Literature DB >> 16522920

Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations.

Rosa-Maria Guéant-Rodriguez1, Jean-Louis Guéant, Renée Debard, Sylvie Thirion, Lu Xiao Hong, Jean-Pierre Bronowicki, Farès Namour, Nicodème W Chabi, Ambaliou Sanni, Guido Anello, Paolo Bosco, Corrado Romano, Emile Amouzou, Heidy R Arrieta, Beatríz E Sánchez, Antonino Romano, Bernard Herbeth, Jean-Claude Guilland, Osvaldo M Mutchinick.   

Abstract

BACKGROUND: Methylenetetrahydrofolate reductase (MTHFR) 677C-->T polymorphism is heterogeneously distributed worldwide, with the highest and lowest frequencies of the T allele in Mexico and Africa, respectively, and a south-to-north gradient in Europe. Distribution of MTHFR 1298A-->C is less well known. It has been hypothesized that 677T frequency could result in part from gene-nutrient interactions.
OBJECTIVE: The objective was to compare the association of 677T and 1298C alleles with plasma concentrations of homocysteine, folate, and vitamin B-12 in geographical areas with contrasting 677T allele frequencies.
DESIGN: Healthy young adults (n = 1277) were recruited in Mexico City, the West African countries of Bénin and Togo, France, and Sicily (Italy). Homocysteine, folate, and vitamin B-12 were measured in plasma, and MTHFR polymorphisms were measured in genomic DNA.
RESULTS: Mexico City and Sicily reported the highest and Bénin and Togo reported the lowest plasma concentrations of folate. Mexico City had the highest 677T allele prevalence and the lowest influence of 677TT genotype on homocysteine, whereas the opposite was observed in Africa. The prevalence of the 1298C allele was lowest in the Mexicans and Africans and highest in the French. The percentage of the 677T genotype was significantly associated with the folate concentrations in 677CC carriers in a univariate analysis (R = 0.976; 95% CI: 0.797, 0.996; P < 0.0002) and in a multiple regression model that included homocysteine, vitamin B-12, and age (P = 0.0002).
CONCLUSION: Our data agree with the hypothesis of a gene-nutrient interaction between MTHFR 677C-->T polymorphism and folate status that may confer a selective advantage of TT-homozygous genotype when dietary intake of folate is adequate, at least in the areas studied.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16522920     DOI: 10.1093/ajcn.83.3.701

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  58 in total

1.  Polymorphism 677C → T MTHFR gene in Mexican mothers of children with complex congenital heart disease.

Authors:  Norma A Balderrábano-Saucedo; Rocio Sánchez-Urbina; José A Sierra-Ramírez; Normand García-Hernández; Adriana Sánchez-Boiso; Miguel Klunder-Klunder; Diego Arenas-Aranda; Gabriela Bravo-Hernández; Penelope Noriega-Zapata; Alfredo Vizcaíno-Alarcón
Journal:  Pediatr Cardiol       Date:  2012-06-04       Impact factor: 1.655

Review 2.  Effects and safety of periconceptional folate supplementation for preventing birth defects.

Authors:  Luz Maria De-Regil; Ana C Fernández-Gaxiola; Therese Dowswell; Juan Pablo Peña-Rosas
Journal:  Cochrane Database Syst Rev       Date:  2010-10-06

3.  Determinants of homocysteine levels in Ivorian rural population.

Authors:  Georges Tiahou; Anne-Marie Dupuy; Isabelle Jaussent; Daniel Sees; Jean-Paul Cristol; Stephanie Badiou
Journal:  Int J Vitam Nutr Res       Date:  2009-09       Impact factor: 1.784

4.  Maternal MTHFR genotype and haplotype predict deficits in early cognitive development in a lead-exposed birth cohort in Mexico City.

Authors:  J Richard Pilsner; Howard Hu; Robert O Wright; Katarzyna Kordas; Adrienne S Ettinger; Brisa N Sánchez; David Cantonwine; Alicia L Lazarus; Alejandra Cantoral; Lourdes Schnaas; Martha Maria Téllez-Rojo; Mauricio Hernández-Avila
Journal:  Am J Clin Nutr       Date:  2010-05-26       Impact factor: 7.045

5.  Role of CLU, PICALM, and TNK1 Genotypes in Aging With and Without Alzheimer's Disease.

Authors:  Davide Seripa; Francesco Panza; Giulia Paroni; Grazia D'Onofrio; Paola Bisceglia; Carolina Gravina; Maria Urbano; Madia Lozupone; Vincenzo Solfrizzi; Alessandra Bizzarro; Virginia Boccardi; Chiara Piccininni; Antonio Daniele; Giancarlo Logroscino; Patrizia Mecocci; Carlo Masullo; Antonio Greco
Journal:  Mol Neurobiol       Date:  2017-06-19       Impact factor: 5.590

Review 6.  Genome-based nutrition: an intervention strategy for the prevention and treatment of obesity and nonalcoholic steatohepatitis.

Authors:  Sonia Roman; Claudia Ojeda-Granados; Omar Ramos-Lopez; Arturo Panduro
Journal:  World J Gastroenterol       Date:  2015-03-28       Impact factor: 5.742

7.  Environmental influence on the worldwide prevalence of a 776C->G variant in the transcobalamin gene (TCN2).

Authors:  Jean-Louis Guéant; Nicodème W Chabi; Rosa-Maria Guéant-Rodriguez; Osvaldo M Mutchinick; Renée Debard; Corinne Payet; Xiaohong Lu; Christian Villaume; Jean-Pierre Bronowicki; Edward V Quadros; Ambaliou Sanni; Emile Amouzou; Bing Xia; Min Chen; Guido Anello; Paolo Bosco; Corrado Romano; Heidy R Arrieta; Beatríz E Sánchez; Antonino Romano; Bernard Herbeth; Wafaa Anwar; Fares Namour
Journal:  J Med Genet       Date:  2007-01-12       Impact factor: 6.318

8.  Relationship of MTHFR gene polymorphisms with renal and cardiac disease.

Authors:  Francesca M Trovato; Daniela Catalano; Angela Ragusa; G Fabio Martines; Clara Pirri; Maria Antonietta Buccheri; Concetta Di Nora; Guglielmo M Trovato
Journal:  World J Nephrol       Date:  2015-02-06

9.  Association of the methylenetetrahydrofolate reductase C677T polymorphism and fracture risk in Chinese postmenopausal women.

Authors:  Xiumei Hong; Yi-Hsiang Hsu; Henry Terwedow; Genfu Tang; Xue Liu; Shanqun Jiang; Xin Xu; Xiping Xu
Journal:  Bone       Date:  2006-12-15       Impact factor: 4.398

Review 10.  The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Authors:  Anne M Molloy; Lawrence C Brody; James L Mills; John M Scott; Peadar N Kirke
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-04
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.