系统性红斑狼疮患者黄斑微血管改变的特点

Lulu Bao, Hong Wang, Yufei Wu, Rong Zhou, M. Shen, Qi Chen
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摘要

目的:应用光学相干断层血管造影(OCTA)观察系统性红斑狼疮患者早期黄斑微血管改变的特点。方法:回顾性分析一系列病例。2018年5月至11月在温州医科大学附属第二医院&育婴儿童医院诊断为SLE的患者31例(62眼),分为狼疮视网膜病变组10例(17眼)和非狼疮视网膜病变组24例(45眼)。同时,招募年龄、性别与疾病组匹配的健康受试者35人(35只眼)作为对照组。所有受试者均对黄斑3 mm×3 mm区域进行OCTA扫描,获得黄斑浅层和深层视网膜微血管图像,并通过定制的自动化算法对视网膜血流密度图进行骨架化和分析。排除中央凹无血管区(FAZ, 0.6 mm)后得到直径为2.5 mm的总环区(TAZ),并将TAZ的浅、深视网膜骨化毛细血管密度(RCD)进一步划分为4个区域(S、T、I、N)。此外,采用SLE疾病活动性指数(SLEDAI)评估患者的疾病活动性。数据分析采用t检验和方差分析。结果:NLR组和LR组视网膜浅毛细血管丛(SRCP) RCD均显著低于对照组,LR组更低于NLR组,差异有统计学意义(P<0.05)。在视网膜深层毛细血管丛(DRCP)上,三组间的差异不如浅层明显。只有N区LR组的RCD显著低于NLR组(P=0.022),除T区均低于对照组(P<0.05)。此外,LR组的SLEDAI评分显著高于NLR组(P=0.006),狼疮肾炎、神经精神性SLE等SLE并发症的发生率LR组更高(分别为50%比25%、10%比4%)。结论:OCTA能有效检测SLE患者黄斑微血管形态的早期变化。在没有明显眼底和视力损害的SLE患者中,SRCP的RCD显著改变,这表明它可能被用作监测SLE视网膜损伤的早期生物标志物。关键词:系统性红斑狼疮;视网膜毛细血管密度;红斑性视网膜病变;系统性红斑狼疮疾病活动指数评分
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Characteristics of Macular Microvascular Changes in Patients with Systemic Lupus Erythematosus
Objective: To observe the characteristics of early macular microvascular changes in patients with systemic lupus erythematosus using optical coherence tomography angiography (OCTA). Methods: This was a retrospective series of case study. Thirty-one patients (62 eyes) who were diagnosed with SLE by the Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University from May to November 2018, were divided into a lupus retinopathy (LR) group of 10 patients (17 eyes) and a non-lupus retinopathy group of 24 patients (45 eyes). At the same time, 35 healthy subjects (35 eyes) who were matched by age and sex with the disease groups were recruited as a control group. All subjects had a 3 mm×3 mm area of the macula scanned by OCTA to obtain superficial and deep retinal microvascular images of the macular area, and retinal blood flow density maps were skeletonized and analyzed by a custom automated algorithm. The total annular zone (TAZ), with a diameter of 2.5 mm, was obtained after excluding the foveal avascular zone (FAZ, 0.6 mm), and the superficial and deep retinal skeletonized capillary densities (RCD) of the TAZ were further divided into 4 regions (S, T, I, N). In addition, disease activity of the patients was assessed using the SLE disease activity index (SLEDAI). Data analysis was performed using a t test and analysis of variance. Results: The RCD of the superficial retinal capillary plexus (SRCP) were found to be significantly lower in the NLR and LR groups than in the control group, and the LR group was even lower than the NLR group and the difference was significant (P<0.05). In the deep retinal capillary plexus (DRCP), the difference between the three groups was not as obvious as that in the superficial layer. Only the RCD of the LR group in the N region was significantly lower than that in the NLR group (P=0.022), which were also lower than those in the control group (P<0.05) except for the T region. In addition, the score of SLEDAI in the LR group was significantly higher than in the NLR group (P=0.006), and the incidence of SLE complications such as lupus nephritis and neuropsychiatric SLE were higher in the LR group (50% vs. 25%, 10% vs. 4% respectively). Conclusions: OCTA can effectively detect early changes in macular microvascular morphology in the patients with SLE. In patients with SLE without significant fundus and visual impairment, the RCD of SRCP is significantly altered, suggesting that it may be used as an early biomarker for monitoring SLE retinal damage. Key words: systemic lupus erythematosus; retinal capillary density; lupus retinopathy; score of systemic lupus erythematosus disease activity index
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