Cerebrovascular pathology in Down syndrome and Alzheimer disease
Acta neuropathologica communications, ISSN: 2051-5960, Vol: 5, Issue: 1, Page: 93-null
2017
- 65Citations
- 153Usage
- 100Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations65
- Citation Indexes65
- 65
- CrossRef63
- Usage153
- Downloads131
- Abstract Views22
- Captures100
- Readers100
- 100
- Mentions1
- News Mentions1
- News1
Most Recent News
Cerebrovascular pathology in Down syndrome and Alzheimer disease.
Acta Neuropathol Commun. 2017 Dec 1;5(1):93. Authors: Head E, Phelan MJ, Doran E, Kim RC, Poon WW, Schmitt FA, Lott IT PubMed: 29195510 Submit Comment
Article Description
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with age. Typically, by age 40 years, most people with DS have sufficient neuropathology for an AD diagnosis. Interestingly, atherosclerosis and hypertension are atypical in DS with age, suggesting the lack of these vascular risk factors may be associated with reduced cerebrovascular pathology. However, because the extra copy of APP leads to increased beta-amyloid peptide (Aβ) accumulation in DS, we hypothesized that there would be more extensive and widespread cerebral amyloid angiopathy (CAA) with age in DS relative to sporadic AD. To test this hypothesis CAA, atherosclerosis and arteriolosclerosis were used as measures of cerebrovascular pathology and compared in post mortem tissue from individuals with DS (n = 32), sporadic AD (n = 80) and controls (n = 37). CAA was observed with significantly higher frequencies in brains of individuals with DS compared to sporadic AD and controls. Atherosclerosis and arteriolosclerosis were rare in the cases with DS. CAA in DS may be a target for future interventional clinical trials.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85048775082&origin=inward; http://dx.doi.org/10.1186/s40478-017-0499-4; http://www.ncbi.nlm.nih.gov/pubmed/29195510; https://actaneurocomms.biomedcentral.com/articles/10.1186/s40478-017-0499-4; https://uknowledge.uky.edu/sbcoa_facpub/81; https://uknowledge.uky.edu/cgi/viewcontent.cgi?article=1080&context=sbcoa_facpub; https://dx.doi.org/10.1186/s40478-017-0499-4
Springer Science and Business Media LLC
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