Cholesterol lowering with bile salt hydrolase-active probiotic bacteria, mechanism of action, clinical evidence, and future direction for heart health applications
Abstract
INTRODUCTION: Cardiovascular diseases (CVD) are the leading cause of global mortality and morbidity. Current CVD treatment methods include dietary intervention, statins, fibrates, niacin, cholesterol absorption inhibitors, and bile acid sequestrants. These formulations have limitations and, thus, additional treatment modalities are needed. Probiotic bacteria, especially bile salt hydrolase (BSH)-active probiotic bacteria, have demonstrated cholesterol-lowering efficacy in randomized controlled trials. AREAS COVERED: This review describes the current treatments for CVD and the need for additional therapeutics. Gut microbiota etiology of CVD, cholesterol metabolism, and the role of probiotic formulations as therapeutics for the treatment and prevention of CVD are described. Specifically, we review studies using BSH-active bacteria as cholesterol-lowering agents with emphasis on their cholesterol-lowering mechanisms of action. Potential limitations and future directions are also highlighted. EXPERT OPINION: Numerous clinical studies have concluded that BSH-active probiotic bacteria, or products containing them, are efficient in lowering total and low-density lipoprotein cholesterol. However, the mechanisms of action of BSH-active probiotic bacteria need to be further supported. There is also the need for a meta-analysis to provide better information regarding the therapeutic use of BSH-active probiotic bacteria. The future of BSH-active probiotic bacteria most likely lies as a combination therapy with already existing treatment options.
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BSH activity has been implicated in the regulation of host cholesterol levels, contributing to a potential cholesterol-lowering effect.
“Among its metabolic benefits, BSH activity has been implicated in the regulation of host cholesterol levels, contributing to its potential cholesterol-lowering effect [11–13].”
From Bile Salt Hydrolase Activity in the Food-Derived Strain Levilactobacillus brevis M3R3: Genomic and Functional Characterization (2026) · cites this paper as [13]
Members of the healthy gut microbiota initiate bile acid catabolism through an ubiquitous reaction catalysed by bacterial bile salt hydrolase enzymes, ending in the production of unconjugated bile acids.
“members of the healthy gut microbiota initiate BA catabolism through an ubiquitous reaction catalysed by bacterial bile salt hydrolase (BSH) enzymes15 that ends in the production of unconjugated BAs.”
From <i>Lactiplantibacillus plantarum</i> strains KABP011, KABP012, and KABP013 modulate bile acids and cholesterol metabolism in humans (2024) · cites this paper as [15]
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References 131 · Cited by 190
- Authors
- Jones, M. L., Tomaro-Duchesneau, C., Martoni, C. J., & Prakash, S.
- Affiliations
- Micropharma (Canada) (CA)
- McGill University (CA)
- Venue
- Expert Opinion on Biological Therapy
- Publisher
- Informa UK Limited
- Published
- 2013-01-28
- Volume
- 13
- Issue
- 5
- Pages
- 631-642
- ISSN
- 1471-2598 (ISSN-L)
- 1744-7682
- OpenAlex
- W2007006020
- Cited by
- 190
- References
- 131
- Citations by year
- 2026: 7 · 2025: 14 · 2024: 17 · 2023: 20 · 2022: 14 · 2021: 25 · 2020: 13 · 2019: 13 · 2018: 12 · 2017: 9 · 2016: 9 · 2015: 9 · 2014: 19 · 2013: 9
- FWCI
- 2.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Expert Opinion on Biological Therapy (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research (MPO64308)
- Natural Sciences and Engineering Research Council of Canada
- Topics
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- bile salt hydrolase, probiotic bacteria, cholesterol lowering, cardiovascular disease, LDL cholesterol, gut microbiota, cholesterol metabolism, bile acid sequestration, probiotic therapy, combination therapy
- MeSH terms
- Amidohydrolases, Animals, Anticholesteremic Agents, Cholesterol, Heart Diseases, Humans, Hypercholesterolemia, Hyperlipidemias, Probiotics, Gastrointestinal Tract, Metagenome
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