Kırşehir Ahi Evran Training and Research Hospital, Department of Opthalmology, Kırşehir, Turkey.
University of Health Sciences, Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey.
Photodiagnosis Photodyn Ther. 2021 Jun;34:102282. doi: 10.1016/j.pdpdt.2021.102282. Epub 2021 Apr 1.
To evaluate and compare the effects of intravitreal ranibizumab and aflibercept treatment on retinal vessel diameters in patients with diabetic macular edema (DME).
Thirty initial-treatment naïve patients with DME who received three loading doses at monthly intervals of intravitreal ranibizumab or aflibercept were retrospectively reviewed. The diameters of the central retinal artery and vein sections at a distance of 1500 microns from the optical disc boundary were measured and evaluated at baseline and after the first, second, and third month of the treatment, using infrared images from optical coherence tomography (OCT) (Heidelberg Engineering, Heidelberg, Germany).
In the superotemporal artery (STA) measurements, the mean basal vessel diameter decreased from 110.00 ± 17.25 μm to 102.60 ± 16.90 μm (p = 0.001) in the third month of the treatment in the ranibizumab group. In the aflibercept group, measurements of the basal STA vessel diameter decreased from 110.20 ± 21.25 μm to 103.93 ± 19.03 μm (p = 0.001) at the third month. The mean basal inferotemporal artery (ITA) vessel diameter was significantly decreased at the third month in both ranibizumab (p = 0.001) and aflibercept groups (p = 0.005). In the superotemporal vein (STV) and inferotemporal vein (ITV) measurements, vessel diameters were found significantly decreased at the end of the third month compared with basal measurements in both the ranibizumab (p = 0.001; p = 0.001, respectively) and aflibercept (p = 0.001; p = 0.004, respectively) treatment groups. The retinal vessel measurements were not found to differ significantly between the two intravitreal treatment agents (p > 0.05).
Both intravitreal ranibizumab and aflibercept agents cause a significant narrowing in the retinal vessel diameters in patients with DME after three loading doses at monthly intervals.
评估和比较玻璃体内雷珠单抗和阿柏西普治疗对糖尿病黄斑水肿(DME)患者视网膜血管直径的影响。
回顾性分析 30 例初始治疗初治的 DME 患者,每月间隔接受 3 次玻璃体内雷珠单抗或阿柏西普负荷剂量。使用来自光学相干断层扫描(OCT)(德国海德堡工程公司,海德堡)的红外图像,在基线和治疗第 1、2 和 3 个月时测量并评估距视盘边界 1500 微米处的视网膜中央动脉和静脉节段的直径。
在超颞动脉(STA)测量中,雷珠单抗组治疗第 3 个月时,平均基础血管直径从 110.00±17.25μm 降至 102.60±16.90μm(p=0.001)。阿柏西普组的基础 STA 血管直径从 110.20±21.25μm 降至 103.93±19.03μm(p=0.001)。在第 3 个月时,雷珠单抗组和阿柏西普组的基础下眼动脉(ITA)平均血管直径均显著降低(p=0.001 和 p=0.005)。在超颞静脉(STV)和下颞静脉(ITV)测量中,与基线相比,在雷珠单抗(p=0.001;p=0.001)和阿柏西普(p=0.001;p=0.004)治疗组,在第 3 个月时,血管直径均显著降低。两种玻璃体内治疗药物之间的视网膜血管测量值无显著差异(p>0.05)。
在每月间隔接受 3 次负荷剂量后,玻璃体内雷珠单抗和阿柏西普均能显著缩小 DME 患者的视网膜血管直径。