S1565 Glucagon-Like Peptide-1 Receptor Agonist Therapy Is Associated With Decreased Risk of Recurrent Pouchitis in Obese Patients With Ulcerative Colitis and IPAA: A Propensity-Matched Cohort Study

Introduction: Obesity is associated with increased pouchitis risk, potentially contributing to chronic intestinal inflammation. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) promote weight loss, improve glycemic control, and exhibit anti-inflammatory properties beneficial in inflammatory bowel disease (IBD). However, their role in recurrent pouchitis remains unclear. Methods: We conducted a retrospective cohort study using the TriNetX database to evaluate the risk of recurrent pouchitis in a cohort of patients with obesity and ileal pouch-anal anastomosis (IPAA) with pouchitis history who initiated GLP-1RA compared to those who did not. The primary outcome was risk of repeat antibiotic use (ciprofloxacin and/or metronidazole) after 30 days and within 1 year. Validated case definitions of IPAA and recurrent pouchitis were used. Patients with advanced therapy (AT) use before the index event and after IPAA were excluded. Secondary outcomes included number of antibiotic prescriptions, AT use, anti-diarrheal use, Crohn’s like disease of pouch (CLDP), pouch excision and healthcare utilization. 1:1 propensity score matching was performed. Results: The GLP-1RA cohort included 43 patients (mean age 51.2 ± 14.7; BMI 35.1 ± 6.4 kg/m2; 62.8% women; 72% White; 44.1% T2DM), matched to 509 control patients. 53.4% had pouchitis and 34.8% had ≥2 episodes in the preceding 1 year in the GLP-1RA cohort. GLP-1RA cohort had a significantly decreased risk of recurrent pouchitis (26.3% vs 52.6%; aHR 0.45, 95% CI 0.21-0.96; log rank P = 0.03) compared to the control cohort. Mean antibiotic prescriptions were numerically lower in the GLP-1RA cohort but not statistically significant (2 vs 4.4, P = 0.16). There was no difference in the risk of AT use or CLDP and no patients required pouch excision. Sensitivity analysis excluding antibiotic prescriptions within 1 and 3 months in the control cohort also showed a decreased risk of recurrent pouchitis in the GLP-1RA cohort. Anti-diarrheal use was lower in the GLP1-RA cohort. Within the GLP-1RA cohort, body mass index (BMI) significantly decreased by 3.2 kg/m² within 12 months (95% CI −5.8 to −0.50; P = 0.03). The mean weight loss was 16 lbs (-39.5 to -6.5). Rates of serious adverse events were low in the GLP-1RA cohort. Conclusion: In patients with obesity and IPAA with history of pouchitis, GLP-1RA use was associated with decrease in pouchitis recurrence, BMI, and body weight, suggesting beneficial effects on pouch inflammation.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001133720.90877.e7
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

S1565 Glucagon-Like Peptide-1 Receptor Agonist Therapy Is Associated With Decreased Risk of Recurrent Pouchitis in Obese Patients With Ulcerative Colitis and IPAA: A Propensity-Matched Cohort Study

Aakash Desai, Francis A. Farraye, Himsikhar Khataniar, Gursimran Kochhar et al.
The American Journal of Gastroenterology
Inflammatory Bowel Disease
article

S1565 Glucagon-Like Peptide-1 Receptor Agonist Therapy Is Associated With Decreased Risk of Recurrent Pouchitis in Obese Patients With Ulcerative Colitis and IPAA: A Propensity-Matched Cohort Study

Aakash Desai, Francis A. Farraye, Himsikhar Khataniar, Gursimran Kochhar, Edward L. Barnes, Jana G. Hashash, Priya Sehgal, Hany Habib
article en

Abstract

Introduction: Obesity is associated with increased pouchitis risk, potentially contributing to chronic intestinal inflammation. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) promote weight loss, improve glycemic control, and exhibit anti-inflammatory properties beneficial in inflammatory bowel disease (IBD). However, their role in recurrent pouchitis remains unclear. Methods: We conducted a retrospective cohort study using the TriNetX database to evaluate the risk of recurrent pouchitis in a cohort of patients with obesity and ileal pouch-anal anastomosis (IPAA) with pouchitis history who initiated GLP-1RA compared to those who did not. The primary outcome was risk of repeat antibiotic use (ciprofloxacin and/or metronidazole) after 30 days and within 1 year. Validated case definitions of IPAA and recurrent pouchitis were used. Patients with advanced therapy (AT) use before the index event and after IPAA were excluded. Secondary outcomes included number of antibiotic prescriptions, AT use, anti-diarrheal use, Crohn’s like disease of pouch (CLDP), pouch excision and healthcare utilization. 1:1 propensity score matching was performed. Results: The GLP-1RA cohort included 43 patients (mean age 51.2 ± 14.7; BMI 35.1 ± 6.4 kg/m2; 62.8% women; 72% White; 44.1% T2DM), matched to 509 control patients. 53.4% had pouchitis and 34.8% had ≥2 episodes in the preceding 1 year in the GLP-1RA cohort. GLP-1RA cohort had a significantly decreased risk of recurrent pouchitis (26.3% vs 52.6%; aHR 0.45, 95% CI 0.21-0.96; log rank P = 0.03) compared to the control cohort. Mean antibiotic prescriptions were numerically lower in the GLP-1RA cohort but not statistically significant (2 vs 4.4, P = 0.16). There was no difference in the risk of AT use or CLDP and no patients required pouch excision. Sensitivity analysis excluding antibiotic prescriptions within 1 and 3 months in the control cohort also showed a decreased risk of recurrent pouchitis in the GLP-1RA cohort. Anti-diarrheal use was lower in the GLP1-RA cohort. Within the GLP-1RA cohort, body mass index (BMI) significantly decreased by 3.2 kg/m² within 12 months (95% CI −5.8 to −0.50; P = 0.03). The mean weight loss was 16 lbs (-39.5 to -6.5). Rates of serious adverse events were low in the GLP-1RA cohort. Conclusion: In patients with obesity and IPAA with history of pouchitis, GLP-1RA use was associated with decrease in pouchitis recurrence, BMI, and body weight, suggesting beneficial effects on pouch inflammation.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 59%
Inflammatory Bowel Disease
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