Literature DB >> 11074217

Effect of heterozygosity for the methionine synthase 2756 A-->G mutation on the risk for recurrent cardiovascular events.

M E Hyndman1, P J Bridge, J W Warnica, G Fick, H G Parsons.   

Abstract

Increased dietary intake of folate has been shown to significantly reduce the risk for fatal myocardial infarction, possibly by lowering homocysteine levels. We therefore investigated the association between recurrent cardiovascular events and a mutation in methionine synthase (2756 A-->G)--an enzyme directly involved in folate and homocysteine metabolism. This mutation significantly reduced the risk for recurrent cardiovascular events and elevated red blood cell folate levels.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11074217     DOI: 10.1016/s0002-9149(00)01177-2

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  7 in total

1.  A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction.

Authors:  Rachel Marceau; Wenbin Lu; Shannon Holloway; Michèle M Sale; Bradford B Worrall; Stephen R Williams; Fang-Chi Hsu; Jung-Ying Tzeng
Journal:  Genet Epidemiol       Date:  2015-07-03       Impact factor: 2.135

Review 2.  Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overview.

Authors:  R Castro; I Rivera; H J Blom; C Jakobs; I Tavares de Almeida
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

3.  Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease.

Authors:  Patrícia Matos Biselli; Alexandre Rodrigues Guerzoni; Moacir Fernandes de Godoy; Marcos Nogueira Eberlin; Renato Haddad; Valdemir Melechco Carvalho; Hélio Vannucchi; Erika Cristina Pavarino-Bertelli; Eny Maria Goloni-Bertollo
Journal:  J Thromb Thrombolysis       Date:  2009-03-13       Impact factor: 2.300

4.  Effects of methionine synthase and methionine synthase reductase polymorphisms on hypertension susceptibility.

Authors:  Young Ree Kim; Sung Ha Kang; Seung-Ho Hong
Journal:  Genes Genomics       Date:  2020-03-07       Impact factor: 1.839

5.  Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.

Authors:  David Watkins; Ming Ru; Hye-Yeon Hwang; Caroline D Kim; Angus Murray; Noah S Philip; William Kim; Helen Legakis; Timothy Wai; John F Hilton; Bing Ge; Carole Doré; Angela Hosack; Aaron Wilson; Roy A Gravel; Barry Shane; Thomas J Hudson; David S Rosenblatt
Journal:  Am J Hum Genet       Date:  2002-05-30       Impact factor: 11.025

6.  Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan.

Authors:  Helmi Yousif Al Farra
Journal:  Indian J Hum Genet       Date:  2010-09

Review 7.  Potential Links between Impaired One-Carbon Metabolism Due to Polymorphisms, Inadequate B-Vitamin Status, and the Development of Alzheimer's Disease.

Authors:  Barbara Troesch; Peter Weber; M Hasan Mohajeri
Journal:  Nutrients       Date:  2016-12-10       Impact factor: 5.717

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.