Cargando…
Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study
BACKGROUND: Arsenic (As) exposure has been associated with increased risk for cardiovascular disease (CVD) and with biomarkers of potential CVD risk and inflammatory processes. However, few studies have evaluated the effects of As on such biomarkers in U.S. populations, which are typically exposed t...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Environmental Health Perspectives
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963594/ https://www.ncbi.nlm.nih.gov/pubmed/29373859 http://dx.doi.org/10.1289/EHP2062 |
_version_ | 1783325051988213760 |
---|---|
author | Farzan, Shohreh F. Howe, Caitlin G. Zens, Michael S. Palys, Thomas Channon, Jacqueline Y. Li, Zhigang Chen, Yu Karagas, Margaret R. |
author_facet | Farzan, Shohreh F. Howe, Caitlin G. Zens, Michael S. Palys, Thomas Channon, Jacqueline Y. Li, Zhigang Chen, Yu Karagas, Margaret R. |
author_sort | Farzan, Shohreh F. |
collection | PubMed |
description | BACKGROUND: Arsenic (As) exposure has been associated with increased risk for cardiovascular disease (CVD) and with biomarkers of potential CVD risk and inflammatory processes. However, few studies have evaluated the effects of As on such biomarkers in U.S. populations, which are typically exposed to low to moderate As concentrations. OBJECTIVES: We investigated associations between As exposures and biomarkers relevant to inflammation, oxidative stress, and CVD risk in a subset of participants from the New Hampshire Health Study, a population with low to moderate As exposure ([Formula: see text]). METHODS: Associations between toenail As, total urine As (uAs), and %uAs metabolites [monomethyl ([Formula: see text]), dimethyl ([Formula: see text]), and inorganic (%iAs) species] and plasma biomarkers, including soluble plasma vascular and cellular adhesion molecules (VCAM-1 and ICAM-1, respectively), matrix metalloproteinase-9 (MMP-9), tumor necrosis [Formula: see text] , plasminogen activator inhibitor-1 (PAI-1), and urinary oxidative stress marker [Formula: see text] ([Formula: see text]), were evaluated using linear regression models. RESULTS: Covariate-adjusted estimates of associations with a doubling of urinary As suggested an 8.8% increase in [Formula: see text] (95% CI: 3.2, 14.7), and a doubling of toenail As was associated with a 1.7% increase in VCAM-1 (95% CI: 0.2, 3.2). Additionally, a 5% increase in %uMMA was associated with a 7.9% increase in [Formula: see text] (95% CI: 2.1, 14.1), and a 5% increase in %uDMA was associated with a 2.98% decrease in [Formula: see text] [(95% CI: [Formula: see text] , 0.21); [Formula: see text]]. However, in contrast with expectations, a doubling of toenail As was associated with a 2.3% decrease (95% CI: [Formula: see text] , [Formula: see text]) in MMP-9, and a 5% increase in %uMMA was associated with a 7.7% decrease (95% CI: [Formula: see text] , [Formula: see text]) in PAI-1. CONCLUSION: In a cross-sectional study of U.S. adults, we observed some positive associations of uAs and toenail As concentrations with biomarkers potentially relevant to CVD pathogenesis and inflammation, and evidence of a higher capacity to metabolize inorganic As was negatively associated with a marker of oxidative stress. https://doi.org/10.1289/EHP2062 |
format | Online Article Text |
id | pubmed-5963594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Environmental Health Perspectives |
record_format | MEDLINE/PubMed |
spelling | pubmed-59635942018-05-30 Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study Farzan, Shohreh F. Howe, Caitlin G. Zens, Michael S. Palys, Thomas Channon, Jacqueline Y. Li, Zhigang Chen, Yu Karagas, Margaret R. Environ Health Perspect Research BACKGROUND: Arsenic (As) exposure has been associated with increased risk for cardiovascular disease (CVD) and with biomarkers of potential CVD risk and inflammatory processes. However, few studies have evaluated the effects of As on such biomarkers in U.S. populations, which are typically exposed to low to moderate As concentrations. OBJECTIVES: We investigated associations between As exposures and biomarkers relevant to inflammation, oxidative stress, and CVD risk in a subset of participants from the New Hampshire Health Study, a population with low to moderate As exposure ([Formula: see text]). METHODS: Associations between toenail As, total urine As (uAs), and %uAs metabolites [monomethyl ([Formula: see text]), dimethyl ([Formula: see text]), and inorganic (%iAs) species] and plasma biomarkers, including soluble plasma vascular and cellular adhesion molecules (VCAM-1 and ICAM-1, respectively), matrix metalloproteinase-9 (MMP-9), tumor necrosis [Formula: see text] , plasminogen activator inhibitor-1 (PAI-1), and urinary oxidative stress marker [Formula: see text] ([Formula: see text]), were evaluated using linear regression models. RESULTS: Covariate-adjusted estimates of associations with a doubling of urinary As suggested an 8.8% increase in [Formula: see text] (95% CI: 3.2, 14.7), and a doubling of toenail As was associated with a 1.7% increase in VCAM-1 (95% CI: 0.2, 3.2). Additionally, a 5% increase in %uMMA was associated with a 7.9% increase in [Formula: see text] (95% CI: 2.1, 14.1), and a 5% increase in %uDMA was associated with a 2.98% decrease in [Formula: see text] [(95% CI: [Formula: see text] , 0.21); [Formula: see text]]. However, in contrast with expectations, a doubling of toenail As was associated with a 2.3% decrease (95% CI: [Formula: see text] , [Formula: see text]) in MMP-9, and a 5% increase in %uMMA was associated with a 7.7% decrease (95% CI: [Formula: see text] , [Formula: see text]) in PAI-1. CONCLUSION: In a cross-sectional study of U.S. adults, we observed some positive associations of uAs and toenail As concentrations with biomarkers potentially relevant to CVD pathogenesis and inflammation, and evidence of a higher capacity to metabolize inorganic As was negatively associated with a marker of oxidative stress. https://doi.org/10.1289/EHP2062 Environmental Health Perspectives 2017-12-15 /pmc/articles/PMC5963594/ /pubmed/29373859 http://dx.doi.org/10.1289/EHP2062 Text en EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted. |
spellingShingle | Research Farzan, Shohreh F. Howe, Caitlin G. Zens, Michael S. Palys, Thomas Channon, Jacqueline Y. Li, Zhigang Chen, Yu Karagas, Margaret R. Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study |
title | Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study |
title_full | Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study |
title_fullStr | Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study |
title_full_unstemmed | Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study |
title_short | Urine Arsenic and Arsenic Metabolites in U.S. Adults and Biomarkers of Inflammation, Oxidative Stress, and Endothelial Dysfunction: A Cross-Sectional Study |
title_sort | urine arsenic and arsenic metabolites in u.s. adults and biomarkers of inflammation, oxidative stress, and endothelial dysfunction: a cross-sectional study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963594/ https://www.ncbi.nlm.nih.gov/pubmed/29373859 http://dx.doi.org/10.1289/EHP2062 |
work_keys_str_mv | AT farzanshohrehf urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT howecaitling urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT zensmichaels urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT palysthomas urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT channonjacqueliney urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT lizhigang urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT chenyu urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy AT karagasmargaretr urinearsenicandarsenicmetabolitesinusadultsandbiomarkersofinflammationoxidativestressandendothelialdysfunctionacrosssectionalstudy |