Cited by 102Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative DiseasesHereditary Neurological Disorders

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C9orf72 intermediate expansions of 24–30 repeats are associated with ALS

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Abstract

The expansion of a hexanucleotide repeat GGGGCC in C9orf72 is the most common known cause of ALS accounting for ~ 40% familial cases and ~ 7% sporadic cases in the European population. In most people, the repeat length is 2, but in people with ALS, hundreds to thousands of repeats may be observed. A small proportion of people have an intermediate expansion, of the order of 20 to 30 repeats in size, and it remains unknown whether intermediate expansions confer risk of ALS in the same way that massive expansions do. We investigated the association of this intermediate repeat with ALS by performing a meta-analysis of four previously published studies and a new British/Alzheimer’s Disease Neuroimaging Initiative dataset of 1295 cases and 613 controls. The final dataset comprised 5071 cases and 3747 controls. Our meta-analysis showed association between ALS and intermediate C9orf72 repeats of 24 to 30 repeats in size (random-effects model OR = 4.2, 95% CI = 1.23–14.35, p -value = 0.02). Furthermore, we showed a different frequency of the repeat between the northern and southern European populations (Fisher’s exact test p -value = 5 × 10 − 3 ). Our findings provide evidence for the association between intermediate repeats and ALS ( p -value = 2 × 10 − 4 ) with direct relevance for research and clinical practice by showing that an expansion of 24 or more repeats should be considered pathogenic.

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Crossref · 10.1186/s40478-019-0724-4

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  • Repeats of 24 or more hexanucleotides in C9orf72 are considered pathogenic, leading to earlier diagnosis of ALS.

    “Repeats of 24 or more hexanucleotides are considered pathogenic, leading to earlier diagnosis of ALS [6, 7].”

    From Lifestyle and medical conditions in relation to ALS risk and progression—an introduction to the Swedish ALSrisc Study (2024) · cites this paper as [6]

    The Discussion (page unavailable) proposes treating C9orf72 expansions of 24 or more repeats as pathogenic. The paper does not report that this threshold leads to earlier ALS diagnosis; its clinical analysis concerns age at onset and survival, not diagnostic timing. (LLM, conf=0.88)

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Metadata

Authors
Initiative, A. D. N., Iacoangeli, A., Al Khleifat, A., Jones, A. R., Sproviero, W., Shatunov, A., Opie-Martin, S., Morrison, K. E., Shaw, P. J., Shaw, C. E., Fogh, I., Dobson, R. J., Newhouse, S. J., & Al-Chalabi, A.
Affiliations
  • San Francisco VA Medical Center (US)
  • King's College London (GB)
  • University Hospital Southampton NHS Foundation Trust (GB)
Corresponding author
Iacoangeli, Alfredo
Venue
Acta Neuropathologica Communications
Published
2019-07-17
Volume
7
Issue
1
Pages
115-115
ISSN
2051-5960 (ISSN-L)
OpenAlex
W2957790560
Cited by
102
References
4
Citations by year
2026: 8 · 2025: 11 · 2024: 17 · 2023: 15 · 2022: 17 · 2021: 17 · 2020: 17
FWCI
1.71
Type
journal article
Language
en
Open access
Locations
  • Acta Neuropathologica Communications (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
  • ePrints Soton (University of Southampton) (acceptedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • UCL Discovery (University College London) (submittedVersion)
  • Research Portal (King's College London) (submittedVersion, cc-by)
  • Research Portal (Queen's University Belfast) (submittedVersion, cc-by)
Funders
  • Motor Neurone Disease Association
  • Medical Research Council (MR/L501529/1, MR/R024804/1)
  • Economic and Social Research Council (ES/L008238/1)
  • Horizon 2020 Framework Programme (633413)
Topics
  • Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
Keywords
C9orf72, hexanucleotide repeat expansion, amyotrophic lateral sclerosis, ALS risk
MeSH terms
Whole Genome Sequencing, C9orf72 Protein, Aged, Amyotrophic Lateral Sclerosis, Female, Humans, Male, Middle Aged, Databases, Genetic, DNA Repeat Expansion, White People

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