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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: Neurobiol Aging. 2020 Sep 3;96:109–116. doi: 10.1016/j.neurobiolaging.2020.08.021

Table 1:

Demographics and Clinical Characteristics

HC (n=10) MCI (n=17) 2-tailed p-value
Age (mean ± SD) b 66.7 ± 7.3 69.6 ± 9.1 0.327
Female (%) c 60.0 % 47.1 % 0.695
Right Handedness (%) c 90% 88.2% 1.000
Years of Education (mean ± SD) a 16.2 ± 2.5 16.9± 2.2 0.447
IQ (mean ± SD)b 117.1 ± 12.4 118.6 ± 6.3 0.578
ADAS-Cog Total (mean ± SD) b 3.3 ± 1.8 11.9 ± 3.4 <0.001
GDS (mean ± SD) b 1.3 ± 2.9 2.3 ± 2.1 0.024
Diabetes (%) c 0% 11.8% 0.516
Hypertension (%) c 20.0% 35.3% 0.666
Hyperlipidemia (%) c 40.0% 76.5% 0.101
Amyloid z-score (mean ± SD) n/a 8.1 ± 3.2 n/a
APOE4 allele ≥ 1 (%) c 62.5% 81.2% 0.362
BDNF-Met allele ≥ 1 (%) c 25% 25% 1.000
Monophasic RMT (mean ± SD) a 57.2 ± 10.2 55.2 ± 9.2 0.623
Biphasic AMT (mean ± SD) a 40.5 ± 7.7 38.5 ± 6.5 0.493
Pre-iTBS MEP (μV) (mean ± SD) b 899.4 ± 676.6 1426.3 ± 1007.2 0.152

Demographic characteristics of HC and MCI participants are shown. MCI participants had impaired global cognition (ADAS-Cog) compared with controls.

Based on age-adjusted WTAR

a

t-test

b

Mann-Whitney U test

c

Fisher’s exact test