AIBILI, Association for Innovation and Biomedical Research on Light and Image Coimbra, Portugal.
School of Allied Health Technologies, Polytechnic Institute of Porto, Porto, Portugal.
Retina. 2018 Jun;38(6):1110-1119. doi: 10.1097/IAE.0000000000001687.
To identify baseline optical coherence tomography morphologic characteristics predicting the visual response to anti-vascular endothelial growth factor therapy in diabetic macular edema.
Sixty-seven patients with diabetic macular edema completed a prospective, observational study (NCT01947881-CHARTRES). All patients received monthly intravitreal injections of Lucentis for 3 months followed by PRN treatment and underwent best-corrected visual acuity measurements and spectral domain optical coherence tomography at Baseline, Months 1, 2, 3, and 6. Visual treatment response was characterized as good (≥10 letters), moderate (5-10 letters), and poor (<5 or letters loss). Spectral domain optical coherence tomography images were graded before and after treatment by a certified Reading Center.
One month after loading dose, 26 patients (38.80%) were identified as good responders, 19 (28.35%) as Moderate and 22 (32.83%) as poor responders. There were no significant best-corrected visual acuity and central retinal thickness differences at baseline (P = 0.176; P = 0.573, respectively). Ellipsoid zone disruption and disorganization of retinal inner layers were good predictors for treatment response, representing a significant risk for poor visual recovery to anti-vascular endothelial growth factor therapy (odds ratio = 10.96; P < 0.001 for ellipsoid zone disruption and odds ratio = 7.05; P = 0.034 for disorganization of retinal inner layers).
Damage of ellipsoid zone, higher values of disorganization of retinal inner layers, and central retinal thickness decrease are good predictors of best-corrected visual acuity response to anti-vascular endothelial growth factor therapy.
确定预测糖尿病性黄斑水肿对血管内皮生长因子治疗反应的基线光相干断层扫描形态学特征。
67 例糖尿病性黄斑水肿患者完成了一项前瞻性、观察性研究(NCT01947881-CHARTRES)。所有患者接受每月一次的 Lucentis 玻璃体内注射,共 3 个月,随后根据需要进行 PRN 治疗,并在基线、第 1、2、3 和 6 个月进行最佳矫正视力测量和光谱域光相干断层扫描。将视力治疗反应特征为好(≥10 个字母)、中(5-10 个字母)和差(<5 个字母或字母丢失)。经认证的阅读中心在治疗前后对光谱域光相干断层扫描图像进行分级。
在负荷剂量后 1 个月,26 例(38.80%)患者被确定为好反应者,19 例(28.35%)为中度反应者,22 例(32.83%)为差反应者。基线时最佳矫正视力和中心视网膜厚度无显著差异(P = 0.176;P = 0.573)。椭圆体带破坏和视网膜内层组织紊乱是治疗反应的良好预测指标,代表抗血管内皮生长因子治疗后视力恢复不良的显著风险(椭圆体带破坏的比值比 = 10.96;P < 0.001,视网膜内层组织紊乱的比值比 = 7.05;P = 0.034)。
椭圆体带损伤、视网膜内层组织紊乱程度较高和中心视网膜厚度降低是抗血管内皮生长因子治疗后最佳矫正视力反应的良好预测指标。