Rebeiz Abdallah G, Mahfoud Ziyad, Abdul Fattah Maamoun, Saad Alain, Safar Ammar, Bashshur Ziad F
Division of Cardiology, Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.
Department of Global and Public Health, Weill Cornell Medical College, Doha, Qatar.
Eur J Ophthalmol. 2020 May;30(3):563-569. doi: 10.1177/1120672119832171. Epub 2019 Feb 27.
Evaluate subclinical myocardial injury associated with intravitreal anti-vascular endothelial growth factor therapy by measuring serum high-sensitivity cardiac troponin T.
This is a prospective pilot comparative study conducted at American University of Beirut Medical Center, Beirut, Lebanon. In total, 40 consecutive patients were randomized to receive either intravitreal bevacizumab or ranibizumab. Patients received three consecutive monthly injections of the assigned drug, then continued treatment as needed. Systemic concentrations of high-sensitivity cardiac troponin T and vascular endothelial growth factor were obtained at baseline, week 9, and week 24. Primary endpoint measure was change in high-sensitivity cardiac troponin T levels compared to baseline. Secondary endpoint measure was change in systemic vascular endothelial growth factor levels.
There was no significant difference in high-sensitivity cardiac troponin T levels over time ( = 0.227) within each treatment group and no significant difference between treatments at any time point ( = 0.276). There was a significant decrease in plasma vascular endothelial growth factor levels at week 9 ( = 0.001) and week 24 ( < 0.001) compared to baseline. In the ranibizumab group, vascular endothelial growth factor levels were not significantly different at weeks 9 and 24 compared to baseline ( = 0.708 and = 0.117, respectively). There was a significant association between the number of bevacizumab injections from weeks 8 to 24 and the decrease in vascular endothelial growth factor levels at week 24 ( = -0.67, = 0.032). This correlation was not observed in the ranibizumab group ( = -0.341, = 0.141).
Repeated intravitreal bevacizumab or ranibizumab did not influence serum high-sensitivity cardiac troponin levels. Intravitreal bevacizumab but not ranibizumab lowered free-systemic vascular endothelial growth factor levels, which was observed in this study to be inversely related to the number of bevacizumab injections.
通过检测血清高敏心肌肌钙蛋白T来评估玻璃体内抗血管内皮生长因子治疗相关的亚临床心肌损伤。
这是一项在黎巴嫩贝鲁特美国大学医学中心进行的前瞻性试点对比研究。总共40例连续患者被随机分配接受玻璃体内贝伐单抗或雷珠单抗治疗。患者连续三个月每月注射一次指定药物,然后根据需要继续治疗。在基线、第9周和第24周获取高敏心肌肌钙蛋白T和血管内皮生长因子的全身浓度。主要终点指标是与基线相比高敏心肌肌钙蛋白T水平的变化。次要终点指标是全身血管内皮生长因子水平的变化。
各治疗组内高敏心肌肌钙蛋白T水平随时间无显著差异(P = 0.227),且在任何时间点治疗组之间也无显著差异(P = 0.276)。与基线相比,第9周(P = 0.001)和第24周(P < 0.001)时血浆血管内皮生长因子水平显著降低。在雷珠单抗组中,第9周和第24周时血管内皮生长因子水平与基线相比无显著差异(分别为P = 0.708和P = 0.117)。第8周至第24周贝伐单抗注射次数与第24周时血管内皮生长因子水平降低之间存在显著关联(r = -0.67,P = 0.032)。在雷珠单抗组中未观察到这种相关性(r = -0.341,P = 0.141)。
重复玻璃体内注射贝伐单抗或雷珠单抗不影响血清高敏心肌肌钙蛋白水平。玻璃体内注射贝伐单抗而非雷珠单抗降低了游离全身血管内皮生长因子水平,本研究观察到这与贝伐单抗注射次数呈负相关。