Abstract
The low-density lipoprotein receptor-related protein (LRP), which interacts with the Alzheimer disease (AD) β-amyloid precursor protein (APP), represents an important pathway in AD pathology. LRP-mediated receptor pathways appear to regulate both the production and the clearance of amyloid β-protein (Aβ), a principal neuropathological product in AD. Several conflicting studies have examined levels of LRP in AD brains, as well as the relationship between the LRP exon 3 (C766T) polymorphism and LRP levels and/or disease susceptibility. In order to further investigate the role of LRP in AD, we examined well-characterized brain samples collected from subjects with varying degrees of cognitive impairment for LRP protein expression levels as well as for the presence of the LRP exon 3 polymorphism. We found no correlation between LRP levels and either presence of the disease or cognitive decline. In addition, we found no correlation between the LRP exon 3 polymorphism and either AD or LRP levels.
Original language | English |
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Pages (from-to) | 999-1005 |
Number of pages | 7 |
Journal | Journal of Neuropathology and Experimental Neurology |
Volume | 62 |
Issue number | 10 |
DOIs | |
State | Published - 1 Oct 2003 |
Keywords
- Alzheimer disease
- Dementia
- LRP polymorphism
- Lipoprotein receptor-related protein (LRP)