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Neovascular age-related macular degeneration: intraocular inflammatory cytokines in the poor responder to ranibizumab treatment

机译:新血管性年龄相关性黄斑变性:兰尼单抗治疗反应差的眼内炎性细胞因子

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Purpose: To determine the levels of interleukin (IL)-6, vascular endothelial growth factor-A, platelet-derived growth factor, placental growth factor (PLGF), and other cytokines in the aqueous fluid of patients with neovascular age-related macular degeneration who respond poorly to ranibizumab. Patients and methods: This is an observational, prospective study. Thirty-two eyes from 30 patients were included in the study: 11 patients who responded poorly to ranibizumab and were switched to aflibercept (AF group), 8 patients who received ranibizumab and photodynamic therapy (PDT group), and 13 patients who responded to ranibizumab (control group). Aqueous fluid samples were collected for analysis of cytokine levels at baseline and after 1, 2, and 3 months of treatment. The effect of treatment on cytokine levels was compared between the study groups and between different time points using a linear mixed-effect regression model. Results: In the AF group, there was an increase in vascular endothelial growth factor-C, IL-7, and angiopoeitin-2 levels ( P =0.01) and a decrease in intercellular adhesion molecule and IL-17 levels ( P =0.01) between baseline and 3 months. After adjustment for age, sex, race, and type of lesion at baseline, the PLGF level was higher ( P =0.02) and the IL-7 level was lower ( P =0.04) in the ranibizumab non-responder group than in the ranibizumab responder group. Conclusion: Switching from ranibizumab to aflibercept did not reduce intraocular levels of angiogenesis cytokines, but resulted in improvement of central subfield thickness. PLGF levels were higher in poor responders to ranibizumab. The response of lesions to medication might be related to the stage of choroidal neovascularization. Trial registration: www.ClinicalTrial.gov (NCT02218177c).
机译:目的:测定新生血管性年龄相关性黄斑变性患者水液中白介素(IL)-6,血管内皮生长因子-A,血小板衍生生长因子,胎盘生长因子(PLGF)和其他细胞因子的水平对兰尼单抗反应差的人。患者和方法:这是一项观察性前瞻性研究。研究纳入了来自30例患者的32只眼:11例对兰尼单抗治疗不良的患者,改用abribercept(AF组),8例接受兰尼单抗和光动力疗法的患者(PDT组),以及13例对兰尼单抗治疗的患者(控制组)。收集基线期和治疗后1、2和3个月后的水样样品,以分析细胞因子水平。使用线性混合效应回归模型比较研究组之间以及不同时间点之间治疗对细胞因子水平的影响。结果:在AF组中,血管内皮生长因子-C,IL-7和血管生成素-2水平升高(P = 0.01),细胞间粘附分子和IL-17水平降低(P = 0.01)在基线到3个月之间。在对基线的年龄,性别,种族和病变类型进行调整之后,与兰尼单抗相比,兰尼单抗无反应者组的PLGF水平较高(P = 0.02),IL-7水平较低(P = 0.04)。响应者组。结论:从兰尼单抗转换为阿柏西普并不能降低眼内血管生成细胞因子的水平,但可以改善中央亚视野的厚度。对兰尼单抗的不良反应者的PLGF水平较高。病变对药物的反应可能与脉络膜新生血管形成阶段有关。试用注册:www.ClinicalTrial.gov(NCT02218177c)。

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