TY - JOUR
T1 - Cerebrovascular pathology in Down syndrome and Alzheimer disease
AU - Head, Elizabeth
AU - Phelan, Michael J.
AU - Doran, Eric
AU - Kim, Ronald C.
AU - Poon, Wayne W.
AU - Schmitt, Frederick A.
AU - Lott, Ira T.
PY - 2017/12/1
Y1 - 2017/12/1
N2 - 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.
AB - 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.
KW - Arteriolosclerosis
KW - Atherosclerosis
KW - Cerebral amyloid angiopathy
KW - Trisomy 21
KW - Vascular risk factors
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U2 - 10.1186/s40478-017-0499-4
DO - 10.1186/s40478-017-0499-4
M3 - Article
C2 - 29195510
AN - SCOPUS:85048775082
VL - 5
SP - 93
JO - Acta neuropathologica communications
JF - Acta neuropathologica communications
IS - 1
ER -