Skip to main content
Erschienen in: Current Diabetes Reports 12/2019

01.12.2019 | Diabetes Epidemiology (E Selvin and K Foti, Section Editors)

Early-Life Arsenic Exposure, Nutritional Status, and Adult Diabetes Risk

verfasst von: Ana Navas-Acien, Miranda J. Spratlen, Ahlam Abuawad, Nancy J. LoIacono, Anne K. Bozack, Mary V. Gamble

Erschienen in: Current Diabetes Reports | Ausgabe 12/2019

Einloggen, um Zugang zu erhalten

Abstract

Purpose of Review

In utero influences, including nutrition and environmental chemicals, may induce long-term metabolic changes and increase diabetes risk in adulthood. This review evaluates the experimental and epidemiological evidence on the association of early-life arsenic exposure on diabetes and diabetes-related outcomes, as well as the influence of maternal nutritional status on arsenic-related metabolic effects.

Recent Findings

Five studies in rodents have evaluated the role of in utero arsenic exposure with diabetes in the offspring. In four of the studies, elevated post-natal fasting glucose was observed when comparing in utero arsenic exposure with no exposure. Rodent offspring exposed to arsenic in utero also showed elevated insulin resistance in the 4 studies evaluating it as well as microRNA changes related to glycemic control in 2 studies. Birth cohorts of arsenic-exposed pregnant mothers in New Hampshire, Mexico, and Taiwan have shown that increased prenatal arsenic exposure is related to altered cord blood gene expression, microRNA, and DNA methylation profiles in diabetes-related pathways. Thus far, no epidemiologic studies have evaluated early-life arsenic exposure with diabetes risk. Supplementation trials have shown B vitamins can reduce blood arsenic levels in highly exposed, undernourished populations. Animal evidence supports that adequate B vitamin status can rescue early-life arsenic-induced diabetes risk, although human data is lacking.

Summary

Experimental animal studies and human evidence on the association of in utero arsenic exposure with alterations in gene expression pathways related to diabetes in newborns, support the potential role of early-life arsenic exposure in diabetes development, possibly through increased insulin resistance. Given pervasive arsenic exposure and the challenges to eliminate arsenic from the environment, research is needed to evaluate prevention interventions, including the possibility of low-cost, low-risk nutritional interventions that can modify arsenic-related disease risk.
Literatur
1.
Zurück zum Zitat Gillman MW, Barker D, Bier D, et al. Meeting report on the 3rd International Congress on Developmental Origins of Health and Disease (DOHaD). Pediatr Res. 2007;61:625–9.PubMed Gillman MW, Barker D, Bier D, et al. Meeting report on the 3rd International Congress on Developmental Origins of Health and Disease (DOHaD). Pediatr Res. 2007;61:625–9.PubMed
2.
Zurück zum Zitat Aerts L, Van Assche FA. Animal evidence for the transgenerational development of diabetes mellitus. Int J Biochem Cell Biol. 2006;38:894–903.PubMed Aerts L, Van Assche FA. Animal evidence for the transgenerational development of diabetes mellitus. Int J Biochem Cell Biol. 2006;38:894–903.PubMed
3.
Zurück zum Zitat Yajnik CS. Transmission of obesity-adiposity and related disorders from the mother to the baby. Ann Nutr Metab. 2014;64(Suppl 1):8–17.PubMed Yajnik CS. Transmission of obesity-adiposity and related disorders from the mother to the baby. Ann Nutr Metab. 2014;64(Suppl 1):8–17.PubMed
4.
Zurück zum Zitat Council USNR. Critical aspects of the EPA’s IRIS assessment of inorganic arsenic: Interim Report. In: Medicine TNAoSE, ed.: The National Acadamies Press; 2013. Council USNR. Critical aspects of the EPA’s IRIS assessment of inorganic arsenic: Interim Report. In: Medicine TNAoSE, ed.: The National Acadamies Press; 2013.
5.
Zurück zum Zitat Chen Y, Graziano JH, Parvez F, et al. Arsenic exposure from drinking water and mortality from cardiovascular disease in Bangladesh: prospective cohort study. BMJ. 2011;342:d2431.PubMedPubMedCentral Chen Y, Graziano JH, Parvez F, et al. Arsenic exposure from drinking water and mortality from cardiovascular disease in Bangladesh: prospective cohort study. BMJ. 2011;342:d2431.PubMedPubMedCentral
6.
Zurück zum Zitat Jiang JY, Liu ML, Parvez F, et al. Association between arsenic exposure from drinking water and longitudinal change in blood pressure among HEALS cohort participants. Environ Health Perspect. 2015;123:806–12.PubMedPubMedCentral Jiang JY, Liu ML, Parvez F, et al. Association between arsenic exposure from drinking water and longitudinal change in blood pressure among HEALS cohort participants. Environ Health Perspect. 2015;123:806–12.PubMedPubMedCentral
7.
Zurück zum Zitat Karagas MR, Gossai A, Pierce B, Ahsan H. Drinking water arsenic contamination, skin lesions, and malignancies: a systematic review of the global evidence. Curr Environ Health Rep. 2015;2:52–68.PubMedPubMedCentral Karagas MR, Gossai A, Pierce B, Ahsan H. Drinking water arsenic contamination, skin lesions, and malignancies: a systematic review of the global evidence. Curr Environ Health Rep. 2015;2:52–68.PubMedPubMedCentral
8.
Zurück zum Zitat Kibriya MG, Jasmine F, Parvez F, et al. Association between genome-wide copy number variation and arsenic-induced skin lesions: a prospective study. Environ Health. 2017;16:75.PubMedPubMedCentral Kibriya MG, Jasmine F, Parvez F, et al. Association between genome-wide copy number variation and arsenic-induced skin lesions: a prospective study. Environ Health. 2017;16:75.PubMedPubMedCentral
9.
Zurück zum Zitat Spratlen MJ, Grau-Perez M, Umans JG, et al. Arsenic, one carbon metabolism and diabetes-related outcomes in the strong heart family study. Environ Int. 2018;121:728–40.PubMedPubMedCentral Spratlen MJ, Grau-Perez M, Umans JG, et al. Arsenic, one carbon metabolism and diabetes-related outcomes in the strong heart family study. Environ Int. 2018;121:728–40.PubMedPubMedCentral
10.
Zurück zum Zitat • Grau-Perez M, Kuo CC, Gribble MO, et al. Association of low-moderate arsenic exposure and arsenic metabolism with incident diabetes and insulin resistance in the Strong Heart Family Study. Environ Health Perspect. 2017;125:127004 This epidemiologic study in children and adolescents in the USA found a possible interaction between folate and vitamin B12 and arsenic metabolism biomarkers on diabetes risk.PubMedPubMedCentral • Grau-Perez M, Kuo CC, Gribble MO, et al. Association of low-moderate arsenic exposure and arsenic metabolism with incident diabetes and insulin resistance in the Strong Heart Family Study. Environ Health Perspect. 2017;125:127004 This epidemiologic study in children and adolescents in the USA found a possible interaction between folate and vitamin B12 and arsenic metabolism biomarkers on diabetes risk.PubMedPubMedCentral
11.
Zurück zum Zitat Wasserman GA, Liu X, Loiacono NJ, et al. A cross-sectional study of well water arsenic and child IQ in Maine schoolchildren. Environ Health. 2014;13:23.PubMedPubMedCentral Wasserman GA, Liu X, Loiacono NJ, et al. A cross-sectional study of well water arsenic and child IQ in Maine schoolchildren. Environ Health. 2014;13:23.PubMedPubMedCentral
12.
Zurück zum Zitat Martin EM, Styblo M, Fry RC. Genetic and epigenetic mechanisms underlying arsenic-associated diabetes mellitus: a perspective of the current evidence. Epigenomics. 2017;9:701–10.PubMedPubMedCentral Martin EM, Styblo M, Fry RC. Genetic and epigenetic mechanisms underlying arsenic-associated diabetes mellitus: a perspective of the current evidence. Epigenomics. 2017;9:701–10.PubMedPubMedCentral
13.
Zurück zum Zitat Andrew AS, Jewell DA, Mason RA, Whitfield ML, Moore JH, Karagas MR. Drinking-water arsenic exposure modulates gene expression in human lymphocytes from a U.S. population. EnvironHealth Perspect. 2008;116:524–31.PubMedPubMedCentral Andrew AS, Jewell DA, Mason RA, Whitfield ML, Moore JH, Karagas MR. Drinking-water arsenic exposure modulates gene expression in human lymphocytes from a U.S. population. EnvironHealth Perspect. 2008;116:524–31.PubMedPubMedCentral
14.
Zurück zum Zitat Rojas D, Rager JE, Smeester L, et al. Prenatal arsenic exposure and the epigenome: identifying sites of 5-methylcytosine alterations that predict functional changes in gene expression in newborn cord blood and subsequent birth outcomes. Toxicol Sci. 2015;143:97–106.PubMed Rojas D, Rager JE, Smeester L, et al. Prenatal arsenic exposure and the epigenome: identifying sites of 5-methylcytosine alterations that predict functional changes in gene expression in newborn cord blood and subsequent birth outcomes. Toxicol Sci. 2015;143:97–106.PubMed
15.
Zurück zum Zitat Rager JE, Bailey KA, Smeester L, et al. Prenatal arsenic exposure and the epigenome: altered microRNAs associated with innate and adaptive immune signaling in newborn cord blood. Environ Mol Mutagen. 2014;55:196–208.PubMed Rager JE, Bailey KA, Smeester L, et al. Prenatal arsenic exposure and the epigenome: altered microRNAs associated with innate and adaptive immune signaling in newborn cord blood. Environ Mol Mutagen. 2014;55:196–208.PubMed
16.
Zurück zum Zitat Kaushal A, Zhang H, Karmaus WJJ, et al. Genome-wide DNA methylation at birth in relation to in utero arsenic exposure and the associated health in later life. Environ Health. 2017;16:50.PubMedPubMedCentral Kaushal A, Zhang H, Karmaus WJJ, et al. Genome-wide DNA methylation at birth in relation to in utero arsenic exposure and the associated health in later life. Environ Health. 2017;16:50.PubMedPubMedCentral
17.
Zurück zum Zitat Davila-Esqueda ME, Morales JM, Jimenez-Capdeville ME, et al. Low-level subchronic arsenic exposure from prenatal developmental stages to adult life results in an impaired glucose homeostasis. Experimental and clinical endocrinology & diabetes. official journal, German Society of Endocrinology [and] German Diabetes Association. 2011;119:613–7. Davila-Esqueda ME, Morales JM, Jimenez-Capdeville ME, et al. Low-level subchronic arsenic exposure from prenatal developmental stages to adult life results in an impaired glucose homeostasis. Experimental and clinical endocrinology & diabetes. official journal, German Society of Endocrinology [and] German Diabetes Association. 2011;119:613–7.
18.
Zurück zum Zitat Ditzel EJ, Nguyen T, Parker P, Camenisch TD. Effects of arsenite exposure during fetal development on energy metabolism and susceptibility to diet-induced fatty liver disease in male mice. Environ Health Perspect. 2016;124:201–9.PubMed Ditzel EJ, Nguyen T, Parker P, Camenisch TD. Effects of arsenite exposure during fetal development on energy metabolism and susceptibility to diet-induced fatty liver disease in male mice. Environ Health Perspect. 2016;124:201–9.PubMed
19.
Zurück zum Zitat Bonaventura MM, Bourguignon NS, Bizzozzero M, et al. Arsenite in drinking water produces glucose intolerance in pregnant rats and their female offspring. Food Chem Toxicol. 2017;100:207–16.PubMed Bonaventura MM, Bourguignon NS, Bizzozzero M, et al. Arsenite in drinking water produces glucose intolerance in pregnant rats and their female offspring. Food Chem Toxicol. 2017;100:207–16.PubMed
20.
Zurück zum Zitat Huang MC, Douillet C, Dover EN, Styblo M. Prenatal arsenic exposure and dietary folate and methylcobalamin supplementation alter the metabolic phenotype of C57BL/6J mice in a sex-specific manner. Arch Toxicol. 2018;92:1925–37.PubMedPubMedCentral Huang MC, Douillet C, Dover EN, Styblo M. Prenatal arsenic exposure and dietary folate and methylcobalamin supplementation alter the metabolic phenotype of C57BL/6J mice in a sex-specific manner. Arch Toxicol. 2018;92:1925–37.PubMedPubMedCentral
21.
Zurück zum Zitat Sanchez-Soria P, Broka D, Quach S, Hardwick RN, Cherrington NJ, Camenisch TD. Fetal exposure to arsenic results in hyperglycemia, hypercholesterolemia, and nonalcoholic fatty liver disease in adult mice. J Toxicol Health. 2014;1. Sanchez-Soria P, Broka D, Quach S, Hardwick RN, Cherrington NJ, Camenisch TD. Fetal exposure to arsenic results in hyperglycemia, hypercholesterolemia, and nonalcoholic fatty liver disease in adult mice. J Toxicol Health. 2014;1.
22.
Zurück zum Zitat Yajnik CS. Obesity epidemic in India: intrauterine origins? Proc Nutr Soc. 2004;63:387–96.PubMed Yajnik CS. Obesity epidemic in India: intrauterine origins? Proc Nutr Soc. 2004;63:387–96.PubMed
23.
Zurück zum Zitat Yajnik CS. Early life origins of insulin resistance and type 2 diabetes in India and other Asian countries. J Nutr. 2004;134:205–10.PubMed Yajnik CS. Early life origins of insulin resistance and type 2 diabetes in India and other Asian countries. J Nutr. 2004;134:205–10.PubMed
24.
Zurück zum Zitat Stewart CP, Christian P, Schulze KJ, et al. Low maternal vitamin B-12 status is associated with offspring insulin resistance regardless of antenatal micronutrient supplementation in rural Nepal. J Nutr. 2011;141:1912–7.PubMed Stewart CP, Christian P, Schulze KJ, et al. Low maternal vitamin B-12 status is associated with offspring insulin resistance regardless of antenatal micronutrient supplementation in rural Nepal. J Nutr. 2011;141:1912–7.PubMed
25.
Zurück zum Zitat Rush EC, Katre P, Yajnik CS. Vitamin B12: one carbon metabolism, fetal growth and programming for chronic disease. Eur J Clin Nutr. 2014;68:2–7.PubMed Rush EC, Katre P, Yajnik CS. Vitamin B12: one carbon metabolism, fetal growth and programming for chronic disease. Eur J Clin Nutr. 2014;68:2–7.PubMed
26.
Zurück zum Zitat Bozack AK, Saxena R, Gamble MV. Nutritional influences on one-carbon metabolism: effects on arsenic methylation and toxicity. Annu Rev Nutr. 2018;38:401–29.PubMedPubMedCentral Bozack AK, Saxena R, Gamble MV. Nutritional influences on one-carbon metabolism: effects on arsenic methylation and toxicity. Annu Rev Nutr. 2018;38:401–29.PubMedPubMedCentral
27.
Zurück zum Zitat Gamble MV, Liu X, Ahsan H, et al. Folate and arsenic metabolism: a double-blind, placebo-controlled folic acid-supplementation trial in Bangladesh. Am J Clin Nutr. 2006;84:1093–101.PubMedPubMedCentral Gamble MV, Liu X, Ahsan H, et al. Folate and arsenic metabolism: a double-blind, placebo-controlled folic acid-supplementation trial in Bangladesh. Am J Clin Nutr. 2006;84:1093–101.PubMedPubMedCentral
28.
Zurück zum Zitat Gamble MV, Liu X, Slavkovich V, et al. Folic acid supplementation lowers blood arsenic. Am J ClinNutr. 2007;86:1202–9. Gamble MV, Liu X, Slavkovich V, et al. Folic acid supplementation lowers blood arsenic. Am J ClinNutr. 2007;86:1202–9.
29.
Zurück zum Zitat Bailey KA, Smith AH, Tokar EJ, et al. Mechanisms underlying latent disease risk associated with early-life arsenic exposure: current research trends and scientific gaps. Environ Health Perspect. 2016;124:170–5.PubMed Bailey KA, Smith AH, Tokar EJ, et al. Mechanisms underlying latent disease risk associated with early-life arsenic exposure: current research trends and scientific gaps. Environ Health Perspect. 2016;124:170–5.PubMed
30.
Zurück zum Zitat Fowler PA, Drake AJ, O’Shaughnessy PJ, et al. Comment on “effects of arsenite during fetal development on energy metabolism and susceptibility to diet-induced fatty liver diseases in male mice” and “mechanisms underlying latent disease risk associated with early-life arsenic exposure: current trends and scientific gaps”. Environ Health Perspect. 2016;124:A99.PubMedPubMedCentral Fowler PA, Drake AJ, O’Shaughnessy PJ, et al. Comment on “effects of arsenite during fetal development on energy metabolism and susceptibility to diet-induced fatty liver diseases in male mice” and “mechanisms underlying latent disease risk associated with early-life arsenic exposure: current trends and scientific gaps”. Environ Health Perspect. 2016;124:A99.PubMedPubMedCentral
31.
Zurück zum Zitat Li Y, He Y, Qi L, et al. Exposure to the Chinese famine in early life and the risk of hyperglycemia and type 2 diabetes in adulthood. Diabetes. 2010;59:2400–6.PubMedPubMedCentral Li Y, He Y, Qi L, et al. Exposure to the Chinese famine in early life and the risk of hyperglycemia and type 2 diabetes in adulthood. Diabetes. 2010;59:2400–6.PubMedPubMedCentral
32.
Zurück zum Zitat Vaiserman AM. Early-life nutritional programming of type 2 diabetes: experimental and quasi-experimental evidence. Nutrients. 2017;9.PubMedCentral Vaiserman AM. Early-life nutritional programming of type 2 diabetes: experimental and quasi-experimental evidence. Nutrients. 2017;9.PubMedCentral
33.
Zurück zum Zitat Reusens B, Theys N, Dumortier O, Goosse K, Remacle C. Maternal malnutrition programs the endocrine pancreas in progeny. Am J Clin Nutr. 2011;94:1824S–9S.PubMed Reusens B, Theys N, Dumortier O, Goosse K, Remacle C. Maternal malnutrition programs the endocrine pancreas in progeny. Am J Clin Nutr. 2011;94:1824S–9S.PubMed
34.
Zurück zum Zitat Martinez JA, Cordero P, Campion J, Milagro FI. Interplay of early-life nutritional programming on obesity, inflammation and epigenetic outcomes. Proc Nutr Soc. 2012;71:276–83.PubMed Martinez JA, Cordero P, Campion J, Milagro FI. Interplay of early-life nutritional programming on obesity, inflammation and epigenetic outcomes. Proc Nutr Soc. 2012;71:276–83.PubMed
35.
Zurück zum Zitat Desai M, Jellyman JK, Ross MG. Epigenomics, gestational programming and risk of metabolic syndrome. Int J Obes. 2015;39:633–41. Desai M, Jellyman JK, Ross MG. Epigenomics, gestational programming and risk of metabolic syndrome. Int J Obes. 2015;39:633–41.
36.
Zurück zum Zitat Young JL, Cai L, States JC. Impact of prenatal arsenic exposure on chronic adult diseases. Syst Biol Reprod Med. 2018:1–15. Young JL, Cai L, States JC. Impact of prenatal arsenic exposure on chronic adult diseases. Syst Biol Reprod Med. 2018:1–15.
37.
Zurück zum Zitat Fry RC, Navasumrit P, Valiathan C, et al. Activation of inflammation/NF-kappaB signaling in infants born to arsenic-exposed mothers. PLoS Genet. 2007;3:e207.PubMedPubMedCentral Fry RC, Navasumrit P, Valiathan C, et al. Activation of inflammation/NF-kappaB signaling in infants born to arsenic-exposed mothers. PLoS Genet. 2007;3:e207.PubMedPubMedCentral
38.
Zurück zum Zitat Farzan SF, Karagas MR, Chen Y. In utero and early life arsenic exposure in relation to long-term health and disease. Toxicol Appl Pharmacol. 2013;272:384–90.PubMedPubMedCentral Farzan SF, Karagas MR, Chen Y. In utero and early life arsenic exposure in relation to long-term health and disease. Toxicol Appl Pharmacol. 2013;272:384–90.PubMedPubMedCentral
39.
Zurück zum Zitat States JC, Singh AV, Knudsen TB, et al. Prenatal arsenic exposure alters gene expression in the adult liver to a proinflammatory state contributing to accelerated atherosclerosis. PLoS One. 2012;7:e38713.PubMedPubMedCentral States JC, Singh AV, Knudsen TB, et al. Prenatal arsenic exposure alters gene expression in the adult liver to a proinflammatory state contributing to accelerated atherosclerosis. PLoS One. 2012;7:e38713.PubMedPubMedCentral
40.
Zurück zum Zitat Ren X, Gaile DP, Gong Z, et al. Arsenic responsive microRNAs in vivo and their potential involvement in arsenic-induced oxidative stress. Toxicol Appl Pharmacol. 2015;283:198–209.PubMedPubMedCentral Ren X, Gaile DP, Gong Z, et al. Arsenic responsive microRNAs in vivo and their potential involvement in arsenic-induced oxidative stress. Toxicol Appl Pharmacol. 2015;283:198–209.PubMedPubMedCentral
41.
Zurück zum Zitat Tsang V, Fry RC, Niculescu MD, et al. The epigenetic effects of a high prenatal folate intake in male mouse fetuses exposed in utero to arsenic. Toxicol Appl Pharmacol. 2012;264:439–50.PubMedPubMedCentral Tsang V, Fry RC, Niculescu MD, et al. The epigenetic effects of a high prenatal folate intake in male mouse fetuses exposed in utero to arsenic. Toxicol Appl Pharmacol. 2012;264:439–50.PubMedPubMedCentral
42.
Zurück zum Zitat Rahman M, Sohel N, Yunus M, et al. Increased childhood mortality and arsenic in drinking water in Matlab. Bangladesh: a population-based cohort study. PLoS One. 2013;8:e55014.PubMedPubMedCentral Rahman M, Sohel N, Yunus M, et al. Increased childhood mortality and arsenic in drinking water in Matlab. Bangladesh: a population-based cohort study. PLoS One. 2013;8:e55014.PubMedPubMedCentral
43.
Zurück zum Zitat Hawkesworth S, Wagatsuma Y, Kippler M, et al. Early exposure to toxic metals has a limited effect on blood pressure or kidney function in later childhood, rural Bangladesh. Int J Epidemiol. 2013;42:176–85.PubMed Hawkesworth S, Wagatsuma Y, Kippler M, et al. Early exposure to toxic metals has a limited effect on blood pressure or kidney function in later childhood, rural Bangladesh. Int J Epidemiol. 2013;42:176–85.PubMed
44.
Zurück zum Zitat Yorifuji T, Tsuda T, Grandjean P. Unusual cancer excess after neonatal arsenic exposure from contaminated milk powder. J Natl Cancer Inst. 2010;102:360–1.PubMedPubMedCentral Yorifuji T, Tsuda T, Grandjean P. Unusual cancer excess after neonatal arsenic exposure from contaminated milk powder. J Natl Cancer Inst. 2010;102:360–1.PubMedPubMedCentral
45.
Zurück zum Zitat Yorifuji T, Tsuda T, Doi H, Grandjean P. Cancer excess after arsenic exposure from contaminated milk powder. Environ Health Prev Med. 2011;16:164–70.PubMed Yorifuji T, Tsuda T, Doi H, Grandjean P. Cancer excess after arsenic exposure from contaminated milk powder. Environ Health Prev Med. 2011;16:164–70.PubMed
46.
Zurück zum Zitat Kuo CC, Su PH, Sun CW, Liu HJ, Chang CL, Wang SL. Early-life arsenic exposure promotes atherogenic lipid metabolism in adolescence: a 15-year birth cohort follow-up study in Central Taiwan. Environ Int. 2018;118:97–105.PubMed Kuo CC, Su PH, Sun CW, Liu HJ, Chang CL, Wang SL. Early-life arsenic exposure promotes atherogenic lipid metabolism in adolescence: a 15-year birth cohort follow-up study in Central Taiwan. Environ Int. 2018;118:97–105.PubMed
47.
Zurück zum Zitat Grau-Perez M, Kuo CC, Spratlen M, et al. The association of arsenic exposure and metabolism with type 1 and type 2 diabetes in youth: the SEARCH case-control study. Diabetes Care. 2017;40:46–53.PubMed Grau-Perez M, Kuo CC, Spratlen M, et al. The association of arsenic exposure and metabolism with type 1 and type 2 diabetes in youth: the SEARCH case-control study. Diabetes Care. 2017;40:46–53.PubMed
48.
Zurück zum Zitat Hall MN, Gamble MV. Nutritional manipulation of one-carbon metabolism: effects on arsenic methylation and toxicity. J Toxicol. 2012;2012:595307.PubMedPubMedCentral Hall MN, Gamble MV. Nutritional manipulation of one-carbon metabolism: effects on arsenic methylation and toxicity. J Toxicol. 2012;2012:595307.PubMedPubMedCentral
49.
Zurück zum Zitat Ducker GS, Rabinowitz JD. One-carbon metabolism in health and disease. Cell Metab. 2017;25:27–42.PubMed Ducker GS, Rabinowitz JD. One-carbon metabolism in health and disease. Cell Metab. 2017;25:27–42.PubMed
50.
Zurück zum Zitat Finer S, Saravanan P, Hitman G, Yajnik C. The role of the one-carbon cycle in the developmental origins of type 2 diabetes and obesity. Diabet Med. 2014;31:263–72.PubMed Finer S, Saravanan P, Hitman G, Yajnik C. The role of the one-carbon cycle in the developmental origins of type 2 diabetes and obesity. Diabet Med. 2014;31:263–72.PubMed
51.
Zurück zum Zitat Lopez-Carrillo L, Gamboa-Loira B, Becerra W, et al. Dietary micronutrient intake and its relationship with arsenic metabolism in Mexican women. Environ Res. 2016;151:445–50.PubMedPubMedCentral Lopez-Carrillo L, Gamboa-Loira B, Becerra W, et al. Dietary micronutrient intake and its relationship with arsenic metabolism in Mexican women. Environ Res. 2016;151:445–50.PubMedPubMedCentral
52.
Zurück zum Zitat Gruber JF, Karagas MR, Gilbert-Diamond D, et al. Associations between toenail arsenic concentration and dietary factors in a New Hampshire population. Nutr J. 2012;11:45.PubMedPubMedCentral Gruber JF, Karagas MR, Gilbert-Diamond D, et al. Associations between toenail arsenic concentration and dietary factors in a New Hampshire population. Nutr J. 2012;11:45.PubMedPubMedCentral
53.
Zurück zum Zitat • Spratlen MJ, Gamble MV, Grau-Perez M, et al. Arsenic metabolism and one-carbon metabolism at low-moderate arsenic exposure: evidence from the Strong Heart Study. Food Chem Toxicol. 2017;105:387–97 This epidemiologic study in a population exposed to low moderate arsenic levels support that one-carbon metabolism nutrients are related to arsenic metabolism, consistent with clinical trials of folate and B vitamin supplementation conducted in Bangladesh.PubMedPubMedCentral • Spratlen MJ, Gamble MV, Grau-Perez M, et al. Arsenic metabolism and one-carbon metabolism at low-moderate arsenic exposure: evidence from the Strong Heart Study. Food Chem Toxicol. 2017;105:387–97 This epidemiologic study in a population exposed to low moderate arsenic levels support that one-carbon metabolism nutrients are related to arsenic metabolism, consistent with clinical trials of folate and B vitamin supplementation conducted in Bangladesh.PubMedPubMedCentral
54.
Zurück zum Zitat Kurzius-Spencer M, da Silva V, Thomson CA, et al. Nutrients in one-carbon metabolism and urinary arsenic methylation in the National Health and Nutrition Examination Survey (NHANES) 2003–2004. Sci Total Environ. 2017;607–608:381–90.PubMed Kurzius-Spencer M, da Silva V, Thomson CA, et al. Nutrients in one-carbon metabolism and urinary arsenic methylation in the National Health and Nutrition Examination Survey (NHANES) 2003–2004. Sci Total Environ. 2017;607–608:381–90.PubMed
55.
Zurück zum Zitat Heck JE, Gamble MV, Chen Y, et al. Consumption of folate-related nutrients and metabolism of arsenic in Bangladesh. Am J Clin Nutr. 2007;85:1367–74.PubMed Heck JE, Gamble MV, Chen Y, et al. Consumption of folate-related nutrients and metabolism of arsenic in Bangladesh. Am J Clin Nutr. 2007;85:1367–74.PubMed
56.
Zurück zum Zitat Aposhian HV, Aposhian MM. Arsenic toxicology: five questions. Chem Res Toxicol. 2006;19:1–15.PubMed Aposhian HV, Aposhian MM. Arsenic toxicology: five questions. Chem Res Toxicol. 2006;19:1–15.PubMed
57.
Zurück zum Zitat Niedzwiecki MM, Hall MN, Liu X, et al. Interaction of plasma glutathione redox and folate deficiency on arsenic methylation capacity in Bangladeshi adults. Free Radic Biol Med. 2014;73:67–74.PubMed Niedzwiecki MM, Hall MN, Liu X, et al. Interaction of plasma glutathione redox and folate deficiency on arsenic methylation capacity in Bangladeshi adults. Free Radic Biol Med. 2014;73:67–74.PubMed
58.
Zurück zum Zitat Vahter ME. Interactions between arsenic-induced toxicity and nutrition in early life. J Nutr. 2007;137:2798–804.PubMed Vahter ME. Interactions between arsenic-induced toxicity and nutrition in early life. J Nutr. 2007;137:2798–804.PubMed
59.
Zurück zum Zitat •• Huang MC, Douillet C, Dover EN, et al. Metabolic phenotype of wild-type and As3mt-knockout C57BL/6J mice exposed to inorganic arsenic: the role of dietary fat and Folate intake. Environ Health Perspect. 2018;126:127003 This experimental study in mice showed that joint exposure to arsenite and folate could rescue the metabolic effects induced by arsenite in male mice but not in female.PubMedPubMedCentral •• Huang MC, Douillet C, Dover EN, et al. Metabolic phenotype of wild-type and As3mt-knockout C57BL/6J mice exposed to inorganic arsenic: the role of dietary fat and Folate intake. Environ Health Perspect. 2018;126:127003 This experimental study in mice showed that joint exposure to arsenite and folate could rescue the metabolic effects induced by arsenite in male mice but not in female.PubMedPubMedCentral
60.
Zurück zum Zitat Fretts AM, Howard BV, McKnight B, et al. Associations of processed meat and unprocessed red meat intake with incident diabetes: the Strong Heart Family Study. Am J Clin Nutr. 2012;95:752–8.PubMedPubMedCentral Fretts AM, Howard BV, McKnight B, et al. Associations of processed meat and unprocessed red meat intake with incident diabetes: the Strong Heart Family Study. Am J Clin Nutr. 2012;95:752–8.PubMedPubMedCentral
61.
Zurück zum Zitat Eilat-Adar S, Mete M, Fretts A, et al. Dietary patterns and their association with cardiovascular risk factors in a population undergoing lifestyle changes: the Strong Heart Study. Nutr Metab Cardiovasc Dis. 2013;23:528–35.PubMed Eilat-Adar S, Mete M, Fretts A, et al. Dietary patterns and their association with cardiovascular risk factors in a population undergoing lifestyle changes: the Strong Heart Study. Nutr Metab Cardiovasc Dis. 2013;23:528–35.PubMed
62.
Zurück zum Zitat Navas-Acien A, Umans JG, Howard BV, et al. Urine arsenic concentrations and species excretion patterns in American Indian communities over a 10-year period: the Strong Heart Study. Environ Health Perspect. 2009;117:1428–33.PubMedPubMedCentral Navas-Acien A, Umans JG, Howard BV, et al. Urine arsenic concentrations and species excretion patterns in American Indian communities over a 10-year period: the Strong Heart Study. Environ Health Perspect. 2009;117:1428–33.PubMedPubMedCentral
63.
Zurück zum Zitat Vahter M. Mechanisms of arsenic biotransformation. Toxicology. 2002;181–182:211–7.PubMed Vahter M. Mechanisms of arsenic biotransformation. Toxicology. 2002;181–182:211–7.PubMed
64.
Zurück zum Zitat Challenger F. Biological Methylation. Chemical Reviews. 1945;36:315–61. Challenger F. Biological Methylation. Chemical Reviews. 1945;36:315–61.
65.
Zurück zum Zitat Cullen WR, Reimer KJ. Arsenic speciation in the environment. Chem Rev. 1989;89:713–64. Cullen WR, Reimer KJ. Arsenic speciation in the environment. Chem Rev. 1989;89:713–64.
66.
Zurück zum Zitat Naranmandura H, Suzuki N, Suzuki KT. Trivalent arsenicals are bound to proteins during reductive methylation. Chem Res Toxicol. 2006;19:1010–8.PubMed Naranmandura H, Suzuki N, Suzuki KT. Trivalent arsenicals are bound to proteins during reductive methylation. Chem Res Toxicol. 2006;19:1010–8.PubMed
67.
Zurück zum Zitat Vahter M. Genetic polymorphism in the biotransformation of inorganic arsenic and its role in toxicity. Toxicol Lett. 2000;112–113:209–17.PubMed Vahter M. Genetic polymorphism in the biotransformation of inorganic arsenic and its role in toxicity. Toxicol Lett. 2000;112–113:209–17.PubMed
68.
Zurück zum Zitat Hernandez A, Marcos R. Genetic variations associated with interindividual sensitivity in the response to arsenic exposure. Pharmacogenomics. 2008;9:1113–32.PubMed Hernandez A, Marcos R. Genetic variations associated with interindividual sensitivity in the response to arsenic exposure. Pharmacogenomics. 2008;9:1113–32.PubMed
69.
Zurück zum Zitat Loffredo CA, Aposhian HV, Cebrian ME, Yamauchi H, Silbergeld EK. Variability in human metabolism of arsenic. Environ Res. 2003;92:85–91.PubMed Loffredo CA, Aposhian HV, Cebrian ME, Yamauchi H, Silbergeld EK. Variability in human metabolism of arsenic. Environ Res. 2003;92:85–91.PubMed
70.
Zurück zum Zitat Tellez-Plaza M, Gribble MO, Voruganti VS, et al. Heritability and preliminary genome-wide linkage analysis of arsenic metabolites in urine. Environ Health Perspect. 2013;121:345–51.PubMedPubMedCentral Tellez-Plaza M, Gribble MO, Voruganti VS, et al. Heritability and preliminary genome-wide linkage analysis of arsenic metabolites in urine. Environ Health Perspect. 2013;121:345–51.PubMedPubMedCentral
71.
Zurück zum Zitat Melak D, Ferreccio C, Kalman D, et al. Arsenic methylation and lung and bladder cancer in a case-control study in northern Chile. Toxicol Appl Pharmacol. 2014;274:225–31.PubMed Melak D, Ferreccio C, Kalman D, et al. Arsenic methylation and lung and bladder cancer in a case-control study in northern Chile. Toxicol Appl Pharmacol. 2014;274:225–31.PubMed
72.
Zurück zum Zitat Chen Y, Wu F, Liu M, et al. A prospective study of arsenic exposure, arsenic methylation capacity, and risk of cardiovascular disease in Bangladesh. Environ Health Perspect. 2013;121:832–8.PubMedPubMedCentral Chen Y, Wu F, Liu M, et al. A prospective study of arsenic exposure, arsenic methylation capacity, and risk of cardiovascular disease in Bangladesh. Environ Health Perspect. 2013;121:832–8.PubMedPubMedCentral
73.
Zurück zum Zitat Chen YC, Guo YL, Su HJ, et al. Arsenic methylation and skin cancer risk in southwestern Taiwan. J Occup Environ Med. 2003;45:241–8.PubMed Chen YC, Guo YL, Su HJ, et al. Arsenic methylation and skin cancer risk in southwestern Taiwan. J Occup Environ Med. 2003;45:241–8.PubMed
74.
Zurück zum Zitat Chen YC, Su HJ, Guo YL, Houseman EA, Christiani DC. Interaction between environmental tobacco smoke and arsenic methylation ability on the risk of bladder cancer. Cancer Causes Control. 2005;16:75–81.PubMed Chen YC, Su HJ, Guo YL, Houseman EA, Christiani DC. Interaction between environmental tobacco smoke and arsenic methylation ability on the risk of bladder cancer. Cancer Causes Control. 2005;16:75–81.PubMed
75.
Zurück zum Zitat Chen YC, Su HJ, Guo YL, et al. Arsenic methylation and bladder cancer risk in Taiwan. Cancer Causes Control. 2003;14:303–10.PubMed Chen YC, Su HJ, Guo YL, et al. Arsenic methylation and bladder cancer risk in Taiwan. Cancer Causes Control. 2003;14:303–10.PubMed
76.
Zurück zum Zitat Hsueh YM, Chiou HY, Huang YL, et al. Serum beta-carotene level, arsenic methylation capability, and incidence of skin cancer. Cancer Epidemiol Biomark Prev. 1997;6:589–96. Hsueh YM, Chiou HY, Huang YL, et al. Serum beta-carotene level, arsenic methylation capability, and incidence of skin cancer. Cancer Epidemiol Biomark Prev. 1997;6:589–96.
77.
Zurück zum Zitat Wu MM, Chiou HY, Hsueh YM, et al. Effect of plasma homocysteine level and urinary monomethylarsonic acid on the risk of arsenic-associated carotid atherosclerosis. Toxicol Appl Pharmacol. 2006;216:168–75.PubMed Wu MM, Chiou HY, Hsueh YM, et al. Effect of plasma homocysteine level and urinary monomethylarsonic acid on the risk of arsenic-associated carotid atherosclerosis. Toxicol Appl Pharmacol. 2006;216:168–75.PubMed
78.
Zurück zum Zitat Chen Y, Wu F, Graziano JH, et al. Arsenic exposure from drinking water, arsenic methylation capacity, and carotid intima-media thickness in Bangladesh. Am J Epidemiol. 2013;178:372–81.PubMedPubMedCentral Chen Y, Wu F, Graziano JH, et al. Arsenic exposure from drinking water, arsenic methylation capacity, and carotid intima-media thickness in Bangladesh. Am J Epidemiol. 2013;178:372–81.PubMedPubMedCentral
79.
Zurück zum Zitat Kuo CC, Moon KA, Wang SL, Silbergeld EK, Navas-Acien A. The association of arsenic metabolism with cancer, cardiovascular disease and diabetes: a systematic review of the epidemiological evidence. Environ Health Perspect 2017;125:087001.PubMedPubMedCentral Kuo CC, Moon KA, Wang SL, Silbergeld EK, Navas-Acien A. The association of arsenic metabolism with cancer, cardiovascular disease and diabetes: a systematic review of the epidemiological evidence. Environ Health Perspect 2017;125:087001.PubMedPubMedCentral
80.
Zurück zum Zitat Kuo CC, Howard BV, Umans JG, et al. Arsenic exposure, arsenic metabolism, and incident diabetes in the Strong Heart Study. Diabetes Care. 2015;38:620–7.PubMedPubMedCentral Kuo CC, Howard BV, Umans JG, et al. Arsenic exposure, arsenic metabolism, and incident diabetes in the Strong Heart Study. Diabetes Care. 2015;38:620–7.PubMedPubMedCentral
81.
Zurück zum Zitat Nizam S, Kato M, Yatsuya H, et al. Differences in urinary arsenic metabolites between diabetic and non-diabetic subjects in Bangladesh. Int J Environ Res Public Health. 2013;10:1006–19.PubMedPubMedCentral Nizam S, Kato M, Yatsuya H, et al. Differences in urinary arsenic metabolites between diabetic and non-diabetic subjects in Bangladesh. Int J Environ Res Public Health. 2013;10:1006–19.PubMedPubMedCentral
82.
Zurück zum Zitat Pang Y, Peng RD, Jones MR, et al. Metal mixtures in urban and rural populations in the US: The Multi-Ethnic Study of Atherosclerosis and the Strong Heart Study. Environ Res. 2016;147:356–64.PubMedPubMedCentral Pang Y, Peng RD, Jones MR, et al. Metal mixtures in urban and rural populations in the US: The Multi-Ethnic Study of Atherosclerosis and the Strong Heart Study. Environ Res. 2016;147:356–64.PubMedPubMedCentral
83.
Zurück zum Zitat Spratlen MJ, Grau-Perez M, Umans JG, et al. Targeted metabolomics to understand the association between arsenic metabolism and diabetes-related outcomes: preliminary evidence from the Strong Heart Family Study. Environ Res. 2018;168:146–57.PubMedPubMedCentral Spratlen MJ, Grau-Perez M, Umans JG, et al. Targeted metabolomics to understand the association between arsenic metabolism and diabetes-related outcomes: preliminary evidence from the Strong Heart Family Study. Environ Res. 2018;168:146–57.PubMedPubMedCentral
Metadaten
Titel
Early-Life Arsenic Exposure, Nutritional Status, and Adult Diabetes Risk
verfasst von
Ana Navas-Acien
Miranda J. Spratlen
Ahlam Abuawad
Nancy J. LoIacono
Anne K. Bozack
Mary V. Gamble
Publikationsdatum
01.12.2019
Verlag
Springer US
Erschienen in
Current Diabetes Reports / Ausgabe 12/2019
Print ISSN: 1534-4827
Elektronische ISSN: 1539-0829
DOI
https://doi.org/10.1007/s11892-019-1272-9

Weitere Artikel der Ausgabe 12/2019

Current Diabetes Reports 12/2019 Zur Ausgabe

Other Forms of Diabetes and Its Complications (JJ Nolan and H Thabit, Section Editors)

Diabetes and Cardiovascular Disease: an Update

Hospital Management of Diabetes (A Wallia and JJ Seley, Section Editors)

Hospitalization as an Opportunity to Optimize Glycemic Control in Oncology Patients

Pathogenesis of Type 1 Diabetes (A Pugliese and SJ Richardson, Section Editors)

What the HLA-I!—Classical and Non-classical HLA Class I and Their Potential Roles in Type 1 Diabetes

Pharmacologic Treatment of Type 2 Diabetes (HE Lebovitz and G Bahtiyar, Section Editors)

Technological Advancements in the Management of Type 2 Diabetes

Health Care Delivery Systems and Implementation in Diabetes (ME McDonnell and AR Sadhu, Section Editors)

mHealth Interventions for Disadvantaged and Vulnerable People with Type 2 Diabetes

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Therapiestart mit Blutdrucksenkern erhöht Frakturrisiko

25.04.2024 Hypertonie Nachrichten

Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.