Evidence map›Paper›PMID 21637034›Full record

GuidelineGut microbes

Responders and non-responders to probiotic interventions: how can we improve the odds?

Gregor Reid, Estelle Gaudier, Francisco Guarner, Gary B Huffnagle, Jean M Macklaim, Alicia M Munoz, Margaret Martini, Tamar Ringel-Kulka, Balfour Sartor, Robert Unal and 3 more

Abstract readConsensus StatementPractice Guideline
In one paragraph

Guideline in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Review
  8. Article
  9. Microorganisms · 2026
    Article
  10. Microorganisms · 2026
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review article: the future of microbiome-based therapeutics.Alimentary pharmacology & therapeutics · 2022
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Gregor ReidLawson Health Research Institute Probiotics, London, Ontario, Canada. gregor@uwo.ca
Estelle Gaudier
Francisco Guarner
Gary B Huffnagle
Jean M Macklaim
Alicia M Munoz
Margaret Martini
Tamar Ringel-Kulka
Balfour Sartor
Robert Unal
Kristin Verbeke
Jens Walter
International Scientific Association for Probiotics and Prebiotics

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As with many clinical studies, trials using probiotics have shown clearly that some patients benefit from the treatment while others do not. For example if treatment with probiotics leads to 36% cure rate of diarrhea, why did the other 64% not have the same result? The issue is important for human and indeed experimental animal studies for two main reasons: (i) Would changing the design of the study result in more subjects responding to treatment? (ii) If a subject does not respond what are the mechanistic reasons? In order to tackle the issue of responders and non-responders to therapy, a workshop was held by the International Scientific Association for Probiotics and Prebiotics (ISAPP). The outcome was four recommendations. 1. Clearly define the end goal: this could be supporting a health claim or having the highest clinical effect and impact. 2. Design the study to maximize the chance of a positive response by identifying precise parameters and defining the level of response that will be tested. 3. Base the selection of the intervention on scientific investigations: which strain(s) and/or product formulation should be used and why. 4. Carefully select the study cohort: use biological or genetic markers when available to stratify the patient population before enrollment and decide at what point intervention will provide the best outcome (for example, in acute phase of disease, or during remission, with or without use of pharmaceutical agents). By following these recommendations and selecting an appropriate primary outcome, it is hoped that clinical data will emerge in the future that expands our knowledge of which probiotics benefits which subjects and by what mechanism.

Indexed as

Clinical Trials as TopicTreatment OutcomeAnimalsDiarrheaHumansProbioticsclinical trial designnon-respondersprebioticsprobioticsresponders

Identifiers

PMID21637034
PMCPMC3023600

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.