Family-based association study of the MTHFR polymorphism C677T in patients with nonsyndromic cleft lip and palate from central Europe

Cleft Palate Craniofac J. 2008 May;45(3):267-71. doi: 10.1597/06-174.

Abstract

Objective: The 677C-->T allele in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene has been implicated in the etiology of nonsyndromic cleft lip and palate (CL/P). This study involved a family-based association study of the MTHFR polymorphism.

Patients/participants: We examined 181 patients with CL/P of central European descent and their parents for this variant.

Results: The transmission disequilibrium test (TDT) did not confirm an association between the MTHFR 677C-->T polymorphism and nonsyndromic CL/P as previously suggested (p = .36). When comparing the offspring of mothers with periconceptional use of folate to those without, no statistically significant differences were found (p = .708).

Conclusion: Our data suggest that the MTHFR 677C-->T polymorphism does not make a major contribution to the occurrence of CL/P among central Europeans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cleft Lip / genetics*
  • Cleft Palate / genetics*
  • Europe
  • Family Health
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Linkage Disequilibrium
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Polymorphism, Single Nucleotide

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)