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Bile acid modifications and microbiota interventions show promise for metabolic and digestive diseases in preclinical models

Bile acid modifications and microbiota interventions show promise for metabolic and digestive…
Photo by National Institute of Allergy and Infectious Diseases / Unsplash
Key Takeaway
Note that most findings are preclinical and clinical translation of bile acids remains uncertain.

This narrative review explores the potential of bile acid modifications, microbiota interventions, and BA-targeted therapies across metabolic, digestive, hepatobiliary, and neoplastic diseases. The scope covers various conditions but relies heavily on preclinical evidence rather than human trials. The authors highlight that most of the findings discussed in this review are derived from preclinical studies in vitro and animal models. This reliance limits the ability to draw firm conclusions about efficacy in patients. The review does not report specific sample sizes, adverse events, or primary outcomes for human populations. Instead, it focuses on the biological plausibility and mechanistic insights gained from laboratory research. The authors suggest that these preclinical results warrant further study before widespread adoption. Current evidence is insufficient to support routine clinical use outside of research settings. The review calls for accelerating the translation of BA-based interventions into clinical practice while acknowledging the current lack of human data. Clinicians should interpret these findings with caution until robust clinical trials are conducted.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
Bile acids (BAs) serve dual roles as lipid-digesting molecules and key signaling mediators in metabolism and immune regulation. This review systematically examines: 1.the molecular mechanisms underlying BA-mediated regulation of glucolipid m5etabolism and energy expenditure; 2.host- and microbiota-driven BA modifications (e.g., 3-acylation); 3. therapeutic targeting of BA signaling pathways (FXR/TGR5). We highlight emerging strategies, including novel BA modifications, microbiota interventions, and BA-targeted therapies, which reshape BA homeostasis and show therapeutic potential for metabolic, digestive, hepatobiliary, and neoplastic diseases. Furthermore, we emphasize the central role of BA modifications in metabolic regulation and their pathological implications. Advances in multi-omics and AI-driven approaches deepen mechanistic insights and accelerate the translation of BA-based interventions into clinical practice. Most of the findings discussed in this review are derived from preclinical studies (in vitro and animal models); clinical translation of bile
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