Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-24T01:45:10.547Z Has data issue: false hasContentIssue false

Treating irritable bowel syndrome with probiotics: the evidence

Published online by Cambridge University Press:  18 March 2010

G. C. Parkes*
Affiliation:
Nutritional Sciences Division, King's College London, 150 Stamford Street, LondonSE1 9NH, UK
J. D. Sanderson
Affiliation:
Nutritional Sciences Division, King's College London, 150 Stamford Street, LondonSE1 9NH, UK
K. Whelan
Affiliation:
Nutritional Sciences Division, King's College London, 150 Stamford Street, LondonSE1 9NH, UK
*
*Corresponding author: Dr G. C. Parkes, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Irritable bowel syndrome (IBS) is a disorder of chronic abdominal pain, altered bowel habit and abdominal distension. It is the commonest cause of referral to gastroenterologists in the developed world and yet current therapeutic strategies are often unsatisfactory. There is now increasing evidence linking alterations in the gastrointestinal (GI) microbiota and IBS. Changes in faecal and mucosa-associated microbiota, post-infectious IBS, a link with small intestinal bacterial overgrowth and an up-regulation of the GI mucosal immune system all suggest a role for the GI microbiota in the pathogenesis of IBS. Given this evidence, therapeutic alteration of the GI microbiota by probiotic bacteria could be beneficial. The present paper establishes an aetiological framework for the use of probiotics in IBS and comprehensively reviews randomised placebo-controlled trials of probiotics in IBS using multiple electronic databases. It highlights safety concerns over the use of probiotics and attempts to establish guidelines for their use in IBS in both primary and secondary care.

Type
Symposium on ‘Dietary management of disease’
Copyright
Copyright © The Authors 2010

Abbreviations:
GI

gastrointestinal

GSS

global symptom score

IBS

irritable bowel syndrome

Irritable bowel syndrome (IBS) is characterised by abdominal pain, bloating and change in bowel habit with an absence of any overt mucosal abnormality(Reference Thompson, Longstreth and Drossman1). Although IBS affects between 10% and 20% of the population in Europe and the USA(Reference Bommelaer, Poynard and Le Pen2), its pathogenesis remains poorly understood. Research into the aetiology of IBS has centred on the interaction between the gastrointestinal (GI) tract and the central and enteric nervous system(Reference Kellow, Azpiroz and Delvaux3). Novel therapeutic agents such as tegaserod(Reference Evans, Clark and Moore4), alosetron(Reference Cremonini, Delgado-Aros and Camilleri5) and more recently corticotrophin-releasing hormone antagonists(Reference Sagami, Shimada and Tayama6) have been based on this research. This emphasis on dysmotility and visceral hypersensitivity in IBS has shifted the focus away from the GI tract, yet there is increasing evidence of GI immune up-regulation and altered microbiota(Reference Parkes, Brostoff and Whelan7). This evidence has highlighted the potential for therapeutic manipulation of the GI microbiota in particular with probiotics. Probiotics are defined as ‘live microorganisms, which, when administered in adequate amounts, confer a health benefit on the host’(8). Probiotics have been shown to be efficacious in a number of GI disorders including the treatment of Clostridium difficile-associated diarrhoea(Reference Parkes, Sanderson and Whelan9), inflammatory bowel disease(Reference Kruis, Fric and Pokrotnieks10), acute gastroenteritis(Reference Van Niel, Feudtner and Garrison11Reference Szajewska, Skorka and Dylag13) and necrotising enterocolitis(Reference Alfaleh and Bassler14). The present paper describes the reasons for the use of probiotics in IBS and their potential mechanisms of action and summarises the clinical evidence for their use to date. Finally, it aims to synthesise guidance for when and how to use probiotics in IBS populations in both primary and secondary care.

The role of the gastrointestinal microbiota in irritable bowel syndrome

Several factors suggest that the GI microbiota might be important in the pathogenesis of IBS. First, several studies have found differences in the faecal and mucosa-associated microbiota of patients with IBS and healthy controls(Reference Balsari, Ceccarelli and Dubini15Reference Si, Yu and Fan19). As a result of the wide range of techniques used, differing patient groups and the complexity of the GI microbiota it is difficult to draw firm conclusions from this series of studies. However, there does appear to be a consistent theme of a relative reduction of the lactobacilli and bifidobacteria(Reference Balsari, Ceccarelli and Dubini15, Reference Malinen, Rinttila and Kajander17Reference Si, Yu and Fan19) in patients with IBS and higher concentrations of species such as enterobacteriaceae(Reference Balsari, Ceccarelli and Dubini15, Reference Si, Yu and Fan19), coliforms(Reference Balsari, Ceccarelli and Dubini15) and bacteroides(Reference Parkes, Rayment and Hudspith18). However, what is less clear, without a greater understanding of the metabolic and immunological roles of the GI microbiota, is whether these changes are a primary or secondary phenomenon.

In addition to differences in the GI microbiota in IBS there is increasing evidence of an activation of the intestinal immune system in IBS, with studies demonstrating increased concentrations of mucosal intra-epithelial lymphocytes(Reference Spiller, Jenkins and Thornley20, Reference Chadwick, Chen and Shu21), mast cells(Reference Chadwick, Chen and Shu21Reference Weston, Biddle and Bhatia24) and 5-hydroxytryptamine-secreting enterochromaffin cells(Reference Spiller, Jenkins and Thornley20). Given the evidence for the role of the GI microbiota in the profound inflammatory state in ulcerative colitis and Crohn's disease, luminal antigens such as the microbiota may play a similar role in IBS.

Many of the studies demonstrating an up-regulation of the GI mucosal immune system have been in post-infectious IBS, in which there is a clear infective trigger(Reference Spiller, Jenkins and Thornley20). A longitudinal study has monitored long-term sequelae following an outbreak of gastroenteritis associated with water contamination in a town in Canada that resulted in >2300 cases of gastroenteritis(Reference Marshall, Thabane and Garg25). Using the unaffected population as controls the study found that over the course of 2 years the OR for developing IBS in the affected population was 4·8 (95% CI 3·4, 6·8; P<0·001).

Finally, there is controversial evidence linking small intestinal bacterial overgrowth and IBS. Bloating and flatulence are common symptoms of IBS(Reference Hungin, Whorwell and Tack26) and bacterial fermentation of undigested carbohydrate leads to production of gases CO2, H2 and CH4. Several studies by the same research group have examined patients with IBS using a lactulose H2 breath test and have found an increased incidence of small intestinal bacterial overgrowth of approximately 78–84%(Reference Hasler27Reference Walters and Vanner30). However, when the incidence of small intestinal bacterial overgrowth is measured using jejunal aspiration and culture (considered to be the gold standard) the incidence has been found to be approximately 4%(Reference Posserud, Stotzer and Bjornsson31).

There are therefore a number of plausible reasons why the GI microbiota may play a role in the aetiology of IBS. However, some of the best evidence is in the success of modulating the host microbiota either with antibiotics(Reference Sharara, Aoun and Abdul-Baki32, Reference Pimentel, Park and Mirocha33) or probiotics.

Probiotics in irritable bowel syndrome: mechanisms of action

In order to be of clinical benefit probiotic bacteria must be able to survive GI transit (e.g. gastric acid and bile acid resistance) and then be able to demonstrate functional efficacy(8). There is substantial evidence demonstrating that probiotic bacteria can interact with the host GI mucosal immune system(Reference Drakes, Blanchard and Czinn34Reference Hudspith, Rouzard and Gibson36). Given the evidence demonstrating an increase in immune cell populations in IBS, it is probable that immunomodulation by probiotics is a key constituent of their mechanism of action. A trial of the probiotic bacteria Bifidobacteria infantis 35624 has found that at baseline patients with IBS have a higher pro-inflammatory IL-12:anti-inflammatory IL-10 than healthy controls(Reference O'Mahony, McCarthy and Kelly37). Administration of the trial probiotic but not placebo reverses these ratios to the levels of the healthy controls. As discussed later, these findings correlate with clinical benefit.

Specific probiotic bacteria appear to directly modulate intestinal pain. Lactobacillus acidophilus has been shown to up regulate μ-opioid and cannaboid receptors in colonic epithelial cell lines and in the colonic epithelium in pretreated rats and mice(Reference Rousseaux, Thuru and Gelot38). Using a rat stress model of visceral hypersensitivity pretreatment with the probiotic was found to ameliorate pain. Similarly, Lactobacillus paracasei attenuates abdominal pain and mucosal inflammation in an antibiotic-induced murine model of visceral hypersensitivity(Reference Verdu, Bercik and Verma-Gandhu39).

Probiotics have also been shown to alter the integrity of the GI mucosa. The probiotic VSL#3® (a combination of nine strains of various bifidobacteria, lactobacilli and Streptococcus thermophilus; VSL Pharmaceuticals, Inc., Gaithersburg, MD, USA) has been shown to induce mucin production in the colon via up-regulation of the gene MUC2 (Reference Caballero-Franco, Keller and De Simone40), thereby increasing barrier protection. In addition, as part of a randomised controlled trial of a probiotic drink containing S. thermophilus, Lactobacillus bulgaricus, L. acidophilus and Bifidobacterium longum in patients with diarrhoea-predominant IBS, intestinal permeability was analysed(Reference Zeng, Li and Zuo41). A significant improvement was found in global symptom score (GSS; patient rating of overall improvement in symptoms post-treatment v. pretreatment(Reference Whitehead, Corazziari and Prizont42)), which was correlated with a significant decrease in small intestinal permeability (measured by lactulose:mannitol urinary excretion; 0·038 v. 0·024; P<0·004). Interestingly, no change in colonic permeability was found when measured by sucralose urinary excretion, suggesting that the effects are specific to the small bowel. As several studies have shown increased GI permeability in IBS(Reference Dunlop, Hebden and Campbell43, Reference Marshall, Thabane and Garg44), therapies that improve barrier function may alleviate symptoms via this mechanism. Although understanding of the exact mechanism of probiotic bacteria is not complete, these examples do provide plausible examples of their efficacy. The data highlight that these effects are often highly species or strain specific and it is therefore important that data from one probiotic are not extrapolated to another.

Probiotics in irritable bowel syndrome: clinical trials

There have now been numerous trials that have investigated the therapeutic benefit of probiotics in IBS, with heterogeneity in dosing regimens, species used and clinical end points. More recently, there have been two systematic reviews(Reference Moayyedi, Ford and Talley45, Reference Brenner, Moeller and Chey46) and two meta-analyses(Reference McFarland and Dublin47, Reference Hoveyda, Heneghan and Mahtani48). Table 1 summarises the important randomised controlled trials over the last 10 years, highlighting the species used, the trial design and results. Several trials have been excluded from this list because of failure to compare with placebo(Reference Hun49), re-analysis of old data(Reference Enck, Zimmermann and Menke50), unclear end points(Reference Bittner, Croffut and Stranahan51) or the use of multiple interventions(Reference Long, Yu and Yang52). Many early studies were small single-centre trials(Reference Bausserman and Michail53Reference Sen, Mullan and Parker57), although more recently a number of much larger multi-centre trials have been undertaken, reflecting the growing interest in the area(Reference Andriulli, Neri and Loguercio58Reference Whorwell, Altringer and Morel61).

Table 1. Summary of recent randomised controlled trials of probiotics in irritable bowel syndrome (IBS)

L., Lactobacillus; B., Bifidobacterium; B. animalis, Bifidobacteria animalis; B. infantis, Bifidobacteria infantis; E. coli; Escherichia coli; S. thermophilus, Streptococcus thermophilus; NCIMB, National Collection of Industrial, Marine and Food Bacteria collection no.; PEP, primary end point; GSS, global symptom score (patient rating of improvement of symptoms overall post-treatment v. pretreatment(Reference Whitehead, Corazziari and Prizont42)).

* Diarrhoea-predominant IBS.

Constipation-predominant IBS.

Subgroup analysis of IBS in a larger cohort of functional abdominal pain disorders.

Lactobacillus plantarum

There are three small single-centre studies using a liquid form of Lactobacillus plantarum in IBS. Two studies show some benefit over placebo, one improving flatulence scores(62 and the other demonstrating reduction in pain(Reference Niedzielin, Kordecki and Birkenfeld55). The third trial shows no significant benefit, although it was underpowered(Reference Sen, Mullan and Parker57). However, these preliminary trials have never been followed up with larger multi-centre studies.

Lactobacillus GG

Lactobacillus GG is a strain of probiotic that has shown efficacy in the treatment of infectious diarrhoea in children(Reference Szajewska, Skorka and Ruszczynski12). There have been two conflicting trials treating childhood IBS and recurrent abdominal pain with L. GG, both of which used resolution of abdominal pain as their primary end point(Reference Bausserman and Michail53, Reference Gawronska, Dziechciarz and Horvath63). The earlier trial found no significant difference in resolution of pain in the treatment arm over placebo (44% v. 40%; P=0·77)(Reference Bausserman and Michail53). The second, however, found that the primary end point was achieved in significantly higher numbers in the treatment arm than placebo (33% v. 5%; P=0·04)(Reference Gawronska, Dziechciarz and Horvath63). A recent Cochrane review of dietary intervention in functional bowel disorders in children has found insufficient evidence to support its use(Reference Huertas-Ceballos, Logan and Bennett64). It should be noted that L. GG is a composite strain in one of the probiotic cocktails that have showed benefit in two larger trials(Reference Kajanda, Myllyluoma and Rajilic-Stojanovic60, Reference Kajanda, Hatakka and Poussa65).

Lactobacillus reuteri ATCC 55730

A single trial of fifty-four patients with IBS using Lactobacillus reuteri ATCC 55730 over a period of 6 months has demonstrated an improvement in the GSS from baseline but because of a large placebo effect failed to show any benefit over controls(Reference Niv, Naftali and Hallak56).

Lactobacillus paracasei B21060

A symbiotic preparation, Flortec® (Bracco spA, Milan, Italy), that contains a combination of prebiotic (xylo-oligosaccharide) and probiotic (Lactobacillus paracasei B21060) has been used in a large (n 267) multi-centre trial, with Flortec® as the treatment arm and xylo-oligosaccharide alone as the control arm(Reference Andriulli, Neri and Loguercio58). The improvement in global relief scores was found to be similar in the study and control arms, albeit Flortec® was shown to significantly reduce stool frequency in patients with diarrhoea-predominant IBS compared with controls (1·18 v. 0·45; P<0·05). A recent placebo-controlled trial of a prebiotic product, trans-galactooligosaccharide, in the treatment of IBS has demonstrated significant reduction in GSS over placebo(Reference Silk, Davis and Vulevic66). Thus, the lack of significant difference compared with controls may be in part related to a beneficial effect of the prebiotic in the control arm.

Lactobacillus acidophilus SDC 2012

A small single-centre study of forty patients with IBS randomised to L. acidophilus SDC 2012 and 2013 or placebo has shown benefit over placebo(Reference Sinn, Song and Kim67). Using any reduction in abdominal pain scores as a primary end-point when comparing L. acidophilus to placebo a reduction in pain of 23·8% v. 0·2% (P=0·003) was reported. However, the study did not use a global symptom-relief score as an end point, and using any reduction in pain as ‘a responder’ is questionable. It is interesting that there appeared to be no appreciable placebo effect in the trial (conducted in South Korea), in contrast to the majority of trials in IBS.

Bifidobacteria infantis 35624

B. infantis 35624 is a probiotic that was initially designed as a treatment for ulcerative colitis but ultimately failed to demonstrate benefit in a multi-centre clinical trial(Reference Shanahan, Guarner and Von Wright68). However, in a trial of seventy-seven patients with IBS randomised to B. infantis, Lactobacillus salivarius or placebo, B. infantis (but not L. salivarius) was shown to reduce pain, bloating and bowel satisfaction scores in comparison with placebo, as well as composite scores(Reference O'Mahony, McCarthy and Kelly37). In addition, as discussed earlier, B. infantis but not placebo or L. salivarius was found to have a profound anti-inflammatory effect in patients with IBS but not in healthy controls. The benefit of B. infantis has been replicated in a large multi-centre dose-finding trial of B. infantis in 362 female patients with IBS, randomised to four groups taking doses of 106, 108 or 1010 colony-forming units per d or placebo(Reference Whorwell, Altringer and Morel61). The group taking B. infantis at 108 colony-forming units per d was reported to have scored significantly better than the placebo group in all symptom groups including a global assessment of IBS relief that was the primary end point (62·3 (se 6·2) v. 42·0 (se 6·4); P<0·02). It was later discovered that the bacteria in the formulation containing 1010 colony-forming units per d were non-viable, perhaps explaining its lack of efficacy.

Bifidobacteria animalis DN 173010

Several well-designed large multi-centre trials of probiotics in IBS have failed to demonstrate benefit, again often in part as a result of a high placebo response(Reference Andriulli, Neri and Loguercio58, Reference Drouault-Holowacz, Bieuvelet and Burckel69, Reference Guyonnet, Chassany and Ducrotte70). A French multi-centre trial of B. animalis DN 173010 in 274 patients with constipation-predominant IBS in primary care has demonstrated symptomatic relief compared with baseline in its primary end point (improvement in a functional bowel disorder quality-of-life score) but not over placebo(Reference Guyonnet, Chassany and Ducrotte70). However, subgroup analysis of patients with less than three bowel motions per week (n 19) at baseline has shown a significant rise in stool frequency compared with controls (P<0·001).

Escherichia coli DSM 17252

A primary-care-based placebo-controlled trial of Escherichia coli (DSM 17252)(Reference Enck, Zimmermann and Menke59) has been conducted in 298 patients with IBS diagnosed by a primary-care (not Rome(Reference Thompson, Drossman and Heaton71) criteria) standard in which response was defined as ‘clinical remission’ with complete resolution of IBS symptoms(Reference Smith, Steinke and Kinnear72). In comparison with placebo the treatment arm was reported to have achieved complete remission in 18·4% v. 4·6% (P<0·0004) of the patients studied (intention-to-treat analysis). In addition, a 50% drop was found in abdominal pain scores (18·9% v. 6·7% in treatment and placebo groups respectively; P=0·001). This trial was based on a much earlier trial of E. coli (DSM 17252) in combination with Enterococcus faecalis (DSM 16440) originally published in 1993(Reference Panijel and Burkhard73) and more recently re-analysed(Reference Enck, Zimmermann and Menke50) by re-defining the clinical end points to give a GSS in accordance with modern guidelines. This re-analysis has demonstrated a significantly better response rate (defined by a drop in GSS by 50%) in the treatment arm than in the placebo arm (68·5% v. 37·8%; P<0·001(Reference Enck, Zimmermann and Menke50); data not included in Table 1). Although both these trials failed to use Rome(Reference Thompson, Drossman and Heaton71) or Manning(Reference Manning, Thompson and Heaton74) definitions in their inclusion criteria, they were otherwise large and well designed. Data from primary care rather than secondary care are particularly useful given the majority of patients with IBS are treated by primary-care physicians.

VSL#3®

The combination probiotic VSL#3® has been used in a number of trials for the treatment of ulcerative colitis(Reference Miele, Pascarella and Giannetti75) and pouchitis(Reference Gionchetti, Rizzello and Venturi76, Reference Gionchetti, Rizzello and Helwig77). However, trials of VSL#3® in IBS, although well designed, have reported mixed results. An initial trial of twenty-five patients with diarrhoea-predominant IBS has used colonic transit (measured by scintography) as the primary end point, with reduction in symptom scores as secondary targets(Reference Kim, Camilleri and McKinzie78). No significant reduction in GI transit was found for the study group, although there was a symptom score reduction in abdominal bloating. Thus, a second, larger, trial was designed using forty-eight patients with a reduction in abdominal bloating as the primary end point and colonic transit and other symptoms as secondary end points(Reference Kim, Vazquez Roque and Camilleri54). Although only a non-significant reduction in abdominal bloating scores was found in the study group v. placebo (31·3 (se 3·1) v. 38·5 (se 3·1); P=0·22), there was a significant reduction in flatulence scores (29·7 (se 2·6) v. 39·5 (se 2·6); P=0·01). In addition, in the larger trial VSL#3® was shown to significantly retard colonic transit (P=0·05), although without a corresponding change in stool frequency or form. Thus, there is only weak evidence supporting the use of VSL#3® in IBS at present.

Lactobacillus rhamnosus GG, Lactobacillus rhamnosus LC705, Bifidobacterium breve, Propionibacterium freudenreichii sppshermanii JS

A multi-species probiotic containing Lactobacillus rhamnosus GG, L. rhamnosus LC705, Bifidobacterium breve and Propionibacterium freudenreichii spp shermanii JS has been used in two trials from the same group. The first 6-month trial of 103 patients with IBS has found a mean difference in reduction of the total symptom scores (the primary end point) of 7·7 points (P=0·015)(Reference Kajanda, Hatakka and Poussa65). These findings were confirmed by a follow-up study of eighty-six patients, with a difference in reduction in GSS of eleven points (P<0·01)(Reference Kajanda, Myllyluoma and Rajilic-Stojanovic60). However, marked differences in baseline severity scores were found between treatment groups and controls, with the treatment group having greater symptom severity and therefore more likely to improve. In addition, a high percentage (22) of both control and treatment arms were prescribed antibiotics in the treatment period. A notable feature in these trials was the longer treatment period of 5 and 6 months respectively with a consistent GSS improvement over the treatment course.

LAB4

A study that used L. acidophilus (NCIMB 30157 and 30156) in combination with Bifidobacterium lactis (NCIMB 30172) and Bifidobacterium bifidum (NCIMB 30153) has also demonstrated benefit in IBS(Reference Williams, Stimpson and Wang79). At the end of the 8-week trial of fifty-two patients with IBS randomised to the probiotic combination (LAB4®; Cultech Ltd, Port Talbot, West Glamorgan, UK) or placebo a significant drop in the symptom severity score was found in the study arm compared with the controls (133 v. 80; P<0·05). However, once again the study arm had a higher baseline severity score than the placebo arm; in addition, the benefit was no longer significant 2 weeks after stopping the probiotic.

Discussion

Although understanding of the GI tract continues to expand, IBS remains a difficult condition to treat. The key to this difficulty is in part the heterogeneous nature of the syndrome. Although the clinical symptoms of altered bowel habit, pain and bloating are frequently similar in different classes of IBS, the underlying aetiologies can be diverse. Clinicians need a range of therapeutic options that reflect this heterogeneity, whether they be neuromotility agents, psychosocial therapy, dietary advice or microbial manipulation with probiotics.

Following the evidence summarised earlier, the probiotics with the greatest efficacy data in treating IBS are B. infantis 35624 and E. coli DSM 17252. Both these probiotics have had initial successful trials supported by larger multi-centre studies(Reference O'Mahony, McCarthy and Kelly37, Reference Enck, Zimmermann and Menke50, Reference Enck, Zimmermann and Menke59, Reference Whorwell, Altringer and Morel61). B. infantis has in vitro and human data supporting a putative mechanism of action. Unfortunately, the second randomised controlled trial of B. infantis was only conducted in women(Reference Whorwell, Altringer and Morel61) and therefore there is little evidence to support its use in men. Although this trial was conducted in all subgroups of IBS, further analysis suggests that B. infantis is most effective in patients with diarrhoea-predominant IBS (reduction in composite symptom score compared with placebo; −0·99, P=0·027) and there is no benefit in patients with IBS with alternating stool pattern (−0·15, P=0·84). In the constipation-predominant IBS group, although the difference in the composite score compared with placebo is not significant (−1·32, P=0·074), this outcome is probably the result of a reduced sample size.

The Finnish probiotic combination of L. rhamnosus GG, L. rhamnosus LC705, B. breve, Propionibacterium freudenreichii spp shermanii JS has also demonstrated benefit in two sequential trials(Reference Kajanda, Myllyluoma and Rajilic-Stojanovic60, Reference Kajanda, Hatakka and Poussa65). However, both trials recruited from a single centre and were conducted by the same investigators. A larger, ideally multi-national, trial would be helpful before making stronger recommendations. Many other products have been hampered by a large placebo effect; in particular, a large trial of B. animalis DN 173010(Reference Guyonnet, Chassany and Ducrotte70). However, given the subgroup analysis showing benefit in patients with a stool frequency of less than three per week, the use of B. animalis DN 173010 could be cautiously recommended in patients with severe constipation-predominant IBS, although clearly further data are needed. There are obviously a number of smaller trials that have demonstrated benefit(Reference Sinn, Song and Kim67, Reference Williams, Stimpson and Wang79, Reference Tsuchiya, Barreto and Okura80), but given the limited numbers and lack of supporting evidence it is difficult to recommend their use at this stage. Single-centre pilot data suggesting benefit for a probiotic agent in treating IBS should be supported by data from larger multi-centre trials.

There have been a number of meta-analyses on probiotics in IBS recently, all of which agree that probiotics are beneficial to varying extents. One meta-analysis has shown a relative risk of not improving the GSS of 0·77 (95% CI 0·62, 0·94)(Reference McFarland and Dublin47), another meta-analysis has reported a relative risk of not improving the GSS of 0·72 (95% CI 0·57, 0·88)(Reference Moayyedi, Ford and Talley45) and another meta-analysis has found an OR of symptomatic improvement of 1·63 (95% CI 1·23, 2·17)(Reference Hoveyda, Heneghan and Mahtani48). However, meta-analyses or systematic reviews that group disparate species of probiotics together always risk diluting evidence of successful trials with studies using entirely different species and vice versa.

Like most therapies in IBS probiotics are unlikely to be beneficial for all patients. However, given their impressive safety profile and their relative low cost, a trial of a probiotic agent is certainly worth considering. Given the wide availability of products to the public, patients need careful guidance as to which product is likely to be of benefit in order not to be frustrated. Care must be taken to recommend the exact strain or species that has shown benefit in treating IBS, and not to extrapolate success of one probiotic species to another. In addition, further research is needed to predict which patient groups are most likely to respond to probiotics, perhaps through faecal microbial profiling. The understanding of the GI microbiota and its interaction with the host is in its infancy; however, its manipulation offers therapeutic benefit in a number of GI disorders including IBS.

Acknowledgements

The author is on an advisory committee for Ferring Pharmaceuticals UK. This work has been supported by a grant from the Foundation for Allergy Information and Research. The paper was researched and written by G. C. P., J. D. S. and K. W. contributed as editors.

References

1.Thompson, WG, Longstreth, GF, Drossman, DA et al. (1999) Functional bowel disorders and functional abdominal pain. Gut 45, Suppl. 2, II43II47.CrossRefGoogle ScholarPubMed
2.Bommelaer, G, Poynard, T, Le Pen, C et al. (2004) Prevalence of irritable bowel syndrome (IBS) and variability of diagnostic criteria. Gastroenterol Clin Biol 28, 554561.CrossRefGoogle ScholarPubMed
3.Kellow, JE, Azpiroz, F, Delvaux, M et al. (2006) Applied principles of neurogastroenterology: physiology/motility sensation. Gastroenterology 130, 14121420.CrossRefGoogle Scholar
4.Evans, BW, Clark, WK, Moore, DJ et al. (2007) Tegaserod for the treatment of irritable bowel syndrome and chronic constipation. Cochrane Database of Systematic Reviews 2007, issue 4, CD003960. Chichester, West Sussex: John Wiley and Sons, Ltd.CrossRefGoogle Scholar
5.Cremonini, F, Delgado-Aros, S & Camilleri, M (2003) Efficacy of alosetron in irritable bowel syndrome: a meta-analysis of randomized controlled trials. Neurogastroenterol Motil 15, 7986.CrossRefGoogle ScholarPubMed
6.Sagami, Y, Shimada, Y, Tayama, J et al. (2004) Effect of a corticotropin releasing hormone receptor antagonist on colonic sensory and motor function in patients with irritable bowel syndrome. Gut 53, 958964.CrossRefGoogle ScholarPubMed
7.Parkes, GC, Brostoff, J, Whelan, K et al. (2008) Gastrointestinal microbiota in irritable bowel syndrome: their role in its pathogenesis and treatment. Am J Gastroenterol 103, 15571567.CrossRefGoogle ScholarPubMed
8.Food and Agriculture Organization/World Health Organization (2001) Evaluation of health and nutritional properties of probiotics in food, including powder milk with the live lactic acid bacteria. Report of a Joint FAO/WHO Expert Consultation on evaluation of health and nutritional properties of probiotics in food including powder milk with live lactic acid bacteria. http://www.who.int/foodsafety/publications/fs_management/en/probiotics.pdfGoogle Scholar
9.Parkes, GC, Sanderson, JD & Whelan, K (2009) The mechanisms and efficacy of probiotics in the prevention of Clostridium difficile-associated diarrhoea. Lancet Infect Dis 9, 237244.CrossRefGoogle ScholarPubMed
10.Kruis, W, Fric, P, Pokrotnieks, J et al. (2004) Maintaining remission of ulcerative colitis with the probiotic Escherichia coli Nissle 1917 is as effective as with standard mesalazine. Gut 53, 16171623.CrossRefGoogle ScholarPubMed
11.Van Niel, CW, Feudtner, C, Garrison, MM et al. (2002) Lactobacillus therapy for acute infectious diarrhea in children: A meta-analysis. Pediatrics 109, 678684.CrossRefGoogle ScholarPubMed
12.Szajewska, H, Skorka, A, Ruszczynski, M et al. (2007) Meta-analysis: Lactobacillus GG for treating acute diarrhoea in children. Aliment Pharmacol Ther 25, 871881.CrossRefGoogle ScholarPubMed
13.Szajewska, H, Skorka, A & Dylag, M (2007) Meta-analysis: Saccharomyces boulardii for treating acute diarrhoea in children. Aliment Pharmacol Ther 25, 257264.CrossRefGoogle ScholarPubMed
14.Alfaleh, K & Bassler, D (2008) Probiotics for prevention of necrotizing enterocolitis in preterm infants. Cochrane Database of Systematic Reviews 2008, issue 1, CD005496. Chichester, West Sussex: John Wiley and Sons, Ltd.CrossRefGoogle Scholar
15.Balsari, A, Ceccarelli, A, Dubini, F et al. (1982) The fecal microbial population in the irritable bowel syndrome. Microbiologica 5, 185194.Google ScholarPubMed
16.Kassinen, A, Krogius-Kurikka, L, Makivuokko, H et al. (2007) The fecal microbiota of irritable bowel syndrome patients differs significantly from that of healthy subjects. Gastroenterology 133, 2433.CrossRefGoogle ScholarPubMed
17.Malinen, E, Rinttila, T, Kajander, K et al. (2005) Analysis of the fecal microbiota of irritable bowel syndrome patients and healthy controls with real-time PCR. Am J Gastroenterol 100, 373382.CrossRefGoogle ScholarPubMed
18.Parkes, GC, Rayment, NB, Hudspith, BN et al. (2007) Investigation of rectal mucosa-associated microbiota in irritable bowel syndrome using fluorescent in-situ hybridisation. Gut 56, Suppl. III, A18.Google Scholar
19.Si, JM, Yu, YC, Fan, YJ et al. (2004) Intestinal microecology and quality of life in irritable bowel syndrome patients. World J Gastroenterol 10, 18021805.CrossRefGoogle ScholarPubMed
20.Spiller, RC, Jenkins, D, Thornley, JP et al. (2000) Increased rectal mucosal enteroendocrine cells, T lymphocytes, and increased gut permeability following acute Campylobacter enteritis and in post-dysenteric irritable bowel syndrome. Gut 47, 804811.CrossRefGoogle ScholarPubMed
21.Chadwick, VS, Chen, W, Shu, D et al. (2002) Activation of the mucosal immune system in irritable bowel syndrome. Gastroenterology 122, 17781783.CrossRefGoogle ScholarPubMed
22.Guilarte, M, Santos, J, de Torres, I et al. (2006) Diarrhoea-predominant IBS patients show mast cell activation and hyperplasia in the jejunum. Gut 56, 203209.CrossRefGoogle ScholarPubMed
23.O'Sullivan, M, Clayton, N, Breslin, NP et al. (2000) Increased mast cells in the irritable bowel syndrome. Neurogastroenterol Motil 12, 449457.CrossRefGoogle ScholarPubMed
24.Weston, AP, Biddle, WL, Bhatia, PS et al. (1993) Terminal ileal mucosal mast cells in irritable bowel syndrome. Dig Dis Sci 38, 15901595.CrossRefGoogle ScholarPubMed
25.Marshall, JK, Thabane, M, Garg, AX et al. (2006) Incidence and epidemiology of irritable bowel syndrome after a large waterborne outbreak of bacterial dysentery. Gastroenterology 131, 445450.CrossRefGoogle ScholarPubMed
26.Hungin, AP, Whorwell, PJ, Tack, J et al. (2003) The prevalence, patterns and impact of irritable bowel syndrome: an international survey of 40,000 subjects. Aliment Pharmacol Ther 17, 643650.CrossRefGoogle Scholar
27.Hasler, WL (2003) Lactulose breath testing, bacterial overgrowth, and IBS: just a lot of hot air? Gastroenterology 125, 18981900.CrossRefGoogle ScholarPubMed
28.Mishkin, D & Mishkin, S (2001) Re: Pimentel et al. – Eradication of small intestinal bacterial overgrowth reduces symptoms of irritable bowel syndrome. Am J Gastroenterol 96, 25052506.CrossRefGoogle ScholarPubMed
29.Riordan, SM, McIver, CJ, Duncombe, VM et al. (2001) Small intestinal bacterial overgrowth and the irritable bowel syndrome. Am J Gastroenterol 96, 25062508.CrossRefGoogle ScholarPubMed
30.Walters, B & Vanner, SJ (2005) Detection of bacterial overgrowth in IBS using the lactulose H2 breath test: comparison with 14C-D-xylose and healthy controls. Am J Gastroenterol 100, 15661570.CrossRefGoogle ScholarPubMed
31.Posserud, I, Stotzer, PO, Bjornsson, ES et al. (2007) Small intestinal bacterial overgrowth in patients with irritable bowel syndrome. Gut 56, 802808.CrossRefGoogle ScholarPubMed
32.Sharara, AI, Aoun, E, Abdul-Baki, H et al. (2006) A randomized double-blind placebo-controlled trial of rifaximin in patients with abdominal bloating and flatulence. Am J Gastroenterol 101, 326333.CrossRefGoogle ScholarPubMed
33.Pimentel, M, Park, S, Mirocha, J et al. (2006) The effect of a nonabsorbed oral antibiotic (rifaximin) on the symptoms of the irritable bowel syndrome: a randomized trial. Ann Intern Med 145, 557563.Google ScholarPubMed
34.Drakes, M, Blanchard, T & Czinn, S (2004) Bacterial probiotic modulation of dendritic cells. Infect Immun 72, 32993309.CrossRefGoogle ScholarPubMed
35.Helwig, U, Lammers, KM, Rizzello, F et al. (2006) Lactobacilli, bifidobacteria and E. coli nissle induce pro- and anti-inflammatory cytokines in peripheral blood mononuclear cells. World J Gastroenterol 12, 59785986.CrossRefGoogle Scholar
36.Hudspith, BN, Rouzard, G, Gibson, GR et al. (2006) Probiotic bacteria inhibit epithelial cell IL-8 production: Role of TLR receptor engagement. Gut 55, Suppl. II, A38.Google Scholar
37.O'Mahony, L, McCarthy, J, Kelly, P et al. (2005) Lactobacillus and bifidobacterium in irritable bowel syndrome: symptom responses and relationship to cytokine profiles. Gastroenterology 128, 541551.CrossRefGoogle ScholarPubMed
38.Rousseaux, C, Thuru, X, Gelot, A et al. (2007) Lactobacillus acidophilus modulates intestinal pain and induces opioid and cannabinoid receptors. Nat Med 13, 3537.CrossRefGoogle ScholarPubMed
39.Verdu, EF, Bercik, P, Verma-Gandhu, M et al. (2006) Specific probiotic therapy attenuates antibiotic induced visceral hypersensitivity in mice. Gut 55, 182190.CrossRefGoogle ScholarPubMed
40.Caballero-Franco, C, Keller, K, De Simone, C et al. (2007) The VSL#3 probiotic formula induces mucin gene expression and secretion in colonic epithelial cells. Am J Physiol Gastrointest Liver Physiol 292, G315G322.CrossRefGoogle ScholarPubMed
41.Zeng, J, Li, YQ, Zuo, XL et al. (2008) Clinical trial: effect of active lactic acid bacteria on mucosal barrier function in patients with diarrhoea-predominant irritable bowel syndrome. Aliment Pharmacol Ther 28, 994–1002.CrossRefGoogle ScholarPubMed
42.Whitehead, WE, Corazziari, E, Prizont, R et al. (1999) Definition of a responder in clinical trials for functional gastrointestinal disorders: report on a symposium. Gut 45, Suppl. 2, II78II79.CrossRefGoogle Scholar
43.Dunlop, SP, Hebden, J, Campbell, E et al. (2006) Abnormal intestinal permeability in subgroups of diarrhea-predominant irritable bowel syndromes. Am J Gastroenterol 101, 12881294.CrossRefGoogle ScholarPubMed
44.Marshall, JK, Thabane, M, Garg, AX et al. (2004) Intestinal permeability in patients with irritable bowel syndrome after a waterborne outbreak of acute gastroenteritis in Walkerton, Ontario. Aliment Pharmacol Ther 20, 13171322.CrossRefGoogle ScholarPubMed
45.Moayyedi, P, Ford, AC, Talley, NJ et al. (2008) The efficacy of probiotics in the therapy of irritable bowel syndrome: a systematic review. Gut (Epublication ahead of print version; doi:10.1136/gut.2008.167270).Google ScholarPubMed
46.Brenner, DM, Moeller, MJ, Chey, WD et al. (2009) The utility of probiotics in the treatment of irritable bowel syndrome: a systematic review. Am J Gastroenterol 104, 10331049.CrossRefGoogle ScholarPubMed
47.McFarland, LV & Dublin, S (2008) Meta-analysis of probiotics for the treatment of irritable bowel syndrome. World J Gastroenterol 14, 26502661.CrossRefGoogle ScholarPubMed
48.Hoveyda, N, Heneghan, C, Mahtani, KR et al. (2009) A systematic review and meta-analysis: probiotics in the treatment of irritable bowel syndrome. BMC Gastroenterol 9, 15.CrossRefGoogle ScholarPubMed
49.Hun, L (2009) Bacillus coagulans significantly improved abdominal pain and bloating in patients with IBS. Postgrad Med 121, 119124.CrossRefGoogle ScholarPubMed
50.Enck, P, Zimmermann, K, Menke, G et al. (2008) A mixture of Escherichia coli (DSM 17252) and Enterococcus faecalis (DSM 16440) for treatment of the irritable bowel syndrome – a randomized controlled trial with primary care physicians. Neurogastroenterol Motil 20, 11031109.CrossRefGoogle ScholarPubMed
51.Bittner, AC, Croffut, RM & Stranahan, MC (2005) Prescript-assist™ probiotic-prebiotic treatment for irritable bowel syndrome: A methodologically oriented, 2-week, randomized, placebo-controlled, double-blind clinical study. Clin Ther 27, 755761.CrossRefGoogle ScholarPubMed
52.Long, ZR, Yu, CH, Yang, Y et al. (2006) [Clinical observation on acupuncture combined with microorganism pharmaceutical preparations for treatment of irritable bowel syndrome of constipation type] (article in Chinese). Zhongguo Zhen Jiu 26, 403405.Google Scholar
53.Bausserman, M & Michail, S (2005) The use of Lactobacillus GG in irritable bowel syndrome in children: a double-blind randomized control trial. J Pediatr 147, 197201.CrossRefGoogle Scholar
54.Kim, HJ, Vazquez Roque, MI, Camilleri, M et al. (2005) A randomized controlled trial of a probiotic combination VSL#3 and placebo in irritable bowel syndrome with bloating. Neurogastroenterol Motil 17, 687696.CrossRefGoogle ScholarPubMed
55.Niedzielin, K, Kordecki, H & Birkenfeld, B (2001) A controlled, double-blind, randomized study on the efficacy of Lactobacillus plantarum 299V in patients with irritable bowel syndrome. Eur J Gastroenterol Hepatol 13, 11431147.CrossRefGoogle Scholar
56.Niv, E, Naftali, T, Hallak, R et al. (2005) The efficacy of Lactobacillus reuteri ATCC 55730 in the treatment of patients with irritable bowel syndrome – a double blind, placebo-controlled, randomized study. Clin Nutr 24, 925931.CrossRefGoogle ScholarPubMed
57.Sen, S, Mullan, MM, Parker, TJ et al. (2002) Effect of Lactobacillus plantarum 299v on colonic fermentation and symptoms of irritable bowel syndrome. Dig Dis Sci 47, 26152620.CrossRefGoogle ScholarPubMed
58.Andriulli, A, Neri, M, Loguercio, C et al. (2008) Clinical trial on the efficacy of a new symbiotic formulation, Flortec, in patients with irritable bowel syndrome: a multicenter, randomized study. J Clin Gastroenterol 42, Suppl. 3, S218S223.CrossRefGoogle ScholarPubMed
59.Enck, P, Zimmermann, K, Menke, G et al. (2009) Randomized controlled treatment trial of irritable bowel syndrome with a probiotic E.-coli preparation (DSM17252) compared to placebo. Z Gastroenterol 47, 209214.CrossRefGoogle ScholarPubMed
60.Kajanda, K, Myllyluoma, E, Rajilic-Stojanovic, M et al. (2008) Clinical trial: multispecies probiotic supplementation alleviates the symptoms of irritable bowel syndrome and stabilizes intestinal microbiota. Aliment Pharmacol Ther 27, 4857.CrossRefGoogle Scholar
61.Whorwell, PJ, Altringer, L, Morel, J et al. (2006) Efficacy of an encapsulated probiotic Bifidobacterium infantis 35624 in women with irritable bowel syndrome. Am J Gastroenterol 101, 15811590.CrossRefGoogle ScholarPubMed
62.Nobaek, S, Johansson, ML, Molin, G et al. (2000) Alteration of intestinal microflora is associated with reduction in abdominal bloating and pain in patients with irritable bowel syndrome. Am J Gastroenterol 95, 12311238.CrossRefGoogle ScholarPubMed
63.Gawronska, A, Dziechciarz, P, Horvath, A et al. (2007) A randomized double-blind placebo-controlled trial of Lactobacillus GG for abdominal pain disorders in children. Aliment Pharmacol Ther 25, 177184.CrossRefGoogle ScholarPubMed
64.Huertas-Ceballos, AA, Logan, S, Bennett, C et al. (2009) Dietary interventions for recurrent abdominal pain (RAP) and irritable bowel syndrome (IBS) in childhood. Cochrane Database of Systematic Reviews 2009, issue 1, CD003019. Chichester, West Sussex: John Wiley and Sons, Ltd.Google Scholar
65.Kajanda, K, Hatakka, K, Poussa, T et al. (2005) A probiotic mixture alleviates symptoms in irritable bowel syndrome patients: a controlled 6-month intervention. Aliment Pharmacol Ther 22, 387394.CrossRefGoogle Scholar
66.Silk, DB, Davis, A, Vulevic, J et al. (2009) Clinical trial: the effects of a trans-galactooligosaccharide prebiotic on faecal microbiota and symptoms in irritable bowel syndrome. Aliment Pharmacol Ther 29, 508518.CrossRefGoogle ScholarPubMed
67.Sinn, DH, Song, JH, Kim, HJ et al. (2008) Therapeutic effect of Lactobacillus acidophilus-SDC 2012, 2013 in patients with irritable bowel syndrome. Dig Dis Sci 53, 27142718.CrossRefGoogle ScholarPubMed
68.Shanahan, F, Guarner, F, Von Wright, A et al. (2006) A one year, randomised, double-blind, placebo controlled trial of a lactobacillus or a bifidobacterium probiotic for maintenance of steroid-induced remission of ulcerative colitis. Gastroenterology 130, Suppl. 2, A44.Google Scholar
69.Drouault-Holowacz, S, Bieuvelet, S, Burckel, A et al. (2008) A double blind randomized controlled trial of a probiotic combination in 100 patients with irritable bowel syndrome. Gastroenterol Clin Biol 32, 147152.CrossRefGoogle ScholarPubMed
70.Guyonnet, D, Chassany, O, Ducrotte, P et al. (2007) Effect of a fermented milk containing Bifidobacterium animalis DN-173 010 on the health-related quality of life and symptoms in irritable bowel syndrome in adults in primary care: a multi-centre, randomized, double-blind, controlled trial. Aliment Pharmacol Ther 26, 475486.CrossRefGoogle Scholar
71.Thompson, WG, Drossman, D, Heaton, KW et al. (1989) Irritable bowel syndrome: guidelines for the diagnosis. Gastroenterology Int 2, 9295.Google Scholar
72.Smith, GD, Steinke, DT, Kinnear, M et al. (2004) A comparison of irritable bowel syndrome patients managed in primary and secondary care: the Episode IBS study. Br J Gen Pract 54, 503507.Google ScholarPubMed
73.Panijel, M & Burkhard, I (1993) Pro-Symbioflor zur Behandlung des irritablen Kolons (Pro-symbioflor for the treatment of irritable colon). Jatros Naturheilkunde 2, 14.Google Scholar
74.Manning, A, Thompson, W, Heaton, K et al. (1978). Towards positive diagnosis of the irritable bowel. Br Med J 2, 653654.CrossRefGoogle ScholarPubMed
75.Miele, E, Pascarella, F, Giannetti, E et al. (2009) Effect of a probiotic preparation (VSL#3) on induction and maintenance of remission in children with ulcerative colitis. Am J Gastroenterol 104, 437443.CrossRefGoogle ScholarPubMed
76.Gionchetti, P, Rizzello, F, Venturi, A et al. (2000) Oral bacteriotherapy as maintenance treatment in patients with chronic pouchitis: a double-blind, placebo-controlled trial. Gastroenterology 119, 305309.CrossRefGoogle ScholarPubMed
77.Gionchetti, P, Rizzello, F, Helwig, U et al. (2003) Prophylaxis of pouchitis onset with probiotic therapy: a double-blind, placebo-controlled trial. Gastroenterology 124, 12021209.CrossRefGoogle ScholarPubMed
78.Kim, HJ, Camilleri, M, McKinzie, S et al. (2003) A randomized controlled trial of a probiotic, VSL#3, on gut transit and symptoms in diarrhoea-predominant irritable bowel syndrome. Aliment Pharmacol Ther 17, 895904.CrossRefGoogle ScholarPubMed
79.Williams, E, Stimpson, J, Wang, D et al. (2009) Clinical trial: a multistrain probiotic preparation significantly reduces symptoms of irritable bowel syndrome in a double-blind placebo-controlled study. Aliment Pharmacol Ther 29, 97–103 (Epublication 9 September 2008).CrossRefGoogle Scholar
80.Tsuchiya, J, Barreto, R, Okura, R et al. (2004) Single-blind follow-up study on the effectiveness of a symbiotic preparation in irritable bowel syndrome. Chin J Dig Dis 5, 169174.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Summary of recent randomised controlled trials of probiotics in irritable bowel syndrome (IBS)