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Arsenic Exposure and Calpain-10 Polymorphisms Impair the Function of Pancreatic Beta-Cells in Humans: A Pilot Study of Risk Factors for T2DM

Overview of attention for article published in PLOS ONE, January 2013
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Title
Arsenic Exposure and Calpain-10 Polymorphisms Impair the Function of Pancreatic Beta-Cells in Humans: A Pilot Study of Risk Factors for T2DM
Published in
PLOS ONE, January 2013
DOI 10.1371/journal.pone.0051642
Pubmed ID
Authors

Andrea Díaz-Villaseñor, Laura Cruz, Arturo Cebrián, Raúl U. Hernández-Ramírez, Marcia Hiriart, Gonzálo García-Vargas, Susana Bassol, Monserrat Sordo, A. Jay Gandolfi, Walter T. Klimecki, Lizbeth López-Carillo, Mariano E. Cebrián, Patricia Ostrosky-Wegman

Abstract

The incidence of type 2 diabetes mellitus (T2DM) is increasing worldwide and diverse environmental and genetic risk factors are well recognized. Single nucleotide polymorphisms (SNPs) in the calpain-10 gene (CAPN-10), which encodes a protein involved in the secretion and action of insulin, and chronic exposure to inorganic arsenic (iAs) through drinking water have been independently associated with an increase in the risk for T2DM. In the present work we evaluated if CAPN-10 SNPs and iAs exposure jointly contribute to the outcome of T2DM. Insulin secretion (beta-cell function) and insulin sensitivity were evaluated indirectly through validated indexes (HOMA2) in subjects with and without T2DM who have been exposed to a gradient of iAs in their drinking water in northern Mexico. The results were analyzed taking into account the presence of the risk factor SNPs SNP-43 and -44 in CAPN-10. Subjects with T2DM had significantly lower beta-cell function and insulin sensitivity. An inverse association was found between beta-cell function and iAs exposure, the association being more pronounced in subjects with T2DM. Subjects without T2DM who were carriers of the at-risk genotype SNP-43 or -44, also had significantly lower beta-cell function. The association of SNP-43 with beta-cell function was dependent on iAs exposure, age, gender and BMI, whereas the association with SNP-44 was independent of all of these factors. Chronic exposure to iAs seems to be a risk factor for T2DM in humans through the reduction of beta-cell function, with an enhanced effect seen in the presence of the at-risk genotype of SNP-43 in CAPN-10. Carriers of CAPN-10 SNP-44 have also shown reduced beta-cell function.

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Mendeley readers

The data shown below were compiled from readership statistics for 58 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Brazil 2 3%
Mexico 1 2%
Ecuador 1 2%
United States 1 2%
Unknown 53 91%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 14%
Student > Master 8 14%
Researcher 7 12%
Student > Bachelor 7 12%
Student > Doctoral Student 6 10%
Other 14 24%
Unknown 8 14%
Readers by discipline Count As %
Medicine and Dentistry 15 26%
Agricultural and Biological Sciences 12 21%
Biochemistry, Genetics and Molecular Biology 4 7%
Nursing and Health Professions 3 5%
Pharmacology, Toxicology and Pharmaceutical Science 2 3%
Other 10 17%
Unknown 12 21%