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. Author manuscript; available in PMC: 2016 Nov 1.
Published in final edited form as: J Neuropathol Exp Neurol. 2015 Nov;74(11):1086–1092. doi: 10.1097/NEN.0000000000000254

Table 1.

Frequency of Clinical and Demographic Characteristics

Characteristic Non-progressor
(n = 141)
Progressors
(n = 173)
Number of visits made
 2 37 (26%) 18 (10%)
 3 24 (17%) 29 (17%)
 4 28 (20%) 34 (19%)
 5 19 (14%) 43 (25%)
 6 17 (12%) 28 (16%)
 7 13 (9%) 15 (9%)
 8 3 (2%) 5 (3%)
 9 0 (0%) 1 (1%)
Age at first UDS visit
 <60 0 (0%) 3 (2%)
 60–69 4 (3%) 4 (2%)
 70–79 25 (18%) 11 (6%)
 80–89 61 (43%) 60 (35%)
 90–94 35 (25%) 44 (25%)
 95+ 16 (11%) 51 (30%)
Educationa
 No college 32 (23%) 39 (23%)
 1 – 4 years of college 66 (47%) 83 (49%)
 At least some graduate school 43 (30%) 48 (28%)
Raceb
 White 136 (97%) 166 (97%)
 Black 2 (1%) 3 (2%)
 Multiracial 3 (2%) 2 (1%)
Sex
 Female 88 (62%) 108 (62%)
 Male 53 (38%) 65 (38%)
APOE ε4c
 Non-carrier 107 (82%) 112 (70%)
 Heterozygous 22 (17%) 46 (29%)
 Homozygous 1 (1%) 1 (1%)
a

3 progressors were missing data on education

b

2 progressors were missing data on race; defined using NACC derived variable “naccnihr”

c

11 non-progressors and 14 progressors were missing data on APOE ε4 allele frequency

NACC, National Alzheimer’s Coordinating Center; UDS, Uniform Data Set.