University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI.
Asia Pac J Ophthalmol (Phila). 2018 Sep-Oct;7(5):345-351. doi: 10.22608/APO.2018298. Epub 2018 Sep 17.
Glaucoma is a chronic disease that can be challenging to treat for both patients and physicians. Most patients will require more than 1 medication over time to maintain their intraocular pressure (IOP) at a physiologically benign level. Patients may become refractory to existing compounds and many struggle with adherence to multiple topical drop regimens. The field of glaucoma therapeutics has been advancing rapidly with an emphasis on compounds comprising multiple molecules/mechanisms of action that offer additivity and are complementary to current therapeutics. Several new topical drop compounds directly targeting the trabecular meshwork (TM)/Schlemm canal/conventional outflow pathway to reduce outflow resistance have obtained US Food and Drug Administration approval in the past year. These include rho kinase inhibitors and nitric oxide donating compounds. Alternative therapies that offer long-term IOP lowering while removing the patient from the drug delivery system are moving forward in development. These include gene therapy and stem cell strategies, which could ease or eliminate the burden of topical drop self-administration for several years. Additionally, a variety of novel formulations and devices are in development that aim for controlled, steady state delivery of therapeutics over periods of months. The future of glaucoma therapy is focusing on an increase in specificity for the individual patient: their type of glaucoma; underlying mechanisms; genetic make-up; comorbid conditions; and rate of progression. Maintaining functional vision and improving patient outcomes remains the goal in glaucoma therapeutics. The current collection of novel therapeutics offers an expanded set of tools to achieve that goal.
青光眼是一种慢性疾病,无论是对患者还是医生来说,治疗都具有挑战性。大多数患者随着时间的推移需要使用 1 种以上的药物来将眼内压(IOP)维持在生理上良性的水平。患者可能会对现有化合物产生抗药性,许多人也难以坚持使用多种局部滴眼方案。青光眼治疗领域发展迅速,重点是包含多种分子/作用机制的化合物,这些化合物具有相加性,与当前的治疗方法互补。过去一年中,几种直接针对小梁网(TM)/施莱姆管/传统流出途径的新型局部滴眼化合物获得了美国食品和药物管理局(FDA)的批准,这些化合物包括 Rho 激酶抑制剂和一氧化氮供体化合物。替代疗法提供了长期降低 IOP 的效果,同时将患者从药物输送系统中解脱出来,目前正在开发中。这些疗法包括基因治疗和干细胞策略,这些策略可以在数年时间内减轻或消除局部滴眼自我给药的负担。此外,各种新的制剂和设备正在开发中,旨在实现数月内药物的持续、稳定输送。青光眼治疗的未来重点是提高对个体患者的特异性:他们的青光眼类型;潜在的发病机制;遗传构成;合并症;以及进展速度。保持功能性视力和改善患者预后仍然是青光眼治疗的目标。目前的一系列新型疗法提供了一套更广泛的工具来实现这一目标。