Malvasi Mariaelena, Calandri Antonella, Pacella Elena, Vingolo Enzo Maria
Department of Sense Organs, Sapienza University of Rome, Rome, Italy.
Department of Ophthalmology, Fiorini Hospital Terracina AUSL, Terracina, Latina, Italy.
Cutan Ocul Toxicol. 2024 Dec;43(4):369-382. doi: 10.1080/15569527.2024.2422914. Epub 2024 Nov 19.
Intravitreal drug administration has become the gold standard for the treatment of many retinal diseases, including age-related macular degeneration (AMD), diabetic retinopathy (DR) and retinal vein occlusion (RVO). The frequency of this procedure has increased significantly after the introduction of anti-VEGF drugs, since the rise in the average age of the population, which is closely correlated with these diseases. In order to ensure therapeutic success in these patients with chronic retinal diseases, intravitreal treatment with anti-VEGF requires a long-term maintenance regimen with repeated administrations. For this reason today, we must consider the risks linked to complications associated with the long-term application of this therapy. Our study aims to investigate whether the intravitreal injection of anti-VEGF may lead to damage to the corneal endothelium, either directly through the administration procedure or indirectly due to the drug's toxicity. We aimed to establish a clear correlation between intravitreal drug administration and a statistically significant reduction in corneal endothelial cell count in the treated eye when compared to the untreated eye. The study also sought to assess whether different toxicities might be present between different types of drugs belonging to the same anti-VEGF family.
The study was conducted by examining a cohort of 133 patients suffering from different diseases: AMD, EMD and RVO. All patients underwent measurement of the endothelial count with CellChek 20, considering the value measured at the first injection as time zero and reassessed at each subsequent treatment session. The measurement of the endothelial count was performed both on the eye under treatment (TE) and in the eye not undergoing intravitreal injection (NTE) with anti-VEGF drugs for each injection cycle. Different anti-VEGF drugs such as Bevacizumab, Ranibizumab, Aflibercept, Brolucizumab were used for intravitreal therapy. The test patients were included in a 12-month follow-up programme, in which the measurement intervals are dictated by the treatment plan.
The statistical analysis performed on the corneal endothelial cell counts showed that the ECD (endothelial cell density) parameter decreases with each administration of the drug. The analysis of the difference in the mean endothelial cell counts of the TE reveals that the difference in the number of endothelial cells between the first and second counts in TE is 54.00; greater than the difference in the number of cells found in NTE, which was 13.42. Both the difference between the TE and NTE cell counts are statistically significant. In the case of the TE, the -value is <0.001, while in the case of the NTE the -value is still significant as <0.05. The hypothesis that the different types of anti-VEGF drugs could determine the decrease in endothelial cell count differently was also evaluated. No statistically significant data emerged from the analyses (-value is >0.05).
The study demonstrated a statistically significant reduction of corneal endothelial cells in patients undergoing intravitreal injection treatment per number of injections with anti-VEGF, this reduction being independent of the type of anti-VEGF used (Bevacizumab, Ranibizumab, Aflibercept and Brolucizumab).
玻璃体内药物注射已成为治疗许多视网膜疾病的金标准,包括年龄相关性黄斑变性(AMD)、糖尿病性视网膜病变(DR)和视网膜静脉阻塞(RVO)。自从引入抗VEGF药物后,由于与这些疾病密切相关的人口平均年龄上升,该治疗方法的频率显著增加。为了确保这些慢性视网膜疾病患者获得治疗成功,抗VEGF玻璃体内治疗需要长期维持方案并反复给药。因此,如今我们必须考虑与该疗法长期应用相关的并发症风险。我们的研究旨在调查玻璃体内注射抗VEGF是否会直接通过给药过程或间接由于药物毒性导致角膜内皮损伤。我们旨在确定玻璃体内给药与治疗眼的角膜内皮细胞计数相比未治疗眼出现统计学显著降低之间的明确相关性。该研究还试图评估同一抗VEGF家族的不同类型药物之间是否可能存在不同的毒性。
该研究通过检查一组133例患有不同疾病(AMD、EMD和RVO)的患者进行。所有患者均使用CellChek 20测量内皮细胞计数,将首次注射时测得的值视为时间零点,并在随后的每次治疗时重新评估。对于每个注射周期,在接受治疗的眼(TE)和未接受抗VEGF药物玻璃体内注射的眼(NTE)上均进行内皮细胞计数测量。玻璃体内治疗使用了不同的抗VEGF药物,如贝伐单抗、雷珠单抗、阿柏西普、布罗利尤单抗。受试患者被纳入一个为期12个月的随访计划,其中测量间隔由治疗计划决定。
对角膜内皮细胞计数进行的统计分析表明,每次给药后内皮细胞密度(ECD)参数都会降低。对TE的平均内皮细胞计数差异分析显示,TE中第一次和第二次计数之间的内皮细胞数量差异为54.00;大于NTE中发现的细胞数量差异,即13.42。TE和NTE细胞计数之间的差异均具有统计学意义。在TE的情况下,P值<0.001,而在NTE的情况下,P值仍具有显著性,为<0.05。还评估了不同类型抗VEGF药物可能以不同方式导致内皮细胞计数降低的假设。分析未得出具有统计学意义的数据(P值>0.05)。
该研究表明,接受抗VEGF玻璃体内注射治疗的患者,每注射一次角膜内皮细胞就会出现统计学显著减少,这种减少与所使用的抗VEGF类型(贝伐单抗、雷珠单抗、阿柏西普和布罗利尤单抗)无关。