4.5 Article

Leukocyte Telomere Length (LTL) is reduced in stable mild cognitive impairment but low LTL is not associated with conversion to Alzheimer's Disease: A pilot study

期刊

EXPERIMENTAL GERONTOLOGY
卷 47, 期 2, 页码 179-182

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exger.2011.12.005

关键词

Leukocyte telomere length; Biological aging; Alzheimer's disease; Mild cognitive impairment; Cerebrospinal fluid

资金

  1. Swedish Research Council
  2. Swedish Foundation for Strategic Research
  3. ALF/LUA in Gothenburg
  4. Lundberg Foundation
  5. Torsten and Ragnar Soderberg's Foundation
  6. Lundbeck Foundation
  7. Sahlgrenska University Hospital
  8. Sahlgrenska Academy
  9. Stiftelsen Psykiatriska Forskningsfonden
  10. Stiftelsen Gamla Tjanarinnor
  11. Uppsala Universitets Medicinska Fakultet stiftelse for psykiatrisk och neurologisk forskning
  12. Alzheimer Foundation, Sweden
  13. Dementia Association, Sweden
  14. Novo Nordisk Foundation

向作者/读者索取更多资源

Leukocyte telomere length (LTL) is associated with the aging process and may be related to cognitive aging. Previous studies have shown conflicting results whether LTL is affected in patients with Alzheimer's disease (AD). In this pilot study, we investigated LTL in a well-defined homogeneous mono-center population. Sixty consecutive patients admitted for cognitive impairment to a memory clinic were recruited. The participants included patients with AD or mild cognitive impairment (MCI) diagnosed with AD upon follow-up (n=32), patients with stable MCI (n=13), patients with other dementias diagnosed at primary evaluation or upon follow-up (n=15), and healthy controls (n=20). LTL was determined using a quantitative PCR assay. Patients with AD had similar LTL as healthy controls. Patients with stable MCI had reduced LTL both compared to AD patients (p=0.02) and controls (p=0.008). Subanalyses within the AD group showed that patients with MCI that later converted to AD had similar LTL as patients with clinical diagnosis of AD at primary evaluation and healthy controls whereas the LTL was longer compared to the stable MCI group (p=0.02). There were no correlations between LTL and the core AD biomarkers A beta(1-42), T-tau and P-tau. In conclusion, in this pilot study, patients with AD or MCI that later converted to AD had similar LTL as healthy controls. Patients with stable MCI that did not progress to dementia had reduced LTL compared to controls, which might suggest a more marked biological aging as a cause of the cognitive symptoms in this group. (C) 2011 Elsevier Inc. All rights reserved.

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