Doheny Image Reading Center, Doheny Eye Institute, Los Angeles, California.
Department of Ophthalmology, David Geffen School of Medicine at UCLA (University of California, Los Angeles), Los Angeles.
JAMA Ophthalmol. 2020 Aug 1;138(8):851-857. doi: 10.1001/jamaophthalmol.2020.2130.
Although previous studies have evaluated the association between anti-vascular endothelial growth factor therapy and macular vessel density, they were confounded by the presence of macular edema, which may be associated with artifacts and segmentation errors in optical coherence tomography angiography (OCTA).
To evaluate the association of intravitreal aflibercept with changes in macular vascular density using OCTA in patients with proliferative diabetic retinopathy without diabetic macular edema.
DESIGN, SETTING, AND PARTICIPANTS: This post hoc analysis of a randomized clinical trial used data on 40 eyes of 40 patients with proliferative diabetic retinopathy without diabetic macular edema who were enrolled in the Intravitreal Aflibercept for Retinal Nonperfusion in Proliferative Diabetic Retinopathy (RECOVERY) clinical trial from August 1, 2016, to June 31, 2017. Three patients were lost to follow-up at month 12, and 5 patients were excluded from analysis because of poor OCTA image quality, leaving 16 patients in each cohort in the final analysis. Data analysis was performed from March 1, 2018, to January 15, 2019.
In the RECOVERY trial, patients were randomized into cohorts receiving 2 mg of aflibercept injections monthly (n = 20) or quarterly (n = 20) and treated for 12 months.
The percentage of vascular density (in total scan and foveal and parafoveal regions) was compared before and after 12 months of therapy.
The sample for this OCTA analysis included 32 eyes from 32 patients (mean [SD] age, 48.37 [12.30] years; 17 [53.1%] male). The mean (SD) total scan vascular density for the superficial vascular complex was 42.28% (4.03%; 95% CI, 40.63%-43.93%) at baseline and 39.64% (4.01%; 95% CI, 37.91%-41.37%) at month 12 (P = .69). For the deep vascular complex, the mean (SD) vascular density was 48.42% (4.99%; 95% CI, 46.36%-50.47%) at baseline and 45.69% (4.63%; 95% CI, 43.69%-47.70%) at month 12 (P = .40). For the choriocapillaris, the mean (SD) vascular density was 64.42% (3.36%; 95% CI, 63.04%-65.81%) at baseline and 62.55% (4.79%; 95% CI, 60.48%-64.62%) at month 12 (P = .16). There was no difference in vascular density parameters between monthly and quarterly injection arms at month 12.
In this study, macular vascular density did not change after 12 months of intravitreal aflibercept therapy. Because nonperfusion is expected to progress in diabetic retinopathy, this finding may represent a beneficial association between anti-vascular endothelial growth factor therapy and macular vascular density.
ClinicalTrials.gov Identifier: NCT02863354.
重要性:尽管之前的研究已经评估了抗血管内皮生长因子治疗与黄斑血管密度之间的关系,但这些研究受到黄斑水肿的影响,黄斑水肿可能与光学相干断层扫描血管造影(OCTA)中的伪影和分割错误有关。
目的:评估玻璃体内注射阿柏西普与无糖尿病性黄斑水肿的增殖性糖尿病性视网膜病变患者黄斑血管密度变化的关系。
设计、地点和参与者:本随机临床试验的事后分析使用了 2016 年 8 月 1 日至 2017 年 6 月 31 日期间在增殖性糖尿病性视网膜病变非灌注的玻璃体内阿柏西普治疗(RECOVERY)临床试验中招募的 40 例无糖尿病性黄斑水肿的增殖性糖尿病性视网膜病变患者的 40 只眼的数据。3 例患者在 12 个月时失访,5 例患者因 OCTA 图像质量差而被排除在分析之外,最终分析中每个队列各有 16 例患者。数据分析于 2018 年 3 月 1 日至 2019 年 1 月 15 日进行。
干预:在 RECOVERY 试验中,患者被随机分为每月(n=20)或每季度(n=20)接受 2mg 阿柏西普注射治疗,并接受 12 个月的治疗。
主要结局和测量指标:在治疗 12 个月前后比较血管密度(总扫描和中心凹及旁中心凹区域)的百分比。
结果:本次 OCTA 分析的样本包括 32 只眼(来自 32 例患者;平均[标准差]年龄为 48.37[12.30]岁;17 例[53.1%]为男性)。浅层血管复合体的总扫描血管密度平均值(标准差)为基线时的 42.28%(4.03%;95%置信区间[CI]:40.63%-43.93%)和 12 个月时的 39.64%(4.01%;95%CI:37.91%-41.37%)(P=.69)。深层血管复合体的血管密度平均值(标准差)为基线时的 48.42%(4.99%;95%CI:46.36%-50.47%)和 12 个月时的 45.69%(4.63%;95%CI:43.69%-47.70%)(P=.40)。脉络膜毛细血管的血管密度平均值(标准差)为基线时的 64.42%(3.36%;95%CI:63.04%-65.81%)和 12 个月时的 62.55%(4.79%;95%CI:60.48%-64.62%)(P=.16)。12 个月时,每月和每季度注射组的血管密度参数没有差异。
结论和相关性:在这项研究中,玻璃体内注射阿柏西普治疗 12 个月后黄斑血管密度没有变化。由于糖尿病性视网膜病变的非灌注预计会进展,这一发现可能代表了抗血管内皮生长因子治疗与黄斑血管密度之间的有益关联。
试验注册:ClinicalTrials.gov 标识符:NCT02863354。