4.5 Article

Plasma β amyloid and the risk of Alzheimer's disease in Down syndrome

Journal

NEUROBIOLOGY OF AGING
Volume 33, Issue 9, Pages 1988-1994

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2011.08.007

Keywords

Down syndrome; Amyloid precursor protein; Abeta; Alzheimer's disease

Funding

  1. Netherlands Organization for Scientific Research (NWO)
  2. Internationale Stichting Alzheimer Onderzoek (ISAO)
  3. Hersenstichting Nederland (HSN)
  4. Centre for Medical Systems Biology (CMSB)
  5. Het Jan Jongmanfonds

Ask authors/readers for more resources

Extracellular deposition of amyloid beta peptide (A beta) has been implicated as a critical step in the pathogenesis of Alzheimer's disease (AD). In Down syndrome (DS), Alzheimer's disease is assumed to be caused by the triplication and overexpression of the gene for amyloid precursor protein (APP), located on chromosome 21. Plasma concentrations of A beta 1-40 and A beta 1-42 were determined in a population based study of 506 persons with DS, who were screened annually for dementia. We used Cox proportional hazards models to determine the risk of dementia. Demented persons with DS have a significantly higher plasma A beta 1-40 concentration than the nondemented (p = 0.05). Those with the highest concentrations of A beta 1-40 and A beta 1-42 have a higher risk to develop dementia. The risk to develop dementia during follow-up (mean 4.7 years) increased to 2.56 (95% confidence interval, 1.39-4.71) for A beta 1-42 and 2.16 (95% confidence interval, 1.14-4.10) for A beta 1-40. High plasma concentration of plasma A beta 1-40 and A beta 1-42 are determinants of the risk of dementia in persons with DS. (C) 2012 Elsevier Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available