Temporal Analysis of Inflammatory Bowel Disease and Pancreatitis Co-Occurrence in Children and Adults in the United States

Author:

Zhang Ke-You1,Siddiqi Ismaeel2,Saad Michelle3,Balabanis Tatiana1,Dehghan Melody S.1,Nasr Alexander3,Tolj Vania4,Habtezion Aida5,Park K.T.1,Abu-El-Haija Maisam3,Sellers Zachary M.1ORCID

Affiliation:

1. Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Stanford University, Palo Alto, California, USA;

2. Department of Medicine, Division of Digestive Diseases, University of Cincinnati, Cincinnati, Ohio, USA;

3. Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Medical Center, Cincinnati, Ohio, USA;

4. Department of Medicine, University of Cincinnati, Cincinnati, Ohio, USA;

5. Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University, Palo Alto, California, USA.

Abstract

INTRODUCTION: Pancreatitis in inflammatory bowel disease has been attributed to peripancreatic intestinal disease and/or drug-induced pancreatic toxicity. We used large cohort analyses to define inflammatory bowel disease and pancreatitis temporal co-occurrence with a detailed descriptive analysis to gain greater insight into the pathophysiological relationship between these 2 diseases. METHODS: Truven Health MarketScan private insurance claims from 141,017,841 patients (younger than 65 years) and 7,457,709 patients from 4 academic hospitals were analyzed. We calculated the prevalence of Crohn's disease or ulcerative colitis (UC) with acute pancreatitis or chronic pancreatitis (CP) and performed temporal and descriptive analyses. RESULTS: Of 516,724 patients with inflammatory bowel disease, 12,109 individuals (2.3%) had pancreatitis. Acute pancreatitis (AP) was 2–6x more prevalent than CP. In adults, AP occurred equally among Crohn's disease and UC (1.8%–2.2% vs 1.6%–2.1%, respectively), whereas in children, AP was more frequent in UC (2.3%–3.4% vs 1.5%–1.8%, respectively). The highest proportion of pancreatitis (21.7%–44.7%) was at/near the time of inflammatory bowel disease diagnosis. Of them, 22.1%–39.3% were on steroids during pancreatitis. Individuals with CP or recurrent pancreatitis hospitalizations had increased risk of a future inflammatory bowel disease diagnosis (odds ratio = 1.52 or 1.72, respectively). DISCUSSION: Pancreatitis in inflammatory bowel disease may not simply be a drug adverse event but may also involve local and/or systemic processes that negatively affect the pancreas. Our analysis of pancreatitis before, during, and after inflammatory bowel disease diagnosis suggests a bidirectional pathophysiologic relationship between inflammatory bowel disease and pancreatitis, with potentially more complexity than previously appreciated.

Funder

NIDDK

Stanford University

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology

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