Kupitz Elke H, Heeren Tjebo F C, Holz Frank G, Charbel Issa Peter
Department of Ophthalmology, University of Bonn, Bonn, Germany.
Retina. 2015 Dec;35(12):2619-26. doi: 10.1097/IAE.0000000000000715.
To investigate long-term effects after intravitreal inhibition of vascular endothelial growth factor in nonproliferative macular telangiectasia type 2.
Nine patients with macular telangiectasia type 2 treated with 12 monthly intravitreal ranibizumab injections in 1 eye were investigated again after a mean follow-up of 6.0 ± 0.4 years. Functional assessment included best-corrected visual acuity and microperimetry testing. Morphologic investigations included optical coherence tomography imaging and fluorescein angiography.
Mean visual acuity at baseline was similar in treated and control eyes (both 20/50; range: 20/32-20/125 in the treated eyes and 20/25-20/100 in the untreated eyes). None of the eyes had a neovascular membrane or a paracentral scotoma. At the last follow-up, more eyes of the treatment group had lost 2 or more lines on best-corrected visual acuity testing (4 vs. 1) and more eyes had developed an absolute paracentral scotoma (7 vs. 2). A secondary neovascular membrane had formed in four of the treated and in none of the untreated eyes.
Vascular endothelial growth factor inhibition with monthly dosing over 1 year had no beneficial effect 5 years after cessation of therapy. The worse outcome in the treated eyes may be due to selection bias, small sample size, or a potential adverse effect of vascular endothelial growth factor inhibition in a degenerative, primarily nonvascular disease as macular telangiectasia type 2.
研究玻璃体内抑制血管内皮生长因子对2型非增生性黄斑毛细血管扩张症的长期影响。
对9例2型黄斑毛细血管扩张症患者的1只眼每月注射1次雷珠单抗,共注射12次,平均随访6.0±0.4年后再次进行研究。功能评估包括最佳矫正视力和微视野检测。形态学研究包括光学相干断层扫描成像和荧光素血管造影。
治疗眼和对照眼的基线平均视力相似(均为20/50;治疗眼范围为20/32 - 20/125,未治疗眼范围为20/25 - 20/100)。所有眼均无新生血管膜或旁中心暗点。在最后一次随访时,治疗组更多眼在最佳矫正视力检测中视力下降2行或更多(4只眼对1只眼),且更多眼出现绝对旁中心暗点(7只眼对2只眼)。4只治疗眼形成了继发性新生血管膜,未治疗眼均未形成。
在治疗停止5年后,每年每月给药抑制血管内皮生长因子没有有益效果。治疗眼较差的结果可能是由于选择偏倚、样本量小或在2型黄斑毛细血管扩张症这种退行性、主要非血管性疾病中抑制血管内皮生长因子的潜在不良反应。