两个关于莉氏综合症谱系治疗创新的故事。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Wei-Sheng Lin
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引用次数: 0

摘要

Leigh综合征谱系是儿童期线粒体脑病最常见的形式,其特征是进行性神经变性。迄今为止,这种疾病的治疗选择仍然有限。尽管如此,在过去的十年中,有两条研究路线显示出令人鼓舞的结果,值得进一步研究。首先,治疗性缺氧似乎可以改善神经系统预后,这有点违反直觉,但有临床前证据支持。此外,烟酸或烟酰胺核苷可以作为一种辅助治疗,增强缺氧的神经保护作用。其次,临床前研究和初步临床经验表明,西地那非对Leigh综合征具有潜在的疾病改善作用。西地那非已被用于治疗肺动脉高压,其用于Leigh综合征的重新用途已得到欧洲药品管理局的认可。这一观点旨在提高对这些进展的认识,并呼吁进行更多的临床研究,以确保在临床实践中安全有效地实施这些治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two tales of therapeutic innovations for Leigh syndrome spectrum.

Leigh syndrome spectrum is the most common form of childhood-onset mitochondrial encephalopathy and is characterized by progressive neurodegeneration. Treatment options for this condition remain limited to date. Nonetheless, two lines of research endeavor in the past decade have shown encouraging results worthy of further investigations. First, therapeutic hypoxia appears to improve neurological outcomes, which is somewhat counterintuitive but supported by preclinical evidence. Furthermore, nicotinic acid or nicotinamide riboside could be an adjunctive therapy that enhances the neuroprotective effect of hypoxia. Second, preclinical studies and preliminary clinical experience suggest that sildenafil is potentially disease-modifying for Leigh syndrome. Sildenafil has already been used to treat pulmonary hypertension, and its repurposing for Leigh syndrome has been endorsed by European Medicines Agency. This perspective aims to raise awareness about these progresses, as well as to call for more clinical studies to ensure safe and effective implementation of these treatment approaches in clinical practice.

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来源期刊
Journal of neurogenetics
Journal of neurogenetics 医学-神经科学
CiteScore
4.40
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms
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