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Elevated whole blood arsenic level is associated with type 2 diabetes in coal-burning areas in Guizhou.

Authors :
Dai L
Lv X
Chen Z
Huang Z
Li B
Xie Y
Duan Y
Zhao H
Wang Y
Yu Q
Li S
Zhou Y
Shen X
Source :
Toxicology and applied pharmacology [Toxicol Appl Pharmacol] 2020 Sep 15; Vol. 403, pp. 115135. Date of Electronic Publication: 2020 Jul 18.
Publication Year :
2020

Abstract

The potential association between coal-burning arsenic exposure and type 2 diabetes (T2D) was examined through a case control study, conducted in coal-burning arsenic poisoning areas in the Guizhou Province. This study included patients diagnosed with type 2 diabetes. Control subjects without type 2 diabetes were recruited randomly after gender and age 1:1 matching. All subjects completed questionnaire surveys and underwent physical examination and whole blood arsenic level testing. The whole blood arsenic level was associated with a significant increase in the risk of type 2 diabetes (75th versus 25th, adjusted OR = 1.76, 95% CI: 1.03-3.01). However, a nonlinear relationship was observed between the blood arsenic level and type 2 diabetes. The risk of type 2 diabetes increased with blood arsenic levels above 3.69 μg/L (Log As ≥0.57). The subgroup analysis revealed that blood arsenic levels were associated with significantly increased risk of type 2 diabetes in people who ever smoked (P < .05), particularly those who smoked ≥15 years (adjusted OR = 3.15, 95% CI: 1.9-7.28). Therefore, prolonged arsenic exposure, even at a low level, is associated with a higher prevalence of type 2 diabetes in a nonlinear pattern. Blood arsenic levels less than 3.69 μg/L may be considered safe with respect to the risk of T2D. However, smoking, particularly smoking ≥15 years, may be associated with the development of diabetes in patients with arsenic exposure.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no conflicts of interest.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1096-0333
Volume :
403
Database :
MEDLINE
Journal :
Toxicology and applied pharmacology
Publication Type :
Academic Journal
Accession number :
32692994
Full Text :
https://doi.org/10.1016/j.taap.2020.115135