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. 2021 Jul 14;12:703481. doi: 10.3389/fpsyt.2021.703481

Table 3.

Proportions of RCD in AD patients at the follow-up.

With COVID-19 pandemic Control OR, 95%CI
Num. RCD proportion (n, %) Num. RCD proportion (n, %)
Overall 131 25 (19.1) 131 48 (36.6)* 0.408 (0.232–0.716)*
Initial CDR
1 49 9 (18.4) 47 19 (40.4)* 0.332 (0.131–0.839)*
2 43 12 (27.9) 47 16 (34.0) ns
3 39 4 (10.3) 37 13 (35.1)* 0.211 (0.061–0.726)*
ApoE genotypes
ApoE ε4 (+) 11 3 (27.3) 19 8 (42.1) ns
ApoE ε4 (–) 30 7 (23.3) 33 12 (36.4) ns
deposition
Positive 39 9 (23.1) 49 20 (40.8) ns
Negative 2 1 (50.0) 3 0 (0.0) ns
ApoE genotypes + Aβ deposition
ApoE ε4 (+), Aβ (+) 10 2 (20.0) 19 8 (42.1) ns
ApoE ε4 (+), Aβ (–) 1 1 (100.0) 0 0 (0.0) ns
ApoE ε4 (-), Aβ (+) 29 7 (24.1) 30 12 (40.0) ns
ApoE ε4 (-), Aβ (–) 1 1 (100.0) 3 0 (0.0) ns

In this study, only 55 patients, including 41 AD patients, in “during COVID-19 pandemic” group, and 52 patients with AD in control group had ApoE genotyping and Aβ deposition records. RCD, rapid cognitive decline; AD, Alzheimer's disease; Num., number of samples; OR, odds ratio; CI, confidence interval; CDR, Clinical Dementia Rate; ApoE, Apolipoprotein E; Aβ, Amyloid β.

*

p < 0.05.