Clinical Gastroenterology and Hepatology
Volume 8, Issue 5 , Pages 433-438, May 2010

Some Patients With Irritable Bowel Syndrome May Have Exocrine Pancreatic Insufficiency

  • John S. Leeds

      Affiliations

    • Department of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom
    • Corresponding Author InformationReprint requests Address requests for reprints to: John S. Leeds, MRCP, Room P39, Department of Gastroenterology and Liver Unit, Royal Hallamshire Hospital, Sheffield, South Yorkshire, S10 2JF, United Kingdom. fax: (0114) 271-2692
  • ,
  • Andrew D. Hopper

      Affiliations

    • Department of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom
  • ,
  • Reena Sidhu

      Affiliations

    • Department of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom
  • ,
  • Alison Simmonette

      Affiliations

    • Department of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom
  • ,
  • Narges Azadbakht

      Affiliations

    • Department of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom
  • ,
  • Nigel Hoggard

      Affiliations

    • Academic Department of Radiology, Royal Hallamshire Hospital, Sheffield, United Kingdom
  • ,
  • Stephen Morley

      Affiliations

    • Department of Clinical Chemistry, Royal Hallamshire Hospital, Sheffield, United Kingdom
  • ,
  • David S. Sanders

      Affiliations

    • Department of Gastroenterology, Royal Hallamshire Hospital, Sheffield, United Kingdom

published online 15 October 2009.

Background & Aims

Patients with irritable bowel syndrome (IBS) might have other underlying pathologies. Pancreatic disease can be elusive—especially in the early stages, and some symptoms overlap with those of IBS. We evaluated the prevalence of exocrine pancreatic insufficiency in diarrhea-predominant IBS (D-IBS) and assessed the effects of pancreatic enzyme supplementation.

Methods

The study included patients who met the Rome II criteria for D-IBS, patients with chronic diarrhea, and subjects without diarrhea (controls). Subjects' baseline weight, stool frequency, stool consistency (using the Bristol score), and fecal elastase-1 (Fel-1) levels were determined. Patients were assessed using British Society of Gastroenterology IBS guidelines. Patients with Fel-1 levels less than 100 μg/g stool (indicating pancreatic exocrine insufficiency; group 1) were compared with age- and sex-matched patients with D-IBS and normal levels of Fel-1 (group 2), given pancreatic enzyme therapy, and reassessed at 12 weeks.

Results

Fel-1 levels were less than 100 μg/g in stool from 19 of 314 patients with D-IBS (6.1%; 95% confidence interval [CI], 3.7%–9.3%), none of the 105 patients with chronic diarrhea (95% CI, 0.0%–3.5%), and none of 95 controls (95% CI, 0.0–3.8%) (P < .001). After enzyme supplementation, improvements in stool frequency (P < .001), stool consistency (P < .001), and abdominal pain (P = .003) were observed in patients in group 1, but not in group 2.

Conclusions

Pancreatic exocrine insufficiency was detected in 6.1% of patients who fulfilled the Rome II criteria for D-IBS. In these patients, pancreatic enzyme therapy might reduce diarrhea and abdominal pain. Pancreatic exocrine insufficiency should be considered in patients with D-IBS.

Keywords: Irritable Bowel Syndrome, Pancreatic Insufficiency, Chronic Pancreatitis, Fecal Elastase

Abbreviations used in this paper: BSS, Bristol stool score, CI, confidence interval, D-IBS, diarrhea-predominant irritable bowel syndrome, Fel-1, fecal elastase-1, Ig, immunoglobulin

 

 Conflicts of interest The authors disclose no conflicts.

 Funding This study was supported by Bardhan Research and Education Trust of Rotherham and Solvay Pharmaceuticals. Dr Leeds' salary was funded partly by Solvay pharmaceuticals; however, Solvay had no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the paper for publication.

PII: S1542-3565(09)01012-X

doi:10.1016/j.cgh.2009.09.032

Clinical Gastroenterology and Hepatology
Volume 8, Issue 5 , Pages 433-438, May 2010