Starita Carla, Patel Manju, Katz Barrett, Adamis Anthony P
Pfizer Ltd., Sandwich, UK.
Dev Ophthalmol. 2007;39:122-148. doi: 10.1159/000098504.
Both clinical and preclinical findings have implicated vascular endothelial growth factor (VEGF) in the pathophysiology of diabetic macular edema (DME). VEGF is both a potent enhancer of vascular permeability and a key inducer of angiogenesis. VEGF levels are elevated in the eyes of patients with DME, and in animal models of diabetes this elevation coincides with the breakdown of the blood-retinal barrier. Moreover, injection of VEGF (the VEGF165 isoform in particular) into healthy eyes of animals can induce diabetes-associated ocular pathologies.Pegaptanib, a novel RNA aptamer currently used in the treatment of agerelated macular degeneration, binds and inactivates VEGF165 and has been shown in animal models to reverse the blood-retinal barrier breakdown associated with diabetes. These findings formed the basis of a phase II trial involving 172 patients with DME, in which intravitreous pegaptanib (0.3 mg, 1 mg, 3 mg) or sham injections were administered every 6 weeks for 12 weeks, with the option of continuing for 18 more weeks or undergoing laser treatment. Compared to sham, patients receiving 0.3 mg displayed superior visual acuity (p = 0.04) as well as a reduction in retinal thickness of 68 micrometers compared to a slight increase under sham treatment (p = 0.021). These data support the use of pegaptanib in the treatment of DME.
临床和临床前研究结果均表明,血管内皮生长因子(VEGF)与糖尿病性黄斑水肿(DME)的病理生理机制有关。VEGF既是血管通透性的强效增强剂,也是血管生成的关键诱导剂。DME患者眼中的VEGF水平升高,在糖尿病动物模型中,这种升高与血视网膜屏障的破坏同时出现。此外,向动物的健康眼睛注射VEGF(特别是VEGF165异构体)可诱发与糖尿病相关的眼部病变。派加他尼是一种目前用于治疗年龄相关性黄斑变性的新型RNA适配体,它能结合并使VEGF165失活,并且在动物模型中已显示可逆转与糖尿病相关的血视网膜屏障破坏。这些发现构成了一项涉及172例DME患者的II期试验的基础,在该试验中,每6周玻璃体内注射派加他尼(0.3mg、1mg、3mg)或进行假注射,持续12周,可选择再持续18周或接受激光治疗。与假注射组相比,接受0.3mg派加他尼治疗的患者视力更佳(p = 0.04),视网膜厚度减少了68微米,而假注射组视网膜厚度略有增加(p = 0.021)。这些数据支持派加他尼用于治疗DME。