Surveillance results and bone effects in the Gulf War depleted uranium-exposed cohort. Issue 20 (18th October 2018)

• Record Type: Journal Article
• Authors: McDiarmid, Melissa A; Cloeren, Marianne; Gaitens, Joanna M; Hines, Stella; Streeten, Elizabeth; Breyer, Richard J.; Brown, Clayton H.; Condon, Marian; Roth, Tracy; Oliver, Marc; Brown, Lawrence; Dux, Moira; Lewin-Smith, Michael R.; Strathmann, Frederick; Velez-Quinones, Maria A.; Gucer, Patricia
• Is Part Of: Journal of toxicology and environmental health. Volume 81:Issue 20(2018)
• Page Start: 1083
• Page End: 1097
• Publication Date: 2018-10-18
• Subjects: Uranium toxicity -- health surveillance -- DU bio-monitoring -- bone mineral density; Toxicology -- Periodicals; Environmental health -- Periodicals; 615.90205
• DOI: 10.1080/15287394.2018.1538914
• Languages: English
• ISSNs: 1528-7394

Abstract

ABSTRACT: A small group of Gulf War I veterans wounded in depleted uranium (DU) friendly-fire incidents have been monitored in a clinical surveillance program since 1993. During the spring of 2017, 42 members of the cohort were evaluated with a protocol which includes exposure monitoring for total and isotopic uranium concentrations in urine and a comprehensive assessment of health outcomes including measures of bone metabolism, and for participants >50 years, bone mineral density (BMD) determination. Elevated urine U concentrations were observed in cohort members with retained DU shrapnel fragments. Only the mean serum estradiol concentration, a marker of bone metabolism, was found to be significantly different for lower-vs- higher urine U (uU) cohort sub-groups. For the first time, a significant deficit in BMD was observed in the over age 50, high uU sub-group. After more than 25 years since first exposure to DU, an aging cohort of military veterans continues to exhibit few U-related adverse health effects in known target organs of U toxicity. The new finding of reduced BMD in older cohort members, while biologically plausible, was not suggested by other measures of bone metabolism in the full (all ages) cohort, as these were predominantly within normal limits over time. Only estradiol was recently found to display a difference as a function of uU grouping. As BMD is further impacted by aging and the U-burden from fragment absorption accrues in this cohort, a U effect may be clarified in future surveillance visits.