Hsieh Yi-Ting, Alam Minhaj Nur, Le David, Hsiao Chia-Chieh, Yang Chang-Hao, Chao Daniel L, Yao Xincheng
Department of Ophthalmology, National Taiwan University Hospital, Taipei, Taiwan.
Department of Bioengineering, University of Illinois at Chicago, Chicago, Illinois.
Ophthalmol Retina. 2019 Oct;3(10):826-834. doi: 10.1016/j.oret.2019.04.027. Epub 2019 May 7.
To correlate quantitative OCT angiography (OCTA) biomarkers with clinical features and to predict the extent of visual improvement after ranibizumab treatment for diabetic macular edema (DME) with OCTA biomarkers.
Retrospective, longitudinal study in Taiwan.
Fifty eyes of 50 patients with DME and 22 eyes of 22 healthy persons, with the exception of cataract and refractive error, from 1 hospital.
Each eye underwent OCT angiography (RTVue XR Avanti System with AngioVue software version 2017.1; Optovue, Fremont, CA), and 3×3-mm en face OCTA images of the superficial layer and the deep layer were obtained at baseline and after 3 monthly injections of ranibizumab in the study group. OCT angiography images also were acquired from the control group.
Five OCTA biomarkers, including foveal avascular zone (FAZ) area (FAZ-A), FAZ contour irregularity (FAZ-CI), average vessel caliber (AVC), vessel tortuosity (VT), and vessel density (VD), were analyzed comprehensively. Best-corrected visual acuity (BCVA) and central retinal thickness (CRT) also were obtained. Student t tests were used to compare the OCTA biomarkers between the study group and the control group. Linear regression models were used to evaluate the correlations between the baseline OCTA biomarkers and the changes of BCVA and CRT after treatment.
Eyes with DME had larger AVC, VT, FAZ-A, and FAZ-CI and lower VD than those in the control group (P < 0.001 for all). After the loading ranibizumab treatment, these OCTA biomarkers improved but did not return to normal levels. Among all biomarkers, higher inner parafoveal VD in the superficial layer at baseline correlated most significantly with visual gain after treatment in the multiple regression model with adjustment for CRT and ellipsoid zone disruption (P < 0.001). To predict visual improvement, outer parafoveal VD in the superficial layer at the baseline showed the largest area under the receiver operating characteristic curve (0.787; P = 0.004). No baseline OCTA biomarkers showed any significant correlation specifically with anatomic improvement.
For eyes with DME, parafoveal VD in the superficial layer at baseline was an independent predictor for visual improvement after the loading ranibizumab treatment.
将定量光学相干断层扫描血管造影(OCTA)生物标志物与临床特征相关联,并利用OCTA生物标志物预测雷珠单抗治疗糖尿病性黄斑水肿(DME)后视力改善程度。
台湾的一项回顾性纵向研究。
来自1家医院的50例DME患者的50只眼以及22名健康人的22只眼,排除白内障和屈光不正。
每只眼均接受光学相干断层扫描血管造影(使用配备AngioVue软件版本2017.1的RTVue XR Avanti系统;Optovue,弗里蒙特,加利福尼亚州),在基线时以及研究组每月注射3次雷珠单抗后,获取表层和深层的3×3 mm正面OCTA图像。对照组也采集了光学相干断层扫描血管造影图像。
综合分析5种OCTA生物标志物,包括黄斑无血管区(FAZ)面积(FAZ-A)、FAZ轮廓不规则性(FAZ-CI)、平均血管管径(AVC)、血管迂曲度(VT)和血管密度(VD)。还获得了最佳矫正视力(BCVA)和中心视网膜厚度(CRT)。采用Student t检验比较研究组和对照组之间的OCTA生物标志物。使用线性回归模型评估基线OCTA生物标志物与治疗后BCVA和CRT变化之间的相关性。
DME患者的眼与对照组相比,具有更大的AVC、VT、FAZ-A和FAZ-CI,以及更低的VD(所有P<0.001)。在进行负荷剂量雷珠单抗治疗后,这些OCTA生物标志物有所改善,但未恢复到正常水平。在所有生物标志物中,在对CRT和椭圆体带破坏进行校正的多元回归模型中,基线时表层视网膜中央凹旁较高的VD与治疗后的视力提高最显著相关(P<0.001)。为了预测视力改善情况,基线时表层视网膜中央凹外的VD在受试者工作特征曲线下显示出最大面积(0.787;P=0.004)。没有基线OCTA生物标志物与解剖学改善有任何显著的特定相关性。
对于DME患者的眼,基线时表层视网膜中央凹旁的VD是负荷剂量雷珠单抗治疗后视力改善的独立预测指标。