Abstract
Objectives. Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene are thought to be associated with a varying risk of cervical dysplasia. The purpose of this trial was to study the role of the two common functional MHTFR polymorphisms in a large multiracial population at risk for cervical dysplasia and cancer. Methods. This is a nested case–control study of 376 subjects obtained from cohorts enrolled in an ongoing prospective cervical carcinogenesis protocol. Cases included invasive cancers ( n = 51), and high ( n = 50) and low ( n = 50) grade dysplasia. There were 225 normal controls. Functional MTHFR 677C→T and 1298A→C genotypes were identified. Follow-up cytology data were reviewed for the control subjects from the time of study entry until August 2004. Results. There is a significant racial difference in allele frequency of the 677C→T polymorphism ( P < 0.005). African–American women had an extremely low prevalence of the 677T allele (8%). There was no significant difference in the frequency of the 677T allele between cases and controls. There is no racial difference in allele frequency of the 1298A→C polymorphism. Also, no significant difference was found between cases and controls. Of the 51 cancers, no case was homozygous for both aberrant polymorphisms (677T, 1298C), and only 3 cases were heterozygous for both. Follow-up data were available for 129 of 225 control subjects (57%). Only 15 (12%) have had a subsequent abnormal pap, and there was no association with the 677C→T polymorphism. Conclusions. We confirm a significant difference in the 677T allele frequencies among racial groups. However, there is no association of either the 677C→T or 1298A→C polymorphisms in cervical carcinogenesis. There is no role of the combined polymorphism effect in cervical cancer or evidence of prediction for future Pap abnormalities.
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