Bile acids as candidate therapies for multiple sclerosis: inverse signal analysis using the FDA adverse event reporting system and preclinical validation

This two-stage investigation highlights the potential utility of pharmacovigilance-guided approaches for identifying therapeutic candidates. Bile acid derivatives, particularly UDCA, are biologically plausible candidates meriting further investigation in the context of MS.

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Publication Details

Journal
Multiple Sclerosis and Related Disorders
Published
2026-03-05
DOI
https://doi.org/10.1016/j.msard.2026.107113
Primary Topic
Drug Transport and Resistance Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Bile acids as candidate therapies for multiple sclerosis: inverse signal analysis using the FDA adverse event reporting system and preclinical validation

Yoshito Zamami, Fuka Aizawa, Takahiro Niimura, Yoshihiro Uesawa et al.
Multiple Sclerosis and Related Disorders
Drug Transport and Resistance Mechanisms
article

Bile acids as candidate therapies for multiple sclerosis: inverse signal analysis using the FDA adverse event reporting system and preclinical validation

Yoshito Zamami, Fuka Aizawa, Takahiro Niimura, Yoshihiro Uesawa, Mitsuhiro Goda, Yuhei Sonoda, Mizuho Asada, Masayuki Chuma, Takahisa Mikami, Keisuke Ishizawa
article en

Abstract

This two-stage investigation highlights the potential utility of pharmacovigilance-guided approaches for identifying therapeutic candidates. Bile acid derivatives, particularly UDCA, are biologically plausible candidates meriting further investigation in the context of MS.

Multiple Sclerosis and Related DisordersVol. 109
Hiroshima University (JP), Asahikawa Medical College Hospital (JP), Harvard University (US), Asahikawa Medical University (JP), Meiji Pharmaceutical University (JP), Massachusetts General Hospital (US), Okayama University Hospital (JP), Tokushima University Hospital (JP), Tokushima University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 32%
Drug Transport and Resistance Mechanisms
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