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Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh

Arsenic contamination of drinking water is a major public health issue in many countries, increasing risk for a wide array of diseases, including cancer. There is inter-individual variation in arsenic metabolism efficiency and susceptibility to arsenic toxicity; however, the basis of this variation...

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Published in:PLoS genetics 2012-02, Vol.8 (2), p.e1002522
Main Authors: Pierce, Brandon L, Kibriya, Muhammad G, Tong, Lin, Jasmine, Farzana, Argos, Maria, Roy, Shantanu, Paul-Brutus, Rachelle, Rahaman, Ronald, Rakibuz-Zaman, Muhammad, Parvez, Faruque, Ahmed, Alauddin, Quasem, Iftekhar, Hore, Samar K, Alam, Shafiul, Islam, Tariqul, Slavkovich, Vesna, Gamble, Mary V, Yunus, Md, Rahman, Mahfuzar, Baron, John A, Graziano, Joseph H, Ahsan, Habibul
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Language:English
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Summary:Arsenic contamination of drinking water is a major public health issue in many countries, increasing risk for a wide array of diseases, including cancer. There is inter-individual variation in arsenic metabolism efficiency and susceptibility to arsenic toxicity; however, the basis of this variation is not well understood. Here, we have performed the first genome-wide association study (GWAS) of arsenic-related metabolism and toxicity phenotypes to improve our understanding of the mechanisms by which arsenic affects health. Using data on urinary arsenic metabolite concentrations and approximately 300,000 genome-wide single nucleotide polymorphisms (SNPs) for 1,313 arsenic-exposed Bangladeshi individuals, we identified genome-wide significant association signals (P
ISSN:1553-7404
1553-7390
1553-7404
DOI:10.1371/journal.pgen.1002522