TY - JOUR
T1 - Efficacy and safety of microbiota-Targeted therapeutics in autoimmune and inflammatory rheumatic diseases
T2 - Protocol for a systematic review and meta-Analysis of randomised controlled trials
AU - Kragsnaes, Maja Skov
AU - Gilbert, Benoit Thomas P.
AU - Sofíudóttir, Bjørk Khaliqi
AU - Rooney, Christopher Michael
AU - Hansen, Sebrina Maj Britt
AU - Mauro, Daniele
AU - Mullish, Benjamin H.
AU - Bergot, Anne Sophie
AU - Mankia, Kulveer Singh
AU - Goel, Niti
AU - Bakland, Gunnstein
AU - Johnsen, Peter Holger
AU - Blanco, Jesus Miguens
AU - Li, Simone
AU - Dumas, Emilie
AU - Lage-Hansen, Philip Rask
AU - Wagenaar, Carlijn
AU - Bakdash, Ghaith
AU - Robinson, Mat
AU - Kristiansen, Karsten
AU - Marchesi, Julian R.
AU - Schett, Georg
AU - Zaiss, Mario M.
AU - Orlu, Mine
AU - Van Schaadenburg, Dirkjan
AU - Scher, Jose U.
AU - McGonagle, Dennis
AU - Elewaut, Dirk
AU - Breban, Maxime
AU - Tugwell, Peter
AU - Finckh, Axel
AU - Ciccia, Francesco
AU - Kriegel, Martin A.
AU - Daien, Claire
AU - Ellingsen, Torkell
AU - Christensen, Robin
N1 - Publisher Copyright:
© 2025 BMJ Publishing Group. All rights reserved.
PY - 2025/12/14
Y1 - 2025/12/14
N2 - Introduction An abnormal composition of gut bacteria along with alterations in microbial metabolites and reduced gut barrier integrity has been associated with the pathogenesis of chronic autoimmune and inflammatory rheumatic diseases (AIRDs). The aim of the systematic review, for which this protocol is presented, is to evaluate the clinical benefits and potential harms of therapies targeting the intestinal microbiota and/or gut barrier function in AIRDs to inform clinical practice and future research. Methods and analysis This protocol used the reporting guidelines from the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocol. We will search Embase (Ovid), Medline (Ovid) and the Cochrane Library (Central) for reports of randomised controlled trials of patients diagnosed with an AIRD. Eligible interventions are therapies targeting the intestinal microbiota and/or gut barrier function including probiotics, synbiotics, faecal microbiota transplantation, live biotherapeutic products and antibiotics with the intent to modify disease activity in AIRDs. The primary outcome of the evidence synthesis will be based on the primary endpoint of each trial. Secondary efficacy outcomes will be evaluated and selected from the existing core domain sets of the individual diseases and include the following domains: disease control, patient global assessment, physician global assessment, health-related quality of life, fatigue, pain and inflammation. Harms will include the total number of withdrawals, withdrawals due to adverse events, number of patients with serious adverse events, disease flares and deaths. A meta-Analysis will be performed for each outcome domain separately. Depending on the type of outcome, the quantitative synthesis will encompass both ORs and standardised mean differences with corresponding 95% CIs. Ethics and dissemination No ethics approval will be needed for this systematic review. We will follow the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines to disseminate the study results through a peer-reviewed publication. PROSPERO registration number CRD42025644244.
AB - Introduction An abnormal composition of gut bacteria along with alterations in microbial metabolites and reduced gut barrier integrity has been associated with the pathogenesis of chronic autoimmune and inflammatory rheumatic diseases (AIRDs). The aim of the systematic review, for which this protocol is presented, is to evaluate the clinical benefits and potential harms of therapies targeting the intestinal microbiota and/or gut barrier function in AIRDs to inform clinical practice and future research. Methods and analysis This protocol used the reporting guidelines from the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocol. We will search Embase (Ovid), Medline (Ovid) and the Cochrane Library (Central) for reports of randomised controlled trials of patients diagnosed with an AIRD. Eligible interventions are therapies targeting the intestinal microbiota and/or gut barrier function including probiotics, synbiotics, faecal microbiota transplantation, live biotherapeutic products and antibiotics with the intent to modify disease activity in AIRDs. The primary outcome of the evidence synthesis will be based on the primary endpoint of each trial. Secondary efficacy outcomes will be evaluated and selected from the existing core domain sets of the individual diseases and include the following domains: disease control, patient global assessment, physician global assessment, health-related quality of life, fatigue, pain and inflammation. Harms will include the total number of withdrawals, withdrawals due to adverse events, number of patients with serious adverse events, disease flares and deaths. A meta-Analysis will be performed for each outcome domain separately. Depending on the type of outcome, the quantitative synthesis will encompass both ORs and standardised mean differences with corresponding 95% CIs. Ethics and dissemination No ethics approval will be needed for this systematic review. We will follow the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines to disseminate the study results through a peer-reviewed publication. PROSPERO registration number CRD42025644244.
KW - Antibiotics
KW - Inflammation
KW - Meta-Analysis
KW - Microbiota
KW - RHEUMATOLOGY
KW - Systematic Review
KW - Meta-Analysis as Topic
KW - Probiotics/therapeutic use
KW - Humans
KW - Gastrointestinal Microbiome
KW - Autoimmune Diseases/therapy
KW - Fecal Microbiota Transplantation
KW - Randomized Controlled Trials as Topic
KW - Systematic Reviews as Topic
KW - Rheumatic Diseases/therapy
KW - Research Design
KW - Anti-Bacterial Agents/therapeutic use
UR - https://www.scopus.com/pages/publications/105024983764
U2 - 10.1136/bmjopen-2025-101593
DO - 10.1136/bmjopen-2025-101593
M3 - Review
C2 - 41397742
AN - SCOPUS:105024983764
SN - 2399-9772
VL - 15
JO - BMJ Open
JF - BMJ Open
IS - 12
M1 - e101593
ER -