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. Author manuscript; available in PMC: 2021 Oct 1.
Published in final edited form as: Neurobiol Aging. 2020 May 29;94:60–70. doi: 10.1016/j.neurobiolaging.2020.05.011

Table 1.

Participant demographics at baseline. Significant findings are baser on three-group ANOVAs or Chi-square tests of independence, with further two-groups post hoc comparisons for significant findings at an alpha level of p<0.05.

NC (n = 238) MCI (n = 185) AD dementia (n = 156) Between-group differences
 Age (SD) 72.38 (7.69) 74.99 (7.24) 76.74 (8.12) NC < MCI < AD
 Sex 62.6% Female 58.4% Female 44.2% Female (NC = MCI) > AD
 Race 89.5% White,
9.7% AA,
0.8% Asian
75.1% White,
23.8% AA,
1.1% Asian
91.0% White,
7.7% AA,
1.3% Asian
(NC = AD) > MCI*
 Education (SD) 16.56 (2.54) 15.51 (2.74) 14.95 (2.95) NC > (MCI = AD)
 MMSE (SD) 29.39 (0.91) 28.20 (1.67) 21.11 (6.17) NC > MCI > AD
 APOE ε4 carrier status 77/235 (32.8%) 59/181 (32.6%) 88/153 (57.5%) (NC = MCI) < AD
 NfL (pg/mL) 15.33 (10.47) 17.77 (10.25) 26.49 (17.30) NC < MCI < AD
 t-tau (pg/mL) 3.22 (2.73) 3.30 (2.39) 3.73 (3.01) not significant
 # with follow-up 206 (86.6%) 150 (81.1%) 120 (76.9%) NC > AD
 Years follow-up (SD) 5.62 (2.64) 5.10 (2.78) 3.20 (2.06) (NC = MCI) > AD

AA=African American.

*

Higher proportion of White participants in NC and AD groups compared to MCI.