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. 2022 Sep 8;12(9):e058810. doi: 10.1136/bmjopen-2021-058810

Table 1.

Selection of demographic, social and clinical characteristics of patients included in the NorCog cohort at baseline

Patients included in NorCog during 2009–2021 Missing data total cohort, n (%)
Total cohort NCI/SCI MCI Dementia Other diagnoses
n (%) 18 120 (100) 2258 (12.5) 6307 (34.8) 8368 (46.2) 1187 (6.6)
Age (years), mean (SD) 73.7 (9.9) 67.3 (11.7) 73.1 (9.7) 76.3 (8.2) 70.5 (10.9) 0
Sex (female), n (%) 9443 (52.1) 1167 (51.7) 3097 (49.1) 4599 (55.0) 580 (48.9) 0
Education (years), mean (SD) 11.3 (3.8) 12.5 (3.9) 11.5 (3.8) 10.8 (3.6) 11.3 (3.9) 1521 (8.4)
Married/cohabiting, n (%) 10 709 (61.6) 1402 (65.0) 3800 (62.7) 4812 (59.9) 695 (61.2) 729 (4.0)
Living alone, n (%) 6589 (36.4) 737 (32.6) 2284 (36.2) 3135 (37.5) 433 (36.5) 687 (3.8)
Public care, n (%) 5639 (32.1) 388 (18.1) 1626 (26.6) 3260 (40.0) 356 (31.6) 597 (3.3)
MMSE score, mean (SD) 23.6 (4.6) 27.1 (3.3) 25.2 (3.4) 21.0 (4.4) 26.2 (3.8) 478 (2.6)
Information from informant obtained, n (%) 17 234 (95.1) 1983 (87.8) 5907 (93.7) 8275 (98.9) 1069 (90.1)

Numbers of patients with missing data are shown in the far right column.

MCI, mild cognitive impairment; MMSE, Mini-Mental State Examination; NCI, no cognitive impairment; NorCog, Norwegian Registry of Persons Assessed for Cognitive Symptoms; SCI, subjective cognitive impairment.