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成人砷暴露和代谢生物标志物随时间的变异性。

Variability in biomarkers of arsenic exposure and metabolism in adults over time.

作者信息

Kile Molly L, Hoffman Elaine, Hsueh Yu-Mei, Afroz Sakila, Quamruzzaman Quazi, Rahman Mahmuder, Mahiuddin Golam, Ryan Louise, Christiani David C

机构信息

Harvard School of Public Health, Boston, Massachusetts 02115, USA.

出版信息

Environ Health Perspect. 2009 Mar;117(3):455-60. doi: 10.1289/ehp.11251. Epub 2008 Nov 19.

Abstract

BACKGROUND

Urinary arsenic metabolites (UAs) are used as biomarkers of exposure and metabolism.

OBJECTIVES

To characterize inter- and intraindividual variability in UAs in healthy individuals.

METHODS

In a longitudinal study conducted in Bangladesh, we collected water and spot urine samples from 196 participants every 3 months for 2 years. Water arsenic (As) was measured by inductively coupled plasma-mass spectrometry and urinary As [arsenite, arsenate, monomethylarsonic acid (MMA), and dimethylarsinic acid (DMA)] were detected using high-performance liquid chromatography-hydride-generated atomic absorption spectrometry. We used linear mixed-effects models to compute variance components and evaluate the association between UAs and selected factors.

RESULTS

The concentrations of UAs were fairly reproducible within individuals, with intraclass correlation coefficients (ICCs) of 0.41, 0.35, 0.47, and 0.49 for inorganic As (InAs), MMA, DMA, and total urinary As (TUA). However, when expressed as a ratio, the percent InAs (%InAs), %MMA, and %DMA were poorly reproducible within individuals, with ICCs of 0.16, 0.16, and 0.17, respectively. Arsenic metabolism was significantly associated with sex, exposure, age, smoking, chewing betel nut, urinary creatinine, and season. Specificity and sensitivity analyses showed that a single urine sample adequately classified a participant's urinary As profile as high or low, but TUA had only moderate specificity for correctly classifying drinking water exposures.

CONCLUSIONS

Epidemiologic studies should use both urinary As concentrations and the relative proportion of UAs to minimize measurement error and to facilitate interpretation of factors that influence As metabolism.

摘要

背景

尿砷代谢产物(UAs)用作暴露和代谢的生物标志物。

目的

描述健康个体中UAs的个体间和个体内变异性。

方法

在孟加拉国进行的一项纵向研究中,我们在2年时间里每3个月从196名参与者中收集水和即时尿样。采用电感耦合等离子体质谱法测定水中砷(As),使用高效液相色谱-氢化物发生原子吸收光谱法检测尿砷[亚砷酸盐、砷酸盐、一甲基胂酸(MMA)和二甲基胂酸(DMA)]。我们使用线性混合效应模型计算方差成分,并评估UAs与选定因素之间的关联。

结果

UAs浓度在个体内具有相当的可重复性,无机砷(InAs)、MMA、DMA和总尿砷(TUA)的组内相关系数(ICC)分别为0.41、0.35、0.47和0.49。然而,当以比率表示时,个体内InAs百分比(%InAs)、%MMA和%DMA的可重复性较差,ICC分别为0.16、0.16和0.17。砷代谢与性别、暴露、年龄、吸烟、嚼槟榔、尿肌酐和季节显著相关。特异性和敏感性分析表明,单个尿样能够充分将参与者的尿砷谱分类为高或低,但TUA对正确分类饮用水暴露的特异性仅为中等。

结论

流行病学研究应同时使用尿砷浓度和UAs的相对比例,以尽量减少测量误差,并便于解释影响砷代谢的因素。

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Dietary arsenic exposure in bangladesh.孟加拉国的膳食砷暴露。
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Sci Total Environ. 2006 Nov 1;370(2-3):294-301. doi: 10.1016/j.scitotenv.2006.06.010. Epub 2006 Jul 27.
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Intraindividual variability in arsenic methylation in a U.S. population.美国人群中砷甲基化的个体内变异性。
Cancer Epidemiol Biomarkers Prev. 2005 Apr;14(4):919-24. doi: 10.1158/1055-9965.EPI-04-0277.
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Arsenic methylation and bladder cancer risk in Taiwan.台湾地区的砷甲基化与膀胱癌风险
Cancer Causes Control. 2003 May;14(4):303-10. doi: 10.1023/a:1023905900171.
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Arsenic methylation and skin cancer risk in southwestern Taiwan.台湾西南部的砷甲基化与皮肤癌风险
J Occup Environ Med. 2003 Mar;45(3):241-8. doi: 10.1097/01.jom.0000058336.05741.e8.
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Intra-individual variation in the metabolism of inorganic arsenic.无机砷代谢的个体内变异。
Int Arch Occup Environ Health. 2002 Oct;75(8):576-80. doi: 10.1007/s00420-002-0361-1. Epub 2002 Jul 9.

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