Evaluation of the Metabolome in Diverticular Disease

Simple Diverticular Disease Clinical Trial

Official title:

Evaluation of the Metabolome in Diverticular Disease and Effects of Probiotic Mixture VSL#3 vs Fibers, Rifaximin and Mesalazine on the Metabolome in Diverticular Disease of the Colon

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01831323
• Other study ID #: TUR-SUDD 2012
• Status: Recruiting
• Phase: N/A
• First received: December 4, 2012
• Last updated: October 16, 2014
• Start date: December 2012
• Est. completion date: May 2015

Study information

• Verified date: October 2014
• Source: S.Eugenio Hospital
• Contact: Gianmarco Giorgetti, MD
• Email: gianmarcogiorgetti[@]gmail.com
• Is FDA regulated: No
• Health authority: Italy: Ethics Committee
• Study type: Observational

Clinical Trial Summary

To evaluate the effect of the probiotic formulation VSL#3 on the metabolome and microbiota of diverticular disease, comparing it with the effects exerted by supplementation with fibers, by rifaximin and by mesalazine, and assessing the evolution over time after each specific treatment

Description:

The incidence of diverticular disease of the colon has increased over the last few years. Since it presents potentially severe complications (both in terms of morbidity and mortality), the most recent studies are focusing on the underlying mechanisms and therapeutic options.

Diverticular disease of the colon presents important etiopathogenetic events. The first is that the severity of microscopic inflammation is correlated to the disease activity. The second is the bacterial overgrowth which is observed in the colon, where the diverticula form "recesses" where bacteria can proliferate. The third is that the "metabolome" plays an important role in the pathogenesis of diseases of the gastrointestinal tract (and not only). An extensive combination of microbial species live permanently in the human gut and participate in the metabolic activities of the gastro-intestinal tract (such as the synthesis of certain vitamins, improvement of the immune system, and balance of the resident bacterial species). There is little published clinical evidence suggesting a direct link between microbiota and diverticular disease; however, an altered microbiota in the flora of patients with colon cancer, irritable bowel syndrome, and IBD has been described.

It is clear that human metabolism and inflammatory response are influenced by genetic information outside our genome. Insights into the influence of microorganisms on the pathogenesis in gastrointestinal function and diverticular disease are in their infancy and often rely on extrapolation from other disease states. Microbiological analysis of fecal microbiota can provide important information on the role that the microbial-mammalian axis might have on the pathogenesis of diverticular disease.

Alteration of the metabolome play an important role in some pathologies of the gastrointestinal tract, from Inflammatory Bowel Diseases (IBD) to Irritable Bowel Syndrome (IBS). Most likely, it plays the same role in diverticular disease. In fact, the current western diet is poor in fibers and can cause an alteration of the resident bacterial species, with a reduction of bifidobacteria and an increase of clostridia.

This alteration might be present in diverticular disease and the manipulation of the microbial flora might represent both a treatment option for diverticular disease and the prevention of its complications.

Recent studies showed that the treatment with probiotics can help reduce the activity index in patients with DDS and as well as reduce the recurrence of the disease.

A new method has now been validated to assess the microbiota: the analysis of the faecal and urinary metabolome by high resolution Nuclear Magnetic Resonance (NMR) spectroscopy. The microbioma is the combination of the DNA of the microorganisms that compose the intestinal microflora (microbiota). Metabolomics allow to assess the metabolic activity of the microbiota and its possible interactions with the host.

The metabolomic analyses of stools and urine offer a new approach to evaluate the metabolome of diverticular disease, and compare it in patients who take a probiotic, fibers, non-absorbable antibiotics or an anti-inflammatory drug.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: May 2015
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Female patients over 18 years of age

• Patient with a diagnosis of uncomplicated symptomatic diverticular disease diagnosed for the first time

• Patient able to comply with the procedures of the Protocol

• Ability to sign written informed consent

Exclusion Criteria:

• Segmental colitis associated with diverticulosis

• Inflammatory Bowel Disease

• Active or recent peptic ulceration

• Chronic renal failure

• Known allergy to products in the study

• Use of lactulose-lactitol in the two weeks prior to enrollment and during the study

• Previous surgery of the colon

• Diverticular disease-related complications (fistulas, abscesses, stenosis)

• Use of probiotics in the 4 weeks prior to enrolment

• Renal, hepatic, hematologic, cardiovascular, pulmonary, neurological, psychiatric, immunological, gastrointestinal or endocrine disease, if found to be clinically significant

• Active malignancy or history of any type of malignancy.

• Recent history or suspicion of abuse of alcohol or drugs

• Women who are pregnant, nursing or of childbearing age not using appropriate contraceptive methods

• Any severe pathology that may interfere with the treatment

• Inability to provide written informed consent

• Not sufficiently reliable or presence of conditions that can result in non-compliance / patient adherence to the Protocol

• Previous participation in another study

• Lack of compliance towards the products in the study

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

• Diverticulum
• Simple Diverticular Disease

Intervention

Dietary Supplement:
• VSL#3
VSL#3

Drug:
• Rifaximin
Rifaximin
• Mesalazine
Mesalazine

Dietary Supplement:
• Psyllium
psyllium

Locations

Country	Name	City	State
Italy	Sant'Eugenio Hospital	Rome	RM

Sponsors (1)

Lead Sponsor	Collaborator
S.Eugenio Hospital

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	identify the metabolome of symptomatic uncomplicated Diverticular Disease (SUDD)	As no studies have ever been conducted or published on this aspect, the main outcome of the study is to analyze and identify the metabolome of patients with SUDD before starting any therapy and after a 2 week therapy of a probiotic, fibers or antibiotics. The metabolomic analysis will allow a precise evaluation of the systemic and organ-specific processes based on low molecular weight components thus providing a profile of the metabolic system of these patients.	12 months	No
Primary	verify changes in the intestinal microbiota following treatment in the different study groups.		12 months	No
Secondary	evaluate the symptomatology and metabolome	Evaluate the difference in symptomatology in the different groups, in particular stool frequency, abdominal pain, mucus or blood in faeces, intestinal gas, and assess possible link to the different metabolome and microbiota	12 months	No
Secondary	evaluate the different metabolomes and microbiota according to the treatment used	Evaluate if the variation in metabolome and microbiota induced by the different treatments modify the symptomatology of the patients and for how long.	12 months	No
Secondary	Evaluate the effects of supplementation with VSL#3 on the metabolome and microbiota of Diverticular Disease	Evaluate the effects of supplementation with VSL#3 on the metabolome and microbiota of Diverticular Disease, comparing it with the effects of supplementation with fibers, or treatment with rifaximin or with mesalazine.	12 months	No
Secondary	evaluate if difference in the symptomatology in the different groups are correlated with changes in the intestinal microbiota		12 months	No