Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 49 min ago
Peer-reviewedCC BY-NC 4.0Crohn's & Colitis 360

Comparative effectiveness of IL-12/23 and IL-23 inhibitors versus JAK inhibitors in patients with inflammatory bowel disease and hidradenitis suppurativa: a real-world propensity-matched analysis

Abstract

Background: Inflammatory bowel disease (IBD) and hidradenitis suppurativa (HS) frequently coexist and share overlapping immune pathways, yet comparative real-world outcomes between IL-12/23 or IL-23 inhibitors and Janus kinase (JAK) inhibitors in this population remain poorly defined.

Methods: We conducted a retrospective cohort study using a large, multicenter, real-world dataset. Adults (≥16 years) with IBD and HS who initiated an IL-12/23 or IL-23 inhibitor after anti-TNF therapy or a JAK inhibitor were included; patients with prior exposure to the opposing drug class were excluded. Propensity score matching (1:1) yielded 150 patients per cohort. Outcomes from 30-365 days included acute care utilization, corticosteroid use, IBD complications, and overall and hidradenitis-specific antibiotic use.

Results: After propensity score matching, 300 patients were included (150 per cohort; mean age 38 years; 75.3% female). Rates of emergency department visits or hospitalization were similar between groups (RR 1.20, 95% CI, 0.82-1.77). Corticosteroid use risk was numerically higher in the IL-12/23 or IL-23 cohort (RR 1.20, 95% CI, 0.98-1.46). IBD-related complications did not differ significantly (RR 1.06, 95% CI, 0.58-1.93). Overall antibiotic use was comparable, while hidradenitis-specific antibiotic use was higher in the IL-12/23 or IL-23 cohort (RR 1.47, 95% CI, 1.11-1.95).

Conclusions: In this real-world analysis, IL-12/23 or IL-23 inhibitor therapy was associated with higher hidradenitis-specific antibiotic use and numerically greater but statistically nonsignificant corticosteroid exposure, while hospitalization and IBD-related complications were comparable. These findings should be interpreted cautiously given the absence of validated disease-activity measures; prospective studies are needed to inform optimal therapeutic selection.

Related

  1. Efferocytosis-Related Transcriptional Dysregulation in Hidradenitis Suppurativa Lesional Macrophages: A Multi-Cohort Single-Cell and Bulk Transcriptomic Study
    BiomedicinesPeer-reviewedCC BYFull textGeneral medicineEurope PMC
  2. Male-predominant, perianal-prone hidradenitis suppurativa in China: A cohort study of 614 patients.
    Yanyu Du, Jingwen Zou, Renliang He +1
    JAAD internationalPeer-reviewedCC BYFull text1 citedGeneral medicineEurope PMC
  3. End-of-Dose Effect as a Guide for Biologic Optimization in Hidradenitis Suppurativa
    Albertine Lynch, Julie Archimbaud, Cécile Lesort +5
    JAMA DermatologyPeer-reviewedLicence not statedFull textGeneral medicinePMC
  4. Real-world patient journey and unmet needs of people with hidradenitis suppurativa: Social media research in China.
    John R Ingram, Wen-Yu Wu, Wenbo Bu +4
    JAAD internationalPeer-reviewedCC BYFull textGeneral medicineEurope PMC
  5. Geospatial Associations of Hidradenitis Suppurativa With Structurally Related Airborne Toxins
    Tara McCaffrey, Beita Badiei, Nina Rossa Haddad +8
    JAMA DermatologyPeer-reviewedLicence not statedFull textGeneral medicinePMC
BibTeX
@article{hafez2026comparative,
  title = {{Comparative effectiveness of IL-12/23 and IL-23 inhibitors versus JAK inhibitors in patients with inflammatory bowel disease and hidradenitis suppurativa: a real-world propensity-matched analysis}},
  author = {Youssef Hafez and Ali Osman and Wing-Kin Syn and Manar Shmais},
  journal = {Crohn's \& Colitis 360},
  year = {2026},
  month = oct,
  doi = {10.1093/crocol/otag086},
  url = {https://doi.org/10.1093/crocol/otag086},
  note = {CC BY-NC 4.0},
}
RIS
TY  - JOUR
TI  - Comparative effectiveness of IL-12/23 and IL-23 inhibitors versus JAK inhibitors in patients with inflammatory bowel disease and hidradenitis suppurativa: a real-world propensity-matched analysis
AU  - Youssef Hafez
AU  - Ali Osman
AU  - Wing-Kin Syn
AU  - Manar Shmais
PY  - 2026
DA  - 2026/10/30
JO  - Crohn's & Colitis 360
DO  - 10.1093/crocol/otag086
UR  - https://doi.org/10.1093/crocol/otag086
AB  - Background: Inflammatory bowel disease (IBD) and hidradenitis suppurativa (HS) frequently coexist and share overlapping immune pathways, yet comparative real-world outcomes between IL-12/23 or IL-23 inhibitors and Janus kinase (JAK) inhibitors in this population remain poorly defined.  Methods: We conducted a retrospective cohort study using a large, multicenter, real-world dataset. Adults (≥16 years) with IBD and HS who initiated an IL-12/23 or IL-23 inhibitor after anti-TNF therapy or a JAK inhibitor were included; patients with prior exposure to the opposing drug class were excluded. Propensity score matching (1:1) yielded 150 patients per cohort. Outcomes from 30-365 days included acute care utilization, corticosteroid use, IBD complications, and overall and hidradenitis-specific antibiotic use.  Results: After propensity score matching, 300 patients were included (150 per cohort; mean age 38 years; 75.3% female). Rates of emergency department visits or hospitalization were similar between groups (RR 1.20, 95% CI, 0.82-1.77). Corticosteroid use risk was numerically higher in the IL-12/23 or IL-23 cohort (RR 1.20, 95% CI, 0.98-1.46). IBD-related complications did not differ significantly (RR 1.06, 95% CI, 0.58-1.93). Overall antibiotic use was comparable, while hidradenitis-specific antibiotic use was higher in the IL-12/23 or IL-23 cohort (RR 1.47, 95% CI, 1.11-1.95).  Conclusions: In this real-world analysis, IL-12/23 or IL-23 inhibitor therapy was associated with higher hidradenitis-specific antibiotic use and numerically greater but statistically nonsignificant corticosteroid exposure, while hospitalization and IBD-related complications were comparable. These findings should be interpreted cautiously given the absence of validated disease-activity measures; prospective studies are needed to inform optimal therapeutic selection.
SN  - 2631-827X
ER  -