Spatial analysis of the etiology of amyotrophic lateral sclerosis among 1991 Gulf War veterans

被引:41
作者
Miranda, Marie Lynn [1 ]
Galeano, M. Alicia Overstreet [1 ]
Tassone, Eric [1 ]
Allen, Kelli D. [2 ,3 ]
Horner, Ronnie D. [4 ,5 ]
机构
[1] Duke Univ, Nicholas Sch Environm, Durham, NC 27708 USA
[2] Vet Adm Med Ctr, Ctr Hlth Serv Res Primary Care, Dept Vet Affairs, Durham, NC 27705 USA
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC 27708 USA
[4] Univ Cincinnati, Med Ctr, Inst Study Hlth, Cincinnati, OH 45267 USA
[5] Univ Cincinnati, Med Ctr, Dept Publ Hlth Sci, Cincinnati, OH 45267 USA
关键词
Geographic information systems; Amyotrophic lateral sclerosis; 1991 Gulf War; Environmental exposure; Spatial analysis;
D O I
10.1016/j.neuro.2008.05.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Veterans of the 1991 Gulf War have an increased risk of amyotrophic lateral sclerosis (ALS), but the etiology is unknown. Objectives: This study sought to identify geographic areas with elevated risk for the later development of ALS among military personnel who served in the first Gulf War. Methods: A unified geographic information system (GIS) was constructed to allow analysis of secondary data on troop movements in the 1991 Gulf War theatre in the Persian Gulf region including Iraq, northern Saudi Arabia, and Kuwait. We fit Bayesian Poisson regression models to adjust for potential risk factors, including one relatively discrete environmental exposure, and to identify areas associated with elevated risk of ALS. Results: We found that service in particular locations of the Gulf was associated with an elevated risk for later developing ALS, both before and after adjustment for branch of service and potential of exposure to chemical warfare agents in and around Khamisiyah, Iraq. Conclusions: Specific geographic locations of troop units within the 1991 Gulf War theatre are associated with an increased risk for the subsequent development of ALS among members of those units. The identified spatial locations represent the logical starting points in the search for potential etiologic factors of ALS among Gulf War veterans. Of note, for locations where the relative odds of subsequently developing ALS are among the highest, specific risk factors, whether environmental or occupationally related, have not been identified. The results of spatial models can be used to subsequently look for risk factors that follow the spatial pattern of elevated risk. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:964 / 970
页数:7
相关论文
共 21 条
[11]   The National Registry of Veterans with Amyotrophic Lateral Sclerosis: Department of Veterans Affairs Cooperative Studies Program (CSP) #500a [J].
Kasarskis, EJ ;
Dominic, K ;
Oddone, EZ .
AMYOTROPHIC LATERAL SCLEROSIS, 2004, 5 :129-132
[12]   Neurological status of Australian veterans of the 1991 Gulf War and the effect of medical and chemical exposures [J].
Kelsall, H ;
Macdonell, R ;
Sim, M ;
Forbes, A ;
McKenzie, D ;
Glass, D ;
Ikin, J ;
Ittak, P .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2005, 34 (04) :810-819
[13]  
PAGE DP, PERIODS RISK GIS EXC
[14]   Health effects in army Gulf War veterans possibly exposed to chemical munitions destruction at Khamisiyah, Iraq: Part I. Morbidity associated with potential exposure [J].
Page, WF ;
Mahan, CM ;
Page, WF ;
Bullman, TA ;
Kang, HK .
MILITARY MEDICINE, 2005, 170 (11) :935-944
[15]  
Proctor S. P., 2005, T GIS, V9, P381
[16]   Effects of sarin and cyclosarin exposure during the 1991 Gulf War on neurobehavioral functioning in US army veterans [J].
Proctor, Susan P. ;
Heaton, Kristin J. ;
Heeren, Tim ;
White, Roberta F. .
NEUROTOXICOLOGY, 2006, 27 (06) :931-939
[17]   Neurological disorders in Gulf War veterans [J].
Rose, MR ;
Brix, KA .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2006, 361 (1468) :605-618
[18]   Neurophysiologic analysis of neuromuscular symptoms in UK Gulf War veterans - A controlled study [J].
Sharief, MK ;
Priddin, J ;
Delamont, RS ;
Unwin, C ;
Rose, MR ;
David, A ;
Wessely, S .
NEUROLOGY, 2002, 59 (10) :1518-1525
[19]  
Smith TC, 2000, AM J EPIDEMIOL, V151, P1053, DOI 10.1093/oxfordjournals.aje.a010147
[20]  
Spencer PS, 1998, TOXICOL LETT, V103, P515