Literature DB >> 27720779

Riboflavin, MTHFR genotype and blood pressure: A personalized approach to prevention and treatment of hypertension.

Helene McNulty1, J J Strain2, Catherine F Hughes2, Mary Ward2.   

Abstract

Hypertension is the leading risk factor contributing to mortality worldwide, primarily from cardiovascular disease (CVD), while effective treatment of hypertension is proven to reduce CVD events. Along with the well recognized nutrition and lifestyle determinants, genetic factors are implicated in the development and progression of hypertension. In recent years genome-wide association studies have identified a region near the gene encoding the folate-metabolizing enzyme methylenetetrahydrofolate reductase (MTHFR) among eight loci associated with blood pressure. Epidemiological studies, which provide a separate line of evidence to link this gene with blood pressure, show that the 677C→T polymorphism in MTHFR increases the risk of hypertension by 24-87% and CVD by up to 40%, albeit with a large geographical variation in the extent of excess disease risk suggestive of a gene-environment interaction. Emerging evidence indicates that the relevant environmental factor may be riboflavin, the MTHFR co-factor, via a novel and genotype-specific effect on blood pressure. Randomized trials conducted in hypertensive patients (with and without overt CVD) pre-screened for this polymorphism show that targeted riboflavin supplementation in homozygous individuals (MTHFR 677TT genotype) lowers systolic blood pressure by 6 to 13 mmHg, independently of the effect of antihypertensive drugs. The latest evidence, that the blood pressure phenotype associated with this polymorphism is modifiable by riboflavin, has important clinical and public health implications. For hypertensive patients, riboflavin supplementation can offer a non-drug treatment to effectively lower blood pressure in those identified with the MTHFR 677TT genotype. For sub-populations worldwide with this genotype, better riboflavin status may prevent or delay the development of high blood pressure. Thus riboflavin, targeted at those homozygous for a common polymorphism in MTHFR, may offer a personalized treatment or preventative strategy for hypertension. Further investigations of this novel gene-nutrient interaction in relation to blood pressure, hypertension and hypertension in pregnancy are required.
Copyright © 2016. Published by Elsevier Ltd.

Entities:  

Keywords:  Blood pressure; Hypertension; Hypertension-in-pregnancy; Methylenetetrahydrofolate reductase (MTHFR) genotype; Personalized medicine; Riboflavin

Mesh:

Substances:

Year:  2016        PMID: 27720779     DOI: 10.1016/j.mam.2016.10.002

Source DB:  PubMed          Journal:  Mol Aspects Med        ISSN: 0098-2997


  18 in total

Review 1.  Riboflavin in Neurological Diseases: A Narrative Review.

Authors:  Domenico Plantone; Matteo Pardini; Giuseppe Rinaldi
Journal:  Clin Drug Investig       Date:  2021-04-22       Impact factor: 2.859

2.  Association of Homocysteine, Methionine, and MTHFR 677C>T Polymorphism With Rate of Cardiovascular Multimorbidity Development in Older Adults in Sweden.

Authors:  Amaia Calderón-Larrañaga; Marguerita Saadeh; Babak Hooshmand; Helga Refsum; A David Smith; Alessandra Marengoni; Davide L Vetrano
Journal:  JAMA Netw Open       Date:  2020-05-01

3.  Improving diabetic and hypertensive retinopathy with a medical food containing L-methylfolate: a preliminary report.

Authors:  Jianhua Wang; Craig Brown; Ce Shi; Justin Townsend; Giovana Rosa Gameiro; Peng Wang; Hong Jiang
Journal:  Eye Vis (Lond)       Date:  2019-07-22

4.  Maternal folate, one-carbon metabolism and pregnancy outcomes.

Authors:  Tanja Jankovic-Karasoulos; Denise L Furness; Shalem Y Leemaqz; Gustaaf A Dekker; Luke E Grzeskowiak; Jessica A Grieger; Prabha H Andraweera; Dylan McCullough; Dale McAninch; Lesley M McCowan; Tina Bianco-Miotto; Claire T Roberts
Journal:  Matern Child Nutr       Date:  2020-07-28       Impact factor: 3.092

5.  A Novel Personalized Systems Nutrition Program Improves Dietary Patterns, Lifestyle Behaviors and Health-Related Outcomes: Results from the Habit Study.

Authors:  Iris M de Hoogh; Barbara L Winters; Kristin M Nieman; Sabina Bijlsma; Tanja Krone; Tim J van den Broek; Barbara D Anderson; Martien P M Caspers; Joshua C Anthony; Suzan Wopereis
Journal:  Nutrients       Date:  2021-05-22       Impact factor: 5.717

6.  Correlation Analysis Between MTHFR C677T Polymorphism and Uterine Fibroids: A Retrospective Cohort Study.

Authors:  Jiahui Shen; Yanhui Jiang; Fengzhi Wu; Hui Chen; Qiujing Wu; Xiaoxiao Zang; Le Chen; Yong Chen; Qiwen Yuan
Journal:  Front Oncol       Date:  2021-06-01       Impact factor: 6.244

7.  Expression of the C677T Polymorphism of the 5, 10-Methylenetetrahydrofolate Reductase (MTHFR) Gene in Patients with Carotid Artery Atherosclerosis.

Authors:  Anying Li; Wei Huang; Qiong Yang; Liping Peng; Qiang Liu
Journal:  Med Sci Monit       Date:  2020-07-17

8.  Methylenetetrahydrofolate Reductase C677T Gene Polymorphism as a Risk Factor for Hypertension in a Rural Population.

Authors:  Rony Mario Candrasatria; Suko Adiarto; Renan Sukmawan
Journal:  Int J Hypertens       Date:  2020-02-13       Impact factor: 2.420

9.  Impact of the common MTHFR 677C→T polymorphism on blood pressure in adulthood and role of riboflavin in modifying the genetic risk of hypertension: evidence from the JINGO project.

Authors:  Mary Ward; Catherine F Hughes; J J Strain; Rosie Reilly; Conal Cunningham; Anne M Molloy; Geraldine Horigan; Miriam Casey; Kevin McCarroll; Maurice O'Kane; Michael J Gibney; Albert Flynn; Janette Walton; Breige A McNulty; Adrian McCann; Laura Kirwan; John M Scott; Helene McNulty
Journal:  BMC Med       Date:  2020-11-11       Impact factor: 8.775

10.  The methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism is associated with breast cancer subtype susceptibility in southwestern China.

Authors:  Zhen Li; Ji Zhang; Wei Zou; Qi Xu; Siyuan Li; Jie Wu; Li Zhu; Yunjiao Zhang; Lei Xu; Ying Zhang; Qingsong Luo; Jianyun Nie; Xingxu Li; Tianning Zou; Ceshi Chen
Journal:  PLoS One       Date:  2021-07-09       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.