Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?

被引:140
作者
van Rooij, IALM
Vermeij-Keers, C
Kluijtmans, LAJ
Ocké, MC
Zielhuis, GA
Goorhuis-Brouwer, SM
van der Biezen, JJ
Kuijpers-Jagtman, AM
Steegers-Theunissen, RPM
机构
[1] Univ Med Ctr Nijmegen, Dept Epidemiol & Biostat, NL-6500 HB Nijmegen, Netherlands
[2] Univ Med Ctr Nijmegen, Dept Obstet & Gynecol, Nijmegen, Netherlands
[3] Erasmus Univ, Med Ctr Rotterdam, Inst Plast Surg, Rotterdam, Netherlands
[4] Univ Med Ctr Nijmegen, Lab Pediat & Neurol, Nijmegen, Netherlands
[5] Natl Inst Publ Hlth & Environm, Dept Chron Dis Epidemiol, NL-3720 BA Bilthoven, Netherlands
[6] Univ Groningen Hosp, Dept Speech & Languages, Groningen, Netherlands
[7] Med Ctr Leeuwarden, Dept Plast Surg, Leeuwarden, Netherlands
[8] Univ Med Ctr Nijmegen, Dept Orthodont & Oral Biol, Nijmegen, Netherlands
关键词
abnormalities; folic acid; genes; nutrition; pregnancy; vitamins;
D O I
10.1093/aje/kwg005
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Periconceptional folic acid supplementation may reduce the risk of cleft lip with or without cleft palate (CL(P)). Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene reduce availability of 5-methyltetrahydrofolate, the predominant circulating form of folate. To determine the effect of MTHFR C677T and MTHFR A 1298C genotypes and haplotypes on CL(P) risk and the interaction with maternal periconceptional dietary folate and folic acid supplement intake, the authors conducted a case-control triad study in the Netherlands (1998-2000) among 179 CL(P) and 204 control families. Infant and parental MTHFR C677T and MTHFR A1298C genotypes and haplotypes were not associated with CL(P) risk in the case-control and transmission disequilibrium test analyses. Mothers carrying the MTHFR 677TT genotype and who either did not use folic acid supplements periconceptionally or had a low dietary folate intake, or both, had an increased risk of delivering a CL(P) child (odds ratio (OR)=5.9, 95% confidence interval (CI): 1.1, 30.9; OR=2.8, 95% CI: 0.7, 10.5; OR=10.0, 95% CI: 1.3, 79.1, respectively). No supplement use, low dietary folate intake, and maternal MTHFR 1298CC genotype increased the risk of CL(P) offspring almost sevenfold (OR=6.5, 95% CI: 1.4, 30.2). Thus, the detrimental effect of low periconceptional folate intake on the risk of giving birth to a CL(P) child was more pronounced in mothers with the MTHFR 677TT or MTHFR 1298CC genotype.
引用
收藏
页码:583 / 591
页数:9
相关论文
共 41 条
[1]   Dextromethorphan and other N-methyl-D-aspartate receptor antagonists are teratogenic in the avian embryo model [J].
Andaloro, VJ ;
Monaghan, DT ;
Rosenquist, TH .
PEDIATRIC RESEARCH, 1998, 43 (01) :1-7
[2]   Testing candidate genes for non-syndromic oral clefts using a case-parent trio design [J].
Beaty, TH ;
Hetmanski, JB ;
Zeiger, JS ;
Fan, YT ;
Liang, KY ;
VanderKolk, CA ;
McIntosh, I .
GENETIC EPIDEMIOLOGY, 2002, 22 (01) :1-11
[3]  
Blanton SH, 2000, AM J MED GENET, V92, P370, DOI 10.1002/1096-8628(20000619)92:5<370::AID-AJMG17>3.0.CO
[4]  
2-4
[5]   DIETARY-FOLATE AND NONNEURAL MIDLINE BIRTH-DEFECTS - NO EVIDENCE OF AN ASSOCIATION FROM A CASE-CONTROL STUDY IN WESTERN-AUSTRALIA [J].
BOWER, C ;
STANLEY, FJ .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (05) :647-650
[6]  
Briggs R M, 1976, Clin Plast Surg, V3, P647
[7]   PREVENTION OF CONGENITAL-ABNORMALITIES BY PERICONCEPTIONAL MULTIVITAMIN SUPPLEMENTATION [J].
CZEIZEL, AE .
BRITISH MEDICAL JOURNAL, 1993, 306 (6893) :1645-1648
[8]   Continuity and change in women's weight orientations and lifestyle practices through pregnancy and the postpartum period: the influence of life course trajectories and transitional events [J].
Devine, CM ;
Bove, CF ;
Olson, CM .
SOCIAL SCIENCE & MEDICINE, 2000, 50 (04) :567-582
[9]   5,10-methylenetetrahydrofolate reductase genotype determines the plasma homocysteine-lowering effect of supplementation with 5-methyltetrahydrofolate or folic acid in healthy young women [J].
Fohr, IP ;
Prinz-Langenohl, R ;
Brönstrup, A ;
Bohlmann, AM ;
Nau, H ;
Berthold, HK ;
Pietrzik, K .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 75 (02) :275-282
[10]  
*FOOD NUTR COUNC, 1993, FOLL REP REL FOL AC