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. 2024 Aug 19;10(3):e004395. doi: 10.1136/rmdopen-2024-004395

Table 1. Demographics of the incident Southeast Norway SLE cohort during 2000–2017 for cases with confirmed SLE diagnosis by chart review.

TotalN=737 FemaleN=619 MaleN=118
Adult onset, n (%) 701 (95.1) 590 (95.3) 111 (94.1)
Juvenile onset, n (%) 36 (4.9) 29 (4.7) 7 (5.9)
Mean age at diagnosis, years (SD) 39.5 (16.5) 38.1 (15.7) 46.7 (18.7)
Mean follow-up time from time of diagnosis to study end in 2017, years (SD) 7.9 (5.2) 7.8 (5.1) 8.5 (5.2)
Median time from first SLE symptom to diagnosis*, years (IQR) 1.0 (0–4) 1.0 (0–4) 1.0 (0–3.3)
Mean time from first SLE symptom to diagnosis*, years (SD) 3.5 (5.5) 3.6 (5.6) 2.9 (4.7)
European descent, n (%) 609 (82.6) 503 (81.3) 106 (89.8)
Asian descent, n (%) 97 (13.2) 87 (14.1) 10 (8.5)
African descent, n (%) 21 (2.8) 19 (3.1) 2 (1.7)
Other descent, n (%) 10 (1.4) 10 (1.6) 0 (0.0)
Number of cases fulfilling the 1997 ACR criteria at diagnosis, n (%) 574 (77.9) 492 (79.5) 82 (69.5)
Number of cases fulfilling the 2019 EULAR/ACR criteria at diagnosis, n (%) 677 (91.9) 574 (92.7) 103 (87.3)
Deceased by end of 2017, n (%) 57 (7.7) 36 (5.8) 21 (17.7)

1997 ACR criteria, 1997 ACR classification criteria for SLE; 2019 EULAR/ACR criteria, 2019 EULAR/ACR classification criteria for SLE.

*

Missing information for 42 of 737 cases.

#, missing information for 42 of 737 cases2019criteria, the 2019 European Alliance of Associations for Rheumatology/American College of Rheumatology classification criteria for Systemic Lupus Erythematous; 1997criteria, the 1997 American College of Rheumatology classification criteria for Systemic Lupus Erythematous; EULAR/ACR, European Alliance of Associations for Rheumatology/American College of Rheumatology; N, number of cases of the incident SLE population; SD, standard deviation; SLE, systemic lupus erythematosus