Skip to main content
Clinical Trials/NCT00418340
NCT00418340UnknownPhase 4

Bacteria and Cytokines as Factors Modulating Visceral Afferent Processing in Irritable Bowel Syndrome: Manipulation of Intestinal Bacteria and Mucosal Cytokines by Probiotic Therapy and the Effect on Visceral Hypersensitivity

London North West Healthcare NHS Trust1 site in 1 country10 target enrollmentStarted: December 1, 2007Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 4
Enrollment
10
Locations
1
Primary Endpoint
The primary outcome measure is the change in physiological rectal sensitivity and before and after probiotic

Study Overview

Brief Summary

Irritable bowel syndrome (IBS) is a common condition. At least 20% of the population suffer from IBS. The symptoms of abdominal pain, diarrhoea, constipation, bloating and difficulty with bowel motions are often disabling. Many of those affected are young and report a poor quality of life (QOL) to a degree that is similar to gut inflammatory conditions like ulcerative colitis and Crohn's disease. Yet the impact of IBS on patients' lives is often underestimated. This is probably because unlike inflammatory bowel disease, in which the bowel is inflammed and bleeds, the bowel in IBS looks normal. Instead the problem is of abnormal functioning of the gut the cause of which is unknown.

Currently therapy for IBS is limited and until recently therapy has focused on treating the symptoms to improve QOL primarily because the underlying mechanism of IBS is poorly understood. However as more processes are being implicated in IBS e.g. visceral hypersensitivity (excessive response to sensory stimuli within the gut), infection, immune activation, dysmotility and abnormal gut fermentation , the potential for new therapies looks promising. The evidence that gut bacteria play a role in inducing IBS symptoms is due to observations of an improvement of IBS symptoms with probiotic therapy (bacterial supplements) and antibiotic therapy.

Patients with IBS are hypersensitive to colorectal distension compared with healthy controls. Studies carried out in our unit have shown that visceral pain thresholds in response to stress are lower in patients with IBS compared with healthy volunteers. This hypersensitivity is apparent in response to both a physical and chemical stimulus but the triggers to visceral hypersensitivity remain largely unknown. Animal models suggest roles for both host immune response and intestinal bacteria in the induction of visceral hypersensitivity. This proposal will focus on further exploration of the mechanisms underlying visceral hypersensitivity to direct future targeting of therapy.

Previous independent studies showed that (a) bacteria reduce visceral hypersensitivity, (b)probiotic therapy can alter gut immune response and (c) gut sensation is affected by the type of immune cells in the gut. Our research proposal will investigate the relationship between gut bacteria, the immune system and the sensory gut nerves in order to understand how IBS symptoms are generated. This understanding will be the critical for effective future drug treatment.

Detailed Description

This research will study

1) probiotic-induced changes in visceral hypersensitivity and immune activity The effects of probiotic therapy will be assessed in a randomised placebo-controlled study. Subjects will be recruited prospectively from outpatient clinics. A flow chart of the study is shown in appendix 1 of the protocol. Patient selection. IBS patients will be selected according to inclusion and exclusion criteria.

Disease severity will be determined at enrolment with a validated IBS symptom questionnaire.

Questionnaires to exclude psychiatric illness: The well-validated Hospital Anxiety Depression Score (HADS)questionniaire will be used to identify patients with anxiety and depression. A SCL-90 questionnaire will also be used to assess the psychological profile of patients as this may have an impact on the response to therapy.

Probiotic therapy. Patients will be randomised to receive either VSL#3 (450 billion lyophilized bacteria/sachet) twice daily for 4 weeks or a placebo powder containing starch but no bacteria. VSL#3 was selected for use in this study because (a) it contains three different Bifidobacteria strains (in addition to lactobaccilli and streptococci) and the limited evidence available Bifidobacteria as the most effective probiotics in IBS 10; (b)it induces IL-10 production by intestinal DC 27 and, in pouchitis studies, stimulated IL-10 production in vivo 38; IBS has been associated with a deficiency in IL-10 production; (c) studies from one group have yielded promising results with this particular probiotic preparation.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •patients fulfilling the Rome II criteria for the diagnosis of IBS
  • •normal blood investigations
  • •normal colonoscopy

Exclusion Criteria

  • •a history of weight loss
  • •rectal bleeding
  • •psychiatric illness (severe depression, anxiety, mania and schizophrenia)
  • •active infection
  • •recent antibiotic therapy or anti-inflammatory medication within previous 4 weeks

Outcomes

Primary Outcomes

The primary outcome measure is the change in physiological rectal sensitivity and before and after probiotic

therapy.

Secondary Outcomes

  • change in the immune response after probiotic therapy.
  • Secondary outcome measures are the change symptoms and QOL induced by probiotic therapy and the

Investigators

Study Sites (1)

Loading locations...

Similar Trials