4.8 Article

Association between maternal urinary speciated arsenic concentrations and gestational diabetes in a cohort of Canadian women

Journal

ENVIRONMENT INTERNATIONAL
Volume 121, Issue -, Pages 714-720

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.envint.2018.10.008

Keywords

Arsenic; Gestational diabetes; Cohort study; Pregnancy

Funding

  1. Canadian Diabetes Association [OG-2-11-3424]
  2. Chemicals Management Plan of Health Canada
  3. Canadian Institutes for Health Research [MOP-81285]
  4. Ontario Ministry of the Environment

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Background: Epidemiological and toxicological evidence suggests that maternal total arsenic (As) levels are associated with an elevated risk of gestational diabetes (GDM). Uncertainty remains regarding the metabolic toxicity of specific arsenic species, comprised of both organic and inorganic sources of arsenic exposure. Objectives: We assessed associations between speciated As and GDM using data from the Maternal-Infant Research on Environmental Chemicals (MIREC) Study. Methods: Concentrations of speciated As [(inorganic (trivalent, pentavalent)), methylated arsenic species metabolites (monomethylarsonic acid (MMA), dimethylarsinic acid (DMA)), and organic (arsenobetaine)] were measured in first trimester maternal urine samples. GDM cases were identified in accordance with Canadian guidelines. Multivariable regression models were used to estimate associations between speciated As and GDM, evaluate potential interaction between speciated As exposures, and assess fetal sex-specific findings. Results: Among 1243 women who had a live, singleton birth and no previous history of diabetes, 4% met the diagnostic criteria for GDM. Our analyses focused on DMA and arsenobetaine as these were the subtypes with detectable concentrations in at least 40% of samples. Compared to women in the lowest tertile of DMA (< 1.49 mu g As/L), women with concentrations exceeding 3.52 mu g As/L (3rd tertile) experienced an increased risk of GDM (aOR = 3.86; 95% CI: 1.18, 12.57) (p-value for trend across tertiles = 0.04). When restricted to women carrying male infants, the magnitude of this association increased (aOR 3rd tertile = 4.71; 95% CI: 1.05, 21.10). Conclusions: These results suggest a positive relation between DMA and GDM; potential differences in risk by fetal sex requires further investigation.

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