Association of APOE with age at onset of sporadic amyotrophic lateral sclerosis
Abstract
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative syndrome with familial and sporadic forms. We conducted a study including 60 sporadic and 19 familial ALS patients, 206 reference patients with other neurological disorders and 1265 neurologically healthy controls to assess the Alzheimer-associated apolipoprotein E (APOE) epsilon4 gene variant as a possible risk factor for ALS. While no major influence of APOE epsilon4 on disease risk was detected, a gene dose-dependent effect with lower age at onset of sporadic ALS in epsilon4 carriers was found (p=0.027). These data support APOE epsilon4 as a subordinate contributing factor in ALS.
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Recently identified functional siRNA sequences target Apolipoprotein E (ApoE), implicated in several neurodegenerative diseases.
“Recently, we identified functional siRNA sequences targeting Apolipoprotein E (ApoE), implicated in several neurodegenerative diseases, including Alzheimer’s disease and Amyotrophic Lateral Sclerosis26–28 (Ferguson et al., manuscript in preparation).”
From A divalent siRNA chemical scaffold for potent and sustained modulation of gene expression throughout the central nervous system (2019) · cites this paper as [28]
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Apolipoprotein E in Alzheimer’s disease and other neurological disorders
Verghese, P. B., Castellano, J. M., & Holtzman, D. M. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(10)70325-2 · Cited by 857 · see citing works
Wang, M.-D., Little, J., Gomes, J., Cashman, N. R., & Krewski, D. (2017) · NeuroToxicology · doi:10.1016/j.neuro.2016.06.015 · Cited by 233 · see citing works
Alterman, J. F., Godinho, B. M. D. C., Hassler, M. R., Ferguson, C. M., Echeverria, D., Sapp, E., Haraszti, R. A., Coles, A. H., Conroy, F., Miller, R., et al. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0205-0 · Cited by 227 · see citing works
- Authors
- Zetterberg, H., Jacobsson, J., Rosengren, L., Blennow, K., & Andersen, P. M.
- Affiliations
- Sahlgrenska University Hospital (SE)
- University Hospital of Umeå (SE)
- Corresponding author
- Zetterberg, Henrik
- Venue
- Journal of the Neurological Sciences
- Publisher
- Elsevier BV
- Published
- 2008-10
- Volume
- 273
- Issue
- 1-2
- Pages
- 67-69
- ISSN
- 0022-510X (ISSN-L)
- OpenAlex
- W1964309555
- Cited by
- 46
- References
- 0
- Citations by year
- 2026: 1 · 2025: 3 · 2023: 1 · 2022: 1 · 2021: 4 · 2019: 2 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 4 · 2014: 4 · 2013: 3 · 2012: 3
- FWCI
- 2.98
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of the Neurological Sciences (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Brain Research Foundation
- Topics
- Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Keywords
- amyotrophic lateral sclerosis, sporadic ALS, familial ALS, apolipoprotein E, APOE ε4, age of onset, genetic risk factors
- MeSH terms
- Superoxide Dismutase-1, Adult, Aged, Aged, 80 and over, Amyotrophic Lateral Sclerosis, Female, Gene Frequency, Genotype, Humans, Male, Middle Aged, Mutation, Superoxide Dismutase, Survival Analysis, Age of Onset, Apolipoprotein E4
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