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治疗与年龄相关的黄斑变性相关性地理萎缩的在研药物。

Investigational Agents in Development for the Treatment of Geographic Atrophy Secondary to Age-Related Macular Degeneration.

机构信息

Retina Consultants of Texas, Retina Consultants of America, 4460 Bissonnet St., Suite 200, Bellaire, Texas, 77401, United States.

Blanton Eye Institute, Houston Methodist Hospital, Houston, TX, USA.

出版信息

BioDrugs. 2021 May;35(3):303-323. doi: 10.1007/s40259-021-00481-y. Epub 2021 Apr 24.

Abstract

Geographic atrophy (GA) is an advanced form of age-related macular degeneration, a late-onset, complex, genetic degenerative disease of the retina. Multiple environmental and genetic factors have been implicated in the development of GA, a pathology ultimately defined by loss of photoreceptors and the underlying retinal pigment epithelium and choriocapillaris. The personal burden of GA has been documented to have a substantial negative impact on quality of life, with progressive and cumulative loss of visual function each year. Currently, there are no treatments to prevent or slow the development or progression of GA. Multiple genetic and histopathologic studies have implicated dysregulation of the complement cascade in GA pathogenesis, leading to the development of several investigational pharmaceuticals targeting key factors in this inflammatory pathway. Several other biochemical pathways have also been implicated in GA development and progression, such as mitochondrial components, mediators of apoptosis and molecules involved in extracellular matrix remodeling, many of which are also being investigated for their potential value as therapeutic targets for GA treatment. Recent advancements in our understanding of GA pathogenesis and the progression of multiple potential therapeutics into later-stage human clinical trials hold great promise for a clinically effective therapeutic for patients with GA to emerge within the near future.

摘要

地理萎缩(GA)是一种与年龄相关的黄斑变性的晚期形式,是一种后天发生的、复杂的、遗传退行性视网膜疾病。多种环境和遗传因素与 GA 的发展有关,GA 的病理学最终定义为光感受器和其下的视网膜色素上皮和脉络膜毛细血管丧失。GA 的个人负担已被证明对生活质量有重大负面影响,每年视觉功能都会逐渐累积丧失。目前,尚无治疗方法可预防或减缓 GA 的发展或进展。多项遗传和组织病理学研究表明,补体级联的失调与 GA 的发病机制有关,导致开发出几种针对该炎症途径关键因素的研究性药物。GA 的发展和进展还涉及其他几种生化途径,如线粒体成分、细胞凋亡介质和细胞外基质重塑分子,其中许多也在研究其作为 GA 治疗潜在治疗靶点的价值。最近对 GA 发病机制的认识进展以及多种潜在治疗药物进入后期人体临床试验,为 GA 患者出现临床有效的治疗方法带来了巨大希望。

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