Microbiota-Driven Strategies for Managing IBD-Associated Risks: From Infections to Mental Health

Inflammatory bowel diseases (IBD) are increasingly acknowledged not merely as confined gastrointestinal disorders but as systemic immunometabolic syndromes. Central to this paradigm is the gut microbiota including non-bacterial components such as the virome, whose functional disruption marked by reduced short-chain fatty acids (SCFAs), increasingly implicated in pathogenic processes extending beyond intestinal mucosa. This review outlines how these alternations compromise the epithelial barrier and immune regulation, increasing the risk of recurrent <i>Clostridioides difficile</i> infections to anemia, neuropsychiatric comorbidities, and extraintestinal manifestations. We critically evaluate emerging microbiota-targeted strategies, including fecal microbiota transplantation (FMT), live biotherapeutic products (LBPs), and precision postbiotics, positioning them as potential adjuncts to conventional immunosuppression. Finally, we discuss the current barriers to clinical translation, such as safety and heterogeneity, and propose a future framework for personalized, functionally integrated IBD care aimed at restoring long-term microbiota homeostasis.

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Publication Details

Journal
Pharmaceuticals
Published
2026-01-09
DOI
https://doi.org/10.3390/ph19010118
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
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article

Microbiota-Driven Strategies for Managing IBD-Associated Risks: From Infections to Mental Health

Pablo Cortegoso Valdivia, Patrycja Krynicka, Anastasios Koulaouzidis, Karolina Skonieczna-Żydecka et al.
Pharmaceuticals
Clostridium difficile and Clostridium perfringens research
article

Microbiota-Driven Strategies for Managing IBD-Associated Risks: From Infections to Mental Health

Pablo Cortegoso Valdivia, Patrycja Krynicka, Anastasios Koulaouzidis, Karolina Skonieczna-Żydecka, Maciej Morawski
article en

Abstract

Inflammatory bowel diseases (IBD) are increasingly acknowledged not merely as confined gastrointestinal disorders but as systemic immunometabolic syndromes. Central to this paradigm is the gut microbiota including non-bacterial components such as the virome, whose functional disruption marked by reduced short-chain fatty acids (SCFAs), increasingly implicated in pathogenic processes extending beyond intestinal mucosa. This review outlines how these alternations compromise the epithelial barrier and immune regulation, increasing the risk of recurrent <i>Clostridioides difficile</i> infections to anemia, neuropsychiatric comorbidities, and extraintestinal manifestations. We critically evaluate emerging microbiota-targeted strategies, including fecal microbiota transplantation (FMT), live biotherapeutic products (LBPs), and precision postbiotics, positioning them as potential adjuncts to conventional immunosuppression. Finally, we discuss the current barriers to clinical translation, such as safety and heterogeneity, and propose a future framework for personalized, functionally integrated IBD care aimed at restoring long-term microbiota homeostasis.

PharmaceuticalsVol. 19(1)
University of Parma (IT), University of Southern Denmark (DK), Military Hospital (PK), Nicolaus Copernicus University (PL), 1 Military Clinical Hospital with Outpatient Clinic (PL), Svendborg Sygehus (DK), Pomeranian Medical University (PL)
Good health and well-being
Openalex Percentile: Top 94%
Clostridium difficile and Clostridium perfringens research
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