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. 2015 Nov 30;50(1):271–282. doi: 10.3233/JAD-150563

Table 1.

Baseline demographics and other clinical characteristics by latent class (mean ± SD unless otherwise specified)

Class 1 n = 162 Class 2 n = 211 Class 3 n = 819 Total n = 1,192 p-value*
Age (years) 74.7 ± 8.31 74.4 ± 7.28 72.9 ± 7.16 73.4 ± 7.38 0.0021
Female (%) 59.3% 62.1% 54.8% 56.7% 0.1287
Race (% Caucasian) 97.5% 96.2% 92.3% 93.7% 0.0612
Education (years) 15.7 ± 2.92 15.8 ± 2.92 16.1 ± 2.75 16.0 ± 2.81 0.0968
EVIQ 114.3 ± 8.83 113.7 ± 9.62 117.8 ± 8.24 116.6 ± 8.75 <0.0001
Amyloid Positive† 92.0% 84.4% 48.2% 60.6% <0.0001
APOE ɛ4 carrier 69.1% 64.0% 38.3% 47.1% <0.0001
Diagnosis (%): <0.0001 (By column)
  HC (n) 0 2 323 325
   % of Column 0.0% 0.9% 39.4% 27.3%
   % of Row 0.0% 0.6% 99.4% 100%
  EMCI (n) 5 29 245 279
   % of Column 3.1% 13.7% 29.9% 23.4%
   % of Row 1.8% 10.4% 87.8% 100%
  LMCI (n) 29 105 238 372
   % of Column 17.9% 49.8% 29.1% 31.2%
   % of Row 7.8% 28.2% 64.0% 100%
  AD (n) 128 75 13 216
   % of Column 79.0% 35.5% 1.6% 18.1%
    % of Row 59.3% 34.7% 6.0% 100%
Medical History
 Alcohol Abuse 8.0% 3.3% 3.9% 4.4% 0.0474
 Smoking 40.1% 37.4% 38.7% 38.7% 0.8699
 Cardiovascular disease 71% 64% 67.9% 67.6% 0.3433
 Endocrine disease 42.6% 42.7% 40.2% 40.9% 0.7261
ADAS-Cog13 29.8 ± 9.55 23.5 ± 7.39 12.5 ± 6.10 16.8 ± 9.54 <0.0001
FAQ 16.1 ± 6.15 6.5 ± 4.41 1.2 ± 2.26 4.1 ± 6.21 <0.0001
Animal Category Fluency 12.0 ± 4.95 15.0 ± 5.10 19.0 ± 5.33 17.4 ± 5.85 <0.0001
CDR-SB 4.9 ± 2.08 2.6 ± 1.25 0.8 ± 0.85 1.7 ± 1.86 <0.0001
Wechsler LM II 1.7 ± 2.32 3.3 ± 3.30 9.2 ± 4.65 7.1 ± 5.20 <0.0001
MMSE 23.5 ± 3.11 25.8 ± 2.44 28.3 ± 1.73 27.2 ± 2.74 <0.0001
MoCA 17.3 ± 4.73 20.3 ± 3.32 24.5 ± 2.89 23.1 ± 4.08 <0.0001
Trail Making Test Part A 68.7 ± 35.91 48.8 ± 26.62 36.7 ± 14.40 43.1 ± 23.70 <0.0001
Trail Making Test Part B 200.8 ± 84.99 160.7 ± 80.08 96.3 ± 52.76 120.9 ± 74.00 <0.0001
NPI-Q 4.4 ± 4.62 2.9 ± 3.50 1.2 ± 1.99 2.0 ± 3.07 <0.0001
GDS Short Form 1.8 ± 1.76 1.7 ± 1.40 1.4 ± 1.47 1.5 ± 1.51 0.0007

Data are presented as mean ± SD unless indicated otherwise. APOE, apolipoprotein E; AD, Alzheimer’s disease; ADAS-Cog13, Alzheimer’s Disease Assessment Scale-Cognitive Subscale, 13-item version; CDR-SB, Clinical Dementia Rating Sum of Boxes; EMCI, early mild cognitive impairment; EVIQ, Estimated Verbal Intelligence Quotient; FAQ, Functional Activities Questionnaire; GDS, Geriatric Depression Scale; HC, healthy controls; LM, Logical Memory; LMCI, late mild cognitive impairment; MMSE, Mini-Mental State Examination; MoCA, Montreal Cognitive Assessment; NPI-Q, Neuropsychiatric Inventory-Questionnaire.  *p-values were from likelihood ratio test in multinomial logit model for categorical measures and from analysis of variance corrected for uncertainty for continuous variables. Uncertainty in latent class assignment is taken into consideration, using a three-step manual calculation as in Asparouhov & Muthén [15].  †31 cases had discrepant amyloid test results (20 out of 31 discrepant cases were CSF positive but FBP-PET negative).