The Effect of Resveratrol, Quercetin, and Curcumin on Drusen Volume in Age-Related Macular Degeneration: A Randomized Clinical Trial
- 1Department of Ophthalmology and Visual Sciences, University of Illinois College of Medicine Chicago, Chicago, IL, USA
- 2Department of Ophthalmology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA
Abstract
Purpose: To evaluate the effect of resveratrol, quercetin, and curcumin (RQC) compared with curcumin alone on drusen volume and clinical outcomes in patients with age-related macular degeneration (AMD).
Methods: In this open-label, randomized phase 2a clinical trial, patients with early and intermediate AMD were randomized 2:1 to oral RQC or curcumin for 24 months. The primary outcome was the mean change in central drusen volume from baseline measured using spectral-domain optical coherence tomography (SD-OCT). Secondary outcomes included analyses of drusen volume and number by baseline size, categorical analyses of individual drusen response, change in best-corrected visual acuity (BCVA), frequency of vision loss, progression to advanced AMD, and safety.
Results: Thirty-eight patients were included in the final analysis. After 24 months, central drusen volume decreased significantly with RQC compared with curcumin (−13.4% vs. +6.9%; P = 0.02). Mean BCVA increased by 0.8 letters in the RQC group and decreased by 2.1 letters in the curcumin group (P = 0.08). The frequencies of both mild and moderate vision loss were lower in the RQC group. Progression to advanced AMD occurred in 3.7% of participants and 2.3% of eligible eyes in the RQC group.
Conclusions: RQC treatment was associated with reductions in drusen volume, low rates of progression to advanced AMD, and maintenance of BCVA over 24 months.
Translational Relevance: This study provides preliminary clinical evidence that this oral therapy may reduce drusen burden and warrants further evaluation as a potential treatment for early to intermediate AMD.
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BibTeX
@article{pfahler2026effect,
title = {{The Effect of Resveratrol, Quercetin, and Curcumin on Drusen Volume in Age-Related Macular Degeneration: A Randomized Clinical Trial}},
author = {Nicholas M. Pfahler and Paul A. Knepper},
journal = {Translational Vision Science \& Technology},
year = {2026},
month = oct,
doi = {10.1167/tvst.15.10.50},
url = {https://doi.org/10.1167/tvst.15.10.50},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - The Effect of Resveratrol, Quercetin, and Curcumin on Drusen Volume in Age-Related Macular Degeneration: A Randomized Clinical Trial
AU - Nicholas M. Pfahler
AU - Paul A. Knepper
PY - 2026
DA - 2026/10/29
JO - Translational Vision Science & Technology
DO - 10.1167/tvst.15.10.50
UR - https://doi.org/10.1167/tvst.15.10.50
AB - Purpose: To evaluate the effect of resveratrol, quercetin, and curcumin (RQC) compared with curcumin alone on drusen volume and clinical outcomes in patients with age-related macular degeneration (AMD). Methods: In this open-label, randomized phase 2a clinical trial, patients with early and intermediate AMD were randomized 2:1 to oral RQC or curcumin for 24 months. The primary outcome was the mean change in central drusen volume from baseline measured using spectral-domain optical coherence tomography (SD-OCT). Secondary outcomes included analyses of drusen volume and number by baseline size, categorical analyses of individual drusen response, change in best-corrected visual acuity (BCVA), frequency of vision loss, progression to advanced AMD, and safety. Results: Thirty-eight patients were included in the final analysis. After 24 months, central drusen volume decreased significantly with RQC compared with curcumin (−13.4% vs. +6.9%; P = 0.02). Mean BCVA increased by 0.8 letters in the RQC group and decreased by 2.1 letters in the curcumin group (P = 0.08). The frequencies of both mild and moderate vision loss were lower in the RQC group. Progression to advanced AMD occurred in 3.7% of participants and 2.3% of eligible eyes in the RQC group. Conclusions: RQC treatment was associated with reductions in drusen volume, low rates of progression to advanced AMD, and maintenance of BCVA over 24 months. Translational Relevance: This study provides preliminary clinical evidence that this oral therapy may reduce drusen burden and warrants further evaluation as a potential treatment for early to intermediate AMD.
SN - 2164-2591
ER -