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. 2022 Feb 8;7(1):e00004-22. doi: 10.1128/msystems.00004-22

TABLE 1.

Demographic and clinical characteristics of the cohort participantsa

Parameter Result for group (n = 125)
Control (n = 51) MCI (n = 27) AD (n = 47)
Sex, % (no. female/total) 45 (23/51) 41 (11/27) 49 (23/47)
Age, mean ± SD yr 67 ± 5.3 69.2 ± 6.4 71.4 ± 5.1
Education, mean ± SD yr 7.2 ± 4.1 10.4 ± 5.2 4.4 ± 4.1
MMSE, mean ± SD 27.1 ± 1.7 25.4 ± 2.7 16.9 ± 5.7
CDR, % (no./total)
 0 100 0 0
 0.5 0 100 (27/27) 29.8 (14/47)
 1 0 0 31.9 (15/47)
 2 0 0 29.8 (14/47)
 3 0 0 8.5 (4/47)
Aβ1–42/p-tau (pg/mL) NA NA 5.97 ± 3.7 (n = 14)
Aβ1–42/t-tau (pg/mL) NA NA 0.91 ± 0.6 (n = 14)
Medication, % (no./total)
 AA NA 37 (10/27) 27.6 (13/47)
 Add NA 81 (22/27) 87 (41/47)
 Adep NA 66.7 (18/27) 27.6 (13/47)
 AE NA 18.5 (5/27) 8.5 (4/47)
 Aht NA 48 (13/27) 29.8 (14/47)
 Apsik NA 11.1 (3/27) 21.2 (10/47)
 Adiab NA 29.6 (8/27) 19.1 (9/47)
 PP NA 7.4 (2/27) 6.3 (3/47)
a

Shown are the demographic characteristics, cognitive performance, concentrations of cerebrospinal fluid biomarkers (Aβ1–42, t-tau, and p-tau), and groups of medicine used by the participants. MCI, mild cognitive impairment group; AD, Alzheimer's disease group; MMSE, Mini-Mental State Exam (MMSE); CDR, Clinical Dementia Rating; AA, antiaggregant; Add, AD treatment; Adep, antidepressant; AE, antiepileptic; Aht, antihypertensive; Apsik, antipsychotic; Adiab, antidiabetic; PP, proton pump inhibitor; NA, not applicable; Aβ1–42, amyloid beta peptide; p-tau, Thr-phosphorylated tau; t-tau, total tau.