APOE-ε2 and APOE-ε4 correlate with increased amyloid accumulation in cerebral vasculature

• Published in: Journal of neuropathology and experimental neurology 2013-07, Vol.72 (7), p.708-715
• Main Authors: Nelson, Peter T, Pious, Nina M, Jicha, Gregory A, Wilcock, Donna M, Fardo, David W, Estus, Steven, Rebeck, G William
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - genetics; Alzheimer Disease - pathology; Amyloid beta-Peptides - metabolism; Apolipoprotein E2 - genetics; Apolipoprotein E4 - genetics; Blood Vessels - metabolism; Cerebral Amyloid Angiopathy - genetics; Cerebral Amyloid Angiopathy - pathology; Cerebral Cortex - pathology; Female; Humans; Logistic Models; Male
• ISSN: 0022-3069; 1554-6578
• DOI: 10.1097/NEN.0b013e31829a25b9

The APOE-ε4 allele correlates with increased risk of Alzheimer disease (AD) and increased parenchymal amyloid plaques. We tested how the APOE genotype correlated with cerebral amyloid angiopathy (CAA) by analyzing 371 brains for parenchymal and meningeal CAA in 4 brain regions (frontal, parietal, temporal, and occipital neocortex). The overall severity of CAA was highest in the occipital lobe. APOE-ε4/4 brains (n = 22) had the highest levels of CAA across regions. In the occipital lobe, nearly all APOE-ε4/4 cases were scored with the highest level of CAA (meninges, 95% of cases; parenchyma, 81%). In this brain region as in others, APOE-ε3/4 brains (n = 115) showed consistently less CAA than APOE-ε4/4 brains (meninges, 43%; parenchyma, 43%). APOE-ε3/3 brains (n = 182) showed even less CAA (meninges, 19%; parenchyma, 19%). Interestingly, APOE-ε2/3 cases (n = 42) had more CAA than APOE-ε3/3 (meninges, 44%; parenchyma, 32%), despite a reduced risk for AD in the APOE-ε2/3 individuals. APOE-ε4/4 brains also had the fewest regions without CAA, whereas APOE-ε3/3 brains had the most. Ordinal regression analyses demonstrated significant impacts of APOE-ε2 and APOE-ε4 on CAA at least in some brain regions. These data demonstrate that APOE genotype correlations with Aβ deposition in CAA only incompletely correspond to other AD-linked brain pathologies.