Skip to main content

Clinical efficacy and safety of faecal microbiota transplantation in the treatment of irritable bowel syndrome: a systematic review, meta-analysis and trial sequential analysis

Abstract

Background

The aim of this study is to evaluate the efficacy and safety of faecal microbiota transplantation (FMT) for the treatment of irritable bowel syndrome (IBS).

Methods

We searched four databases for randomised controlled trials (RCTs) that compared FMT with a control intervention in patients with IBS. The revised Cochrane risk-of-bias (RoB) tool was chosen for appraisal. Meta-analysis with trial sequential analysis (TSA) was conducted. Grading of Recommendations Assessment Development and Evaluation (GRADE) methodology was used to assess the certainty of evidence (CoE).

Results

We included 12 RCTs with a total of 615 participants. Meta-analyses showed no significant difference between the FMT and control groups in terms of clinical responses (relative risk [RR] = 1.44, 95% confidence interval [CI] 0.88–2.33) and changes in IBS Severity Scoring System (IBS-SSS) scores (standardised mean difference [SMD] =  − 0.31, 95% CI  − 0.72 to 0.09) and IBS Quality of Life (IBS-QOL) scores (SMD = 0.30, 95% CI  − 0.09 to 0.69). Subgroup analysis revealed that in studies with low RoB and using endoscopy, nasojejunal tube and rectal enema delivery, FMT led to a significant improvement in clinical responses and changes in IBS-SSS and IBS-QOL scores. TSA suggested that the current evidence is inconclusive and that the CoE is very low.

Conclusion

This study suggests that patients with IBS may benefit from FMT especially when it is administered via endoscopy, nasojejunal tube or rectal enema. However, the certainty of evidence is very low. Further research is needed to confirm the efficacy and safety of FMT for IBS treatment.

Trial Registration: PROSPERO registration number CRD42020211002.

Introduction

Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder characterised by abdominal pain and altered bowel habits, leading to considerable discomfort and impairing quality of life [1]. It affects a large proportion of the population, with prevalence rates ranging from 7 to 21% worldwide [2]. Despite its high prevalence, its underlying mechanisms are not yet fully understood, making developing effective treatments difficult [3].

Faecal microbiota transplantation (FMT) is a therapeutic intervention that involves the transfer of faecal microbiota from a healthy donor to a recipient with dysbiotic gut microbiota [4]. FMT is thought to work by restoring gut microbial diversity and function, which leads to an improvement in gastrointestinal and nongastrointestinal symptoms [5]. It has been used to treat a variety of disorders, including recurrent Clostridioides difficile infection (CDI), IBS, Parkinson’s disease and various inflammatory disorders [6]. In 2022, the FDA approved the first FMT therapy to prevent recurrent CDI in adults who previously completed antibiotic treatment [7]. This event represents a major milestone of FMT therapy.

Recent studies have suggested that alterations in gut microbiota may play a key role in the development and exacerbation of IBS symptoms [8]. The gut microbiota is a complex ecosystem of microorganisms that live in the gastrointestinal tract and has been shown to play a crucial role in maintaining gut homeostasis and overall health [9]. Dysbiosis or an imbalance in the gut microbiota has been associated with a variety of gastrointestinal disorders, including IBS [10]. This association has led to increasing interest in FMT as a potential therapy for IBS.

Although previous randomised controlled trials (RCTs) have evaluated the efficacy of FMT in IBS treatment, their results were inconsistent and limited by their small sample sizes [11,12,13,14,15,16,17,18,19,20,21,22]. Prior systematic reviews with meta-analyses of RCTs also have some limitations. Firstly, continuous outcomes, such as the IBS Severity Scoring System (IBS-SSS) and IBS Quality of Life (IBS-QOL), were pooled on the basis of their scores at the follow-up endpoint instead of the change in their scores from baseline [23, 24]. Furthermore, despite the existence of two different scoring systems for IBS-QOL in enrolled RCTs, the original scores, rather than the standardised mean difference (SMD), from each RCT were combined [24,25,26]. Last but not least, several new RCTs and full-text articles were not enrolled in previous meta-analyses [18,19,20]. We conducted an updated meta-analysis to provide a comprehensive and precise analysis of the available evidence on the efficacy and safety of FMT in treating IBS to address the above limitations. Our study also utilised trial sequential analysis (TSA) to provide a cautious evaluation of the data through repetitive and cumulative testing.

Methods

Literature searches and data sources

This systematic review and meta-analysis was conducted in accordance with the guidelines of the Cochrane Handbook of systematic reviews and followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement [27]. We comprehensively searched online literature by using Embase, MEDLINE, Cochrane CENTRAL, CINAHL and Scopus. All the searches were completed on June 20, 2024. In addition, we searched clinicaltrials.gov manually for potential unpublished trials. The database search terms consisted of ‘irritable colon’ OR ‘irritable bowel syndrome’ AND ‘faecal microbiota transplantation’. We limited the results to ‘randomised controlled trials’ and ‘human’. The detailed search methods are available in the Supplementary Materials (supplementary Table 1). No language restrictions were imposed. We also manually searched the references of the included studies for additional relevant citations. Any further information required from the original author was requested through written correspondence (e.g. emailing the corresponding or first author).

Study selection

Two authors (Shao-Wei, Lo and Tsung-Hsuan, Hung) independently screened the titles and abstracts then reviewed full texts and assessed the relevant studies for compliance with inclusion criteria. Any disagreement was resolved by discussion.

The inclusion criteria are as follows: (1) RCTs enrolling patients diagnosed with IBS by a clinician or on the basis of specific criteria, such as Rome Criteria or Manning. (2) Intervention with FMT at any dosage and through any route of administration and control group treated with a placebo or autologous transfer. (3) Primary outcomes included clinical response and changes in the severity of IBS symptoms, including IBS-SSS and IBS-QOL scores, and secondary outcomes included the safety and side effects of the intervention. The clinical response was the proportion of patients with clinical responses to the total examined patients and was defined as decreases of at least > 50 in IBS-SSS or > 30% in GSRS-IBS or adequate relief of global symptoms after 12 weeks.

The study design and protocol for this research were registered with PROSPERO. Approval was granted by its editorial team under registration number CRD42020211002.

Data extraction and quality assessment

Two authors (Yen-Tsen Lin and Tsung-Hsuan Hung) independently extracted the data, including publication year, origin country, study design, sample size, patients’ baseline characteristics, IBS diagnosis criteria and subtype, intervention type, primary and secondary outcomes, adverse events, follow-up information and exclusion and inclusion criteria from the included studies. Two authors (Shao-Wei Lo and Chun-Shen Lee) independently assessed quality by using the revised Cochrane Risk-of-Bias tool for Randomised Trials (RoB 2) [28]. The confidence levels of the outcome effect estimates were evaluated by grading the quality of evidence as low risk, some concern for risk or high risk. Any disagreement was resolved by discussion.

Statistical analysis

We used random-effects models to analyse pooled effect sizes and 95% confidence intervals (CIs) for all outcomes. For binary data, such as clinical response and adverse events, the meta-analysis used relative risk (RR). We analysed continuous data by using the standard mean difference (SMD) for the changes in IBS-SSS and IBS-QOL due to discrepancies amongst scales in the included studies. P-value < 0.05 was considered statistically significant. Heterogeneity was evaluated by using the I2 statistic [29].

TSA is a recently described cumulative frequentist meta-analysis method used to weigh type I and II errors and to provide information on the precision and uncertainty of the meta-analysis results. TSA also provides monitoring boundaries or futility boundaries to providing information on whether ongoing trials are necessary [30]. TSA version 0.9.5.10 beta was used in this study, and the details of model setting were mentioned in a previous report [31]. In summary, we analysed the data using a random-effects model via the Biggerstaff–Tweedie method, with a 5% type I error rate, 80% statistical power, and an improvement with a relative risk of 50%. The TSA result was presented as MD and α-spending adjusted CIs. We performed subgroup analysis on the basis of the following variables to explore possible causes leading to the heterogeneity of treatment effects: (1) the route of FMT delivery; (2) single or mixed donor samples; (3) fresh or frozen donor stool and (4) risk of bias (RoB) in the included studies. The differences in treatment effect were tested between subgroups, and P < 0.1 indicated a potential subgroup effect [27]. We detected publication bias with Egger’s test and funnel plots where more than 10 studies were present [32]. Data analysis and RoB plots were completed with Review Manager version 5.4 (Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2020).

Grading of the certainty of evidence

The certainty of evidence is the extent to which we can be confident that what the research tells us about a particular treatment effect is likely to be accurate. The levels of evidence of all outcomes were assessed on the basis of the Grading of Recommendations Assessment Development and Evaluation (GRADE) methodology [33]. The overall certainty of evidence (CoE) was evaluated in accordance with the GRADE handbook by downgrading it to five domains [33]. The CoE was judged as high, moderate, low or very low and was constructed by using the online GRADE Profiler (available from http://www.gradepro.org).

Results

Search results and study characteristics

Study selection is illustrated in Fig. 1. The initial literature search identified 639 potentially eligible articles. A total of 576 unique, relevant studies were retrieved after duplicate removal. After the titles and abstracts of the articles were screened, 71 eligible studies were retrieved and then subjected to full-text assessment. A total of 59 studies were excluded for various reasons, and 12 randomised trials were ultimately included in data extraction [11,12,13,14,15,16,17,18,19,20,21,22] (Fig. 1).

Fig. 1
figure 1

PRISMA 2020 flow diagram of study selection

The included trials were published between 2018 and 2023. When all the studies were combined, the total numbers of patients in the FMT and control groups were 356 and 259, respectively. A summary of the included studies and the baseline characteristics of the enrolled participants are presented in Table 1.

Table 1 The characteristics of included studies

RoB

The RoB assessment domains and authors’ judgments with justifications based on the RoB 2.0 tool were summarised (Supplementary Fig. 1). Five studies were of some concern for allocation bias because no information was available about concealment, [11, 16,17,18, 20]Additionally, one study [22] exhibited imbalanced baseline characteristics between the two groups post-randomisation, including age and baseline IBS severity, which could potentially confound the true effect. Only one study was rated with high RoB for the domain of performance bias because information about the blinding of the participants and personnel was unavailable and the authors did not appropriately analyse the effect of adherence. [18] Four studies were of some concern for RoB in the attrition bias domain due to their relatively high and unequal dropout rates without available explanations [12, 14, 19, 20]. Two studies were of some concern for detection bias because no information was available about the assessors being blinded. [16, 18] Overall, two of the included studies had low RoB [13, 15]; six were of some concern for RoB [12, 14, 17, 19, 20, 22]; and three had high RoB [11, 16, 18]. The RoB of the study of Aumpan et al., 2022 could not be assessed because only its abstract was published.

Outcome

Comparison of the clinical response of the FMT group with that of the control group after 12 weeks

The pooled effect showed no significant difference between the FMT and control groups in clinical response rate with high heterogeneity (RR = 1.44, 95% CI 0.88–2.33, I2 = 79%) (Fig. 2a). We further conducted subgroup analyses in accordance with the route of FMT delivery (Fig. 2a), the RoB of each study (Fig. 2b), the use of a single or mixed donor sample (Supplementary Fig. 2a) and fresh or frozen donor stool (Supplementary Fig. 2b) to explore potential heterogeneity. The clinical response of the group that received FMT via endoscopy (colonoscopy [12, 13, 16] and gastroscopy [15, 22]), nasojejunal tube [17] and rectal enema [21] was superior to that of the control group with moderate heterogeneity (RR = 1.91, 95% CI 1.26–2.91, I2 = 61%) (Fig. 2a). The pooled effect showed no statistically significant difference between FMT and the control administered via oral capsule [11, 14, 18, 20] (RR = 0.73, 95% CI 0.32–1.68, I2 = 70%) (Fig. 2a). Pooled data from RCTs with a low RoB revealed that the FMT group was superior to the control groups with low heterogeneity (RR = 3.53, 95% CI 2.21–5.64, I2 = 0%) (Fig. 2b) [13, 15]. By contrast, the pooled effect showed no statistically significant difference between the FMT and control groups in studies with some concerns [11, 12, 14, 17, 22] or high RoB [16, 18, 20] (RR = 1.07, 95% CI 0.69–1.65, I2 = 69%) (Fig. 2b).

Fig. 2
figure 2

Forest plot of the clinical responses of patients with IBS to FMT or the placebo. a Subgroup analysis based on the route of FMT delivery. b Subgroup analysis based on the RoB of a study. c TSA of the FMT treatment effect on patients with IBS

Because the subgroup analysis of FMT via direct delivery methods (including endoscopy, nasojejunal tube and rectal enema) showed more promising results, we performed further post hoc analysis by TSA in this subgroup. The Z-curves crossed the O'Brien–Fleming α-spending monitoring boundaries, indicating a potentially significant effect. Nevertheless, the sample size included in this subgroup analysis did not exceed the required information size, limiting the findings' strength (Fig. 2c).

Change in IBS‐SSS scores from the baseline after 8–12 weeks

The overall pooled estimates revealed no statistically significant difference in IBS-SSS scores after 8–12 weeks between the FMT and control groups with high heterogeneity (SMD =  − 0.31, 95% CI  − 0.72 to 0.09, I2 = 77%) (Fig. 3a). Subgroup analyses showed that FMT delivered via endoscopy [12, 13, 15, 16, 19, 22], nasojejunal tube and rectal enema had significantly reduced IBS-SSS scores after 8–12 weeks compared with the control with low heterogeneity (SMD =  − 0.43, 95% CI  − 0.73 to  − 0.13, I2 = 43%) (Fig. 3a). No statistically significant difference was found between the FMT and control groups treated with oral capsules [11, 14, 18, 20] (SMD =  − 0.16, 95% CI  − 1.22 to 0.90, I2 = 86%) (Fig. 3a). Pooled data from RCTs with a low RoB [13, 15] indicated that FMT was superior to the control with low heterogeneity (SMD =  − 0.66, 95% CI  − 0.99 to  − 0.33, I2 = 2%) (Fig. 3b).

Fig. 3
figure 3

Forest plot of the change in the IBS-SSS of patients with IBS in response to FMT or the placebo. a Subgroup analysis based on the route of FMT delivery. b Subgroup analysis based on the RoB in a study

Change in IBS‐QOL scores from the baseline after 8–12 weeks

Pooled estimates showed no statistically significant difference in IBS-QOL scores after 8–12 weeks between the FMT and control groups (SMD = 0.30, 95% CI  − 0.09 to 0.69, I2 = 68%) (Fig. 4a). Subgroup analyses demonstrated that FMT delivered via endoscopy [13, 15, 16], nasojejunal tube [17] and rectal enema significantly improved IBS-QOL scores after 8–12 weeks compared with the control (SMD = 0.53, 95% CI 0.20–0.86, I2 = 34%) (Fig. 4a). However, the pooled effect showed no statistically significant difference between the FMT and control delivered via oral capsule [11, 14, 18, 20] (SMD = 0.03, 95% CI  − 0.78 to 0.85, I2 = 79%) (Fig. 4a). Pooled data from RCTs with a low RoB [13, 15] showed that FMT was superior to the control with low heterogeneity (SMD = 0.77, 95% CI 0.45–1.09, I2 = 0%) (Fig. 4b).

Fig. 4
figure 4

Forest plot of the change in the IBS-QOL of patients with IBS in response to FMT or the placebo. a Subgroup analysis based on the route of FMT delivery. b Subgroup analysis based on the RoB of a study

Adverse events

Pooled analysis revealed no significant difference between the FMT and control groups in adverse events, including nausea, abdominal pain/cramping/tenderness, diarrhoea, constipation, bloating/flatulence and fever (Fig. 5).

Fig. 5
figure 5

Forest plot of the adverse events in patients with IBS in response to FMT or the placebo: a abdominal pain, b bloating/flatulence, c constipation, d diarrhea, e fever, f nausea

GRADE assessment

The certainty of evidence in consideration of the outcomes with clinical response and changes in IBS-SSS and IBS-QoL scores were all judged as ‘very low’ in accordance with GRADE criteria. We downgraded the CoE in the domain of risk of bias because more than half of the included studies were judged as having some concern to high RoB. We also downgraded in the domain of inconsistency due to high heterogeneity, and in the domain of imprecision due to wide confidence intervals. (Supplementary Table 2). Indirectness and publication bias were not considered with the Egger’s regression test (P = 0.72725) and the funnel plot showed no evidence of publication bias (Supplementary Fig. 3).

Discussion

IBS is a prevalent gastrointestinal disorder that significantly impacts patients' quality of life and imposes substantial economic burdens globally [34, 35]. Recent research has delved into the potential of microbiota-targeting treatments for IBS sufferers [36]. The rationale behind these interventions hinges on the direct influence of microbiota on the gut’s mucosal environment and their regulatory impact on the gut–brain communication pathway [36], aiming to preserve gut mucosal integrity, alter gut microbiome composition and mitigate inflammatory cytokine release [37, 38]. However, the definitive effectiveness and safety of FMT in IBS patients remain inconclusive.

To address this gap, our study performed a comprehensive systematic review and meta-analysis to explore the efficacy and safety of FMT in patients with IBS. We included updated studies and eventually identified 12 RCTs. In addition, we combined various scoring systems in IBS-QOL by using SMD while considering the changes in IBS-SSS and IBS-QOL scores from the baseline. We further strengthened our analysis by applying the rigorous TSA method to test the robustness of our findings. As a result, our study provides a highly reliable and insightful perspective on the effectiveness of FMT in IBS treatment.

Consistent with the meta-analyses published recently in 2022 and 2023, our study revealed no significant differences between the FMT and control groups in terms of clinical responses after 12 weeks [23, 24, 26, 39]. A similar result was shown in terms of the changes in IBS-SSS and IBS-QOL after 8–12 weeks. We also observed high heterogeneity amongst studies, suggesting that caution is needed in interpreting results. No serious adverse events were related to FMT in IBS. The GRADE assessments indicated that the CoE for all clinical outcomes in our study was very low.

Various delivery routes are currently utilised for FMT. They include oesophagogastroduodenoscopy; nasogastric, nasojejunal or nasoduodenal tube; colonoscopy; rectal enema and oral capsule delivery. Our subgroup analyses revealed that the route of FMT delivery significantly influenced its efficacy. FMT delivered via routes with more direct delivery to the gut, such as endoscopy, nasojejunal tube, or rectal enema, significantly improved all three outcomes, including clinical response, change in IBS-SSS and change in IBS-QOL compared to control. In contrast, oral capsule FMT did not demonstrate any benefits, suggesting that direct delivery to the target site may be more effective. Several biological and physiological factors may explain the superiority of direct delivery routes. Firstly, the live bacterial counts of FMT capsules range widely from 100 million bacteria per capsule to 100 billion bacteria per capsule and decline rapidly over time, reaching only 10% of their initial values after 24 hours [40]. This rapid decline in bacterial viability can significantly impact the effectiveness of the treatment. Secondly, the capsules expose bacteria to harsh gastric conditions, reducing bacterial viability and colonisation potential in the gut [41, 42]. Direct delivery methods like endoscopic, nasojejunal and rectal enema bypass the stomach, allowing for better survival and engraftment of the transplanted microbiota. [43] Thirdly, the gastrointestinal tract, particularly the lower intestines, is an anaerobic environment. Many of the beneficial gut microorganisms, such as obligate anaerobes, are highly sensitive to oxygen exposure [44]. Oral capsules may expose these anaerobic microorganisms to oxygen during transit through the upper gastrointestinal tract, potentially compromising their viability and functionality. Direct delivery minimises exposure to oxygen, maintaining the anaerobic environment necessary for these microorganisms to thrive. [45] Lastly, deviations from recommended protocols, such as using suboptimal doses or improper storage conditions, may have decreased the efficacy of oral capsule FMT in some studies. As noted previously by Rodrigues et al. [39] the recommended dose for a faecal transplant is 30 g. However, Aroniadis et al. administered less than the recommended dose. [14] In addition, Halkjaer et al. stored their final faecal suspensions at − 20 °C [11], whereas guidelines suggest storage at − 80 °C [46]. These deviations from the recommended protocol may have decreased the efficacy of oral capsule FMT, thereby diminishing the overall pooled effect of its efficacy.

Another emerging way to deliver FMT is colonic transendoscopic enteral tubing (TET), which has shown potential in treating various gut disorders, including IBS [47]. This procedure involves inserting a long, soft tube through the rectum into the colon using a colonoscope to infuse the faecal suspension directly into the colonic region. This tube allows for targeted infusion of the faecal suspension throughout the colonic region [47]. Compared to traditional colonoscopic delivery, TET is less invasive, better tolerated by patients and eliminates the need for full colon preparation [47]. Growing evidence suggests that administering FMT through a colonic TET could serve as a promising and more patient-friendly treatment strategy for patients with inflammatory bowel disease [47]. A recent prospective observational study by Zhang et al. demonstrated that washed microbiota transplantation delivered via mid-gut TET in 12 patients (16.4%) and colonic TET in 61 patients (83%) effectively improved both gastrointestinal and extraintestinal symptoms in individuals with IBS [48]. Despite these promising findings, further research through rigorous clinical trials specifically evaluating colonic TET-delivered FMT for IBS treatment is necessary.

The quality of the pooled studies could affect the reported effectiveness of FMT treatment. In our study, subgroup analysis based on overall RoB showed that in studies with a low RoB, the patients who received FMT had a significant improvement in all clinical outcomes, suggesting that methodological rigour is crucial in evaluating the true efficacy of FMT. Potential biases like inadequate allocation concealment, lack of blinding and high dropout rates may have obscured true effects in lower-quality studies. Further large-scale, high-quality RCTs are warranted to confirm the therapeutic role of FMT in the management of IBS.

Our study also analysed the effect of different faecal origins on FMT and its efficacy in patients with IBS. The results of subgroup analysis did not reveal a significant clinical response to FMT samples from single or mixed donors and in patients who received FMT using fresh, frozen or mixed stool samples. However, due to the limited sample size of our study, further research is needed to reach a conclusion on the preferable type of faeces.

The present study has several limitations. One major limitation is the heterogeneity of the enrolled participants, which persisted even after extensive subgroup analyses. This heterogeneity can be attributed to several factors. Firstly, the enrolled participants exhibited high heterogeneity, with variations in the diagnostic criteria employed IBS as well as the specific IBS subtypes represented. These RCTs included participants with different IBS subtypes (IBS-C, IBS-D, IBS-M, IBS-U) and most of the RCTs included a mixture of patients with differing IBS subtypes, which may respond differently to FMT due to varying underlying pathophysiologies. This variation makes it challenging to determine whether FMT efficacy differs among IBS subtypes. Future studies should focus on specific IBS subtypes to identify patient populations most likely to benefit from FMT.

Secondly, the inclusion criteria for symptom severity varied across studies. Some included participants with more severe IBS symptoms (e.g. IBS Symptom Severity Score (IBS-SSS) ≥ 175) [11, 12, 14, 15, 20], while others did not specify symptom severity criteria, potentially leading to differences in treatment response [13, 16, 18, 19, 21]. Furthermore, utilising different diagnostic criteria, Rome IV versus Rome III, leads to the inclusion of distinct patient populations with varying disease severities, as Rome IV criteria tend to identify individuals with a more severe clinical presentation of IBS [48, 49]. This discrepancy in the recruited cohorts based on diagnostic criteria introduces a fundamental difference in the study populations, complicating the interpretation and comparison of treatment outcomes across studies. Future studies should focus on implementing standardised symptom severity criteria and unified diagnostic standards (preferably Rome IV) across all trials. Studies are recommended to incorporate pre-planned subgroup and sensitivity analyses to evaluate the impact of different inclusion criteria on outcomes.

Thirdly, the FMT interventions differed in terms of their origin, dosage, therapy duration, frequency, comparators and study protocols, making it difficult to analyse and compare the results. The dosages of donor stool ranged from 25 capsules (50g) to a single dose of 30-80g, and the frequency of administration varied from a single dose to multiple doses over several days. The placebo interventions varied across studies, with some using autologous stool transplantation and others using inert capsules or solutions. These variations may differently impact the gut microbiota, placebo response and the relative efficacy of FMT. Additionally, several studies lacked clear reporting of the inclusion and exclusion criteria used for donor selection, which may limit the generalisability of the findings. To enhance consistency and reproducibility, future trials should adopt a comprehensive, standardised protocol that includes donor screening and selection, FMT dosage, frequency, duration and placebo interventions, all guided by the latest consensus statements on best practices for FMT [50,51,52].

The heterogeneity observed in our meta-analysis, arising from the diverse features discussed, underscores the complex and multifaceted nature of both IBS and FMT as a therapeutic intervention. Although this heterogeneity limits the robustness of our conclusions, it also offers valuable insights into the factors that may influence the efficacy of FMT in treating IBS.

Another limitation of our study is that the included RCTs primarily focused on gut-specific symptoms like abdominal pain, bloating and bowel habits (i.e. IBS-SSS) and their impacts on quality of life (i.e. IBS-QOL). However, it’s crucial to recognise that IBS is a multifaceted condition that affects more than just the gastrointestinal system, and these broader effects can significantly impair a patient’s quality of life [53]. Psychological distress, including anxiety and depression, is common among IBS patients, influencing various aspects like gut physiology and immune response through the gut–brain axis [54]. Unfortunately, most RCTs do not adequately capture these outcomes, leading to a high degree of variability among studies that do include them. Guo et al. focused on patients with IBS-D who also suffered from depression and anxiety [18]. Their findings revealed that FMT therapy reduced not only gastrointestinal symptoms but also anxiety and depression. [18] Conversely, studies by Aroniadis et al., Mazzawi et al., Holster et al. and Lahtinen et al. reported no significant effect of FMT on depression and anxiety [13, 14, 16, 19]. Notably, Mazzawi et al. and Lahtinen et al. did not provide baseline data on depression and anxiety [16, 19], and Holster et al. explicitly excluded patients with depression prior to intervention [13]. Factors like concurrent psychological disorders, diet variations, co-medications and follow-up care are often overlooked in current RCTs, potentially limiting the efficacy evaluation of FMT for IBS [55]. Future research should adopt a comprehensive approach, including standardised tools to assess not only gastrointestinal symptoms but also psychological health and other relevant outcomes.

Despite these limitations, our study provides valuable insights into the effectiveness of FMT for IBS treatment. While the overall pooled estimates did not show a significant benefit of FMT, the subgroup analyses suggest that FMT, particularly when delivered via endoscopy, nasojejunal tube, or rectal enema, and in well-designed studies, may be an effective treatment option for improving symptoms and quality of life in IBS patients. However, the certainty of evidence was rated as “very low” due to concerns about bias, heterogeneity and imprecision, indicating limited confidence in the effect estimates. The true effect may differ from the estimates presented in our meta-analysis. Although the TSA results for the most important outcome, clinical response, suggest that the current evidence is a true positive, the sample size remains insufficient to draw a definitive conclusion. This inadequacy in sample size leads to a downgrade in the GRADE assessment in the domain of imprecision. Further well-designed studies with more participants should strive to standardise study designs, donor screening, treatment protocols, outcome metrics and the stratification of participants by IBS subtype to enhance the consistency and applicability of FMT research in IBS. It is imperative to explore potential effect modifiers through pre-specified subgroup analyses and meta-regression, as well as to examine the long-term effects and safety of FMT, to effectively integrate these findings into clinical practice.

Conclusion

This study revealed that while the overall pooled estimates did not show a significant benefit of FMT for IBS, subgroup analyses revealed that FMT delivered via routes with more direct delivery to the gut, such as endoscopy, nasojejunal tube, or rectal enema, and in well-designed studies, may be an effective treatment option for improving symptoms and quality of life in IBS patients. The overall certainty of evidence was very low and the TSA indicated that the current evidence is inconclusive. Therefore, larger well-designed randomised controlled trials with rigorous methodology are warranted. Future studies should aim to standardise protocols for donor screening, treatment regimens and outcome assessments to enhance the consistency and clinical applicability of findings.

Availability of data and materials

Most of the data generated or analysed during this study are included in this published article and its supplementary information flies. Other datasets associated with the current study are available from the corresponding author on reasonable request.

References

  1. Lacy BE, Mearin F, Chang L, Chey WD, Lembo AJ, Simren M, et al. Bowel disorders. Gastroenterology. 2016;150(6):1393–407.

    Article  Google Scholar 

  2. Sperber AD, Dumitrascu D, Fukudo S, Gerson C, Ghoshal UC, Gwee KA, et al. The global prevalence of IBS in adults remains elusive due to the heterogeneity of studies: a Rome Foundation working team literature review. Gut. 2017;66(6):1075–82.

    Article  PubMed  Google Scholar 

  3. Glynn E, Galambosi G, Boland K. Resolution of weight loss, systemic illness, and fever after triple therapy: a surprising response to treatment of positive urease test. Gastroenterology. 2021;160(5):e1–3.

    Article  PubMed  CAS  Google Scholar 

  4. Kim KO, Gluck M. Fecal microbiota transplantation: an update on clinical practice. Clinical endoscopy. 2019;52(2):137–43.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Staley C, Khoruts A, Sadowsky MJ. Contemporary applications of fecal microbiota transplantation to treat intestinal diseases in humans. Arch Med Res. 2017;48(8):766–73.

    Article  PubMed  Google Scholar 

  6. Borody T, Fischer M, Mitchell S, Campbell J. Fecal microbiota transplantation in gastrointestinal disease: 2015 update and the road ahead. Expert Rev Gastroenterol Hepatol. 2015;9(11):1379–91.

    Article  PubMed  CAS  Google Scholar 

  7. U.S. Food and Drug Administration. Enforcement Policy Regarding Investigational New Drug Requirements for Use of Fecal Microbiota for Transplantation to Treat Clostridium difficile Infection Not Responsive to Standard Therapies. 2022. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/enforcement-policy-regarding-investigational-new-drug-requirements-use-fecal-microbiota.

  8. Wang L, Alammar N, Singh R, Nanavati J, Song Y, Chaudhary R, et al. Gut microbial dysbiosis in the irritable bowel syndrome: a systematic review and meta-analysis of case–control studies. J Acad Nutr Diet. 2020;120(4):565–86.

    Article  PubMed  Google Scholar 

  9. Ghaisas S, Maher J, Kanthasamy A. Gut microbiome in health and disease: linking the microbiome–gut–brain axis and environmental factors in the pathogenesis of systemic and neurodegenerative diseases. Pharmacol Ther. 2016;158:52–62.

    Article  PubMed  CAS  Google Scholar 

  10. Chang C, Lin H. Dysbiosis in gastrointestinal disorders. Best Pract Res Clin Gastroenterol. 2016;30(1):3–15.

    Article  PubMed  Google Scholar 

  11. Halkjær SI, Christensen AH, Lo BZS, Browne PD, Günther S, Hansen LH, et al. Faecal microbiota transplantation alters gut microbiota in patients with irritable bowel syndrome: results from a randomised, double-blind placebo-controlled study. Gut. 2018;67(12):2107–15.

    Article  PubMed  Google Scholar 

  12. Johnsen PH, Hilpüsch F, Cavanagh JP, Leikanger IS, Kolstad C, Valle PC, et al. Faecal microbiota transplantation versus placebo for moderate-to-severe irritable bowel syndrome: a double-blind, randomised, placebo-controlled, parallel-group, single-centre trial. Lancet Gastroenterol Hepatol. 2018;3(1):17–24.

    Article  PubMed  Google Scholar 

  13. Holster S, Lindqvist CM, Repsilber D, Salonen A, de Vos WM, König J, et al. The effect of allogenic versus autologous fecal microbiota transfer on symptoms, visceral perception and fecal and mucosal microbiota in irritable bowel syndrome: a randomized controlled study. Clin Transl Gastroenterol. 2019;10(4):e00034.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Aroniadis OC, Brandt LJ, Oneto C, Feuerstadt P, Sherman A, Wolkoff AW, et al. Faecal microbiota transplantation for diarrhoea-predominant irritable bowel syndrome: a double-blind, randomised, placebo-controlled trial. Lancet Gastroenterol Hepatol. 2019;4(9):675–85.

    Article  PubMed  Google Scholar 

  15. El-Salhy M, Hatlebakk JG, Gilja OH, Kristoffersen AB, Hausken T. Efficacy of faecal microbiota transplantation for patients with irritable bowel syndrome in a randomised, double-blind, placebo-controlled study. Gut. 2020;69(5):859–67.

    Article  PubMed  CAS  Google Scholar 

  16. Lahtinen P, Jalanka J, Hartikainen A, Mattila E, Hillilä M, Punkkinen J, et al. Randomised clinical trial: faecal microbiota transplantation versus autologous placebo administered via colonoscopy in irritable bowel syndrome. Aliment Pharmacol Ther. 2020;51(12):1321–31.

    Article  PubMed  CAS  Google Scholar 

  17. Holvoet T, Joossens M, Vázquez-Castellanos JF, Christiaens E, Heyerick L, Boelens J, et al. Fecal microbiota transplantation reduces symptoms in some patients with irritable bowel syndrome with predominant abdominal bloating: short-and long-term results from a placebo-controlled randomized trial. Gastroenterology. 2021;160(1):145–57.

    Article  PubMed  CAS  Google Scholar 

  18. Guo Q, Lin H, Chen P, Tan S, Wen Z, Lin L, et al. Dynamic changes of intestinal flora in patients with irritable bowel syndrome combined with anxiety and depression after oral administration of enterobacteria capsules. Bioengineered. 2021;12(2):11885–97.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  19. Mazzawi T, Hausken T, Refsnes PF, Hatlebakk JG, Lied GA. The effect of anaerobically cultivated human intestinal microbiota compared to fecal microbiota transplantation on gut microbiota profile and symptoms of irritable bowel syndrome, a double-blind placebo-controlled study. Microorganisms. 2022;10(9):1819.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  20. Singh P, Alm EJ, Kelley JM, Cheng V, Smith M, Kassam Z, et al. Effect of antibiotic pretreatment on bacterial engraftment after Fecal Microbiota Transplant (FMT) in IBS-D. Gut microbes. 2022;14(1):2020067.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Aumpan N, Pornthisarn B, Chonprasertsuk S, Siramolpiwat S, Bhanthumkomol P, Nunanan P, et al. Effect of fecal microbiota transplantation (FMT) on irritable bowel syndrome (IBS): a randomized, placebo-controlled, double-blind study. Gastroenterology. 2022;162(7):S936–7.

    Article  Google Scholar 

  22. Yau YK, Su Q, Xu Z, Lin H, Chen P, Tan S, et al. Randomised clinical trial: faecal microbiota transplantation for irritable bowel syndrome with diarrhoea. Aliment Pharmacol Ther. 2023;58(8):795–804. https://doi.org/10.1111/apt.17703.

    Article  PubMed  CAS  Google Scholar 

  23. Samuthpongtorn C, Kantagowit P, Pittayanon R, Patcharatrakul T, Gonlachanvit S. Fecal microbiota transplantation in irritable bowel syndrome: a meta-analysis of randomized controlled trials. Front Med. 2022. https://doi.org/10.3389/fmed.2022.1039284.

    Article  Google Scholar 

  24. Wu J, Lv L, Wang C. Efficacy of fecal microbiota transplantation in irritable bowel syndrome: a meta-analysis of randomized controlled trials. Front Cell Infect Microbiol. 2022. https://doi.org/10.3389/fcimb.2022.827395.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Elhusein AM, Fadlalmola HA. Efficacy of fecal microbiota transplantation in irritable bowel syndrome patients: an updated systematic review and meta-analysis. Gastroenterol Nurs. 2022;45(1):11–20.

    Article  PubMed  Google Scholar 

  26. Abdelghafar YA, AbdelQadir YH, Motawea KR, Nasr SA, Omran HAM, Belal MM, et al. Efficacy and safety of fecal microbiota transplant in irritable bowel syndrome: an update based on meta-analysis of randomized control trials. Health Sci Rep. 2022;5(5):e814.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Balduzzi S, Rücker G, Schwarzer G. How to perform a meta-analysis with R: a practical tutorial. BMJ Ment Health. 2019;22(4):153–60.

    Google Scholar 

  28. Sterne JA, Savović J, Page MJ, Elbers RG, Blencowe NS, Boutron I, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019. https://doi.org/10.1136/bmj.l4898.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Higgins J, Tompson S, Deeks J, Altman D. A meta-analysis on the effectiveness of smart-learning. BMJ. 2003;327(1):557–60.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Kang H. Trial sequential analysis: novel approach for meta-analysis. Anesth Pain Med. 2021;16(2):138–50.

    Article  Google Scholar 

  31. Chen P-C, Lai C-H, Fang C-J, Lai PC, Huang YT. Intravenous infusion of lidocaine for bowel function recovery after major colorectal surgery: a critical appraisal through updated meta-analysis, trial sequential analysis, certainty of evidence, and meta-regression. Front Med. 2022. https://doi.org/10.3389/fmed.2021.759215.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Sterna J, Sutton A, Ioannidis J, Terrin N, Jones D, Lau J, et al. Recommendations for examining und interpreting funnel plot asymmetry in metaanalyses of randomized controlled trials. BMJ. 2011;343:d4002.

    Article  Google Scholar 

  33. Group GW. Grading quality of evidence and strength of recommendations. BMJ. 2004;328(7454):1490.

    Article  Google Scholar 

  34. Peery AF, Crockett SD, Murphy CC, et al. Burden and cost of gastrointestinal, liver, and pancreatic diseases in the United States: update 2021. Gastroenterology. 2022;162(2):621–44.

    Article  PubMed  Google Scholar 

  35. Black CJ, Ford AC. Global burden of irritable bowel syndrome: trends, predictions and risk factors. Nat Rev Gastroenterol Hepatol. 2020;17(8):473–86.

    Article  PubMed  Google Scholar 

  36. Ghaffari P, Shoaie S, Nielsen LK. Irritable bowel syndrome and microbiome; switching from conventional diagnosis and therapies to personalized interventions. J Transl Med. 2022;20(1):173.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Simon E, Călinoiu LF, Mitrea L, Vodnar DC. Probiotics, prebiotics, and synbiotics: implications and beneficial effects against irritable bowel syndrome. Nutrients. 2021;13(6):2112.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  38. Singh P, Lembo A. Emerging role of the gut microbiome in irritable bowel syndrome. Gastroenterol Clin North Am. 2021;50(3):523–45.

    Article  PubMed  Google Scholar 

  39. Rodrigues T, Rodrigues Fialho S, Araújo JR, Rocha R, Moreira-Rosário A. Procedures in fecal microbiota transplantation for treating irritable bowel syndrome: systematic review and meta-analysis. J Clin Med. 2023;12(5):1725.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Verdier C, Denis S, Gasc C, Boucinha L, Uriot O, Delmas D, et al. An oral FMT capsule as efficient as an enema for microbiota reconstruction following disruption by antibiotics, as assessed in an in vitro human gut model. Microorganisms. 2021;9(2):358.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  41. Gulati M, Singh SK, Corrie L, Kaur IP, Chandwani L. Delivery routes for faecal microbiota transplants: available, anticipated and aspired. Pharmacol Res. 2020;159:104954.

    Article  PubMed  Google Scholar 

  42. Furuya-Kanamori L, Paterson DL, Helms SK, Yakob L, McKenzie SJ, Garborg K, et al. Upper versus lower gastrointestinal delivery for transplantation of fecal microbiota in recurrent or refractory Clostridium difficile infection. J Clin Gastroenterol. 2017;51(2):145–50.

    Article  PubMed  Google Scholar 

  43. Ianiro G, Maida M, Burisch J, et al. Efficacy of different faecal microbiota transplantation protocols for Clostridium difficile infection: a systematic review and meta-analysis. United Eur Gastroenterol J. 2018;6(8):1232–44.

    Article  Google Scholar 

  44. Maier E, Anderson RC, Roy NC. Understanding how commensal obligate anaerobic bacteria regulate immune functions in the large intestine. Nutrients. 2014;7(1):45–73.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Fadda HM. The route to palatable fecal microbiota transplantation. AAPS PharmSciTech. 2020;21(3):114.

    Article  PubMed  Google Scholar 

  46. Costello SP, Conlon MA, Vuaran MS, Roberts-Thomson IC, Andrews JM. Faecal microbiota transplant for recurrent Clostridium difficile infection using long-term frozen stool is effective: clinical efficacy and bacterial viability data. Aliment Pharmacol Ther. 2015;42(8):1011–8.

    Article  PubMed  CAS  Google Scholar 

  47. Wang W, Lu G, Wu X, Wen Q, Zhang F. Colonic transendoscopic enteral tubing is a new pathway to microbial therapy, colonic drainage, and host-microbiota interaction research. J Clin Med. 2023;12(3):780.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  48. Keller JJ, Ooijevaar RE, Hvas CL, et al. A standardised model for stool banking for faecal microbiota transplantation: a consensus report from a multidisciplinary UEG working group. United Eur Gastroenterol J. 2021;9(2):229–47.

    Article  Google Scholar 

  49. Barberio B, Houghton LA, Yiannakou Y, et al. Symptom stability in Rome IV vs. Rome III irritable bowel syndrome. Am J Gastroenterol. 2021;116:362–71.

    Article  PubMed  Google Scholar 

  50. Zhang Z, Li Q, Zhang S, et al. Washed microbiota transplantation targeting both gastrointestinal and extraintestinal symptoms in patients with irritable bowel syndrome. Prog Neuropsychopharmacol Biol Psychiatry. 2023;127:110839.

    Article  PubMed  Google Scholar 

  51. Cammarota G, Ianiro G, Kelly CR, et al. International consensus conference on stool banking for faecal microbiota transplantation in clinical practice. Gut. 2019;68(12):2111–21.

    Article  PubMed  CAS  Google Scholar 

  52. Haifer C, Kelly CR, Paramsothy S, et al. Australian consensus statements for the regulation, production and use of faecal microbiota transplantation in clinical practice. Gut. 2020;69(5):801–10.

    Article  PubMed  Google Scholar 

  53. Goodoory VC, Houghton LA, Yiannakou Y, et al. Natural history and disease impact of Rome IV vs. Rome III irritable bowel syndrome: a longitudinal follow-up study. Clin Gastroenterol Hepatol. 2022;20:569–77.

    Article  PubMed  Google Scholar 

  54. Hillestad EMR, van der Meeren A, Nagaraja BH, et al. Gut bless you: the microbiota–gut–brain axis in irritable bowel syndrome. World J Gastroenterol. 2022;28(4):412–31.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  55. Camilleri M. Diagnosis and treatment of irritable bowel syndrome: a review. JAMA. 2021;325(9):865–77.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

None.

Funding

This work was supported by the Higher Education Sprout Project, Ministry of Education to the Headquarters of University Advancement at National Cheng Kung University; National Cheng Kung University Hospital under Grant NCKUH-11209002, NCKUH-11203014.

Author information

Authors and Affiliations

Authors

Contributions

Chiung-Yu Chen and Pei Chun Lai conducted the concept of the study. Sha-Wei Lo, Tsung Hsuan Hung and Ching-Ju Fang performed the search. Sha-Wei Lo and Chun-Shen Lee performed quality assessment. Yen Tsen Lin and Tsung Hsuan Hung extract the data and prepared the figures. Sha-Wei Lo, Tsung Hsuan Hung and Pei Chun Lai wrote the main manuscript text. All authors reviewed the manuscript.

Corresponding author

Correspondence to Pei-Chun Lai.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

All authors have agreed to the publication of this manuscript.

Competing interests

The authors report there are no competing interests to declare.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Supplementary material 1: Table 1. Search strategy

Supplementary material 2: Table 2. GRADE evidence profile: FMT for patients with IBS

Supplementary material 3: Figure 1. RoB summary

40001_2024_2046_MOESM4_ESM.tif

Supplementary material 4: Figure 2. Forest plot of the clinical responses of patients with IBS to FMT or the placeboSubgroup analysis based on FMT samples from single or mixed donor stoolSubgroup analysis based on FMT stool from a fresh, frozen or mixed sample

Supplementary material 5: Figure 3. Funnel plot with Egger’s test

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lo, SW., Hung, TH., Lin, YT. et al. Clinical efficacy and safety of faecal microbiota transplantation in the treatment of irritable bowel syndrome: a systematic review, meta-analysis and trial sequential analysis. Eur J Med Res 29, 464 (2024). https://doi.org/10.1186/s40001-024-02046-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s40001-024-02046-5

Keywords