Genetic epidemiology of amyotrophic lateral sclerosis
Open accessAbstract
Amyotrophic lateral sclerosis (ALS) is a late onset, rapidly progressive and ultimately fatal neurological disorder, caused by the loss of motor neurons in the brain and spinal cord. Familial aggregation of ALS, with an age-dependent but high penetrance, is a major risk factor for ALS. Familial ALS (FALS) is clinically and genetically heterogeneous. Three genes and linkage to four additional gene loci have been identified so far and may either predominantly lead to ALS (ALSI-ALS6) or cause multisystem neurodegeneration with ALS as an occasional symptom (tauopathies, ALS-dementia complex). This review presents a tentative classification of the "major" ALS genes and ALS "susceptibility" genes, that may act as susceptibility factors for neurodegeneration in interaction with other genetic or environmental risk factors. Considering that mutations in ALS genes explain approximately 10% of familial as well as sporadic ALS, and most remaining cases of the discase are thought to result form the interaction of several genes and environmental factors, ALS is a paradigm for multifactorial discases.
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Approximately 20% of familial ALS and 5% of sporadic ALS cases are caused by mutations in the SOD1 gene.
“Approximately 20% of fALS and 5% of sALS cases are caused by mutations in the SOD1 gene (Majoor-Krakauer et al., 2003; Robberecht and Philips, 2013).”
From Downregulation of MicroRNA-193b-3p Promotes Autophagy and Cell Survival by Targeting TSC1/mTOR Signaling in NSC-34 Cells (2017) · cites this paper as Majoor-Krakauer et al., 2003
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References 363 · Cited by 147
- Authors
- Majoor‐Krakauer, D., Willems, P., & Hofman, A.
- Affiliations
- Erasmus MC (NL)
- Corresponding author
- Majoor‐Krakauer, D
- ORCID
- Majoor‐Krakauer, D
- Venue
- Clinical Genetics
- Publisher
- Wiley
- Published
- 2003-02
- Volume
- 63
- Issue
- 2
- Pages
- 83-101
- ISSN
- 0009-9163 (ISSN-L)
- 1399-0004
- OpenAlex
- W2121632523
- Cited by
- 147
- References
- 363
- Citations by year
- 2025: 2 · 2024: 3 · 2022: 4 · 2021: 4 · 2020: 3 · 2019: 4 · 2018: 5 · 2017: 8 · 2016: 6 · 2015: 1 · 2014: 7 · 2013: 2 · 2012: 8
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- green
- pure.eur.nl
- Licence
- Locations
- Clinical Genetics (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion, other-oa)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- RePub (Erasmus University Rotterdam) (submittedVersion)
- Topics
- Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- amyotrophic lateral sclerosis, familial aggregation, ALS gene, susceptibility genes, motor neuron degeneration, genetic linkage, tauopathy, complex diseases, gene-environment interaction, sporadic ALS
- MeSH terms
- Age Factors, Amyotrophic Lateral Sclerosis, Female, Humans, Male, Mutation, Risk Factors, Causality, Inheritance Patterns
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