Am J Epidemiol 2003; 157:1083-1091.
Copyright © 2003 by Johns
Hopkins Bloomberg School of Public Health
ORIGINAL CONTRIBUTIONS |
Exploring the Effects of Methylenetetrahydrofolate Reductase Gene Variants C677T and A1298C on the Risk of Orofacial Clefts in 261 Norwegian Case-Parent Triads
1 Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
2 Section for Medical Statistics and Medical Birth Registry of Norway, University of Bergen, Bergen, Norway.
3 Epidemiology Branch, National Institute of Environmental Health Sciences, Durham, NC.
4 Department of Pediatrics, University of Iowa, Iowa City, IA.
5 Locus for Homocysteine and Related Vitamins, University of Bergen, Bergen, Norway.
6 Institute for Nutrition Research, University of Oslo, Oslo, Norway.
7 Department of Plastic Surgery, Haukeland University Hospital, Bergen, Norway.
8 Department of Plastic Surgery, Rikshospitalet, Oslo, Norway.
Folic acid and the methylenetetrahydrofolate reductase (MTHFR) gene have both been implicated in the etiology of orofacial clefts. The authors selected 261 case-parent triads (173 cases with cleft lip with or without cleft palate (CL/P) and 88 cases with cleft palate only (CPO)) from a Norwegian population-based study of orofacial clefts (May 1996–1998). A case-parent triad design was used to examine whether MTHFR variants C677T and A1298C, and their haplotypes, are risk factors for orofacial clefts. Among CL/P cases, the child’s genotype at C677T or A1298C did not influence the risk. However, children of mothers carrying the C677T variant allele had a lower risk of CL/P. For CPO, children carrying the C677T variant allele had about a twofold increased risk, whereas the mother’s genotypes did not contribute to the risk. The haplotype-based transmission/disequilibrium test showed that except for 677T/1298A (p = 0.06), none of the other haplotypes showed evidence of excess transmission to the offspring. The authors also explored interaction of C677T with maternal use of folic acid among children with CPO. Surprisingly, the risk associated with the child’s carrying either CT or TT was higher (fourfold) when the mother used folic acid. These findings suggest a possible role of MTHFR and folic acid in the causation of orofacial clefts, but the strength and direction of these effects remain to be clarified.
abnormalities; cleft lip; cleft palate; folic acid; genes; genetic predisposition to disease; haplotypes; vitamins
Abbreviations: Abbreviations: CI, confidence interval; CL/P, cleft lip with or without cleft palate; CPO, cleft palate only; MTHFR, methylenetetrahydrofolate reductase; PCR, polymerase chain reaction.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  C. Y Johnson and J. Little Folate intake, markers of folate status and oral clefts: is the evidence converging? Int. J. Epidemiol., June 26, 2008; (2008) dyn098v1. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. Sharp, Z. Miedzybrodzka, A. H. Cardy, J. Inglis, L. Madrigal, S. Barker, D. Chesney, C. Clark, and N. Maffulli The C677T Polymorphism in the Methylenetetrahydrofolate Reductase Gene (MTHFR), Maternal Use of Folic Acid Supplements, and Risk of Isolated Clubfoot: A Case-Parent-Triad Analysis Am. J. Epidemiol., November 1, 2006; 164(9): 852 - 861. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P Leoyklang, P Siriwan, and V Shotelersuk A mutation of the p63 gene in non-syndromic cleft lip. J. Med. Genet., June 1, 2006; 43(6): e28 - e28. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 T. Tamura and M. F. Picciano Folate and human reproduction Am. J. Clinical Nutrition, May 1, 2006; 83(5): 993 - 1016. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C A Hobbs, S J James, A Parsian, P A Krakowiak, S Jernigan, J J Greenhaw, Y Lu, and M A Cleves Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene J. Med. Genet., February 1, 2006; 43(2): 162 - 166. [Abstract] [Full Text] [PDF]
|
|