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Vitreous and plasma concentrations of apelin and vascular endothelial growth factor after intravitreal bevacizumab in eyes with proliferative diabetic retinopathy.

机译:玻璃体腔注射贝伐单抗治疗增生性糖尿病性视网膜病变后,玻璃体和血浆中apelin和血管内皮生长因子的浓度。

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PURPOSE: To evaluate vitreous and plasma concentrations of vascular endothelial growth factor (VEGF) and apelin and to detect the expressions of VEGF and apelin on epiretinal fibrovascular membranes obtained during vitrectomy in eyes with proliferative diabetic retinopathy after intravitreal bevacizumab injection. METHODS: Forty-four eyes of 44 patients affected by active proliferative diabetic retinopathy were investigated. The bevacizumab study group consisted of 20 eyes that received an intravitreal bevacizumab injection (1.25 mg) 7 days before pars plana vitrectomy. The control group included 24 eyes that underwent pars plana vitrectomy without previous intravitreal bevacizumab injection. Using enzyme-linked immunosorbent assay, the concentrations of VEGF and apelin were measured in vitreous and plasma samples. The expressions of VEGF and apelin in the excised epiretinal membranes were examined by fluorescence immunostaining. RESULTS: Vitreous and plasma concentrations of VEGF were significantly lower in the bevacizumab group than in the control group (P , 0.001 and P = 0.003, respectively), while the vitreous and plasma concentrations of apelin did not vary significantly between the 2 groups (P = 0.62 and P = 0.09, respectively). In the epiretinal fibrovascular membranes of both the groups, a colocalization of the endothelial marker CD31 with the markers for apelin was observed. CONCLUSION: Intravitreal bevacizumab injection may lead to a decrease in the intraocular and systemic concentrations of VEGF, suggesting a local and potentially a systemic effect on VEGF but may have no effect on apelin. Apelin may be associated with the development of epiretinal membranes in proliferative diabetic retinopathy and may not directly correlate with VEGF.
机译:目的:评估玻璃体腔注射贝伐单抗注射后增生性糖尿病视网膜病变患者玻璃体切除术中获得的视网膜前纤维膜上的血管内皮生长因子(VEGF)和apelin的玻璃体和血浆浓度,并检测VEGF和apelin的表达。方法:调查了44例活动性糖尿病性视网膜病变患者的44只眼。贝伐单抗研究组由20只眼睛组成,在平视玻璃体切除术前7天接受玻璃体内贝伐单抗注射(1.25 mg)。对照组包括24眼接受了平视玻璃体切除术而未事先注射玻璃体内贝伐单抗的眼睛。使用酶联免疫吸附测定,在玻璃体和血浆样品中测量VEGF和apelin的浓度。通过荧光免疫染色检查切除的视网膜前膜中VEGF和apelin的表达。结果:贝伐单抗组玻璃体和血浆中的VEGF浓度显着低于对照组(分别为P,0.001和P = 0.003),而两组的玻璃体和血浆中apelin的浓度无显着差异(P = 0.62和P = 0.09)。在两组的视网膜上纤维血管膜中,观察到内皮标记物CD31与apelin标记物共定位。结论:玻璃体内贝伐单抗注射可能导致眼内和全身VEGF浓度降低,提示对VEGF有局部或全身性作用,但可能对apelin无效。 Apelin可能与增生性糖尿病视网膜病变中视网膜前膜的发育有关,并且可能与VEGF不直接相关。

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