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Genetic association of the low-density lipoprotein receptor-related protein gene (LRP), and apolipoprotein E receptor, with late-onset Alzheimer's disease
Abstract
The presence of the APOE epsilon 4 allele encoding apolipoprotein E4 (apoE4) is the major genetic risk factor for late-onset Alzheimer's disease (AD). However, the molecular and cellular mechanisms by which APOE epsilon 4 renders AD risk are unclear. In this report, we present genetic evidence that an apoE receptor, LRP, may be associated with the expression of late-onset AD. Using a biallelic genetic marker in exon 3 of LRP, late-onset AD cases markedly differed from the control subjects in the distribution of LRP genotypes, and this difference was highly accentuated among AD cases with positive family history of senile dementia. Furthermore, the numbers of neutritic plaques were significantly altered as a consequence of different LRP genotypes in postmortem AD cases. Taken together, our results implicate the pathophysiology of LRP in the expression of late-onset AD.
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Polymorphisms in LRP or α2-macroglobulin increase the risk of late onset familial AD.
“genetic evidence suggests that polymorphisms in either LRP or ␣ 2 -macroglobulin increase the risk of late onset familial AD (35,36).”
From Apolipoprotein E Receptors Mediate the Effects of β-Amyloid on Astrocyte Cultures (2000) · cites this paper as [35]
Levels of LRP decrease with age.
“Furthermore, levels of LRP decrease with age”
From Increased Extracellular Amyloid Deposition and Neurodegeneration in Human Amyloid Precursor Protein Transgenic Mice Deficient in Receptor-Associated Protein (2002) · cites this paper as Kang et al., 1997
A polymorphism in exon 3 of the LRP gene (C776T) has been associated with increased risk for late onset AD.
“and a polymorphism in exon 3 of the LRP gene (C776T) has been associated with increased risk for late onset AD (Kang et al., 1997(Kang et al., , 2000)).”
From Increased Extracellular Amyloid Deposition and Neurodegeneration in Human Amyloid Precursor Protein Transgenic Mice Deficient in Receptor-Associated Protein (2002) · cites this paper as Kang et al., 1997
Polymorphisms in the LRP and SorLA/LR11 genes have been associated with increased risk for Alzheimer's disease.
“Polymorphisms in the LRP and SorLA/LR11 genes have also been associated with increased risk for Alzheimer's disease [3], [4].”
From Receptor-Associated Protein (RAP) Plays a Central Role in Modulating Aβ Deposition in APP/PS1 Transgenic Mice (2008) · cites this paper as [3]
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Metadata
- Authors
- Kang, D. E., Saitoh, T., Chen, X., Xia, Y., Masliah, E., Hansen, L. A., Thomas, R. G., Thal, L. J., & Katzman, R.
- Venue
- Neurology
- Published
- 1997-07
- Volume
- 49
- Issue
- 1
- Pages
- 56-61
- ISSN
- 0028-3878
- 1526-632X
- Cited by
- 211
- References
- 3
- Language
- en
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