A perspective on persistent toxicants in veterans and amyotrophic lateral sclerosis: identifying exposures determining higher ALS risk
- PMID: 34973105
- PMCID: PMC9021134
- DOI: 10.1007/s00415-021-10928-5
A perspective on persistent toxicants in veterans and amyotrophic lateral sclerosis: identifying exposures determining higher ALS risk
Abstract
Multiple studies indicate that United States veterans have an increased risk of developing amyotrophic lateral sclerosis (ALS) compared to civilians. However, the responsible etiological factors are unknown. In the general population, specific occupational (e.g. truck drivers, airline pilots) and environmental exposures (e.g. metals, pesticides) are associated with an increased ALS risk. As such, the increased prevalence of ALS in veterans strongly suggests that there are exposures experienced by military personnel that are disproportionate to civilians. During service, veterans may encounter numerous neurotoxic exposures (e.g. burn pits, engine exhaust, firing ranges). So far, however, there is a paucity of studies investigating environmental factors contributing to ALS in veterans and even fewer assessing their exposure using biomarkers. Herein, we discuss ALS pathogenesis in relation to a series of persistent neurotoxicants (often emitted as mixtures) including: chemical elements, nanoparticles and lipophilic toxicants such as dioxins, polycyclic aromatic hydrocarbons and polychlorinated biphenyls. We propose these toxicants should be directly measured in veteran central nervous system tissue, where they may have accumulated for decades. Specific toxicants (or mixtures thereof) may accelerate ALS development following a multistep hypothesis or act synergistically with other service-linked exposures (e.g. head trauma/concussions). Such possibilities could explain the lower age of onset observed in veterans compared to civilians. Identifying high-risk exposures within vulnerable populations is key to understanding ALS etiopathogenesis and is urgently needed to act upon modifiable risk factors for military personnel who deserve enhanced protection during their years of service, not only for their short-term, but also long-term health.
Keywords: Amyotrophic lateral sclerosis; Etiology; Exposure; Neurotoxicant; Persistent; Veterans.
© 2021. The Author(s).
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Similar articles
-
Military service, deployments, and exposures in relation to amyotrophic lateral sclerosis etiology.Environ Int. 2016 May;91:104-15. doi: 10.1016/j.envint.2016.02.014. Epub 2016 Feb 23. Environ Int. 2016. PMID: 26923711 Free PMC article.
-
Military service and related risk factors for amyotrophic lateral sclerosis.Acta Neurol Scand. 2021 Jan;143(1):39-50. doi: 10.1111/ane.13345. Epub 2020 Oct 12. Acta Neurol Scand. 2021. PMID: 32905613 Free PMC article.
-
Military service, deployments, and exposures in relation to amyotrophic lateral sclerosis survival.PLoS One. 2017 Oct 10;12(10):e0185751. doi: 10.1371/journal.pone.0185751. eCollection 2017. PLoS One. 2017. PMID: 29016608 Free PMC article.
-
Military service, deployments, and exposures in relation to amyotrophic lateral sclerosis etiology and survival.Epidemiol Rev. 2015;37(1):55-70. doi: 10.1093/epirev/mxu001. Epub 2014 Oct 31. Epidemiol Rev. 2015. PMID: 25365170 Free PMC article. Review.
-
Retrospective Assessment of Occupational Exposures for the GENEVA Study of ALS among Military Veterans.Ann Work Expo Health. 2017 Apr 1;61(3):299-310. doi: 10.1093/annweh/wxw028. Ann Work Expo Health. 2017. PMID: 28355414 Free PMC article.
Cited by
-
TDP-43 CSF Concentrations Increase Exponentially with Age in Metropolitan Mexico City Young Urbanites Highly Exposed to PM2.5 and Ultrafine Particles and Historically Showing Alzheimer and Parkinson's Hallmarks. Brain TDP-43 Pathology in MMC Residents Is Associated with High Cisternal CSF TDP-43 Concentrations.Toxics. 2022 Sep 24;10(10):559. doi: 10.3390/toxics10100559. Toxics. 2022. PMID: 36287840 Free PMC article.
-
An Update on Parkinson's Disease and its Neurodegenerative Counterparts.Curr Med Chem. 2024;31(19):2770-2787. doi: 10.2174/0929867330666230403085733. Curr Med Chem. 2024. PMID: 37016529 Review.
-
Guidance for clinical management of pathogenic variant carriers at elevated genetic risk for ALS/FTD.J Neurol Neurosurg Psychiatry. 2025 Mar 13;96(3):209-218. doi: 10.1136/jnnp-2024-334339. J Neurol Neurosurg Psychiatry. 2025. PMID: 39572211 Free PMC article. Review.
-
Update on recent advances in amyotrophic lateral sclerosis.J Neurol. 2024 Jul;271(7):4693-4723. doi: 10.1007/s00415-024-12435-9. Epub 2024 May 27. J Neurol. 2024. PMID: 38802624 Free PMC article. Review.
-
Military Service Roles and ALS Among Veterans: A Matched Case-Control Study.Ann Clin Transl Neurol. 2025 May 19;12(8):1702-5. doi: 10.1002/acn3.70079. Online ahead of print. Ann Clin Transl Neurol. 2025. PMID: 40386966 Free PMC article.
References
-
- Rowland LP, Mitsumoto H, Przedborski S. Amyotrophic lateral sclerosis, progressive muscular atrophy, and primary lateral sclerosis. In: Rowland LP, Pedley TA, editors. Merritt's neurology. Lippincott: Williams & Wilkins; 2010. pp. 802–808.
-
- Mathis S, et al. Genetics of amyotrophic lateral sclerosis: A review. J Neurol Sci. 2019;399:217–226. - PubMed
-
- Nguyen HP, et al. ALS genes in the genomic era and their implications for FTD. Trends Genet. 2018;34(6):404–423. - PubMed
-
- Harms MM et al (1993) TARDBP-related amyotrophic lateral sclerosis. In: Adam MP (eds) GeneReviews [Internet]. University of Washington, Seattle, WA
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous