The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Prevalence of amyotrophic lateral sclerosis in the United States, 2018
Open accessAbstract
OBJECTIVE: To estimate prevalent ALS cases in the United States for calendar year 2018. METHODS: The National ALS Registry (Registry) compiled data from national administrative databases (from the Centers for Medicare and Medicaid Services, the Veterans Health Administration, and the Veterans Benefits Administration) and enrollment data voluntarily submitted through a web portal (www.cdc.gov/als). We used log-linear capture-recapture (CRC) model-based methodology to estimate the number of cases not ascertained by the Registry. RESULTS: The Registry identified 21,655 cases of ALS in 2018, with an age-adjusted prevalence of 6.6 per 100,000 U.S. population. When CRC methods were used, an estimated 29,824 cases were identified, for an adjusted prevalence of 9.1 per 100,000 U.S. population. The demographics of cases of ALS did not change from previous year's reports. ALS continues to impact Whites, males, and persons over 50 years of age more so than other comparison groups. The results from the present report suggest case ascertainment for the Registry has improved, with the estimate of missing prevalent cases decreasing from 44% in 2017 to 27% in in 2018. DISCUSSION: Consistent with previous estimates that used CRC, ALS prevalence in the United States is about 29,824 cases per year.
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“The proportion of patients younger than age 50 years (12.8%) was slightly overrepresented in our sample when compared with the National ALS Registry as a whole (10.5%) [86].”
From Head Injury and Amyotrophic Lateral Sclerosis: Population-Based Study from the National ALS Registry (2025) · cites this paper as [86]
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“racial diversity appeared to be underrepresented in the sample. Only 3.6% of respondents were Non-White compared with 11.6% in the Registry as a whole [86].”
From Head Injury and Amyotrophic Lateral Sclerosis: Population-Based Study from the National ALS Registry (2025) · cites this paper as [86]
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Cites
Risk factors for amyotrophic lateral sclerosis: A regional United States case‐control study
Andrew, A. S., Bradley, W. G., Peipert, D., Butt, T., Amoako, K., Pioro, E. P., Tandan, R., Novak, J., Quick, A., Pugar, K. D., et al. (2021) · Muscle & Nerve · doi:10.1002/mus.27085 · Cited by 54
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Dinov, I. D., Heavner, B., Tang, M., Glusman, G., Chard, K., Darcy, M., Madduri, R., Pa, J., Spino, C., Kesselman, C., et al. (2016) · PLOS ONE · doi:10.1371/journal.pone.0157077 · Cited by 145
Head Injury and Amyotrophic Lateral Sclerosis: Population-Based Study from the National ALS Registry
Raymond, J., Howard, I. M., Berry, J., Larson, T., Horton, D. K., & Mehta, P. (2025) · Brain Sciences · doi:10.3390/brainsci15020143 · Cited by 4
Self-citationLester, E. G., Vitolo, O. V., Flaherty, A., Beaussant, Y., Cramer, M., Harley, R., & Cohen, J. N. (2023) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.23ct15038 · Cited by 2
Metadata
- Authors
- Mehta, P., Raymond, J., Zhang, Y., Punjani, R., Han, M., Larson, T., Muravov, O., Lyles, R. H., & Horton, D. K.
- Affiliations
- Centers for Disease Control and Prevention (US)
- Emory University (US)
- Corresponding author
- Mehta, Paul
- ORCID
- Venue
- Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Publisher
- Informa UK Limited
- Published
- 2023-08-21
- Volume
- 24
- Issue
- 7-8
- Pages
- 702-708
- ISSN
- 2167-8421 (ISSN-L)
- 2167-9223
- OpenAlex
- W4386020250
- Cited by
- 86
- References
- 1
- Citations by year
- 2026: 6 · 2025: 24 · 2024: 16 · 2023: 9
- FWCI
- 9.07
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- public-domain
- creativecommons.org/publicdomain/mark/1.0/ (vor)
- Locations
- Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (publishedVersion, public-domain)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Physical Sciences › Mathematics › Statistics and Probability › Census and Population Estimation
- Health Sciences › Medicine › Internal Medicine › Amyloidosis: Diagnosis, Treatment, Outcomes
- Keywords
- amyotrophic lateral sclerosis, prevalence, National ALS Registry, case ascertainment, United States
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