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...

Descripción completa

Detalles Bibliográficos
Autores principales: Farzan, Shohreh F., Howe, Caitlin G., Zens, Michael S., Palys, Thomas, Channon, Jacqueline Y., Li, Zhigang, Chen, Yu, Karagas, Margaret R.
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