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

Hoet, Perrine;Buchet, Jean-Pierre;Decerf, Laurence;Lavalleye, Benoît;Lison, Dominique;et.al.
(2006) Clinical Chemistry : international journal of molecular diagnostics and laboratory medicine — Vol. 52, n° 1, p. 88-96 (2006)

Files

22350.pdf
  • Restricted Access
  • Adobe PDF
  • 156.26 KB

Details

Authors
  • Hoet, PerrineUCLouvain
    Author
  • Buchet, Jean-PierreUCLouvain
    Author
  • Decerf, LaurenceUCLouvain
    Author
  • Lavalleye, BenoîtUCLouvain
    Author
  • Author
  • Lison, Dominiqueorcid-logoUCLouvain
    Author
Show more
Abstract
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 microg/L] and 40 lead-exposed individuals (315 microg/L). 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 microg/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 microg/4 h is proposed for Belgian reference individuals. The diagnostic value of DMSA-PbU is likely to be contributive for PbB >300 microg/L.
Affiliations

Citations

Hoet, P., Buchet, J.-P., Decerf, L., Lavalleye, B., Haufroid, V., & Lison, D. (2006). Clinical evaluation of a lead mobilization test using the chelating agent dimercaptosuccinic acid. Clinical Chemistry : international journal of molecular diagnostics and laboratory medicine, 52(1), 88-96. https://doi.org/10.1373/clinchem.2005.051128 (Original work published 2006)