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Autor(en) / Beteiligte
Titel
C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition
Ist Teil von
  • Neurobiology of aging, 2019-12, Vol.84, p.242.e7-242.e12
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2019
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • The hexanucleotide repeat expansion in C9orf72 is a common cause of amyotrophic lateral sclerosis/frontotemporal dementia and also rarely found in other psychiatric and neurodegenerative conditions. Alleles with >30 repeats are often considered an expansion, but the pathogenic repeat length threshold is still unclear. It is also unclear whether intermediate repeat length alleles (often defined either as 7–30 or 20–30 repeats) have clinically significant effects. We determined the C9orf72 repeat length distribution in 3142 older Finns (aged 60–104 years). The longest nonexpanded allele was 45 repeats. We found 7–45 repeats in 1036/3142 (33%) individuals, 20–45 repeats in 56/3142 (1.8%), 30–45 repeats in 12/3142 (0.38%), and expansion (>45 repeats) in 6/3142 (0.19%). There was no apparent clustering of neurodegenerative or psychiatric diseases in individuals with 30–45 repeats indicating that 30–45 repeats are not pathogenic. None of the 6 expansion carriers had a diagnosis of amyotrophic lateral sclerosis/frontotemporal dementia but 4 had a diagnosis of a neurodegenerative or psychiatric disease. Intermediate length alleles (categorized as 7–45 and 20–45 repeats) did not associate with Alzheimer's disease or cognitive impairment. •C9orf72 hexanucleotide repeat expansion is the most common cause of ALS/FTD.•Pathogenic threshold and effects of intermediate repeats on cognition are unclear.•Analysis of 3142 older Finns indicates pathologic threshold of at least 45 repeats.•Intermediate repeat lengths do not predispose to Alzheimer's disease.•Expansions and repeats of over 20 seem more common in Finland than elsewhere.
Sprache
Englisch
Identifikatoren
ISSN: 0197-4580
eISSN: 1558-1497
DOI: 10.1016/j.neurobiolaging.2019.02.026
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8981799

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