Cross-sectional studycited by the Tayebat archiveabstract only checked A-PPI-16 standard review

PPIs and the gut microbiome (Netherlands)

Proton pump inhibitors affect the gut microbiome.

Overview

Imhann F et al.. Gut 2016 · PMID 26657899 · DOI 10.1136/gutjnl-2015-310376

PPI users had less diverse gut bacteria and more potentially harmful bacteria.

Does the study support the specific claim? Yes · Methodological quality: moderate

Original publication

Plain-language summary

Study explained simply
What did the researchers want to find out?

Microbiome.

How was the study done?

3 cohorts.

How many people, animals or samples were studied?

1,815.

What was actually found?

Shifts in 20% of taxa.

What do the results mean in everyday life?

Possible infection link.

What are the study's limitations?

Cross-sectional.

What does it say about Elawady's specific claim?

Supports.

Do the results apply to Germany and Europe?

Dutch.

What can explicitly not be concluded from this study?

Disease.

Scientific in-depth review

1. Full reference

Authors
Imhann F, Bonder MJ, Vich Vila A, Fu J, Mujagic Z, Vork L, Tigchelaar EF, Jankipersadsing SA, Cenit MC, Harmsen HJ, Dijkstra G, Franke L, Xavier RJ, Jonkers D, Wijmenga C, Weersma RK, Zhernakova A
Journal
Gut
Year
2016
Identifier
PMID 26657899 DOI 10.1136/gutjnl-2015-310376 · PMC4853569
Verification
verified – PubMed E-utilities efetch, 2026-10-25
Retracted
no
Corrections
none
Extent checked
abstract only
Conflicts of interest and funding

not stated in abstract; grants: NIDDK NIH HHS

2. Research question

Influence of PPI use on gut microbiome

3. Study design and population

Study design
Cross-sectional study – Three population cohorts, 16S rRNA sequencing, meta-analysis
Population

Three Dutch cohorts

Country

Netherlands

Sample size

1,815 (211 PPI users)

Inclusion and exclusion criteria

see abstract

4. Methods and endpoints

Exposure / intervention

Current PPI use

Comparator

Non-use

Endpoints

Microbiome diversity and taxa

Statistical methods

Per-cohort analysis then meta-analysis; FDR

5. Actual results

Results

Decreased Shannon diversity; changes in 20% of taxa; oral bacteria (Rothia, p=9.8×10⁻³⁸); more Enterococcus, Streptococcus, Staphylococcus, E. coli.

Absolute risks

not reported in abstract

Authors' conclusion

PPI-associated changes point toward a less healthy microbiome; effects more prominent than antibiotics at population level.

6. Strengths

  • Three cohorts
  • Meta-analysis

7. Weaknesses

  • Cross-sectional
  • Composition ≠ outcome

8. Risk of bias

Orienting tool
ROBINS-E
Type of assessment
simplified assessment (abstract only)
Full formal assessment
no
Overall risk of bias
some concerns
Rationale

Cross-sectional; confounding possible.

9. Assessment of the statistical interpretation

Modest relative risks from observational data; see bias notes.

10. Relevance to the specific claim

C-PPI-02.

11. Independent contrary findings

12. Transferability to Germany and Europe

High: European (Swedish, UK, Dutch, German) data show similar associations; PPIs are widely used in Germany.

13. Overall methodological judgement

Consistent with A-PPI-15.

Multidimensional assessment
Multidimensional assessment
Authenticity of the sourceverified
Methodological qualitymoderate
Risk of biassome concerns
Precision of resultsnot applicable
Directnessindirect
Reproducibilityreplicated
Consistency with the overall evidenceconsistent
Regional transferabilityhigh
Adequacy of the interpretation (by the archive)correctly reported

14. Open questions

15. Linked fact checks

Use by the Tayebat archive

Note: according to the archive, the studies were compiled by the archive operators. Whether Dr. Elawady himself cited this study is not established.

What the archive says about the study

Listed in the archive bibliography of the acid-blockers rule without its own interpretation; used implicitly to support the rule summary ('long-term suppression turns against the body: CKD, bacterial overgrowth, C. difficile, pneumonia, B12 and magnesium deficiency, hip fractures, microbiome change, excess mortality').

A. What was actually studied?

Influence of PPI use on gut microbiome

B. What did the authors find?

Decreased Shannon diversity; changes in 20% of taxa; oral bacteria (Rothia, p=9.8×10⁻³⁸); more Enterococcus, Streptococcus, Staphylococcus, E. coli.

C. What conclusions do the authors themselves draw?

PPI-associated changes point toward a less healthy microbiome; effects more prominent than antibiotics at population level.

D. What does the archive derive from it?

Supports microbiome change.

E. Is this derivation scientifically justified?

Yes.

Adequacy of the interpretation (by the archive)
correctly reported