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© 2002 The American Society for Nutritional Sciences J. Nutr. 132:1872-1878, 2002


Human Nutrition and Metabolism

Vitamin B-12 Status Is Inversely Associated with Plasma Homocysteine in Young Women with C677T and/or A1298C Methylenetetrahydrofolate Reductase Polymorphisms1

Lynn B. Bailey2, Robert L. Duhaney, David R. Maneval, Gail P.A. Kauwell, Eoin P. Quinlivan, Steven R. Davis, Aisha Cuadras, Alan D. Hutson* and Jesse F. Gregory, III.

Food Science and Human Nutrition Department, and * Department of Statistics, University of Florida, Gainesville, FL 32611

2To whom correspondence should be addressed. E-mail: LBBailey{at}mail.IFAS.UFL.EDU.

Methylenetetrahydrofolate reductase (MTHFR) polymorphisms may negatively influence one-carbon metabolism and increase health risks in women of reproductive age. The effect of MTHFR single nucleotide polymorphisms at bp 677 and/or 1298 and differences in folate and vitamin B-12 status on plasma homocysteine concentration in women of reproductive age (20–30 y; n = 186) were investigated. From the multivariate regression model, homozygotes (n = 23) for the C677T MTHFR variant had plasma homocysteine concentrations that were higher (P < 0.05) than those observed in the other 5 genotype groups, including those who were heterozygous for both variants (677CT/1298AC; n = 32). Plasma homocysteine was negatively associated with plasma vitamin B-12 concentration (P = 0.015) and serum folate (P = 0.049), with the degree of correlation between plasma vitamin B-12 and homocysteine concentrations dependent on MTHFR genotype. The C677T and A1298C MTHFR polymorphisms were significant predictors (P < 0.05) of plasma homocysteine when regression analysis was used to model plasma homocysteine concentration as a function of genotype, supplement use, serum folate and plasma vitamin B-12 concentration. Plasma homocysteine decreased as vitamin B-12 concentration increased (P = 0.0005) in individuals who were heterozygous for both the C677T and A1298C variants with nonsignificant trends (P = 0.114–0.128) in individuals homozygous for either the C677T or A1298C variants. In contrast, within the group of individuals with the wild-type genotype for both the C677T and A1298C MTHFR variants, homocysteine was not associated with changes in plasma vitamin B-12 concentrations. These data suggest that enhancing vitamin B-12 status may significantly decrease homocysteine in young women with C677T and/or A1298C MTHFR polymorphisms, even when vitamin B-12 concentrations are within the normal range.


KEY WORDS: • vitamin B-12 • methylenetetrahydrofolate reductase • polymorphisms • homocysteine • folate • women




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