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Scientific article
English

Telomere length is not predictive of dementia or MCI conversion in the oldest old

Published inNeurobiology of aging, vol. 31, no. 4, p. 719-720
Publication date2010
Abstract

The contribution of telomere shortening to the onset of certain age-related diseases, such as dementia, and its role as a predictor of cognitive impairment remain unclear. We tested these hypotheses by analyzing telomere length in 449 inpatients in a large cohort of the oldest old (mean age 85 years) followed up yearly. No significant difference in telomere length was observed between cognitively normal patients (205), demented patients (195; 82 mixed dementia, 77 Alzheimer's disease and 21 vascular dementia) and patients (49) with mild cognitive impairment (MCI). Similarly, no significant differences in telomere length were found between patients with different etiologies or severities of dementia. Telomere length and change in cognitive status (from normal to MCI or dementia, or from MCI to dementia) were not associated after two years of follow-up. This longitudinal study in very old patients provided no evidence to suggest that telomere length could be used to distinguish between demented and non demented patients, regardless of the type of dementia, or to predict dementia or MCI conversion.

Keywords
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease/genetics
  • Cell Aging/genetics
  • Cognition Disorders/ genetics
  • Cohort Studies
  • DNA Mutational Analysis
  • Dementia/ genetics
  • Dementia, Vascular/genetics
  • Disease Progression
  • Female
  • Frontotemporal Dementia/genetics
  • Genetic Markers/ genetics
  • Genetic Predisposition to Disease/ genetics
  • Genetic Testing
  • Genotype
  • Humans
  • Longitudinal Studies
  • Male
  • Prognosis
  • Risk Factors
  • Telomere/ genetics
Affiliation Not a UNIGE publication
Citation (ISO format)
ZEKRY BERGER, Dina Selma et al. Telomere length is not predictive of dementia or MCI conversion in the oldest old. In: Neurobiology of aging, 2010, vol. 31, n° 4, p. 719–720. doi: 10.1016/j.neurobiolaging.2008.05.016
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ISSN of the journal0197-4580
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