Clinical evaluation of a lead mobilization test using the chelating agent dimercaptosuccinic acid

被引:15
作者
Hoet, P [1 ]
Buchet, JP [1 ]
Decerf, L [1 ]
Lavalleye, E [1 ]
Haufroid, V [1 ]
Lison, D [1 ]
机构
[1] Catholic Univ Louvain, Fac Med, Unit Ind Toxicol & Occupat Med, B-1200 Brussels, Belgium
关键词
D O I
10.1373/clinchem.2005.051128
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 [基础医学];
摘要
Background: The lead mobilization test reflects the mobilizable and likely toxicologically active fraction of the lead body burden. We propose a safe and convenient protocol for this test, to assess concomitant copper and zinc excretion and to determine the size of the chelatable lead pool in nonoccupationally exposed adults. Methods: The study population included 80 white adults: 40 controls [median blood lead concentration (PbB), 25 mu g/L] and 40 lead-exposed individuals (315 mu g/U. After collection of 4- and 24-h baseline urine specimens and a blood sample, dimercaptosuccinic acid (DMSA) was administered orally (1 g), and additional 4-and 24-h urine specimens were obtained. Determinants of the chelatable urinary lead (DMSA-PbU) were traced by linear regression analysis. Results: Urinary DMSA and lead excretion peaked within 2-3 h after DMSA administration. The amounts of DMSA, lead, copper, and zinc recovered in the 4-h urinary collections were highly correlated with those in 24-h collections. (r = 0.857, 0.859, 0.958, and 0.757, respectively). At PbB concentrations > 300 mu g/L, the relationship between DMSA-PbU and PbB showed a steep increase and a widespread dispersion of DMSA-PbU around the regression line. After DMSA, copper and zinc excretion rates were increased up to 91- and 33-fold, respectively. No side effects were reported after DMSA. Conclusions: Determination of DMSA-PbU in a 4-h collection after DMSA is convenient, apparently safe, and inexpensive. An upper reference limit value of 22 mu g/4 h is proposed for Belgian reference individuals. The diagnostic value of DMSA-PbU is likely to be contributive for PbB > 300 mu g/L. (c) 2006 American Association for Clinicai Chemistry.
引用
收藏
页码:88 / 96
页数:9
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