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. Author manuscript; available in PMC: 2014 Aug 14.
Published in final edited form as: J Alzheimers Dis. 2014 Jan 1;42(1):275–289. doi: 10.3233/JAD-140276

Table 2.

Demographic, clinical, genetic, CSF biomarker, and neuropsychological characteristics of MCI subtypes resulting from cluster analyses of participants diagnosed via conventional ADNI MCI criteria (left) and actuarial neuropsychological criteria (right)

Conventional Petersen/Winblad ADNI MCI criteria
Actuarial Jak/Bondi neuropsychological MCI criteria
Amnestic (n = 477) Dysexec/ Mixed (n = 104) Cluster derived normal (n = 265) F Sig Amnestic (n = 236) Impaired language (n = 86) Dysexec/Mixed (n = 79) F Sig
Demographic Characteristics
Age 73.1 (7.2) 74.1 (7.9) 72.9 (8.3) 1.0 p = 0.36 72.6 (7.4) 75.9 (6.5) 74.5 (7.9) 6.9 p = 0.001
Education 16.0 (2.8) 14.8 (3.4) 16.5 (2.5) 14.5 p < 0.001 16.0 (2.8) 14.9 (3.0) 14.5 (3.5) 8.4 p < 0.001
Gender (F/M) 171/306 41/63 131/134 χ2 = 13.1 p = 0.001 86/150 40/46 30/49 χ2 = 2.7 p = 0.26
Cluster Analysis Measures
Language
Animal Fluency −0.6 (0.8) 1.3 (0.7) −0.1 (0.9) 90.79 p < 0.001 −0.7 (0.9) 1.2 (0.7) 1.4 (0.7) 33.88 p < 0.001
Boston Naming Test −0.3 (1.1) 1.1 (1.5) 0.2 (0.7) 56.25 p < 0.001 −0.2 (0.8) 1.4 (1.5) 1.5 (1.6) 61.36 p < 0.001
Speed/Executive Function
Trail Making Test, Part A −0.2 (0.8) 2.7 (2.2) −0.1 (0.8) 246.78 p < 0.001 −0.3 (0.8) 1.0 (0.9) 3.0 (2.4) 130.76 p < 0.001
Trail Making Test, Part B −0.3 (0.8) 3.6 (1.1) 0.1 (0.7) 806.55 p < 0.001 −0.4 (0.9) 1.1 (1.1) 3.8 (0.9) 355.12 p < 0.001
Memory
AVLT Recall 1.4 (0.7) 1.3 (0.8) 0.4 (0.9) 449.43 p < 0.001 1.7 (0.6) −0.8 (1.0) 1.2 (0.8) 48.99 p < 0.001
AVLT Recognition 1.1 (0.8) 1.1 (1.1) 0.4 (0.6) 303.67 p < 0.001 1.7 (0.7) −0.1 (0.9) 1.4 (0.9) 118.69 p < 0.001
Genetic / CSF Biomarkers*
APOE (ε4/non-ε4) 261/210 60/43 100/162 χ2 = 23.0 p < 0.001 140/92 51/35 41/37 χ2 = 1.5 p = 0.48
1–42 (pg/ml) 177.4 (68.7) 164.9 (59.1) 230.9 (68.5) 33.3 p < 0.001 170.8 (68.0) 173.8 (71.2) 164.3 (62.3) 0.3 P = 0.75
Total tau (pg/ml) 99.4 (63.4) 104.4 (56.6) 77.6 (47.7) 7.8 p < 0.001 100.4 (68.1) 101.3 (58.7) 98.2 (53.6) 0.0 p = 0.96
p-tau (pg/ml) 31.9 (17.7) 36.8 (16.1) 22.9 (11.3) 21.4 p < 0.001 33.2 (19.1) 27.8 (15.0) 37.6 (15.5) 2.8 p = 0.06
p-tau/Aβ1–42 0.22 (0.18) 0.25 (0.13) 0.12 (0.10) 24.7 p < 0.001 0.23 (0.18) 0.20 (0.15) 0.26 (0.13) 1.2 p = 0.30
Clinical Characteristics
GDS 1.4 (1.4) 1.5 (1.5) 1.8 (1.6) 5.3 p < 0.01 1.4 (1.5) 1.7 (1.5) 1.5 (1.6) 3.0 p = 0.05
NPI-Q 1.9 (2.6) 2.1 (2.9) 2.0 (3.1) 0.3 p = 0.77 2.0 (2.9) 2.5 (3.2) 2.2 (3.1) 0.6 p = 0.55
FAQ 3.6 (4.4) 4.7 (4.6) 1.7 (2.8) 25.5 p < 0.001 5.2 (5.1) 4.3 (5.1) 4.5 (4.5) 1.2 p = 0.31
6-month MMSE follow-up 26.8 (2.4) 25.0 (3.0) 28.5 (1.5) 83.1 p < 0.001 26.3 (2.2) 26.0 (2.8) 24.9 (3.2) 6.7 p = 0.001

1–42, amyloid-β protein; ADNI, Alzheimer’s Disease Neuroimaging Initiative; AVLT, Rey Auditory Verbal Learning Test; APOE, apolipoprotein E; CSF, cerebrospinal fluid; FAQ, Functional Activity Questionnaire; GDS, Geriatric Depression Scale; MCI, mild cognitive impairment; MMSE, Mini-Mental State Examination; NPI-Q, Neuropsychiatric Inventory; p-tau, hyperphosphorylated tau; pg/ml, picograms/milliliters.

*

Information regarding APOE genotype was not available for 10 participants classified as MCI by conventional ADNI criteria and 5 participants classified as MCI by actuarial neuropsychological criteria. For MCI participants classified using conventional ADNI criteria, CSF biomarker data were available for 244 participants in the Amnestic MCI subgroup (51.2%), 53 participants in the Dysexecutive/Mixed MCI subgroup (51.0%), and 146 participants in the Cluster-Derived Normal subgroup (55.1%). For MCI participants identified using the actuarial neuropsychological criteria, CSF biomarker data were available for 130 participants from the Amnestic subgroup (55.1%), 38 participants from the Impaired Language subgroup (44.2%), and 38 participants from the Dysexecutive/Mixed subgroup (48.1%).