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. Author manuscript; available in PMC: 2018 May 1.
Published in final edited form as: Neurobiol Aging. 2017 Jan 30;53:83–92. doi: 10.1016/j.neurobiolaging.2017.01.017

Table 5.

Demographic and clinical characteristics of ACT participants with Alzheimer’s disease neuropathologic change (ADNC) with and without co-occurring Lewy body disease (LBD) or vascular brain injury (VBI)*

Characteristics ADNC only ADNC+LBD ADNC+VBI
ADNC+LBD
+VBI
Total autopsies, N 68 18 103 25
Age at death, mean (SD) 89.1 (6.7) 88.9 (5.8) 90.6 (5.9) 87.8 (6.3)
Female 43 (63.2) 7 (38.9) 60 (58.3) 13 (52.0)
Non-white 5 (7.4) 1 (5.6) 7 (6.8) 1 (4.0)
College graduate 26 (38.2) 9 (50.0) 31 (30.1) 11 (44.0)
History of stroke 2 (3.4) 1 (6.7) 25 (26.9) 1 (4.5)
APOE ε4 allele 20 (33.3) 6 (37.5) 33 (34.4) 12 (60.0)
Demented 35 (51.5) 14 (77.8) 76 (73.8) 17 (68.0)
  Clinical AD dementia 33 (94.3) 10 (71.4) 61 (80.2) 14 (82.3)

ACT, Adult Changes in Thought study

*

ADNC = moderate/frequent neuritic plaques & Braak stage III-VI; LBD = Lewy bodies in any brain region examined; VBI = gross infarcts and cortical microinfarcts.

N,% unless otherwise specified. Relative frequencies presented for complete data. Number of participants missing data: stroke=25 (11.7%), and APOE genotype=22 (10.3%).