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Leber遗传性视神经病变的治疗:从理论到实践

Treatment of Leber's hereditary optic neuropathy: theory to practice.

作者信息

Johns Donald R, Colby Kathryn A

机构信息

Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Semin Ophthalmol. 2002 Mar;17(1):33-8. doi: 10.1076/soph.17.1.33.10288.

Abstract

Dramatic advances in our understanding of the molecular genetic basis of Leber's hereditary optic neuropathy (LHON) have revolutionized our ability to diagnose and prognosticate this disease. Unfortunately no corresponding advances in the treatment of LHON have emerged. Glaucoma is a prevalent form of optic neuropathy that has been studied extensively. Lessons learned from treatment of LHON and glaucoma may have important implications for both diseases. LHON presents formidable challenges to the design and conduct of clinical trials. The acutely symptomatic LHON patient with monocular vision loss provides a unique clinical situation in which to test an agent during a critical therapeutic window. Advances in neuroprotection, apoptosis, and neurodegenerative diseases may provide important clues for potential therapeutic agents for LHON. Antioxidants and agents that interfere with the critical steps of mitochondrial-dependent, oxidative stress-induced apoptosis are candidates for future LHON therapy. A variety of neuroprotective agents, under active investigation in other diseases, may be useful in LHON therapy. Effective pharmacotherapy will complement the current management approach that has changed little in the 130 years since LHON was originally described.

摘要

我们对莱伯遗传性视神经病变(LHON)分子遗传基础的理解取得了巨大进展,彻底改变了我们诊断和预测这种疾病的能力。不幸的是,在LHON治疗方面并未取得相应进展。青光眼是一种广泛研究的视神经病变形式。从LHON和青光眼治疗中吸取的经验教训可能对这两种疾病都有重要意义。LHON给临床试验的设计和实施带来了巨大挑战。患有单眼视力丧失的急性症状性LHON患者提供了一种独特的临床情况,可在关键治疗窗口期间测试一种药物。神经保护、细胞凋亡和神经退行性疾病方面的进展可能为LHON的潜在治疗药物提供重要线索。抗氧化剂和干扰线粒体依赖性、氧化应激诱导细胞凋亡关键步骤的药物是未来LHON治疗的候选药物。目前正在其他疾病中积极研究的多种神经保护药物可能对LHON治疗有用。有效的药物治疗将补充自最初描述LHON以来130年中变化不大的当前管理方法。

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