Table 1

Phenotype at initiation

All patients (n=93)
Male sex51 (55%)
Age, years, median (IQR)36 (26–49)
Disease duration, years, median (IQR)12 (6–16)
Smoking status
 Never72 (77%)
 Current10 (11%)
Previous IBD-related luminal surgery29 (31%)
Age at diagnosis
 ≤16 years (A1)23 (25%)
 17–40 years (A2)57 (61%)
 >40 years (A3)13 (13%)
Disease location
 Ileal (L1)15 (16%)
 Colon (L2)35 (38%)
 Ileocolonic (L3)43 (46%)
 Upper gastrointestinal involvement (L4)24 (26%)
Disease behaviour
 Non-stricturing, non-penetrating (B1)54 (58%)
 Stricturing (B2)26 (28%)
 Penetrating (B3)13 (14%)
Perianal disease (p)24 (26%)
Extraintestinal manifestations (EIM)
Total number of patients with EIMs50 (54%)
 Enteropathic arthritis24 (26%)
 Dermatological11 (12%)
 Oral8 (9%)
 Primary sclerosing cholangitis4 (7%)
 Ocular3 (3%)
Comorbidities
Total number of patients with comorbidities37 (40%)
 Immune-mediated inflammatory diseases13 (14%)
 Metabolic syndrome/obesity/dyslipidaemia11 (12%)
 Respiratory10 (11%)
 Cardiac/vascular6 (6%)
 Renal4 (4%)
 Venous thromboembolism3 (4%)
 Other14 (15%)
Prior advanced therapy class exposure*
 Anti-TNF91 (98%)
 IL-12/23 and IL-23 inhibitors71 (76%)
 Anti-integrin49 (53%)
 JAK inhibitor11 (12%)
 Calcineurin inhibitor2 (2%)
Upadacitinib induction dose
 45 mg92 (99%)
 15 mg†1 (1%)
Corticosteroid use during induction32 (34%)
Baseline disease severity
 Median HBI (n=37)‡8 (5–11)
 Median CRP, mg/L (n=62)10 (3–30)
 Median albumin, g/L (n=62)35 (32–40)
 Median FCAL, µg/g (n=50)615 (211–1229)
  • *Prior drug exposure listed in online supplemental table 4.

  • †13 patients had a stoma, therefore, HBI could not be calculated.

  • ‡Induction dose of 15 mg due to stage 4 chronic kidney disease.

  • Anti-TNF, anti-tumour necrosis factor; CD, Crohn’s disease; CRP, C-reactive protein; EIM, extraintestinal manifestations; FCAL, faecal calprotectin; HBI, Harvey-Bradshaw Index; IL, interleukin; JAK, Janus kinase.