTHFR gene as a genetic risk factor for idiopathic RA. Molecular analysis was performed in 80 DNA samples from 30 patients with RA and among 50 healthy control subjects. Using the Polymerase Chain Reaction (PCR), a 198 bp (bases pairs) fragment, was digested with the restriction enzyme HinfI, which can recognize the C > T substitution responsible for the polymorphism. 677T MTHFR allele frequencies for group with RA and the control group were 35% and 33%, respectively and 677C MTHFR allele frequencies were 65% and 67%, respectively. There was no significant difference in allele frequency between these two groups. The data presented in this study fail to support the relationship between MTHFR C677T polymorphism and risk in women with RA.

Palabras clave : MTHFR C677T polymorphism; recurrent unexplained spontaneous abortion.

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