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糖尿病性黄斑水肿治疗眼糖尿病视网膜病变严重程度波动的相关性及其预后意义。

Associations and Prognostic Significance of Fluctuations in Diabetic Retinopathy Severity in Eyes Treated for Diabetic Macular Edema.

机构信息

School of Medicine, Vita-Salute San Raffaele University, Milan, Italy.

Eye Clinic, University Hospital Maggiore della Carità, Novara, Italy.

出版信息

Ophthalmologica. 2023;246(2):131-140. doi: 10.1159/000530417. Epub 2023 Mar 30.

Abstract

INTRODUCTION

The aim of our study was to investigate factors associated with diabetic retinopathy (DR) severity fluctuations in patients undergoing intravitreal injections for diabetic macular edema and to explore risk factors for proliferative DR (PDR).

METHODS

We graded ultra-widefield fundus photography imaging at each visit using the Early Treatment Diabetic Retinopathy Study Severity Scale (DRSS). We calculated the deviation from the mode (DM) of DRSS values as a proxy of DR severity fluctuations, and we analyzed its clinical associations with linear models. We computed risk factors for PDR with Cox hazard models. We included the DRSS area-under-the-curve (AUC) of DRSS scores as a covariate in all analyses.

RESULTS

We included 111 eyes with a median follow-up of 44 months. Higher DRSS-AUC values (β = +0.03 DRSS DM for unitary DRSS/month increase, p = 0.01) and a higher number of anti-VEGF injections (β = +0.07 DRSS DM for injection, p = 0.045) were associated with wider DR severity fluctuations. Higher DRSS-AUC values (HR = 1.45 for unitary DRSS/month increase, p = 0.001) and wider DR severity fluctuations (HR = 22.35 4th quartile vs. 1st-3rd quartile of DRSS DM, p = 0.01) were risk factors for PDR.

CONCLUSION

Patients with larger DR variability in response to intravitreal injections may be at higher risk of DR progression. We advocate attentive follow-up in these patients to recognize PDR early.

摘要

简介

本研究旨在探讨接受抗血管内皮生长因子(VEGF)治疗的糖尿病黄斑水肿患者中,与糖尿病性视网膜病变(DR)严重程度波动相关的因素,并探讨增生性糖尿病性视网膜病变(PDR)的危险因素。

方法

我们使用糖尿病性视网膜病变早期治疗研究严重程度分级(DRSS),在每次就诊时对超广角眼底照相进行分级。我们计算 DRSS 值模式偏差(DM),作为 DR 严重程度波动的替代指标,并使用线性模型分析其临床相关性。我们使用 Cox 风险模型计算 PDR 的危险因素。在所有分析中,我们均将 DRSS 评分的曲线下面积(AUC)作为协变量。

结果

我们纳入了 111 只眼,中位随访时间为 44 个月。DRSS-AUC 值较高(DRSS 每增加 0.03,DM 增加 0.01,p = 0.01)和抗 VEGF 注射次数较多(DRSS 每增加 0.07,DM 增加 0.045,p = 0.045)与 DR 严重程度波动较大相关。DRSS-AUC 值较高(DRSS 每月增加 1 单位,HR = 1.45,p = 0.001)和 DR 严重程度波动较大(DRSS DM 四分位间距第 4 四分位间距与第 1-3 四分位间距比较,HR = 22.35,p = 0.01)是 PDR 的危险因素。

结论

对玻璃体内注射反应中 DR 变异性较大的患者,DR 进展的风险可能更高。我们主张对这些患者进行密切随访,以便及早发现 PDR。

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