Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry & Biomedical Sciences, Queen's University Belfast, United Kingdom.
The Department of Anatomy, Faculty of Medicine-Rabigh, King Abdulaziz University, Saudi Arabia.
Invest Ophthalmol Vis Sci. 2021 Jun 1;62(7):10. doi: 10.1167/iovs.62.7.10.
To evaluate anatomic-functional associations at sites of retinal lesions in retinal vein occlusion (RVO).
This pilot, prospective, observational study was conducted at the Northern Ireland Clinical Research Facility (NICRF) of Queen's University and the Belfast Health and Social Care Trust, Northern Ireland, between August 1, 2018, and September 30, 2019. The study included 10 treatment-naïve patients with RVO (10 RVO eyes and 10 fellow eyes). There were 81 points/sites assessed for each eye at baseline; six patients were re-assessed 6 months after anti-vascular endothelial growth factor therapy at the same locations. We investigated associations between retinal sensitivity and presence of structural RVO lesions, including retinal ischemia, hemorrhages, intraretinal fluid (IRF) and subretinal fluid outside the foveal/parafoveal regions. Comparisons were made between RVO eyes and fellow eyes at baseline, and between RVO eyes at baseline and at 6 months after treatment. Regression models were used to investigate anatomic-functional associations.
At baseline, strong associations were found between reduced retinal sensitivity and presence of ischemia (estimate = -2.08 dB; P < 0.001), intraretinal fluid (estimate = -7.82 dB; P < 0.001), and subretinal fluid (estimate = -8.66 dB; P < 0.001). Resolution of subretinal fluid but not intraretinal fluid was associated with improved function (estimate = 2.40 dB [P = 0.022]; estimate = 1.16 dB [P = 0.228], respectively). However, reperfusion of ischemic retina, observed in 31 of 486 points (6%) 6 months after anti-vascular endothelial growth factor therapy, was associated with a further decrease in retinal sensitivity (estimate = -2.34 dB; P = 0.035).
Retinal sensitivity was decreased at sites of RVO lesions. Decreased function at sites of retinal ischemia did not recover after treatment, even when reperfusion occurred.
评估视网膜静脉阻塞(RVO)病变部位的解剖-功能相关性。
本研究为前瞻性观察性研究,在北爱尔兰女王大学临床研究中心(NICRF)和北爱尔兰贝尔法斯特健康与社会保健信托基金进行,于 2018 年 8 月 1 日至 2019 年 9 月 30 日期间纳入 10 例未经治疗的 RVO 患者(10 只 RVO 眼和 10 只对侧眼)。每只眼在基线时有 81 个点/部位进行评估;6 例患者在抗血管内皮生长因子治疗后 6 个月在相同部位进行了重新评估。我们调查了视网膜敏感性与结构性 RVO 病变(包括视网膜缺血、出血、视网膜内液(IRF)和黄斑/旁黄斑区外的视网膜下液)之间的相关性。在基线时比较 RVO 眼和对侧眼,以及治疗后 6 个月时 RVO 眼和基线时的相关性。使用回归模型研究解剖-功能相关性。
基线时,发现视网膜敏感性与缺血(估计值=-2.08dB;P<0.001)、视网膜内液(估计值=-7.82dB;P<0.001)和视网膜下液(估计值=-8.66dB;P<0.001)的存在密切相关。尽管视网膜下液的消退与功能的改善相关(估计值=2.40dB[P=0.022];估计值=1.16dB[P=0.228]),但仅在治疗后发现的视网膜内液消退与功能改善无关。然而,在抗血管内皮生长因子治疗后 6 个月时,观察到的 486 个点中的 31 个点(6%)出现缺血性视网膜再灌注,与视网膜敏感性进一步下降相关(估计值=-2.34dB;P=0.035)。
RVO 病变部位的视网膜敏感性降低。即使发生再灌注,视网膜缺血部位的功能下降在治疗后也无法恢复。