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Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study

BACKGROUND: High arsenic exposure has been related to diabetes, but at low-moderate levels the evidence is mixed. Arsenic metabolism, which is partly genetically controlled and may rely on certain B vitamins, plays a role in arsenic toxicity. OBJECTIVE: We evaluated the prospective association of ar...

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Autores principales: Grau-Perez, Maria, Kuo, Chin-Chi, Gribble, Matthew O., Balakrishnan, Poojitha, Jones Spratlen, Miranda, Vaidya, Dhananjay, Francesconi, Kevin A., Goessler, Walter, Guallar, Eliseo, Silbergeld, Ellen K., Umans, Jason G., Best, Lyle G., Lee, Elisa T., Howard, Barbara V., Cole, Shelley A., Navas-Acien, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Environmental Health Perspectives 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963590/
https://www.ncbi.nlm.nih.gov/pubmed/29373862
http://dx.doi.org/10.1289/EHP2566
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author Grau-Perez, Maria
Kuo, Chin-Chi
Gribble, Matthew O.
Balakrishnan, Poojitha
Jones Spratlen, Miranda
Vaidya, Dhananjay
Francesconi, Kevin A.
Goessler, Walter
Guallar, Eliseo
Silbergeld, Ellen K.
Umans, Jason G.
Best, Lyle G.
Lee, Elisa T.
Howard, Barbara V.
Cole, Shelley A.
Navas-Acien, Ana
author_facet Grau-Perez, Maria
Kuo, Chin-Chi
Gribble, Matthew O.
Balakrishnan, Poojitha
Jones Spratlen, Miranda
Vaidya, Dhananjay
Francesconi, Kevin A.
Goessler, Walter
Guallar, Eliseo
Silbergeld, Ellen K.
Umans, Jason G.
Best, Lyle G.
Lee, Elisa T.
Howard, Barbara V.
Cole, Shelley A.
Navas-Acien, Ana
author_sort Grau-Perez, Maria
collection PubMed
description BACKGROUND: High arsenic exposure has been related to diabetes, but at low-moderate levels the evidence is mixed. Arsenic metabolism, which is partly genetically controlled and may rely on certain B vitamins, plays a role in arsenic toxicity. OBJECTIVE: We evaluated the prospective association of arsenic exposure and metabolism with type 2 diabetes and insulin resistance. METHODS: We included 1,838 American Indian men and women free of diabetes (median age, 36 y). Arsenic exposure was assessed as the sum of inorganic arsenic (iAs), monomethylarsonate (MMA), and dimethylarsinate (DMA) urine concentrations ([Formula: see text]). Arsenic metabolism was evaluated by the proportions of iAs, MMA, and DMA over their sum (iAs%, MMA%, and DMA%). Homeostasis model assessment for insulin resistance (HOMA2-IR) was measured at baseline and follow-up visits. Incident diabetes was evaluated at follow-up. RESULTS: Median [Formula: see text] , iAs%, MMA%, and DMA% was [Formula: see text] creatinine, 9.5%, 14.4%, and 75.6%, respectively. Over 10,327 person-years of follow-up, 252 participants developed diabetes. Median HOMA2-IR at baseline was 1.5. The fully adjusted hazard ratio [95% confidence interval (CI)] for incident diabetes per an interquartile range increase in [Formula: see text] was 1.57 (95% CI: 1.18, 2.08) in participants without prediabetes at baseline. Arsenic metabolism was not associated with incident diabetes. [Formula: see text] was positively associated with HOMA2-IR at baseline but negatively with HOMA2-IR at follow-up. Increased MMA% was associated with lower HOMA2-IR when either iAs% or DMA% decreased. The association of arsenic metabolism with HOMA2-IR differed by B-vitamin intake and AS3MT genetics variants. CONCLUSIONS: Among participants without baseline prediabetes, arsenic exposure was associated with incident diabetes. Low MMA% was cross-sectional and prospectively associated with higher HOMA2-IR. Research is needed to confirm possible interactions of arsenic metabolism with B vitamins and AS3MT variants on diabetes risk. https://doi.org/10.1289/EHP2566
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spelling pubmed-59635902018-05-30 Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study Grau-Perez, Maria Kuo, Chin-Chi Gribble, Matthew O. Balakrishnan, Poojitha Jones Spratlen, Miranda Vaidya, Dhananjay Francesconi, Kevin A. Goessler, Walter Guallar, Eliseo Silbergeld, Ellen K. Umans, Jason G. Best, Lyle G. Lee, Elisa T. Howard, Barbara V. Cole, Shelley A. Navas-Acien, Ana Environ Health Perspect Research BACKGROUND: High arsenic exposure has been related to diabetes, but at low-moderate levels the evidence is mixed. Arsenic metabolism, which is partly genetically controlled and may rely on certain B vitamins, plays a role in arsenic toxicity. OBJECTIVE: We evaluated the prospective association of arsenic exposure and metabolism with type 2 diabetes and insulin resistance. METHODS: We included 1,838 American Indian men and women free of diabetes (median age, 36 y). Arsenic exposure was assessed as the sum of inorganic arsenic (iAs), monomethylarsonate (MMA), and dimethylarsinate (DMA) urine concentrations ([Formula: see text]). Arsenic metabolism was evaluated by the proportions of iAs, MMA, and DMA over their sum (iAs%, MMA%, and DMA%). Homeostasis model assessment for insulin resistance (HOMA2-IR) was measured at baseline and follow-up visits. Incident diabetes was evaluated at follow-up. RESULTS: Median [Formula: see text] , iAs%, MMA%, and DMA% was [Formula: see text] creatinine, 9.5%, 14.4%, and 75.6%, respectively. Over 10,327 person-years of follow-up, 252 participants developed diabetes. Median HOMA2-IR at baseline was 1.5. The fully adjusted hazard ratio [95% confidence interval (CI)] for incident diabetes per an interquartile range increase in [Formula: see text] was 1.57 (95% CI: 1.18, 2.08) in participants without prediabetes at baseline. Arsenic metabolism was not associated with incident diabetes. [Formula: see text] was positively associated with HOMA2-IR at baseline but negatively with HOMA2-IR at follow-up. Increased MMA% was associated with lower HOMA2-IR when either iAs% or DMA% decreased. The association of arsenic metabolism with HOMA2-IR differed by B-vitamin intake and AS3MT genetics variants. CONCLUSIONS: Among participants without baseline prediabetes, arsenic exposure was associated with incident diabetes. Low MMA% was cross-sectional and prospectively associated with higher HOMA2-IR. Research is needed to confirm possible interactions of arsenic metabolism with B vitamins and AS3MT variants on diabetes risk. https://doi.org/10.1289/EHP2566 Environmental Health Perspectives 2017-12-20 /pmc/articles/PMC5963590/ /pubmed/29373862 http://dx.doi.org/10.1289/EHP2566 Text en EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted.
spellingShingle Research
Grau-Perez, Maria
Kuo, Chin-Chi
Gribble, Matthew O.
Balakrishnan, Poojitha
Jones Spratlen, Miranda
Vaidya, Dhananjay
Francesconi, Kevin A.
Goessler, Walter
Guallar, Eliseo
Silbergeld, Ellen K.
Umans, Jason G.
Best, Lyle G.
Lee, Elisa T.
Howard, Barbara V.
Cole, Shelley A.
Navas-Acien, Ana
Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study
title Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study
title_full Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study
title_fullStr Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study
title_full_unstemmed Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study
title_short Association of Low-Moderate Arsenic Exposure and Arsenic Metabolism with Incident Diabetes and Insulin Resistance in the Strong Heart Family Study
title_sort association of low-moderate arsenic exposure and arsenic metabolism with incident diabetes and insulin resistance in the strong heart family study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963590/
https://www.ncbi.nlm.nih.gov/pubmed/29373862
http://dx.doi.org/10.1289/EHP2566
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