Division of Research, Qatar Foundation, Weill Cornell Medicine-Qatar, Doha, Qatar.
Araim Pharmaceuticals, Tarrytown, New York, USA.
Clin Exp Optom. 2020 May;103(3):265-277. doi: 10.1111/cxo.12887. Epub 2019 Mar 4.
Corneal confocal microscopy is a non-invasive ophthalmic imaging modality, which was initially used for the diagnosis and management of corneal diseases. However, over the last 20 years it has come to the forefront as a rapid, non-invasive, reiterative, cost-effective imaging biomarker for neurodegeneration. The human cornea is endowed with the densest network of sensory unmyelinated axons, anywhere in the body. A robust body of evidence shows that corneal confocal microscopy is a reliable and reproducible method to quantify corneal nerve morphology. Changes in corneal nerve morphology precede or relate to clinical manifestations of peripheral and central neurodegenerative conditions. Moreover, in clinical intervention trials, corneal nerve regeneration occurs early and predicts functional gains in trials of neuroprotection. In view of these findings, it is timely to summarise the knowledge in this area of research and to explain why the case for corneal confocal microscopy is sufficiently compelling to argue for its inclusion as a Food and Drug Administration endpoint in clinical trials of peripheral and central neurodegenerative conditions.
角膜共焦显微镜是一种非侵入性的眼科成像方式,最初用于诊断和管理角膜疾病。然而,在过去的 20 年中,它已成为一种快速、非侵入性、可重复、具有成本效益的神经退行性病变成像生物标志物。人体角膜拥有身体任何部位最密集的感觉无髓神经轴突网络。大量证据表明,角膜共焦显微镜是一种可靠且可重复的方法,可以定量分析角膜神经形态。角膜神经形态的变化先于或与周围和中枢神经退行性疾病的临床表现相关。此外,在临床干预试验中,角膜神经再生发生得较早,并预测神经保护试验中的功能增益。鉴于这些发现,及时总结这一研究领域的知识,并解释为什么角膜共焦显微镜的情况足够令人信服,可以认为它应该作为食品和药物管理局在周围和中枢神经退行性疾病临床试验中的终点纳入其中。