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Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México
Environmental arsenic exposure in adults and children has been associated with a reduction in the expression of club cell secretory protein (CC16) and an increase in the expression of matrix metalloproteinase-9 (MMP-9), both biomarkers of lung inflammation and negative respiratory outcomes. The obje...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919633/ https://www.ncbi.nlm.nih.gov/pubmed/33650048 http://dx.doi.org/10.1007/s11356-021-13070-x |
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author | Vega-Millán, Christian B. Dévora-Figueroa, Ana G. Burgess, Jefferey L. Beamer, Paloma I. Furlong, Melissa Lantz, R. Clark Meza-Figueroa, Diana O´Rourke, Mary Kay García-Rico, Leticia Meza-Escalante, Edna R. Balderas-Cortés, José J. Meza-Montenegro, Maria M. |
author_facet | Vega-Millán, Christian B. Dévora-Figueroa, Ana G. Burgess, Jefferey L. Beamer, Paloma I. Furlong, Melissa Lantz, R. Clark Meza-Figueroa, Diana O´Rourke, Mary Kay García-Rico, Leticia Meza-Escalante, Edna R. Balderas-Cortés, José J. Meza-Montenegro, Maria M. |
author_sort | Vega-Millán, Christian B. |
collection | PubMed |
description | Environmental arsenic exposure in adults and children has been associated with a reduction in the expression of club cell secretory protein (CC16) and an increase in the expression of matrix metalloproteinase-9 (MMP-9), both biomarkers of lung inflammation and negative respiratory outcomes. The objectives of this study were to determine if the levels of serum CC16 and MMP-9 and subsequent respiratory infections in children are associated with the ingestion of arsenic by drinking water. This cross-sectional study included 216 children from three Yaqui villages, Potam, Vicam, and Cocorit, with levels of arsenic in their ground water of 70.01 ± 21.85, 23.3 ± 9.99, and 11.8 ± 4.42 μg/L respectively. Total arsenic in water and urine samples was determined by inductively coupled plasma/optical emission spectrometry. Serum was analyzed for CC16 and MMP-9 using ELISA. The children had an average urinary arsenic of 79.39 μg/L and 46.8 % had levels above of the national concern value of 50 μg/L. Increased arsenic concentrations in drinking water and average daily arsenic intake by water were associated with decreased serum CC16 levels (β = − 0.12, 95% CI − 0.20, − 0.04 and β = − 0.10, 95% CI − 0.18, − 0.03), and increased serum MMP-9 levels (β = 0.35, 95% CI 0.22, 0.48 and β = 0.29, 95% CI 0.18, 0.40) at significant levels (P < 0.05). However, no association was found between levels of these serum biomarkers and urinary arsenic concentrations. In these children, reduced serum CC16 levels were significantly associated with increased risk of respiratory infections (OR = 0.34, 95% CI 0.13, 0.90). In conclusion, altered levels of serum CC16 and MMP-9 in the children may be due to the toxic effects of arsenic exposure through drinking water. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-021-13070-x. |
format | Online Article Text |
id | pubmed-7919633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-79196332021-03-02 Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México Vega-Millán, Christian B. Dévora-Figueroa, Ana G. Burgess, Jefferey L. Beamer, Paloma I. Furlong, Melissa Lantz, R. Clark Meza-Figueroa, Diana O´Rourke, Mary Kay García-Rico, Leticia Meza-Escalante, Edna R. Balderas-Cortés, José J. Meza-Montenegro, Maria M. Environ Sci Pollut Res Int Research Article Environmental arsenic exposure in adults and children has been associated with a reduction in the expression of club cell secretory protein (CC16) and an increase in the expression of matrix metalloproteinase-9 (MMP-9), both biomarkers of lung inflammation and negative respiratory outcomes. The objectives of this study were to determine if the levels of serum CC16 and MMP-9 and subsequent respiratory infections in children are associated with the ingestion of arsenic by drinking water. This cross-sectional study included 216 children from three Yaqui villages, Potam, Vicam, and Cocorit, with levels of arsenic in their ground water of 70.01 ± 21.85, 23.3 ± 9.99, and 11.8 ± 4.42 μg/L respectively. Total arsenic in water and urine samples was determined by inductively coupled plasma/optical emission spectrometry. Serum was analyzed for CC16 and MMP-9 using ELISA. The children had an average urinary arsenic of 79.39 μg/L and 46.8 % had levels above of the national concern value of 50 μg/L. Increased arsenic concentrations in drinking water and average daily arsenic intake by water were associated with decreased serum CC16 levels (β = − 0.12, 95% CI − 0.20, − 0.04 and β = − 0.10, 95% CI − 0.18, − 0.03), and increased serum MMP-9 levels (β = 0.35, 95% CI 0.22, 0.48 and β = 0.29, 95% CI 0.18, 0.40) at significant levels (P < 0.05). However, no association was found between levels of these serum biomarkers and urinary arsenic concentrations. In these children, reduced serum CC16 levels were significantly associated with increased risk of respiratory infections (OR = 0.34, 95% CI 0.13, 0.90). In conclusion, altered levels of serum CC16 and MMP-9 in the children may be due to the toxic effects of arsenic exposure through drinking water. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-021-13070-x. Springer Berlin Heidelberg 2021-03-01 2021 /pmc/articles/PMC7919633/ /pubmed/33650048 http://dx.doi.org/10.1007/s11356-021-13070-x Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Research Article Vega-Millán, Christian B. Dévora-Figueroa, Ana G. Burgess, Jefferey L. Beamer, Paloma I. Furlong, Melissa Lantz, R. Clark Meza-Figueroa, Diana O´Rourke, Mary Kay García-Rico, Leticia Meza-Escalante, Edna R. Balderas-Cortés, José J. Meza-Montenegro, Maria M. Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México |
title | Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México |
title_full | Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México |
title_fullStr | Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México |
title_full_unstemmed | Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México |
title_short | Inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three Yaqui villages in southern Sonora, México |
title_sort | inflammation biomarkers associated with arsenic exposure by drinking water and respiratory outcomes in indigenous children from three yaqui villages in southern sonora, méxico |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919633/ https://www.ncbi.nlm.nih.gov/pubmed/33650048 http://dx.doi.org/10.1007/s11356-021-13070-x |
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