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Advances in glaucoma treatment and management: Neurotrophic agents

机译:青光眼治疗和管理的进展:神经营养剂

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摘要

The causes of glaucoma are complex and so are its treatment regimens. It is almost as if glaucoma were several separate diseases. Controlling intraocular pressure (IOP) in the anterior segment is certainly a prime consideration, but the pathologic endpoint of glaucoma is the death of the retinal ganglion cell in the posterior segment. The disease itself is probably best called an optic neuropathy, one of many diseases that can affect neuronal cells. However, it is unique as to the cell affected (the ganglion cell) and the endpoints of the disease process. Biologically and physically, glaucoma is characterized by changes in the optic disc, optic nerve, and brain and by ganglion cell death. Functionally, the changes lead to visual impairment, as best exemplified by a decrease in visual field. Thus, developing methods of preserving ganglion cell function and lifespan are the ultimate goals in maintaining vision in glaucoma. One way to achieve preservation is through neuroprotection—the use of neuron-survival (neurotrophic) agents.
机译:青光眼的病因很复杂,其治疗方案也很复杂。青光眼几乎是几种不同的疾病。控制前段的眼内压(IOP)当然是首要考虑因素,但青光眼的病理终点是后段视网膜神经节细胞的死亡。这种疾病本身最好被称为视神经病变,它是可以影响神经元细胞的许多疾病之一。但是,对于受影响的细胞(神经节细胞)和疾病过程的终点,它是唯一的。从生物学和物理上讲,青光眼的特征在于视盘,视神经和大脑的变化以及神经节细胞死亡。从功能上讲,这些变化会导致视力障碍,最好的例子是视野减少。因此,开发保持神经节细胞功能和寿命的方法是维持青光眼视力的最终目标。实现保存的一种方法是通过神经保护-使用神经元存活(神经营养)药物。

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