Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts

被引:59
作者
Boyles, Abee L. [1 ]
Wilcox, Allen J. [1 ]
Taylor, Jack A. [1 ]
Meyer, Klaus [2 ,3 ]
Fredriksen, Ase [2 ,3 ]
Ueland, Per Magne [2 ,3 ]
Drevon, Christian A. [4 ]
Vollset, Stein Emil [5 ]
Lie, Rolv Terje [5 ]
机构
[1] NIEHS, NIH, Epidemiol Branch, Durham, NC 27709 USA
[2] Univ Bergen, Pharmacol Sect, Inst Med, Bergen, Norway
[3] Haukeland Hosp, N-5021 Bergen, Norway
[4] Univ Oslo, Inst Basic Med Sci, Dept Nutr, Fac Med, Oslo, Norway
[5] Univ Bergen, Dept Publ Hlth & Primary Hlth Care, Sect Epidemiol & Med Stat, Bergen, Norway
关键词
alleles; cleft lip; cleft palate; dietary supplements; folic acid; metabolism; humans; single nucleotide polymorphisms;
D O I
10.1002/ajmg.a.32162
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Folare metabolism plays a critical role in embryonic development. Prenatal folate supplementation reduces the risk of neural tube defects and probably oral facial clefts. Previous studies of related metabolic genes have associated polymorphisms in cystathionine-beta-synthase (CBS) and 5,10-methylenetetrahydrofolate reductase (MTHFR) with cleft risk. We explored associations between genes related to one-carbon metabolism and clefts in a Norwegian population-based study that included 362 families with cleft lip with Or without cleft palate (CUP) and 191 families with cleft palate only, (CPO). We previously showed a 39% reduction in risk of CUP with folic acid supplementation in this population. In the present study we genotyped 12 polymorphisms in nine genes related to one-carbon metabolism and looked for associations of clefting risk with fetal polymorphisms, maternal polymorphisms, as well as parent-of-origin effects, using combined likelihood-ratio tests (LRT). We also stratified by maternal periconceptional intake of folic acid (> 400 mu g) to explore gene-exposure interactions. We found a reduced risk of CUP with mothers who carried the CBS C699T variant (rs234706); relative risk was 0.94 with one copy of the T allele (95% Cl 0.63-1.4) and 0.50 (95% Cl 0.26-0.96) with two copies (P=0.008). We found no evidence of interaction of this variant with folate status. We saw no evidence of risk from the MTHFR C677T variant (rs1801133) either overall or after stratifying by maternal folate intake. No associations were found between any of the polymorphisms and CPO. Genetic variations in the nine metabolic genes examined here do not confer a substantial degree of risk for clefts. Published 2008 Wiley-Liss. Inc.(dagger)
引用
收藏
页码:440 / 449
页数:10
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