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基于光学相干断层扫描血管造影的抗血管内皮生长因子治疗期间活动性近视性脉络膜新生血管形态学变化的定量评估

Optical Coherence Tomography Angiography-Based Quantitative Assessment of Morphologic Changes in Active Myopic Choroidal Neovascularization During Anti-vascular Endothelial Growth Factor Therapy.

作者信息

Wang Yao, Hu Zhongli, Zhu Tiepei, Su Zhitao, Fang Xiaoyun, Lin Jijian, Chen Zhiqing, Su Zhaoan, Ye Panpan, Ma Jian, Zhang Li, Li Jinyu, Feng Lei, Sun Chuan-Bin, Zhang Zhiyong, Shentu Xingchao

机构信息

Eye Center of the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

Department of Ophthalmology, Zhuji People's Hospital of Zhejiang Province, Zhuji, China.

出版信息

Front Med (Lausanne). 2021 May 7;8:657772. doi: 10.3389/fmed.2021.657772. eCollection 2021.

DOI:10.3389/fmed.2021.657772
PMID:34026789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8137977/
Abstract

To establish quantitative profile of the morphologic changes among patients with active myopic choroidal neovascularization (mCNV) before and after anti-vascular endothelial growth factor (VEGF) therapy using optical coherence tomography angiography (OCTA) to assess the therapeutic response. Patients with active mCNV who received anti-VEGF injections between February 2017 to October 2020 and fit the study criteria were retrospectively reviewed. Quantitative analysis of their OCTA images were carried out to evaluate the morphologic features and vascular changes of mCNV lesions in response to anti-VEGF therapy. For further quantitative profiling, mCNV area, fractal dimension, vessel area, vessel density, vessel diameter, vessel length, vessel junction, junction density, and vessel tortuosity were obtained by means of advanced skeletonization postprocessing analyses. Thirty-one eyes of 29 consecutive patients with OCTA-positive mCNV lesions (mean spherical equivalent: -12.55 ± 3.24 diopters) were included. The 31 cases were divided into two phenotypes at baseline: organized interlacing pattern (83.87%) and disorganized vascular loops pattern (16.13%). The values of mCNV area, fractal dimension, vessel area, vessel length, vessel junction, and junction density decreased remarkably 1 month after the initial anti-VEGF injection ( < 0.001). Although, vessel density, vessel diameter, and vessel tortuosity increased meanwhile, only vessel diameter displayed statistical significance ( = 0.027). Of note, relative ratio analysis showed that vessel junction was the most sensitive biomarker in response to anti-VEGF therapy, reflecting a mean decrease of 50.36%. Sensitivity lowered successively in biomarkers of vessel length, vessel area, junction density, mCNV area, and fractal dimension. In addition, percent change of mCNV area ( = 0.552, = 0.002), fractal dimension ( = 0.446, = 0.017), vessel area ( = 0.518, = 0.005), and vessel length ( = 0.440, = 0.019) were moderately associated with that of central retinal thickness. The study showed morphological as well as quantitative changes on OCTA responding to anti-VEGF treatment in mCNV patients, among which vessel junctions might be the most predictive biomarker. OCTA-based analysis, providing intuitive images and a large spectrum of quantitative data at the same time, could promote new insights into the therapeutic response assessment in mCNV patients.

摘要

利用光学相干断层扫描血管造影(OCTA)建立活动性近视性脉络膜新生血管(mCNV)患者在抗血管内皮生长因子(VEGF)治疗前后形态学变化的定量特征,以评估治疗反应。对2017年2月至2020年10月期间接受抗VEGF注射且符合研究标准的活动性mCNV患者进行回顾性分析。对其OCTA图像进行定量分析,以评估抗VEGF治疗后mCNV病变的形态学特征和血管变化。为进行进一步的定量分析,通过先进的骨架化后处理分析获得mCNV面积、分形维数、血管面积、血管密度、血管直径、血管长度、血管连接、连接密度和血管迂曲度。纳入29例连续患者的31只OCTA阳性mCNV病变眼(平均球镜等效度:-12.55±3.24屈光度)。31例患者在基线时分为两种表型:有组织的交织模式(83.87%)和无组织的血管环模式(16.13%)。首次抗VEGF注射后1个月,mCNV面积、分形维数、血管面积、血管长度、血管连接和连接密度值显著下降(<0.001)。虽然同时血管密度、血管直径和血管迂曲度增加,但只有血管直径具有统计学意义(=0.027)。值得注意的是,相对比率分析显示,血管连接是对抗VEGF治疗反应最敏感的生物标志物,平均下降50.36%。血管长度、血管面积、连接密度、mCNV面积和分形维数的生物标志物敏感性依次降低。此外,mCNV面积(=0.552,=0.002)、分形维数(=0.446,=0.017)、血管面积(=0.518,=0.005)和血管长度(=0.440,=0.019)的百分比变化与中心视网膜厚度的百分比变化中度相关。该研究显示了mCNV患者抗VEGF治疗后OCTA上的形态学和定量变化,其中血管连接可能是最具预测性的生物标志物。基于OCTA的分析同时提供直观图像和大量定量数据,可促进对mCNV患者治疗反应评估的新认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/160205bc3cf7/fmed-08-657772-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/56720949de8b/fmed-08-657772-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/2022abab1096/fmed-08-657772-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/160205bc3cf7/fmed-08-657772-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/56720949de8b/fmed-08-657772-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/2022abab1096/fmed-08-657772-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9d/8137977/160205bc3cf7/fmed-08-657772-g0003.jpg

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