{"title":"Resveratrol Supplementation in Wet AMD: Association With Fewer Intravitreal Injections and Reduced Macular Fibrosis.","authors":"Ioannis Datseris, Alexandros Rouvas, Malvina-Efthymia Tzanidaki, Marina Kardara, Vasileios Geros, Nikolaos Gouliopoulos","doi":"10.2147/OPTH.S494595","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the 2-year outcomes of resveratrol oral supplement given as an adjunctive treatment in patients with wet age-related macular degeneration (AMD) that were treated with intravitreal injections of aflibercept.</p><p><strong>Patients and methods: </strong>In our retrospective study, 50 treatment-naïve patients suffering from wet-AMD were included. They were assigned to two subgroups of 25 patients each. Every participant was treated according to \"Pro Re Nata\" protocol; 3 monthly intravitreal injections of 2.0 mg aflibercept were applied followed by injections according to need. The patients in the second group also consumed daily two tablets of resveratrol enriched oral supplement (60 mg of resveratrol in total). For 2 years, the patients were monthly assessed with best corrected visual acuity (BCVA) measurement, fundus autofluorescence, optical coherence tomography (OCT) scans and OCT-angiography. The main endpoints were the change of BCVA, the number of anti-VEGF injections, the change of central foveal thickness values, and the expansion or new development of fibrosis.</p><p><strong>Results: </strong>Between the studied groups, no significant differences were detected in the baseline demographic and clinical data (p>0.05 for all). Over the 24-month study period, both BCVA and central foveal thickness values did not differ significantly between the two groups. As for the number of applied injections, they were significantly fewer in the group of patients that were treated with the resveratrol supplement (9.32±1.37 vs 7.40±1.88, p<0.001). Notably, the frequency of fibrosis progression was significantly lower in the resveratrol group (p=0.04).</p><p><strong>Conclusion: </strong>In conclusion, our findings suggest that resveratrol oral supplement could be considered as a useful adjunctive aid to the established treatment in cases suffering from wet AMD, highlighting the superiority of the combination treatment regimen, since it was accompanied by lower rates of both intravitreal aflibercept injections and progression of macular fibrosis.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"19 ","pages":"217-225"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11762261/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical ophthalmology (Auckland, N.Z.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/OPTH.S494595","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: To evaluate the 2-year outcomes of resveratrol oral supplement given as an adjunctive treatment in patients with wet age-related macular degeneration (AMD) that were treated with intravitreal injections of aflibercept.
Patients and methods: In our retrospective study, 50 treatment-naïve patients suffering from wet-AMD were included. They were assigned to two subgroups of 25 patients each. Every participant was treated according to "Pro Re Nata" protocol; 3 monthly intravitreal injections of 2.0 mg aflibercept were applied followed by injections according to need. The patients in the second group also consumed daily two tablets of resveratrol enriched oral supplement (60 mg of resveratrol in total). For 2 years, the patients were monthly assessed with best corrected visual acuity (BCVA) measurement, fundus autofluorescence, optical coherence tomography (OCT) scans and OCT-angiography. The main endpoints were the change of BCVA, the number of anti-VEGF injections, the change of central foveal thickness values, and the expansion or new development of fibrosis.
Results: Between the studied groups, no significant differences were detected in the baseline demographic and clinical data (p>0.05 for all). Over the 24-month study period, both BCVA and central foveal thickness values did not differ significantly between the two groups. As for the number of applied injections, they were significantly fewer in the group of patients that were treated with the resveratrol supplement (9.32±1.37 vs 7.40±1.88, p<0.001). Notably, the frequency of fibrosis progression was significantly lower in the resveratrol group (p=0.04).
Conclusion: In conclusion, our findings suggest that resveratrol oral supplement could be considered as a useful adjunctive aid to the established treatment in cases suffering from wet AMD, highlighting the superiority of the combination treatment regimen, since it was accompanied by lower rates of both intravitreal aflibercept injections and progression of macular fibrosis.
目的:评价白藜芦醇口服补充剂作为湿性年龄相关性黄斑变性(AMD)患者玻璃体内注射阿伯西普的辅助治疗的2年结果。患者和方法:我们回顾性研究了50例treatment-naïve湿性amd患者。他们被分为两个亚组,每组25名患者。每个参与者都按照“Pro Re Nata”协议受到待遇;每3个月玻璃体内注射阿布西普2.0 mg,根据需要再注射一次。第二组患者也每天服用两片富含白藜芦醇的口服补充剂(总共60毫克白藜芦醇)。2年来,患者每月接受最佳矫正视力(BCVA)测量、眼底自身荧光、光学相干断层扫描(OCT)扫描和OCT血管造影评估。主要终点为BCVA变化、抗vegf注射次数、中央中央凹厚度值变化、纤维化扩大或新发。结果:在研究组之间,基线人口学和临床资料没有发现显著差异(p < 0.05)。在24个月的研究期间,两组间BCVA和中央中央凹厚度值无显著差异。在注射次数方面,白藜芦醇补充组明显少于对照组(9.32±1.37 vs 7.40±1.88)。总之,我们的研究结果表明,白藜芦醇口服补充剂可以被认为是湿性AMD患者现有治疗方法的有效辅助,突出了联合治疗方案的优势,因为它伴随着玻璃体内注射阿非利西普和黄斑纤维化进展的较低发生率。