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Table 4. Post-mortem neuropathological findings.

CAA = cerebral amyloid angiopathy, APOE = apolipoprotein E, NA = not available, ADNC = Alzheimer’s disease neuropathological change (NIA-AA [24]), PART = primary age-related tauopathy, PSP = progressive supranuclear palsy, CBD = corticobasal degeneration, Aβ = Amyloid-β deposition, ICH = Intracerebral hematoma, SAH = subarachnoidal hematoma, SDH = subdural hematoma.

Cognitive status at death n Sex Age at death ± (SD) Brain weight (g) CAA (n) APOE Neurodegenerative lesions Cerebrovascular pathology contributing to cognitive status Other cerebrovascular lesions
ADNC Non-ADNC
Normal or mild cognitive impairment (MCI) 11 M 3 F 8 73±9 1413±19 1/11 10/11 ε3/3 (8/10) ε4/3 (1/10) ε3/2 (1/10) 1 NA Low (3/11) Intermediate (1/11) High - PART 6/11 PSP 1/11 Cerebrovascular atherosclerosis 5/11 Infarct(s) 4/11 Postoperative ICH (2/11) SAH (1/11) Acute SDH (1/11)
Moderate dementia 9 M 5 F 4 73±7 1428±17 2/9 3/9 ε4/3 (2/3) ε3/3 (1/3) Low - Intermediate (3/9) High - PART 4/9 Cerebrovascular atherosclerosis (5/9) Infarct(s) (2/9) Acute SDH (4/9) SAH (1/9)
Severe dementia 9 M 4 F 5 76±5 1349±19 4/9 2/9 ε3/3 (1) ε4/4 (1) Low (4/9) Intermediate (1/9) High (1/9) PART 2/9 CBD 1/9 PSP 1/9 Aβ 1/9 Synucleinopathy 1/9 Infarct(s) 4/9 Cerebrovascular atherosclerosis (9/9)