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Abstract Details

Use of ALS cases from the ATSDR/CDC National ALS Registry and a population based control group to investigate ambient air pollution and suspected neurotoxicants as risk factors for ALS
General Neurology
P9 - Poster Session 9 (12:00 PM-1:00 PM)
6-008
To investigate associations between exposure to neurotoxicants/air pollution (AP) and risk of ALS among ALS cases from the ATSDR/CDC National ALS Registry/Biorepository and population-based controls. 

Little is known about risk factors for ALS ; 90%-95% of cases are sporadic. We linked USEPA modeled AP data to residences of ALS cases and controls to explore relationships of AP, especially particulate matter (PM) and other ambient air toxics and risk of ALS.  

Of 280 cases recruited by the ALS Registry/Biorepository, the current analysis includes cases and controls matched by age, gender, and county, with blood specimens for separate pesticide analysis.  USEPA modeled AP estimates (PM2.5 and O3) for 2002-2015 and NATA (National Air Toxics Assessment) data for 2011 and 2014 were linked to the census tract centroid of the individual’s ZCTA residence.  NATA compounds represent five classes: volatile organics, chlorinated hydrocarbons, pesticides, metals, and other hazardous air pollutants. Matched pair analysis and multivariate conditional analysis will be performed with adjustment and the study is ongoing.   

Preliminary analysis is available on the 83 matched-pairs to date. The majority of cases and controls were male (63.9% vs. 65.1%, respectively).  Cases were primarily white (97.6% and 1.2% black), mean age at diagnosis: 58.5±9.7.  For 2011, mean PM25 levels: 9.28 ug/m3 for cases, and 9.27 ug/m3 for controls; ozone levels were 40.1 ppb and 40.4 ppb, respectively.  NATA 2011 levels for selected air toxicants include: benzene: 0.48±0.26 and .50±0.27 ug/m3, toluene: 1.34±1.02 and 1.49±1.61 ug/m3, and methylene chloride: .04±0.16 and .02±.06 ug/m3 for cases and controls, respectively. Conditional logistic analysis without adjustment revealed no significant differences in ozone or PM25 between cases and controls.

This is the first study to consider both AP and neurotoxicant exposures at a national level in cases and controls that can be correlated with serum levels of the same neurotoxicants.

Authors/Disclosures

PRESENTER
No disclosure on file
Angela M. Malek, PhD (Medical University of South Carolina, Department of Public Health Sciences) No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
Fan Wu, PhD No disclosure on file