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Air Quality Criteria for Lead Volume II of II - (NEPIS)(EPA) - US ...

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AX6-65<br />

Table AX6-3.8 (cont’d). Occupational Exposure to Organolead and Inorganic <strong>Lead</strong> in Adults<br />

Reference, Study<br />

Location, and Period Study Description Pb Measurement Findings, Interpretation<br />

United States (cont’d)<br />

Stewart et al. (2002)<br />

U.S.<br />

Tassler et al. (2001)<br />

U.S.<br />

Bolla et al. (1995)<br />

U.S.<br />

Mitchell et al. (1996)<br />

U.S.<br />

Population as described in Stewart et al.<br />

(1999) and Schwartz et al. (2000b). Data<br />

on 20 neurobehavioral tests from 529<br />

<strong>for</strong>mer organolead workers were<br />

evaluated to determine if the previously<br />

described relationship with bone Pb<br />

levels is influenced by the apolipoprotein<br />

E (ApoE) genotype.<br />

490 <strong>for</strong>mer organolead workers, mean<br />

age 58 (7.5) yrs. The peripheral nervous<br />

system was examined with sensory<br />

pressure thresholds, and pinch and grip<br />

strength.<br />

190 current workers in organolead<br />

manufacturing (from the 222 described in<br />

Schwartz et al., 1993) mean age 45 (8)<br />

yrs compared to 52 referents, mean age<br />

45 (8) yrs and 144 solvent exposed<br />

workers, mean age 42 (8) yrs.<br />

58 organolead workers, self-selected <strong>for</strong><br />

a clinical evaluation. Mean age 45 (7.1)<br />

yrs.<br />

Mean (SD) blood Pb 5<br />

(2.6) µg/dL<br />

Mean (SD) DMSA-chelatable Pb<br />

19 (16.3) µg<br />

Mean (SD) current tibia Pb<br />

15 (9.4) µg/g<br />

Mean (SD) peak tibia Pb 24<br />

(17.6) µg/g<br />

IH found organic Pb was 65 to<br />

70% <strong>of</strong> exposure in production<br />

area.<br />

Mean (SD) weighted avg blood<br />

Pb 24 (9.4) µg/dL<br />

Mean (SD) blood Pb 19<br />

(6.5) µg/dL<br />

Mean (SD) lifetime blood Pb 26<br />

(9.1) µg/dL<br />

Mean (SD) lifetime urine Pb 51<br />

(18.8) µg/L<br />

In 20 linear regression models, coefficients <strong>for</strong> the ApoE and tibia Pb<br />

interaction term were negative in 19 with significance reached <strong>for</strong> digit<br />

symbol (∃ = !0.109 [SE 0.054], p # 0.05), Purdue pegboard dominant<br />

(∃ = 0.068 [SE 0.028], p # 0.05) and complex reaction time (∃ = !0.003<br />

[SE 0.001], p#0.05) and borderline significance existed <strong>for</strong> symbol digit<br />

(∃ = !0.046 [SE 0.026], p # 0.10), Trails A (∃ = !0.303, [SE 0.164]<br />

p # 0.10) and Stroop (∃ = !0.013 [SE 0.008], p # 0.10). The slope <strong>of</strong> the<br />

relation between tibia Pb and neurobehavioral outcome was more<br />

negative in those individuals with at least one ε4 allele than individuals<br />

without this allele. It is suggested that the presence <strong>of</strong> one Apo-ε-4 allele<br />

increases the risk <strong>of</strong> persistent central nervous system effects <strong>of</strong> Pb.<br />

No strong association was found between Pb biomarkers and measures<br />

<strong>of</strong> sensory and motor function after adjusting <strong>for</strong> age. The authors<br />

attributed the findings to decreased sensitivity <strong>of</strong> the peripheral nerves in<br />

this dose range <strong>of</strong> inorganic Pb or the possibility <strong>of</strong> differential repair in<br />

the peripheral nervous system compared to the central nervous system.<br />

Pb and solvent exposure associated with adverse effects on tests <strong>of</strong><br />

manual dexterity. When compared to the solvent group Pb exposure had<br />

greater impairment on memory and learning and less on executive/motor<br />

tests. An elevated neuropsychiatric score was present in 43% <strong>of</strong> the Pb<br />

group, 15% <strong>of</strong> the solvent and 7% <strong>of</strong> the referent group.<br />

The most common symptoms were memory loss 74%, joint pain 56%,<br />

trouble sleeping 54%, irritability 51%, paresthesia 49%, fatigue 49%,<br />

nightmares 35%, moodiness 28%, headaches 21% and depression 21%.<br />

Of the 31 workers receiving nerve conduction studies, 29% were normal,<br />

carpal tunnel syndrome 36%, cubital tunnel syndrome 3%, median<br />

neuropathy 3%, ulnar neuropathy 23%, mononeuropathy in lower<br />

extremity 5%, tarsal tunnel syndrome 7% and sensorimotor<br />

polyneuropathy 36%. 39 workers had neurobehavioral evaluation with<br />

64% had abnormal tests <strong>of</strong> which 46% were considered to be consistent<br />

with a toxic exposure.

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