Cited by 46Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatmentsHereditary Neurological Disorders

Association of APOE with age at onset of sporadic amyotrophic lateral sclerosis

Zetterberg, Henrik, Jacobsson, Johan, Rosengren, Lars, Blennow, Kaj, Andersen, Peter M.·2008·Journal of the Neurological Sciences

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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Crossref · 10.1016/j.jns.2008.06.025

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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
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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