Campos António, Campos Elisa J, do Carmo Anália, Patrício Miguel, Castro de Sousa João P, Ambrósio António Francisco, Silva Rufino
Coimbra Institute for Clinical and Biomedical Research (iCBR), Faculty of Medicine, University of Coimbra, Azinhaga de Santa Comba, Celas, 3000-548, Coimbra, Portugal.
CNC.IBILI Consortium, University of Coimbra, Coimbra, Portugal.
Graefes Arch Clin Exp Ophthalmol. 2018 Oct;256(10):1857-1865. doi: 10.1007/s00417-018-4072-z. Epub 2018 Jul 23.
The aim of this study was to evaluate subfoveal choroidal thickness (SFCT) as a marker of outcome in real-world treatment of diabetic macular edema (DME) and to correlate it with choroidal thicknesses (CT) collected around the fovea.
Prospective interventional case series included a total of 126 eyes from 126 patients with recently diagnosed DME treated with a 3-monthly loading dose of ranibizumab or aflibercept and PRN thereafter until 24 months (M). CT was manually measured in the central 3500 μm area, subfoveally (SFCT), at 1750 μm right and left from the center in the horizontal plane and at 1750 μm up and down from the center in the vertical plane, by OCT. Anatomic (10% decrease in central retinal thickness) and functional (gain ≥ 5 letters) responses were assessed using univariate and multivariate analyses. The areas under ROC curves were used to assess whether baseline SFCT was a predictor of outcome.
CT significantly decreased in all follow-ups (3 months after the 3 injections' loading dose (3M), 6 months (6M), 12 months (12M), 18 months (18M), 24 months (24M)). SFCT and other CT parameters are correlated. SFCT decrease from baseline was related with treatment (p = 0.003 to p < 0.001) but not with anatomic (3M, p = 0.858; 6M p = 0.762) or functional response (3M, p = 0.746; 6M, p = 0.156). SFCT was not found to be predictive of anatomic (AUC = 0.575, p = 0.172) or functional (AUC = 0.515, p = 0.779) outcome.
SFCT is a reliable marker of choroidal thickness. Baseline SFCT decreased with anti-VEGF treatment but did not predict DME outcome.
本研究旨在评估黄斑中心凹下脉络膜厚度(SFCT)作为糖尿病性黄斑水肿(DME)实际治疗效果的标志物,并将其与黄斑中心凹周围收集的脉络膜厚度(CT)进行关联。
前瞻性干预性病例系列研究共纳入126例近期诊断为DME患者的126只眼,给予每月1次负荷剂量的雷珠单抗或阿柏西普治疗3个月,之后按需治疗直至24个月(M)。通过光学相干断层扫描(OCT)在中心3500μm区域手动测量黄斑中心凹下(SFCT)、水平方向距中心1750μm处左右以及垂直方向距中心1750μm处上下的CT。使用单因素和多因素分析评估解剖学(中心视网膜厚度降低10%)和功能学(视力提高≥5个字母)反应。ROC曲线下面积用于评估基线SFCT是否为治疗效果的预测指标。
在所有随访中(3次注射负荷剂量后3个月(3M)、6个月(6M)、12个月(12M)、18个月(18M)、24个月(24M))CT均显著降低。SFCT与其他CT参数相关。SFCT相对于基线的降低与治疗相关(p = 0.003至p < 0.001),但与解剖学反应(3M,p = 0.858;6M,p = 0.762)或功能学反应(3M,p = 0.746;6M,p = 0.156)无关。未发现SFCT可预测解剖学(AUC = 0.575,p = 0.172)或功能学(AUC = 0.515,p = 0.779)结局。
SFCT是脉络膜厚度的可靠标志物。基线SFCT随抗VEGF治疗而降低,但不能预测DME的治疗效果。