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Effect of riboflavin supplementation on blood pressure and possible effect modification by the MTHFR C677T polymorphism: a randomised trial in rural Gambia [version 1; peer review: 1 approved, 1 approved with reservations]

Authors :
Modou Jobe
Mary Ward
Bakary Sonko
Abdul Khalie Muhammad
Ebrima Danso
Helene McNulty
Andrew M Prentice
Author Affiliations :
<relatesTo>1</relatesTo>Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Atlantic Boulevard, Fajara, Banjul, PO Box 273, The Gambia<br /><relatesTo>2</relatesTo>Northern Ireland Centre for Food and Health, University of Ulster, Ulster, UK
Source :
F1000Research. 9:1034
Publication Year :
2020
Publisher :
London, UK: F1000 Research Limited, 2020.

Abstract

Introduction: Emerging evidence links a functional polymorphism in the methylenetetrahydrofolate reductase ( MTHFR) gene (rs1801133) with hypertension in adults. This variant reduces the affinity of MTHFR for its cofactor flavin-adenine dinucleotide (FAD) which is derived from riboflavin. Previous work has demonstrated a blood pressure (BP)-lowering effect of riboflavin in Irish adults with the MTHFR 677TT variant. We hypothesize that the almost-universal severe riboflavin deficiency seen in rural Gambia mimics the BP phenotypic effect of the TT variant and exacerbate the effect of the CT variant. We will test this in a randomised, placebo-controlled trial, whether intervention with riboflavin can decrease BP in adults in rural Gambia. Methods: This is a phase 2 recall-by-genotype randomised single-blind placebo-controlled riboflavin supplementation trial. We will use the Keneba biobank to recruit approximately 102 individuals aged between 18-70, previously genotyped for the MTHFR C677T polymorphism and identified as carrying the T allele; these individuals will be age- and sex-matched to a similar number of homozygotes for the C allele. The participants will be randomised to a 16-week supplementation trial of 5 mg/day riboflavin or placebo, supplied every 14 days. The primary outcome, BP, will be measured at baseline and at weeks 8 and 16. Blood samples, collected at baseline and week 16, will be analysed for riboflavin, homocysteine, red cell folate, cobalamin (vitamin B12) and pyridoxine (vitamin B6). Discussion: The study will evaluate the role of riboflavin supplementation in BP control within a population with high levels of riboflavin deficiency and will test a possible gene-nutrient interaction with the MTHFR C677T polymorphism. If improvements in BP are observed in this study, and proven in subsequent large-scale interventions, riboflavin could offer a cost-effective, safe and accessible option for the prevention and control of hypertension in this population. Trial registration: ClinicalTrials.gov Identifier NCT03151096. Registered on 12 May 2017.

Details

ISSN :
20461402
Volume :
9
Database :
F1000Research
Journal :
F1000Research
Notes :
[version 1; peer review: 1 approved, 1 approved with reservations]
Publication Type :
Academic Journal
Accession number :
edsfor.10.12688.f1000research.25113.1
Document Type :
study-protocol
Full Text :
https://doi.org/10.12688/f1000research.25113.1