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用于年龄相关性黄斑变性的新型药物。

Emerging drugs for age-related macular degeneration.

作者信息

Augustin Albert J, Offermann Indre

机构信息

Eye Clinic, Department of Ophthalmology, Moltkestrasse 90, 76133 Karlsruhe, Germany.

出版信息

Expert Opin Emerg Drugs. 2006 Nov;11(4):725-40. doi: 10.1517/14728214.11.4.725.

DOI:10.1517/14728214.11.4.725
PMID:17064228
Abstract

Age-related macular degeneration (AMD) is a leading cause of blindness that until recently had no recognised drug treatment. In wet AMD, choroidal neovascularisation (CNV) causes a profound loss of central vision. CNV is a complex process in which tissue ischaemia and/or inflammation is thought to trigger production of angiogenic signal molecules. The release of VEGF appears to be particularly important. Verteporfin photodynamic therapy was the first drug therapy to be licensed for the treatment of some types of wet AMD. Other treatments directly targeting VEGF or other aspects of angiogenesis, such as pegaptanib, ranibizumab and anecortave acetate, have either recently been licensed or are in the advanced stages of development. These and other promising treatment options such as combination strategies are reviewed.

摘要

年龄相关性黄斑变性(AMD)是导致失明的主要原因,直到最近都没有公认的药物治疗方法。在湿性AMD中,脉络膜新生血管形成(CNV)会导致严重的中心视力丧失。CNV是一个复杂的过程,其中组织缺血和/或炎症被认为会触发血管生成信号分子的产生。血管内皮生长因子(VEGF)的释放似乎尤为重要。维替泊芬光动力疗法是首个被批准用于治疗某些类型湿性AMD的药物疗法。其他直接靶向VEGF或血管生成其他方面的治疗方法,如培加尼布、雷珠单抗和醋酸阿奈可他韦,要么最近已获得批准,要么正处于研发的后期阶段。本文对这些以及其他有前景的治疗选择(如联合策略)进行了综述。

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Emerging drugs for age-related macular degeneration.用于年龄相关性黄斑变性的新型药物。
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Verteporfin photodynamic therapy and anti-angiogenic drugs: potential for combination therapy in exudative age-related macular degeneration.维替泊芬光动力疗法与抗血管生成药物:用于渗出性年龄相关性黄斑变性联合治疗的潜力
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Evolving European guidance on the medical management of neovascular age related macular degeneration.不断发展的欧洲关于新生血管性年龄相关性黄斑变性医疗管理的指南。
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A view on new drugs for macular degeneration.关于黄斑变性新药的观点。
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Expert Opin Biol Ther. 2015;15(9):1349-58. doi: 10.1517/14712598.2015.1057565. Epub 2015 Jun 16.

引用本文的文献

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Identification of pathogenic genes and upstream regulators in age-related macular degeneration.年龄相关性黄斑变性中致病基因及上游调节因子的鉴定
BMC Ophthalmol. 2017 Jun 26;17(1):102. doi: 10.1186/s12886-017-0498-z.
2
VEGFA and VEGFR2 gene polymorphisms and response to anti-vascular endothelial growth factor therapy: comparison of age-related macular degeneration treatments trials (CATT).VEGFA 和 VEGFR2 基因多态性与抗血管内皮生长因子治疗反应:年龄相关性黄斑变性治疗试验(CATT)比较。
JAMA Ophthalmol. 2014 May;132(5):521-7. doi: 10.1001/jamaophthalmol.2014.109.
3
Progress and perspectives on the role of RPE cell inflammatory responses in the development of age-related macular degeneration.
视网膜色素上皮细胞炎症反应在年龄相关性黄斑变性发展中的作用的研究进展与展望。
J Inflamm Res. 2008;1:49-65. doi: 10.2147/jir.s4354. Epub 2008 Dec 2.
4
Anti-sphingosine-1-phosphate monoclonal antibodies inhibit angiogenesis and sub-retinal fibrosis in a murine model of laser-induced choroidal neovascularization.抗1-磷酸鞘氨醇单克隆抗体在激光诱导脉络膜新生血管小鼠模型中抑制血管生成和视网膜下纤维化。
Exp Eye Res. 2009 Mar;88(3):367-77. doi: 10.1016/j.exer.2008.07.012. Epub 2008 Aug 6.
5
Video monitoring of neovessel occlusion induced by photodynamic therapy with verteporfin (Visudyne), in the CAM model.在鸡胚绒毛尿囊膜(CAM)模型中,使用维替泊芬(Visudyne)进行光动力疗法诱导新生血管闭塞的视频监测。
Angiogenesis. 2008;11(3):235-43. doi: 10.1007/s10456-008-9106-4. Epub 2008 Mar 7.
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