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High Incidence of Two Methylenetetrahydrofolate Reductase Mutations (C677T and A1298C) in Hispanics
11
Citations
29
References
2003
Year
GeneticsGenetic EpidemiologyHuman PolymorphismMolecular BiologyPathologyMolecular GeneticsGenomicsClinical GeneticsPublic HealthVariant InterpretationMethylenetetrahydrofolate Reductase MutationsCardiovascular EpidemiologyMthfr MutationsGenetic FactorGenetic VariationEpidemiologyGenetic DeterminantGenetic DisorderMedical GeneticsHigh IncidenceMedicineCoagulation Factors IiCardiovascular GeneticsWomen's HealthMutagenesisAmerican Hispanics
Mutations in the 5,10-methylenetetrahydrofolate reductase (MTHFR) and coagulation factors II and V genes have been found at high frequencies in European and American Caucasian populations and are associated with increased risk for thrombophilia, premature coronary artery disease, and a variety of adverse pregnancy outcomes. Hispanic populations in the United States exhibit high levels of some of these conditions, so we initiated a population-based study to determine the frequency of these mutations (MTHFR C677T and A1298C, Factor II G20210A and Factor V G1691A) in this group. We find comparable frequencies of the Factors II and V mutations, but a high incidence of the two MTHFR mutations in a diverse sample of American Hispanics compared to those reported in Caucasians. Prospective studies of Hispanic women with these mutations and pregnancy outcomes will establish if there is a causal relationship.
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