Departments of Environmental Health Sciences.
Epidemiology.
Am J Clin Nutr. 2019 Feb 1;109(2):380-391. doi: 10.1093/ajcn/nqy148.
Arsenic exposure through drinking water persists in many regions. Inorganic As (InAs) is methylated to monomethyl-arsenical species (MMAs) and dimethyl-arsenical species (DMAs), facilitating urinary excretion. Arsenic methylation is dependent on one-carbon metabolism, which is influenced by nutritional factors such as folate and creatine.
This study investigated the effects of folic acid (FA) and/or creatine supplementation on the proportion of As metabolites in urine.
In a 24-wk randomized, double-blinded, placebo-controlled trial, 622 participants were assigned to receive FA (400 or 800 μg per day), 3 g creatine per day, 400 μg FA + 3 g creatine per day, or placebo. The majority of participants were folate sufficient; all received As-removal water filters. From wk 12-24, half of the participants receiving FA received placebo.
Among groups receiving FA, the mean decrease in ln(%InAs) and %MMAs and increase in %DMAs exceeded those of the placebo group at wk 6 and 12 (P < 0.05). In the creatine group, the mean decrease in %MMAs exceeded that of the placebo group at wk 6 and 12 (P < 0.05); creatine supplementation did not affect change in %InAs or %DMAs. The decrease in %MMAs at wk 6 and 12 was larger in the 800 µg FA than in the 400 µg FA group (P = 0.034). There were no differences in treatment effects between the 400 µg FA and creatine + FA groups. Data suggest a rebound in As metabolite proportions after FA cessation; at wk 24, log(%InAs) and %DMAs were not significantly different than baseline levels among participants who discontinued FA supplementation.
The results of this study confirm that FA supplementation rapidly and significantly increases methylation of InAs to DMAs. Further research is needed to understand the strong cross-sectional associations between urinary creatinine and As methylation in previous studies. This trial was registered at https://clinicaltrials.gov as NCT01050556.
通过饮用水暴露于砷的情况在许多地区仍然存在。无机砷(InAs)被甲基化为一甲基砷(MMAs)和二甲基砷(DMAs),有利于尿液排泄。砷的甲基化依赖于一碳代谢,而一碳代谢受叶酸和肌酸等营养因素的影响。
本研究旨在探讨叶酸(FA)和/或肌酸补充对尿液中砷代谢产物比例的影响。
在一项为期 24 周的随机、双盲、安慰剂对照试验中,622 名参与者被分配接受 FA(每天 400 或 800μg)、每天 3g 肌酸、每天 400μg FA+3g 肌酸或安慰剂。大多数参与者叶酸充足;所有人都使用了除砷水过滤器。从第 12 周到第 24 周,接受 FA 的一半参与者接受安慰剂。
在接受 FA 的组中,与安慰剂组相比,ln(%InAs)和%MMAs 的平均下降以及%DMAs 的平均增加在第 6 周和第 12 周时更为显著(P<0.05)。在肌酸组中,与安慰剂组相比,%MMAs 的平均下降在第 6 周和第 12 周时更为显著(P<0.05);肌酸补充并未影响%InAs 或%DMAs 的变化。与 400μg FA 组相比,800μg FA 组第 6 周和第 12 周时%MMAs 的下降幅度更大(P=0.034)。400μg FA 组和肌酸+FA 组之间的治疗效果没有差异。数据表明,FA 停止后砷代谢产物比例出现反弹;在第 24 周时,停止 FA 补充的参与者的 log(%InAs)和%DMAs 与基线水平没有显著差异。
本研究结果证实,FA 补充可迅速显著增加 InAs 向 DMAs 的甲基化。需要进一步研究以了解先前研究中尿肌酐与砷甲基化之间的强横断面关联。该试验在 https://clinicaltrials.gov 注册,编号为 NCT01050556。