The methylenetetrahydrofolate reductase 677C→T polymorphism and dietary folate restriction affect plasma one-carbon metabolites and red blood cell folate concentrations and distribution in women

被引:29
作者
Davis, SR
Quinlivan, EP
Shelnutt, KP
Maneval, DR
Ghandour, H
Capdevila, A
Coats, BS
Wagner, C
Selhub, J
Bailey, LB
Shuster, JJ
Stacpoole, PW
Gregory, JF [1 ]
机构
[1] Univ Florida, Coll Med, Inst Food & Agr Sci, Dept Food Sci & Human Nutr, Gainesville, FL 32611 USA
[2] Univ Florida, Coll Med, Dept Med, Div Endocrinol & Metab, Gainesville, FL 32611 USA
[3] Univ Florida, Coll Med, Dept Biochem & Mol Biol, Gainesville, FL 32611 USA
[4] Univ Florida, Coll Med, Dept Stat, Gainesville, FL 32611 USA
[5] Tufts Univ, USDA, Human Nutr Res Ctr Aging, Jean Mayer US Dept Agr, Boston, MA 02111 USA
[6] Vanderbilt Univ, Dept Biochem, Nashville, TN 37232 USA
[7] Dept Vet Affairs Med Ctr, Nashville, TN 37232 USA
关键词
homocysteine; methionine; S-adenosylmethionine; S-adenosylhomocysteine; women;
D O I
10.1093/jn/135.5.1040
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Whether folate status and the methylenetetrahydrofolate reductase (MTHFR) 677C -> T polymorphism interact to affect methionine-cycle metabolite concentrations is uncertain. We evaluated the effects of dietary folate restriction on relations among folate status indices and plasma concentrations of methionine cycle metabolites in women with the MTHFR 677 C/C and T/T genotypes. Healthy, normohomocysteinemic women (n = 18; 20-30 y old) of adequate B vitamin status, and equally divided according to MTHFR 677C -> T genotype (9 C/C and 9 T/T) were recruited. Folate status indices and methionine cycle metabolites were measured in blood samples collected at baseline and after 7 wk of dietary folate restriction (115 mu g dietary folate equivalents/d). Significant negative correlations between plasma total homocysteine concentrations and total or 5-methyl folate concentrations (P = 0.041 and 0.023, respectively) in RBCs were found only in T/T subjects. Formylated folates were detected in RBCs of T/T subjects only, and their abundance was predictive of plasma total homocysteine concentration despite no significant alteration by folate restriction. Plasma concentrations of S-adenosylmethionine and S-adenosylhomocysteine were not significantly affected by dietary folate restriction and the MTHFR 677 T/T genotype. In conclusion, plasma total homocysteine concentrations in subjects with the MTHFR 677 T/T genotype were inversely related to 5-methyl folate concentrations and directly related to formylated folate concentrations in RBCs, even though the latter were not significantly affected by moderate folate restriction.
引用
收藏
页码:1040 / 1044
页数:5
相关论文
共 32 条
[1]  
Bagley PJ, 2000, CLIN CHEM, V46, P404
[2]   A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells [J].
Bagley, PJ ;
Selhub, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13217-13220
[3]   Polymorphisms of methylenetetrahydrofolate reductase and other enzymes: Metabolic significance, risks and impact on folate requirement [J].
Bailey, LB ;
Gregory, JF .
JOURNAL OF NUTRITION, 1999, 129 (05) :919-922
[4]   A QUANTITATIVE ASSESSMENT OF PLASMA HOMOCYSTEINE AS A RISK FACTOR FOR VASCULAR-DISEASE - PROBABLE BENEFITS OF INCREASING FOLIC-ACID INTAKES [J].
BOUSHEY, CJ ;
BERESFORD, SAA ;
OMENN, GS ;
MOTULSKY, AG .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (13) :1049-1057
[5]   FOLIC-ACID RESPONSIVE POSTMENOPAUSAL HOMOCYSTEINEMIA [J].
BRATTSTROM, LE ;
HULTBERG, BL ;
HARDEBO, JE .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1985, 34 (11) :1073-1077
[6]   Measurement of plasma S-adenosylmethionine and S-adenosylhomocysteine as their fluorescent isoindoles [J].
Capdevila, A ;
Wagner, C .
ANALYTICAL BIOCHEMISTRY, 1998, 264 (02) :180-184
[7]   The effect of 677C → T and 1298A → C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects [J].
Chango, A ;
Boisson, F ;
Barbé, F ;
Quilliot, D ;
Droesch, S ;
Pfister, M ;
Fillon-Emery, N ;
Lambert, D ;
Frémont, S ;
Rosenblatt, DS ;
Nicolas, JP .
BRITISH JOURNAL OF NUTRITION, 2000, 83 (06) :593-596
[8]   Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease [J].
Christensen, B ;
Frosst, P ;
LussierCacan, S ;
Selhub, J ;
Goyette, P ;
Rosenblatt, DS ;
Genest, J ;
Rozen, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (03) :569-573
[9]   Homocysteine and risk of ischemic heart disease and stroke -: A meta-analysis [J].
Clarke, R ;
Collins, R ;
Lewington, S ;
Donald, A ;
Alfthan, G ;
Tuomilehto, J ;
Arnesen, E ;
Bonaa, K ;
Blacher, J ;
Boers, GHJ ;
Bostom, A ;
Bots, ML ;
Grobee, DE ;
Brattström, L ;
Breteler, MMB ;
Hofman, A ;
Chambers, JC ;
Kooner, JS ;
Coull, BM ;
Evans, RW ;
Kuller, LH ;
Evers, S ;
Folsom, AR ;
Freyburger, G ;
Parrot, F ;
Genst, J ;
Dalery, K ;
Graham, IM ;
Daly, L ;
Hoogeveen, EK ;
Kostense, PJ ;
Stehouwer, CDA ;
Hopknis, PN ;
Jacques, P ;
Selhub, J ;
Luft, FC ;
Jungers, P ;
Lindgren, A ;
Lolin, YI ;
Loehrer, F ;
Fowler, B ;
Mansoor, MA ;
Malinow, MR ;
Ducimetiere, P ;
Nygard, O ;
Refsum, H ;
Vollset, SE ;
Ueland, PM ;
Omenn, GS ;
Beresford, SAA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (16) :2015-2022
[10]  
Clarke S, 2001, HOMOCYSTEINE IN HEALTH AND DISEASE, P63