Modification of vitamin B6 on the associations of blood lead levels and cardiovascular diseases in the US adults.

Journal Article (Journal Article)

Background

Cardiovascular disease (CVD) is a leading cause of death in the US population. Lead exposure is an important risk factor of CVDs, as is associated with elevated homocysteine level and oxidative stress. We aim to examine whether vitamin B6, which has been shown to reduce homocysteine level, can modify the relationship between blood lead and the risk of CVDs.

Methods

Cross-sectional data on ever-report CVDs (congestive heart failure, coronary heart disease, angina pectoris, heart attack and stroke), blood lead level (BLL) and vitamin B6 in the form of plasma pyridoxal 5'-phosphate were obtained from US National Health and Nutrition Examination Survey 2005-2006 for adults≥20 years old. The association between CVDs and quartiles of BLL was estimated using multivariate logistic regression models adjusted for demographics factors, lifestyle variables, stress variables, comorbidities and CVD biomarkers (C reactive protein, homocysteine, cholesterol) and was stratified by vitamin B6 deficiency level (<20 nmol/L) and median value of vitamin B6 (42.5 nmol/L).

Results

Positive associations between BLL and CVDs only appeared in the vitamin B6 deficiency group, with quartile 2 to quartile 4 of BLL showing higher risk of CVDs (OR=3.1, 95% CI 0.9 to 10.6; OR=6.5, 95% CI 1.4 to 30.8; OR=5.5, 95% CI 1.4 to 21.7) compared with quartile 1. When stratified by median value of vitamin B6, a significant association between higher CVD risk with higher BLL was only observed in subjects with low vitamin B6 (p trend=0.004).

Conclusions

Vitamin B6 could modify the association between BLL and CVDs, which suggests a potential value of vitamin B6 in influencing the effects of lead exposure on the cardiovascular system.

Full Text

Duke Authors

Cited Authors

  • Wei, J; Ji, JS

Published Date

  • December 2020

Published In

Volume / Issue

  • 3 / 2

Start / End Page

  • 180 - 187

PubMed ID

  • 33521527

Pubmed Central ID

  • PMC7841818

Electronic International Standard Serial Number (EISSN)

  • 2516-5542

International Standard Serial Number (ISSN)

  • 2516-5542

Digital Object Identifier (DOI)

  • 10.1136/bmjnph-2020-000088

Language

  • eng