Emerson M Vaughn, Lauer Andreas K
Casey Eye Institute, Oregon Health and Science University, Portland, OR, USA.
Clin Ophthalmol. 2008 Jun;2(2):377-88. doi: 10.2147/opth.s1485.
Age-related macular degeneration (AMD) is the leading cause of vision loss in the industrialized world. In the last few decades, the mainstay of treatment for choroidal neovascularization (CNV) due to AMD has been thermal laser photocoagulation. In the last decade, photodynamic therapy with verteporfin extended treatment for more patients. While both of these treatments have prevented further vision loss in a subset of patients, improvement in visual acuity is rare. Anti-vascular endothelial growth factor A (VEGF) therapy has revolutionized the treatment of AMD-related CNV. Pegaptanib, an anti-VEGF aptamer prevents vision loss in CNV, although the performance is similar to that of photodynamic therapy. Ranibizumab, an antibody fragment and bevacizumab, a full-length humanized monoclonal antibody against VEGF have both shown promising results with improvements in visual acuity with either agent. VEGF trap, a modified soluble VEGF receptor analogue, binds VEGF more tightly than all other anti-VEGF agents and has also shown promising results in early trials. Other treatment strategies to decrease the effect of VEGF have used small interfering ribonucleic acid (RNA) to inhibit VEGF production and VEGF receptor production. Steroids, including anecortave acetate in the treatment and prevention of CNV, have shown promise in controlled trials. Receptor tyrosine kinase inhibitors, such as vatalanib, inhibit downstream effects of VEGF, and have been effective in the treatment of CNV in early studies. Squalamine lactate inhibits plasma membrane ion channels with downstream effects on VEGF, and has shown promising results with systemic administration. Other growth factors, including pigment epithelium-derived growth factor that has been administered via an adenoviral vector has shown promising initial results. In some patients ciliary neurotrophic factor is currently being studied for the inhibition of progression of geographic atrophy. Combination therapy has been investigated, and may prove to be more effective in the management of AMD-associated CNV. Ongoing and future studies will be crucial for optimizing the treatment of patients with AMD.
年龄相关性黄斑变性(AMD)是工业化国家视力丧失的主要原因。在过去几十年中,针对AMD所致脉络膜新生血管(CNV)的主要治疗方法一直是热激光光凝术。在过去十年中,维替泊芬光动力疗法使更多患者得到了治疗。虽然这两种治疗方法都在一部分患者中防止了视力进一步丧失,但视力提高的情况很少见。抗血管内皮生长因子A(VEGF)疗法彻底改变了AMD相关CNV的治疗方式。抗VEGF适配体培加他尼可防止CNV导致的视力丧失,但其效果与光动力疗法相似。雷珠单抗(一种抗体片段)和贝伐单抗(一种针对VEGF的全长人源化单克隆抗体)都显示出了令人鼓舞的结果,使用任一药物均可提高视力。VEGF陷阱(一种改良的可溶性VEGF受体类似物)比所有其他抗VEGF药物更紧密地结合VEGF,并且在早期试验中也显示出了令人鼓舞的结果。其他降低VEGF作用的治疗策略使用小干扰核糖核酸(RNA)来抑制VEGF生成和VEGF受体生成。类固醇,包括醋酸阿奈可他用于治疗和预防CNV,在对照试验中已显示出前景。受体酪氨酸激酶抑制剂,如瓦他拉尼,可抑制VEGF的下游效应,并且在早期研究中对CNV的治疗有效。乳酸角鲨胺可抑制质膜离子通道,对VEGF产生下游效应,全身给药已显示出令人鼓舞的结果。其他生长因子,包括通过腺病毒载体给药的色素上皮衍生生长因子,已显示出令人鼓舞的初步结果。目前正在对一些患者研究睫状神经营养因子对地图样萎缩进展的抑制作用。联合治疗已得到研究,可能证明对AMD相关CNV的管理更有效。正在进行的和未来的研究对于优化AMD患者的治疗至关重要。