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. 2020 Dec 29;6(1):e12116. doi: 10.1002/trc2.12116

TABLE 2.

Demographics, mean performance, and survey results of “scorable” participants

Age Sex Education Test preference (%)
Participant source n (years) (%women) (years) MoCA SATURN %Report SATURN “Easy to Use” MoCA No Pref. SATURN
Study partner 37 65.5 ± 9.2 59 16.3 ± 2.5 27.0 ± 1.8 27.1 ± 2.6 97 8 30 62
Dementia clinic 24 71.5 ± 10.3 46 15.5 ± 3.0 19.1 ± 6.1 17.5 ± 6.4 63 42 38 21
 Not Demented a 4 74.3 ± 6.1 50 15.8 ± 1.6 24.8 ± 3.8 24.3 ± 4.1 75 25 75 0
 Alzheimer's b 13 68.5 ± 11.3 46 16.4 ± 2.6 18.5 ± 5.6 16.4 ± 6.0 54 54 31 15
Other Dementia c 7 75.6 ± 9.2 29 13.7 ± 3.8 16.9 ± 6.6 15.7 ± 6.2 71 29 29 43
Other Clinic 14 65.9 ± 7.6 36 15.5 ± 3.6 24.8 ± 3.3 23.6 ± 3.6 79 21 29 50
 Multiple Sclerosis 2 62.5 ± 7.8 100 15.0 ± 1.4 28.0 ± 1.4 26.5 ± 2.1 100 50 50
 Essential Tremor 1 66 100 14 27 25 100 100
 Parkinson 11 66.5 ± 8.2 18 15.7 ± 4.0 24.0 ± 3.3 23.0 ± 3.7 73 18 36 45

Shaded rows break down patients from each clinic into more specific diagnoses. Other than group sizes (n), data are presented as percentages or as mean ± standard deviation. The MoCA and SATURN are scored out of 30 points.

a

Includes three patients with mild cognitive impairment, and a cognitively normal carrier of an apolipoprotein E (APOE) ε4 allele

b

The clinical diagnosis was Alzheimer's disease for all but one, for whom cerebrospinal fluid implicated Alzheimer's disease as the cause of corticobasal syndrome

c

Includes one case of Lewy body dementia, three cases predominantly or exclusively caused by cerebrovascular disease, and another three of mixed or uncertain cause. To simplify presentation, this row includes a patient with known dementia who was seen in general neurology clinic for peripheral neuropathy on the day of testing (and therefore not assigned CDR scores).