کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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331223 | 1433656 | 2007 | 6 صفحه PDF | دانلود رایگان |
Cerebral accumulation of β-amyloid peptide (Aβ) is a central event in the pathogenesis of Alzheimer's disease (AD). Several proteases were shown to hydrolyze Aβ in vitro or in cell-based assays, and are likely candidates for a role in Aβ clearance in brain. Previous reports suggest that matrix metalloproteinases (MMPs) could be involved in such a mechanism. A functional polymorphism at position −1171 (5A/6A) in MMP-3 was examined in two independent studies to investigate the impact of this polymorphism on the risk of developing dementia. We found that subjects APOE ɛ4 non-carriers and 6A/6A homozygous for the MMP-3 polymorphism were at increased risk of dementia. Our findings support the hypothesis that MMPs may influence the risk of dementia.
Journal: Neurobiology of Aging - Volume 28, Issue 8, August 2007, Pages 1215–1220