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Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study

BACKGROUND: To examine the relationship between cadmium, lead, and mercury concentrations with high-sensitivity C-reactive protein (hs-CRP) and homocysteine in women. METHODS: Metals were measured at enrollment in whole blood. Homocysteine and hs-CRP were measured in one (N = 9) or two (N = 250) men...

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Autores principales: Pollack, Anna Z., Mumford, Sunni L., Sjaarda, Lindsey, Perkins, Neil J., Malik, Farah, Wactawski-Wende, Jean, Schisterman, Enrique F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549434/
https://www.ncbi.nlm.nih.gov/pubmed/28789684
http://dx.doi.org/10.1186/s12940-017-0293-6
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author Pollack, Anna Z.
Mumford, Sunni L.
Sjaarda, Lindsey
Perkins, Neil J.
Malik, Farah
Wactawski-Wende, Jean
Schisterman, Enrique F.
author_facet Pollack, Anna Z.
Mumford, Sunni L.
Sjaarda, Lindsey
Perkins, Neil J.
Malik, Farah
Wactawski-Wende, Jean
Schisterman, Enrique F.
author_sort Pollack, Anna Z.
collection PubMed
description BACKGROUND: To examine the relationship between cadmium, lead, and mercury concentrations with high-sensitivity C-reactive protein (hs-CRP) and homocysteine in women. METHODS: Metals were measured at enrollment in whole blood. Homocysteine and hs-CRP were measured in one (N = 9) or two (N = 250) menstrual cycles up to 3 and 8 times per cycle, respectively. Linear mixed models with inverse probability of exposure weights to account for time varying confounding were used and models were stratified by dietary and serum vitamin status (dietary: vitamin B(6), B(12), folate; serum: folate). RESULTS: Geometric mean (95% confidence interval (CI)) concentrations for cadmium, lead, and mercury were 0.29 (0.26–0.31) μg/L, 0.91 (0.86–0.96) μg/dL, and 1.05 (0.93–1.18) μg/L, respectively. Lead was associated with increased homocysteine (0.08; 95% CI: 0.01, 0.15) and this persisted among those in the lower three quartiles of consumption of vitamin B(6), B(12), folate, and serum folate but was not significant among those in the upper quartile. No associations were observed between metals and hs-CRP. CONCLUSIONS: Blood lead was associated with increased homocysteine in a cohort of healthy, premenopausal women but these associations did not persist among those consuming ≥75th percentile of essential micronutrients. Cadmium, lead, and mercury were not associated with hs-CRP concentrations.
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spelling pubmed-55494342017-08-11 Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study Pollack, Anna Z. Mumford, Sunni L. Sjaarda, Lindsey Perkins, Neil J. Malik, Farah Wactawski-Wende, Jean Schisterman, Enrique F. Environ Health Research BACKGROUND: To examine the relationship between cadmium, lead, and mercury concentrations with high-sensitivity C-reactive protein (hs-CRP) and homocysteine in women. METHODS: Metals were measured at enrollment in whole blood. Homocysteine and hs-CRP were measured in one (N = 9) or two (N = 250) menstrual cycles up to 3 and 8 times per cycle, respectively. Linear mixed models with inverse probability of exposure weights to account for time varying confounding were used and models were stratified by dietary and serum vitamin status (dietary: vitamin B(6), B(12), folate; serum: folate). RESULTS: Geometric mean (95% confidence interval (CI)) concentrations for cadmium, lead, and mercury were 0.29 (0.26–0.31) μg/L, 0.91 (0.86–0.96) μg/dL, and 1.05 (0.93–1.18) μg/L, respectively. Lead was associated with increased homocysteine (0.08; 95% CI: 0.01, 0.15) and this persisted among those in the lower three quartiles of consumption of vitamin B(6), B(12), folate, and serum folate but was not significant among those in the upper quartile. No associations were observed between metals and hs-CRP. CONCLUSIONS: Blood lead was associated with increased homocysteine in a cohort of healthy, premenopausal women but these associations did not persist among those consuming ≥75th percentile of essential micronutrients. Cadmium, lead, and mercury were not associated with hs-CRP concentrations. BioMed Central 2017-08-08 /pmc/articles/PMC5549434/ /pubmed/28789684 http://dx.doi.org/10.1186/s12940-017-0293-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Pollack, Anna Z.
Mumford, Sunni L.
Sjaarda, Lindsey
Perkins, Neil J.
Malik, Farah
Wactawski-Wende, Jean
Schisterman, Enrique F.
Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study
title Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study
title_full Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study
title_fullStr Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study
title_full_unstemmed Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study
title_short Blood lead, cadmium and mercury in relation to homocysteine and C-reactive protein in women of reproductive age: a panel study
title_sort blood lead, cadmium and mercury in relation to homocysteine and c-reactive protein in women of reproductive age: a panel study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549434/
https://www.ncbi.nlm.nih.gov/pubmed/28789684
http://dx.doi.org/10.1186/s12940-017-0293-6
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