Optical Coherence Tomography-Based Grading of Diabetic Macular Edema Is Associated with Systemic Inflammatory Indices and Imaging Biomarkers.

IF 2 4区 医学 Q2 OPHTHALMOLOGY
Ophthalmic Research Pub Date : 2024-01-01 Epub Date: 2024-01-11 DOI:10.1159/000535199
Chen Yanxia, Yang Xiongyi, Fu Min, Ke Xiaoyun
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引用次数: 0

Abstract

Introduction: Objectives of the study were to investigate the correlation between optical coherence tomography (OCT)-based grading of diabetic macular edema (DME) and systemic inflammatory indices, imaging biomarkers, and early anti-vascular endothelial growth factor (VEGF) treatment response.

Methods: A total of 111 eyes from 111 patients with DME treated with intravitreous anti-VEGF therapy for 3 consecutive months every month were enrolled in this retrospective study. According to a protocol termed "TCED," DME was divided into early, advanced, severe, and atrophic stages. The best-corrected visual acuity (BCVA), subretinal fluid (SRF), and the number of hyperreflective foci (HRF) in the whole retinal layers were analyzed at baseline and 3 months after the first injection. Peripheral blood inflammatory indices were calculated, including neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio (MLR), platelet (PLT)-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), and C-reactive protein (CRP). Statistical analysis was performed to compare the visual and anatomical results and evaluate HRF and SRF in different stages of DME before and after treatment.

Results: There were significant differences in systemic inflammatory indices among the four groups, including NLR, PLR, MLR, SII, and CRP (all p < 0.05). The CRP, NLR, PLR, MLR, and SII were significantly higher in the atrophic stage compared to the advanced stage (all p < 0.05). Conversely, the CRP, NLR, PLR, MLR, and SII were significantly lower in the advanced stage compared to the early stage (all p < 0.05). Except for the atrophic stage, BCVA and central retinal thickness (CRT) were significantly improved after treatment in early, advanced and severe stages (all p < 0.05), especially in the severe stage. The decline in the proportion of SRF and HRF ≥20 was the most significant in the advanced stage after anti-VEGF treatment (p < 0.001, p = 0.016), but not in the early and severe stages (all p > 0.05).

Conclusion: Systemic inflammatory indices and the decline in the proportion of SRF and HRF ≥20 were closely associated with different stages of DME based on "TCED." Meanwhile, the "TCED" grading system can predict visual and anatomical prognosis of DME after anti-VEGF treatment, which may be a biomarker for identifying risk stratification and management of DME.

基于 OCT 的糖尿病黄斑水肿分级与全身炎症指数和成像生物标志物有关。
简介:本研究旨在探讨基于 OCT 的糖尿病性黄斑水肿(DME)分级与全身炎症指数、成像生物标志物和早期抗血管内皮生长因子之间的相关性:该研究旨在探讨基于OCT的糖尿病黄斑水肿(DME)分级与全身炎症指数、影像生物标志物和早期抗血管内皮生长因子治疗反应之间的相关性:这项回顾性研究共纳入了111名DME患者的111只眼睛,这些患者每月接受连续3个月的玻璃体内抗血管内皮生长因子治疗。根据 "TCED "方案,DME 被分为早期、进展期、重度和萎缩期。在基线和首次注射三个月后,分析了最佳矫正视力(BCVA)、视网膜下积液(SRF)和视网膜全层高反射灶(HRF)的数量。计算了外周血炎症指数,包括中性粒细胞与淋巴细胞比值(NLR)、单核细胞与淋巴细胞比值(MLR)、血小板(PLT)与淋巴细胞比值(PLR)、全身免疫炎症指数(SII)和 C 反应蛋白(CRP)。通过统计分析,比较视觉和解剖结果,并评估治疗前后不同阶段 DME 的 HRF 和 SRF:结果:四组患者的全身炎症指标,包括NLR、PLR、MLR、SII和CRP,均有明显差异(均P<0.05)。与晚期相比,萎缩期的 CRP、NLR、PLR、MLR 和 SII 均明显升高(均 P <0.05)。相反,与早期相比,晚期的 CRP、NLR、PLR、MLR 和 SII 明显降低(均 P <0.05)。除萎缩期外,早期、晚期和重度期的 BCVA 和 CRT 在治疗后均明显改善(均 P < 0.05),尤其是重度期。抗 VEGF 治疗后,SRF 和 HRF ≥ 20 比例的下降在晚期最为明显(P < 0.001,P = 0.016),但在早期和重度期则不明显(均 P > 0.05):结论:根据 "TCED",全身炎症指数以及SRF和HRF≥20比例的下降与DME的不同分期密切相关。同时,"TCED "分级系统可预测抗血管内皮生长因子治疗后DME的视觉和解剖预后,可作为DME风险分层和管理的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmic Research
Ophthalmic Research 医学-眼科学
CiteScore
3.80
自引率
4.80%
发文量
75
审稿时长
6-12 weeks
期刊介绍: ''Ophthalmic Research'' features original papers and reviews reporting on translational and clinical studies. Authors from throughout the world cover research topics on every field in connection with physical, physiologic, pharmacological, biochemical and molecular biological aspects of ophthalmology. This journal also aims to provide a record of international clinical research for both researchers and clinicians in ophthalmology. Finally, the transfer of information from fundamental research to clinical research and clinical practice is particularly welcome.
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