Patel Sanjay V
Ophthalmology, Mayo Clinic, Rochester, Minnesota, USA.
BMJ Open Ophthalmol. 2019 Jul 11;4(1):e000321. doi: 10.1136/bmjophth-2019-000321. eCollection 2019.
The surgical treatment of Fuchs endothelial corneal dystrophy (FECD) has advanced dramatically over the last two decades. Penetrating keratoplasty has been superseded by various iterations of endothelial keratoplasty, and currently, surgical removal of host Descemet membrane without keratoplasty is being investigated. These surgical advances have been accompanied by significant improvement of our understanding of the underlying disease mechanisms, not least the discovery that FECD in western populations is predominantly an intronic trinucleotide repeat expansion disorder in the gene that results in RNA toxicity and mis-splicing. Understanding the disease mechanisms augurs well for developing targeted molecular medical therapies, which will require careful clinical investigation through trials to prove their efficacy and safety. As the field advances towards clinical trials, investigators should carefully define the disease state being treated and consider the options for outcome measures relevant to the type of intervention. FECD, and the outcomes of interventions to treat the disease, can be measured in terms of corneal morphology, corneal function and clinical impact. Standardising the approach for defining FECD and careful thought about the outcomes of intervention that are reported will help make the results of future trials for FECD applicable in clinical practice.
在过去二十年中,富克斯内皮性角膜营养不良(FECD)的外科治疗取得了显著进展。穿透性角膜移植术已被各种内皮角膜移植术所取代,目前,正在研究不进行角膜移植而手术切除宿主后弹力层的方法。这些手术进展伴随着我们对潜在疾病机制的理解有了显著改善,尤其是发现西方人群中的FECD主要是一种基因内含子三核苷酸重复扩增疾病,这会导致RNA毒性和错误剪接。了解疾病机制对于开发靶向分子医学疗法很有帮助,而这需要通过试验进行仔细的临床研究以证明其有效性和安全性。随着该领域向临床试验迈进,研究人员应仔细定义所治疗的疾病状态,并考虑与干预类型相关的结局测量选项。FECD以及治疗该疾病的干预结果可以从角膜形态、角膜功能和临床影响方面进行测量。标准化定义FECD的方法并仔细考虑所报告的干预结果将有助于使未来FECD试验的结果适用于临床实践。