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Author Notes:

Chin-Chi Kuo, MD, PhD., Kidney Division and Big Data Center, China Medical University Hospital and College of Medicine, China Medical University, Taichung, Taiwan, Address: 2, Yude Rd., North Dist., Taichung City 404, Tel: 886-4-22052121 ext. 2501. Email: chinchik@gmail.com

The authors thank Nancy LoIacono for the substantive editorial comments to this manuscript.

Subjects:

Research Funding:

This study was supported by grants from the U.S. National Heart, Lung, and Blood Institute (R01-HL-090863, HL-41642, HL-41652, HL-41654, and HL-65521), the U.S. National Institute of Environmental Health Sciences (R01-ES-021367 and P30-ES-03819), and the China Medical University Hospital, Taiwan (DMR-HHC-110-5).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Environmental Sciences
  • Environmental Sciences & Ecology
  • American Indians
  • Arsenic
  • Arsenic species
  • Arsenic methylation
  • Arsenic metabolism
  • Mortality
  • Cardiovascular disease
  • Cancer
  • Strong Heart Study
  • AMERICAN-INDIANS
  • DRINKING-WATER
  • DOSE-RESPONSE
  • DISEASE
  • RISK
  • METHYLATION
  • ACID
  • LEVEL
  • SUPPLEMENTATION
  • METAANALYSIS

The association of arsenic exposure and arsenic metabolism with all-cause, cardiovascular and cancer mortality in the Strong Heart Study

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Journal Title:

ENVIRONMENT INTERNATIONAL

Volume:

Volume 159

Publisher:

, Pages 107029-107029

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The effect of low-moderate levels of arsenic exposure and of arsenic metabolism on mortality remains uncertain. We used data from a prospective cohort study in 3600 men and women aged 45 to 75 years living in Arizona, Oklahoma, and North and South Dakota. The biomarker of inorganic arsenic exposure was the sum of urine inorganic (iAs), monomethylated (MMA) and dimethylated (DMA) arsenic compounds (ƩAs) at baseline. The proportions of urine iAs, MMA and DMA over the ƩiAs, expressed as iAs%, MMA%, and DMA%, respectively, were used as biomarkers of arsenic metabolism. Arsenic exposure and arsenic metabolism were associated with all-cause, cardiovascular, and cancer mortality. For each interquartile range (IQR) increase in ƩAs (12.5 μg/L, overall range 0.7–194.1 μg/L), the adjusted hazard ratios (aHRs) were 1.28 (95% CI 1.16–1.41) for all-cause mortality, 1.28 (1.08–1.52) for cardiovascular mortality and 1.15 (0.92–1.44) for cancer mortality. The aHR for mortality for each IQR increase in MMA%, when iAs% is decreasing, was 1.52 (95% CI 1.16–1.99) for cardiovascular disease, 0.73 (0.55–0.98) for cancer, and 1.03 (0.90–1.19) for all-cause mortality. These findings at low-moderate levels of arsenic exposure highlight the need to implement public health measures to protect populations from involuntary arsenic exposure and for research to advance the biological and clinical understanding of arsenic-related health effects in general populations.

Copyright information:

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/rdf).
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