Literature DB >> 18452350

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

Heiko Reutter1, Stefanie Birnbaum, Amalia Diaz Lacava, Meinhard Mende, Henning Henschke, Stefaan Bergé, Bert Braumann, Carola Lauster, Franziska Schiefke, Matthias Wenghoefer, Mitra Saffar, Rudolf Reich, Martin Scheer, Franz-Josef Kramer, Michael Knapp, Elisabeth Mangold.   

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.

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Year:  2008        PMID: 18452350     DOI: 10.1597/06-174

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  6 in total

1.  Association between Maternal MTHFR Polymorphisms and Nonsyndromic Cleft Lip with or without Cleft Palate in Offspring, A Meta-Analysis Based on 15 Case-Control Studies.

Authors:  Xinjuan Pan; Ping Wang; Xinjuan Yin; Xiaozhuan Liu; Di Li; Xing Li; Yongchao Wang; Hongle Li; Zengli Yu
Journal:  Int J Fertil Steril       Date:  2015-02-07

2.  Maternal Supplementary Folate Intake, Methylenetetrahydrofolate Reductase (MTHFR) C677T and A1298C Polymorphisms and the Risk of Orofacial Cleft in Iranian Children.

Authors:  Asghar Ebadifar; Hamid Reza KhorramKhorshid; Koorosh Kamali; Mehdi Salehi Zeinabadi; Tayyebeh Khoshbakht; Nazila Ameli
Journal:  Avicenna J Med Biotechnol       Date:  2015 Apr-Jun

3.  Methylenetetrahydrofolate reductase C677T variant in Indian children with craniosynostosis: Its role in the pathogenesis, risk of craniosynostosis.

Authors:  Rajeev Kumar Pandey; Abid Ali; Amit Singh; Sukanya Gayan; Minu Bajpai
Journal:  Indian J Hum Genet       Date:  2014-04

4.  MTHFR C677T polymorphism and risk of nonsyndromic cleft lip with or without cleft palate in the Moroccan population.

Authors:  Amine Rafik; Laila Rachad; Abdou-Samad Kone; Sellama Nadifi
Journal:  Appl Clin Genet       Date:  2019-03-07

5.  Incidence Assessment of MTHFR C677T and A1298C Polymorphisms in Iranian Non-syndromic Cleft Lip and/or Palate Patients.

Authors:  Asghar Ebadifar; Nazila Ameli; Hamid Reza Khorramkhorshid; Mehdi Salehi Zeinabadi4; Kourosh Kamali; Tayyebeh Khoshbakht
Journal:  J Dent Res Dent Clin Dent Prospects       Date:  2015-06-10

6.  Association of Transforming Growth Factor Alpha and Methylenetetrahydrofolate reductase gene variants with nonsyndromic cleft lip and palate in the Indian population.

Authors:  Asavari L Desai; M R Dinesh; B C Amarnath; R M Dharma; K R Akshai; C S Prashanth
Journal:  Contemp Clin Dent       Date:  2014-07
  6 in total

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