Arsenic exposure-related hyperglycemia is linked to insulin resistance with concomitant reduction of skeletal muscle mass. (October 2020)

• Record Type: Journal Article
• Authors: Mondal, Victor; Hosen, Zubaer; Hossen, Faruk; Siddique, Abu Eabrahim; Tony, Selim Reza; Islam, Zohurul; Islam, Md. Shofikul; Hossain, Shakhawoat; Islam, Khairul; Sarker, Md. Khalequzzaman; Hasibuzzaman, M.M.; Liu, Ling-Zhi; Jiang, Bing-Hua; Hoque, Md Mominul; Saud, Zahangir Alam; Xin, Lian; Himeno, Seiichiro; Hossain, Khaled
• Is Part Of: Environment international. Volume 143(2020)
• Publication Date: 2020-10
• Subjects: Arsenic -- Diabetes -- Bangladesh -- Hyperglycemia -- Insulin resistance -- Muscle mass; Environmental protection -- Periodicals; Environmental health -- Periodicals; Environmental monitoring -- Periodicals; Environmental Monitoring -- Periodicals; Environnement -- Protection -- Périodiques; Hygiène du milieu -- Périodiques; Environnement -- Surveillance -- Périodiques; Environmental health; Environmental monitoring; Environmental protection; Periodicals; 333.705
• DOI: 10.1016/j.envint.2020.105890
• Languages: English
• ISSNs: 0160-4120

Abstract

Highlights: Arsenic exposure increases fasting blood glucose levels and insulin resistance. Arsenic exposure causes the reduction of skeletal muscle mass. Arsenic exposure increased the risk of hyperglycemia. Females are more susceptible to arsenic -related hyperglycemia than males. Risk of hyperglycemia is increased with reduction of skeletal muscle mass. Abstract: Background: A large body of evidence has shown a link between arsenic exposure and diabetes, but the underlying mechanisms have not yet been clarified. Objective: We explored the association between arsenic exposure and the reduction of skeletal muscle mass as a potential mechanism of insulin resistance for developing arsenic-related hyperglycemia. Methods: A total of 581 subjects were recruited from arsenic-endemic and non-endemic areas in Bangladesh and their fasting blood glucose (FBG), serum insulin, and serum creatinine levels were determined. Subjects' arsenic exposure levels were assessed by arsenic concentrations in water, hair, and nails. HOMA-IR and HOMA-β were used to calculate insulin resistance and β-cell dysfunction, respectively. Serum creatinine levels and lean body mass (LBM) were used as muscle mass indicators. Results: Water, hair and nail arsenic concentrations showed significant positive associations with FBG, serum insulin and HOMA-IR and inverse associations with serum creatinine and LBM in a dose-dependent manner both in males and females. Water, hair and nail arsenic showed significant inverse associations with HOMA-β in females but not in males. FBG and HOMA-IR were increased with the decreasing levels of serum creatinine and LBM. Odds ratios (ORs) of hyperglycemia were significantly increased with the increasing concentrations of arsenic in water, hair and nails and with the decreasing levels of serum creatinine and LBM. Females' HOMA-IR showed greater susceptibility to the reduction of serum creatinine and LBM, possibly causing the greater risk of hyperglycemia in females than males. Path analysis revealed the mediating effect of serum creatinine level on the relationship of arsenic exposure with HOMA-IR and hyperglycemia. Conclusion: Arsenic exposure elevates FBG levels and the risk of hyperglycemia through increasing insulin resistance with greater susceptibility in females than males. Additionally, arsenic exposure-related reduction of skeletal muscle mass may be a mechanism underlying the development of insulin resistance and hyperglycemia.