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基于姜黄素的治疗罕见病因性黄斑水肿:疗效和安全性评估。

Curcumin-Based Treatment for Macular Edema from Uncommon Etiologies: Efficacy and Safety Assessment.

机构信息

Eye Center, Humanitas, Bergamo, Italy.

Department of Biomedical Sciences, Humanitas University, Milano, Italy.

出版信息

J Med Food. 2020 Aug;23(8):834-840. doi: 10.1089/jmf.2019.0241. Epub 2020 Jan 8.

Abstract

The aim of this study was to investigate the efficacy and safety of curcumin formulation with a polyvinylpyrrolidone-hydrophilic carrier (CHC*; Diabec-AlfaIntes, Italy) for the treatment of macular edema (ME) from uncommon etiologies. We conducted retrospective interventional case series, reviewing the medical records of patients referred to the Eye Center, Humanitas Hospital, Bergamo due to persistent ME related to uncommon causes and treated by oral administration of CHC. The main outcomes assessed were best-corrected visual acuity (BCVA), central macular thickness (CMT), and the presence of intraretinal and/or subretinal fluid (SRF). Only patients with a minimum follow-up (f/u) of 6 months were included. The occurrence of any adverse effect was registered. Thirty-one eyes of 30 patients were included, with a mean f/u of 8.32 ± 1.77 months. Of them, 9 patients (10 eyes) were affected by postoperative ME and 21 by chronic central serous chorioretinopathy. Median BCVA significantly improved after treatment, changing from 0.3 [0.16-0.5] to 0.1 [0-0.3] logarithm of the minimum angle of resolution ( < .001). Also CMT was significantly improved, as it decreased from 400 [364-438] m before treatment to 280 [242-307] m at the last f/u visit ( < .001). The complete absorption of intraretinal/SRF was detected in 23 of 31 eyes (74%) at the final f/u. No adverse effects were registered. In conclusion, treatment with CHC was effective and safe for eyes affected by ME of various uncommon etiologies, resulting in significant improvement of both functional and anatomical outcomes, with the complete resolution of the edema in the majority of cases (74%).

摘要

本研究旨在探讨姜黄素制剂与亲水性载体聚乙烯吡咯烷酮(CHC*;意大利 Diabec-AlfaIntes)联合治疗罕见病因引起的黄斑水肿(ME)的疗效和安全性。我们进行了回顾性干预性病例系列研究,回顾了因罕见原因引起的持续性 ME 而转诊至 Bergamo 的 Humanitas 医院眼科中心的患者的病历,并给予 CHC 口服治疗。主要评估的结局包括最佳矫正视力(BCVA)、中心黄斑厚度(CMT)以及视网膜内和/或视网膜下液(SRF)的存在。仅纳入了随访时间至少为 6 个月的患者。记录了任何不良反应的发生情况。共纳入了 30 例患者的 31 只眼,平均随访时间为 8.32±1.77 个月。其中,9 例患者(10 只眼)患有术后 ME,21 例患者患有慢性中心性浆液性脉络膜视网膜病变。治疗后,中位 BCVA 显著提高,从治疗前的 0.3[0.16-0.5]logMAR 变为治疗后的 0.1[0-0.3]logMAR( < .001)。CMT 也显著改善,从治疗前的 400[364-438]μm 降至最后一次随访时的 280[242-307]μm( < .001)。31 只眼中有 23 只(74%)在最后一次随访时检测到视网膜内/视网膜下液完全吸收。未发现不良反应。总之,CHC 治疗各种罕见病因引起的 ME 有效且安全,可显著改善功能和解剖学结局,大多数情况下(74%)水肿完全消退。

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