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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: Dement Geriatr Cogn Disord. 2014 Nov 8;39(0):92–104. doi: 10.1159/000366411

Table 2.

Findings of ischemic, hemorrhagic and vascular pathology, according to the groups at the clinical enrollment

Control (n=14) CVD risk (n=17)
DAT (n=26) p value*
SHEP (n=11) CS (n=6)
Vascular pathology
    Large artery cerebralinfarcts 1 (7.14%) 3 (17.65%) 1 (9.09%) 2 (33.33%) 2 (7.69%) 0.5 44
    Cortical microinfarcts 5 (35.71%) 5 (29.41%) 2 (18.18%) 3 (50.00%) 5 (19.23%) 0.550
    Lacunes 5 (35.71%) 6 (35.29%) 3 (27.27%) 3 (50.00%) 8 (30.77%) 0.933
    Cerebral hemorrhages 1 (7.14%) 2 (11.76%) 1 (9.09%) 1 (16.67%) 5 (19.23%) 0.627
    Subcortical arteriosclerotic leukoencephalopathy 0 (0.00%) 1 (5.88%) 0 (0.00%) 1 (16.67%) 1 (3.85%) 0.675
    Atherosclerosis (of the circle of Willis) 14 (100.00%) 16 (94.12%) 10 (90.91%) 6 (100.00%) 22 (84.62%) 0.307
    Arteriosclerosis 14 (100.00%) 17 (100.00%) 11 (100.00%) 6 (100.00%) 25 (96.15%) 0.551
    Cerebral amyloid angiopathy 11 (78.57%) 9 (52.94%) 7 (63.64%) 2 (33.33%) 22 (84.62%) 0.071
AD pathology 6 (42.867%) 3 (17.65%) 2 (18.18%) 1 (16.67%) 21 (80.77%)

Values are presented as number (percentage).

*

Comparisons among the groups on clinical enrollment by using the Fisher's exact test.

Age upon clinical evaluation and the duration to death were adjusted for the analyses.

CVD, cerebrovascular disease; SHEP, Systolic Hypertension in the Elderly Program; CS, Carotid stenosis; DAT, dementia of the Alzheimer type; AD, Alzheimer's disease.