Resveratrol for the Management of Human Health: How Far Have We Come? A Systematic Review of Resveratrol Clinical Trials to Highlight Gaps and Opportunities
Overview
Chemistry
Molecular Biology
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Resveratrol has long been proposed as being beneficial to human health across multiple morbidities, yet there is currently no conclusive clinical evidence to advocate its recommendation in any healthcare setting. A large cohort with high-quality clinical data and clearly defined biomarkers or endpoints are required to draw meaningful conclusions. This systematic review compiles every clinical trial conducted using a defined dose of resveratrol in a purified form across multiple morbidities to highlight the current 'state-of-play' and knowledge gaps, informing future trial designs to facilitate the realisation of resveratrol's potential benefits to human health. Over the last 20 years, there have been almost 200 studies evaluating resveratrol across at least 24 indications, including cancer, menopause symptoms, diabetes, metabolic syndrome, and cardiovascular disease. There are currently no consensus treatment regimens for any given condition or endpoint, beyond the fact that resveratrol is generally well-tolerated at a dose of up to 1 g/day. Additionally, resveratrol consistently reduces inflammatory markers and improves aspects of a dysregulated metabolism. In conclusion, over the last 20 years, the increasing weight of clinical evidence suggests resveratrol can benefit human health, but more large, high-quality clinical trials are required to transition this intriguing compound from health food shops to the clinic.
Pifferi F, Terrien J, Marchal J, Dal-Pan A, Djelti F, Perret M Commun Biol. 2025; 8(1):331.
PMID: 40021720 PMC: 11871233. DOI: 10.1038/s42003-024-07387-9.
Vera-Juarez G, Vazquez-Martinez E, Gomez-Pliego R, Lopez-Martinez M, Espinosa-Raya J Brain Sci. 2025; 15(2).
PMID: 40002544 PMC: 11853727. DOI: 10.3390/brainsci15020210.
Molecular Docking Study and 3D-QSAR Model for Trans-Stilbene Derivatives as Ligands of CYP1B1.
Dutkiewicz Z, Mikstacka R Int J Mol Sci. 2025; 26(3).
PMID: 39940769 PMC: 11817148. DOI: 10.3390/ijms26031002.
Lawinski M, Zadka K, Ksepka N, Matin M, Wysocki K, Karkocha D Nutrients. 2025; 17(3).
PMID: 39940362 PMC: 11819975. DOI: 10.3390/nu17030504.
Resveratrol-driven macrophage polarization: unveiling mechanisms and therapeutic potential.
Wang P, Li Z, Song Y, Zhang B, Fan C Front Pharmacol. 2025; 15:1516609.
PMID: 39872049 PMC: 11770351. DOI: 10.3389/fphar.2024.1516609.