Table 1

Characteristics of TNFi-treated patients with psoriatic arthritis at start of follow-up, grouped by country

Sweden
2006–2019
Denmark
2006–2016
Finland
2006–2017
Norway
2006–2019
Iceland
2006–2017
All, n65052429474879334
Male, n (%)3158 (48.6)1098 (45.2)256 (54.0)425 (48.7)136 (40.7)
Age (years), mean (SD)49.4 (12.9)47.2 (12.3)48.3 (11.6)47.5 (12.2)48.4 (13.2)
BMI (kg/m2)N/A27.7 (24.2 to 30.9)27.8 (25.1 to 31.2)N/A29.6 (26.1 to 33.1)
BMI missing (n, %)6505 (100)2036 (83.8)86 (18.1)879 (100)206 (61.7)
Smoking status, n (%)
 Current295 (4.5)296 (12.2)12 (2.5)176 (20.0)33 (9.9)
 Previous833 (12.8)240 (9.9)N/A271 (30.8)59 (17.7)
 Never915 (14.1)487 (20.0)88 (18.6)299 (34.0)98 (29.3)
 Missing4462 (68.6)1406 (57.9)374 (78.9)133 (15.1)144 (43.1)
Disease-related characteristics at start of first TNFi
 DAS28-CRP (0–10)4.1 (3.3–4.8)4.0 (3.0–5.0)3.7 (2.5–4.7)3.5 (2.7–4.3)4.4 (3.9–5)
 Missing n (%)2613 (40.2)745 (30.7)128 (27.0)110 (12.5)189 (56.6)
 CRP (mg/L)5 (2–13)6 (2–15)7 (3–15)5 (2–11)N/A
 Swollen joint count (0–28)2 (0–5)2 (0–4)1 (0–4)1 (0–3)4 (2–6)
 Tender joint count (0–28)4 (2–8)5 (2–11)1 (0–4)2 (1–6)5 (2–8)
 HAQ Score (0–3)0.9 (0.5–1.3)1 (0.6–1.5)0.8 (0.4–1.2)0.6 (0.3–0.9)1.2 (0.6–1.6)
 Missing n (%)2415 (37.1)1174 (48.3)100 (21.1)51 (5.8)192 (57.5)
First TNFi, n (%)
 Adalimumab1996 (30.7)939 (38.7)188 (39.7)147 (16.7)25 (7.5)
 Certolizumab pegol248 (3.8)215 (8.9)15 (3.2)184 (20.9)1 (0.3)
 Etanercept2697 (41.5)527 (21.7)148 (31.2)302 (34.4)65 (19.5)
 Golimumab450 (6.9)217 (8.9)38 (7.9)142 (16.2)42 (12.6)
 Infliximab1114 (17.1)531 (21.9)85 (17.9)104 (11.8)199 (59.6)
Other antirheumatic treatment, n (%) at start of first TNFi
 Methotrexate, n (%)2726 (41.9)1233 (50.8)269 (56.8)520 (59.2)147 (44)
 Oral steroid, n (%)909 (14.0)506 (20.8)128 (26.7)300 (34.1)12 (3.6)
Calendar year at start of first TNFi, n (%)
 2006–20101536 (23.6)1034 (42.6)165 (34.8)258 (29.4)73 (21.9)
 2011—end of follow-up4969 (76.4)1395 (57.4)309 (65.2)621 (70.6)261 (78.1)
Comorbidities and extra-articular manifestations, as registered in national patient registers up to 10 years prior to start of first TNFi, n (%)
 Cardiovascular disease360 (5.5)167 (6.9)33 (6.9)N/AN/A
 COPD97 (1.5)39 (1.6)2 (0.4)N/AN/A
 Diabetes mellitus430 (6.6)104 (4.3)36 (7.6)N/AN/A
 Hypertension964 (14.8)231 (9.5)73 (15.4)N/AN/A
 Inflammatory bowel disease120 (1.8)44 (1.8)14 (2.9)N/AN/A
 Uveitis170 (2.6)32 (1.3)14 (2.9)N/AN/A
 Urethritis38 (0.6)≤30 (0)N/AN/A
 Hospitalisations, n, mean (range)1 (0–2)4 (1–7)2 (1–4)N/AN/A
 Hip and/or knee replacement any time prior to start of first TNFi286 (4.4)72 (3.0)48 (10.1)N/AN/A
Mean time of follow-up in years (SD)5.7 (3.8)5.1 (2.9)6.1 (3.3)6.8 (3.5)4.9 (3.4)
Median time of follow-up in years (Q1–Q3)5.2 (2.3–8.7)5.1 (2.7–7.4)6.2 (3.2–9.0)6.6 (3.9–9.6)4.2 (1.9–7.2)
  • Values are median and IQR if not stated otherwise. Patients who shifted from biological disease-modifying anti-rheumatic drug (bDMARD)-naïve to TNFi-treated appear in both TNFi-treated and bDMARD-naïve groups because all switchers have two baseline records.

  • BMI, body mass index; COPD, chronic obstructive pulmonary disease; CRP, C reactive protein; DAS28, Disease Activity Score in 28 joints; HAQ, Health Assessment Questionnaire; N/A, not available; Q1, percentile 25; Q3, percentile 75; TNFi, tumour necrosis factor inhibitor; VAS, visual analogue scale.