Effects of faecal microbiota transplantation on glycaemic outcomes in adults with metabolic disorders: a systematic review and meta-analysis of randomised controlled trials
6 affiliations
- 1Physiology Department, Danylo Halytsky Lviv National Medical University , ,
- 2Bogomolets National Medical University , ,
- 3Department of Therapy and Family Medicine, I. Horbachevsky Ternopil National Medical University , ,
- 4Department of Medical Rehabilitation, I. Horbachevsky Ternopil National Medical University , ,
- 5Department of Biochemistry and Pharmacology, Uzhhorod National University , ,
- 6Department of Microbiology, Virology, and Immunology, I. Horbachevsky Ternopil National Medical University , ,
Abstract
Background: Faecal microbiota transplantation (FMT) may improve glucose metabolism, but findings from randomised trials and previous meta-analyses are inconsistent. We evaluated the effects of FMT on glycaemic outcomes in adults with type 2 diabetes, prediabetes, insulin resistance or related metabolic disorders.
Methods: We searched PubMed and Scopus for English-language randomised controlled trials published from January 2000 to May 2026. The primary outcome was change from baseline in HOMA-IR. Secondary outcomes included HbA1c, fasting glucose and clamp-derived peripheral insulin sensitivity. Random-effects meta-analyses used Paule–Mandel estimation with Hartung–Knapp–Sidik–Jonkman confidence intervals. Sensitivity analyses evaluated comparator type, data reconstruction, the assumed baseline–follow-up correlation and individual-study influence. Risk of bias was assessed using RoB 2.
Results: The searches identified 887 records, and 18 studies met the eligibility criteria. Six trials involving 120 participants included to the primary analysis. FMT did not significantly reduce HOMA-IR compared with control (MD, −1.29; 95% CI [−3.04, 0.47]; I2 = 72%). The sensitivity analysis combining HOMA-IR and HOMA2-IR also produced a non-significant result (MD, −1.11; 95% CI [−2.50, 0.29]). HbA1c data were sparse and were not pooled across comparator types. Clamp-derived findings suggested a possible donor-phenotype effect but remained inconclusive. The certainty of evidence was very low for HOMA-IR and HbA1c and low for peripheral insulin sensitivity.
Conclusions: FMT did not demonstrate a clear benefit for glycaemic outcomes. The estimates were imprecise, heterogeneous and influenced by comparator design. Larger trials with standardised outcomes and predefined donor phenotypes are required.
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BibTeX
@article{savytska2026effects,
title = {{Effects of faecal microbiota transplantation on glycaemic outcomes in adults with metabolic disorders: a systematic review and meta-analysis of randomised controlled trials}},
author = {Maryana Savytska and Viktoriya-Svitlana Halich and Liudmyla Kuzmenko and Iryna Halabitska and Iryna Kamyshna and Pavlo Petakh and Oleksandr Kamyshnyi and Nazarii Kobyliak},
journal = {Frontiers in medicine},
year = {2026},
month = oct,
doi = {10.3389/fmed.2026.1983162},
url = {https://europepmc.org/article/PMC/PMC13719402},
note = {CC BY},
}
RIS
TY - JOUR
TI - Effects of faecal microbiota transplantation on glycaemic outcomes in adults with metabolic disorders: a systematic review and meta-analysis of randomised controlled trials
AU - Maryana Savytska
AU - Viktoriya-Svitlana Halich
AU - Liudmyla Kuzmenko
AU - Iryna Halabitska
AU - Iryna Kamyshna
AU - Pavlo Petakh
AU - Oleksandr Kamyshnyi
AU - Nazarii Kobyliak
PY - 2026
DA - 2026/10/16
JO - Frontiers in medicine
DO - 10.3389/fmed.2026.1983162
UR - https://europepmc.org/article/PMC/PMC13719402
AB - Background: Faecal microbiota transplantation (FMT) may improve glucose metabolism, but findings from randomised trials and previous meta-analyses are inconsistent. We evaluated the effects of FMT on glycaemic outcomes in adults with type 2 diabetes, prediabetes, insulin resistance or related metabolic disorders. Methods: We searched PubMed and Scopus for English-language randomised controlled trials published from January 2000 to May 2026. The primary outcome was change from baseline in HOMA-IR. Secondary outcomes included HbA1c, fasting glucose and clamp-derived peripheral insulin sensitivity. Random-effects meta-analyses used Paule–Mandel estimation with Hartung–Knapp–Sidik–Jonkman confidence intervals. Sensitivity analyses evaluated comparator type, data reconstruction, the assumed baseline–follow-up correlation and individual-study influence. Risk of bias was assessed using RoB 2. Results: The searches identified 887 records, and 18 studies met the eligibility criteria. Six trials involving 120 participants included to the primary analysis. FMT did not significantly reduce HOMA-IR compared with control (MD, −1.29; 95% CI [−3.04, 0.47]; I2 = 72%). The sensitivity analysis combining HOMA-IR and HOMA2-IR also produced a non-significant result (MD, −1.11; 95% CI [−2.50, 0.29]). HbA1c data were sparse and were not pooled across comparator types. Clamp-derived findings suggested a possible donor-phenotype effect but remained inconclusive. The certainty of evidence was very low for HOMA-IR and HbA1c and low for peripheral insulin sensitivity. Conclusions: FMT did not demonstrate a clear benefit for glycaemic outcomes. The estimates were imprecise, heterogeneous and influenced by comparator design. Larger trials with standardised outcomes and predefined donor phenotypes are required.
SN - 2296-858X
ER -