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. 2021 Mar 22;3(2):fcab045. doi: 10.1093/braincomms/fcab045

Table 1.

Demographic data of patients with DLB or AD/DLB and non-DLB following the disclosure of clinical data

Final clinical diagnosis
Probable DLB (n = 32) Prodromal DLB (n = 5) DLB/AD (n = 6) AD (n = 10) Probable CJD a (n = 10) PSP (n = 8) CBS (n = 1) FTD (n = 3) Others b (n = 6)
Gender M/F 23/9 3/2 3/3 7/3 5/5 4/4 0/1 3/0 2/4
Age (years) 73.9 ± 6.0 75.4 ± 4.0 66.3 ± 9.6 69.3 ± 9.6 66 ± 16 73.5 ± 5.0 70 72.0 ± 1.6 53 ± 24.4
MMSE score at diagnosis 23.2 ± 4.5 28.0 ± 1.6 18.3 ± 7.4 23.9 ± 1.4 N.E. 27.6 ± 2.9 28 23.3 ± 1.0 27.2 ± 4.2
Interval between clinical onset and OM swabbing (mo) 39.0 ± 27.2 26.2 ± 14.9 31.8 ± 31.0 26.0 ± 15.0 3.3 ± 1.8 20.7 ± 14.9 36 37.3 ± 9.6 33.6 ± 43
MMSE score at OM brushing 19.7 ± 5.6 27.8 ± 1.5 16.2 ± 8.0 22.7 ± 3.0 N.E. 25.6 ± 4.6 30 16.7 ± 5.0 26.5 ± 3.7
Interval between clinical onset and lumbar puncture (mo) 25.6 ± 27.4 (n = 10) 24 (n = 1) 17.7 ± 12.6 (n = 6) 23.8 ± 14.2 (n = 10) 3.3 ± 1.8 (n = 10) 22.4 ± 17.1 (n = 5) 30 31.3 ± 12.7 (n = 3) 18.7 ± 6.2 (n = 4)
Alzheimer’s disease CSF profile § 0/10 0/1 5/5 9/10 0/10 0/4 0 0/3 0/4
a

All CJD patients received a definite diagnosis.

b

Clinical diagnoses included: Psychosis (n = 2), Down syndrome (n = 1), vascular dementia (n = 1); mild cognitive impairment (n = 1) and Arnold-Chiari malformation type 1 (n = 1);

§

CSF biomarkers were considered positive for AD. pathology when the ratio of Aβ42 and p-tau was lower than 6.5 (see Ref.28) or when the ratio T-tau/Aβ42 was lower than 0.52 (see Ref.29); N.E. denotes not evaluated; mo denotes month.