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

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AX6-67<br />

Table AX6-3.9 (cont’d). Other Neurological Outcomes Associated with <strong>Lead</strong> Exposure in Adults<br />

Reference, Study<br />

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

United States (cont’d)<br />

Kamel et al. (2003)<br />

Massachusetts<br />

Armon et al. (1991)<br />

Minnesota<br />

Europe<br />

Chancellor et al.<br />

(1993)<br />

Scotland<br />

1990-1991<br />

Gunnarsson et al.<br />

(1992)<br />

Sweden<br />

1990<br />

As above, the same data was used to<br />

determine the associations <strong>of</strong> ALS with<br />

polymorphism in ALAD and the vitamin D<br />

receptor (VDR) and the influence <strong>of</strong><br />

genotype.<br />

A case-control design with 47 ALS patients,<br />

mean age 61 with involvement <strong>of</strong> upper and<br />

lower motor neurons and 201 controls, mean<br />

age 62. For the Pb exposure analysis 45 male<br />

matched pairs were examined.<br />

A case-control design 103 ALS patients from<br />

the Scottish Motor Neuron Disease Register<br />

and matched community controls.<br />

Differences in potential occupational<br />

exposures were determined between cases<br />

and controls.<br />

A case-control study <strong>of</strong> 92 cases <strong>of</strong> MND<br />

and 372 controls. MND included ALS,<br />

progressive bulbar paresis (PBP), and<br />

progressive muscular atrophy (PMA).<br />

Relation <strong>of</strong> MND to risk factors including<br />

occupational exposure examined.<br />

Same as above The ALAD2 allele was associated with a 2-fold increase risk <strong>of</strong> ALS<br />

after adjustment <strong>for</strong> the covariates, age, sex, region, education and<br />

physical activity adjusted (OR = 1.9 [95% CI: 0.60, 6.3]).<br />

Additionally adjusting <strong>for</strong> blood Pb strengthened the association <strong>of</strong><br />

ALAD2 and ALS risk adjusted (OR = 3.6 [95% CI: 0.9, 15]). This<br />

was not found <strong>for</strong> bone Pb or occupational history <strong>of</strong> Pb exposure<br />

(patella-adjusted OR = 2.1 [95% CI: 0.61, 6.9]; tibial-adjusted (OR =<br />

2.2 [95% CI: 0.66, 7.3]; occupational history-adjusted<br />

(OR = 2.4 [95% CI: 0.67, 8.7]). VDR was not associated with Pb or<br />

ALS risk.<br />

Lifetime exposure to Pb <strong>of</strong><br />

200 hrs or more (yrs on job x<br />

hrs spent per wk)<br />

Exposure to Pb obtained by<br />

lifetime employment history<br />

from Office <strong>of</strong> Population and<br />

Censuses and Surveys.<br />

Physician’s record review and<br />

direct interview questionnaire.<br />

Exposure in<strong>for</strong>mation<br />

obtained by self-administered<br />

questionnaire.<br />

Of 13 discordant pairs <strong>for</strong> Pb exposure, 11 were in ALS patient. The<br />

relative risk was 5.5 (95% CI: 1.44, 21.0). A dose-response was<br />

weakened by 3 controls with highest lifetime exposure. Men with<br />

ALS worked more <strong>of</strong>ten at blue collar jobs and significantly more<br />

time welding (p < 0.01). These results expanded a prior pilot study<br />

that found a higher incidence <strong>of</strong> heavy metal exposure in ALS cases.<br />

Odds ratio <strong>for</strong> manual labor in ALS patients was 2.6 (95% CI: 1.1,<br />

6.3). Occupational exposure to Pb was more common in ALS<br />

patients (OR = 5.7 [95% CI: 1.6, 30]).<br />

Exposure to heavy metals primarily from welding had an increased<br />

Mantel-Haenszel OR = 3.7 [95% CI: 1.1, 13.0].

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