Department of Environmental Health and Engineering, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, New York.
Am J Epidemiol. 2018 Aug 1;187(8):1598-1612. doi: 10.1093/aje/kwy048.
Inorganic arsenic exposure is ubiquitous, and both exposure and interindividual differences in its metabolism have been associated with cardiometabolic risk. However, the associations of arsenic exposure and arsenic metabolism with the metabolic syndrome (MetS) and its individual components are relatively unknown. We used Poisson regression with robust variance to evaluate the associations of baseline arsenic exposure (urinary arsenic levels) and metabolism (relative percentage of arsenic species over their sum) with incident MetS and its individual components (elevated waist circumference, elevated triglycerides, reduced high-density lipoprotein cholesterol, hypertension, and elevated fasting plasma glucose) in 1,047 participants from the Strong Heart Family Study, a prospective family-based cohort study in American Indian communities (baseline visits were held in 1998-1999 and 2001-2003, follow-up visits in 2001-2003 and 2006-2009). Over the course of follow-up, 32% of participants developed MetS. An interquartile-range increase in arsenic exposure was associated with a 1.19-fold (95% confidence interval: 1.01, 1.41) greater risk of elevated fasting plasma glucose concentration but not with other individual components of the MetS or MetS overall. Arsenic metabolism, specifically lower percentage of monomethylarsonic acid and higher percentage of dimethylarsinic acid, was associated with higher risk of overall MetS and elevated waist circumference but not with any other MetS component. These findings support the hypothesis that there are contrasting and independent associations of arsenic exposure and arsenic metabolism with metabolic outcomes which may contribute to overall diabetes risk.
无机砷暴露普遍存在,其暴露和个体间代谢差异均与心血管代谢风险相关。然而,砷暴露和砷代谢与代谢综合征(MetS)及其各组分之间的关联尚不清楚。我们采用稳健方差的泊松回归,评估基线砷暴露(尿砷水平)和代谢(砷形态相对比例与其总和)与新发代谢综合征及其各组分(腰围升高、甘油三酯升高、高密度脂蛋白胆固醇降低、高血压和空腹血糖升高)之间的关联,研究对象为来自美国印第安人社区的前瞻性家族队列研究——“强壮心脏家族研究”中的 1047 名参与者(基线访视于 1998-1999 年和 2001-2003 年进行,随访于 2001-2003 年和 2006-2009 年进行)。在随访期间,32%的参与者发生了代谢综合征。砷暴露的四分位距增加与空腹血糖浓度升高的风险增加 1.19 倍(95%置信区间:1.01,1.41)相关,但与代谢综合征的其他各组分或总体代谢综合征无关。砷代谢,特别是单甲基砷酸的比例降低和二甲基砷酸的比例升高,与总体代谢综合征和腰围升高的风险增加相关,但与代谢综合征的任何其他组分无关。这些发现支持了以下假说,即砷暴露和砷代谢与代谢结果之间存在相反且独立的关联,这可能导致总体糖尿病风险增加。