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遗传性神经病的新型治疗方法:系统评价

Novel Therapeutic Approaches in Inherited Neuropathies: A Systematic Review.

作者信息

Hustinx Manon, Shorrocks Ann-Marie, Servais Laurent

机构信息

Department of Paediatrics, MDUK Oxford Neuromuscular Centre and, NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford OX1 3DW, UK.

Centre de Référence des Maladies Neuromusculaires, Department of Neurology, University Hospital Liège, and University of Liège, 4000 Liège, Belgium.

出版信息

Pharmaceutics. 2023 May 30;15(6):1626. doi: 10.3390/pharmaceutics15061626.

Abstract

The management of inherited neuropathies relies mostly on the treatment of symptoms. In recent years, a better understanding of the pathogenic mechanisms that underlie neuropathies has allowed for the development of disease-modifying therapies. Here, we systematically review the therapies that have emerged in this field over the last five years. An updated list of diseases with peripheral neuropathy as a clinical feature was created based on panels of genes used clinically to diagnose inherited neuropathy. This list was extended by an analysis of published data by the authors and verified by two experts. A comprehensive search for studies of human patients suffering from one of the diseases in our list yielded 28 studies that assessed neuropathy as a primary or secondary outcome. Although the use of various scales and scoring systems made comparisons difficult, this analysis identified diseases associated with neuropathy for which approved therapies exist. An important finding is that the symptoms and/or biomarkers of neuropathies were assessed only in a minority of cases. Therefore, further investigation of treatment efficacy on neuropathies in future trials must employ objective, consistent methods such as wearable technologies, motor unit indexes, MRI or sonography imaging, or the use of blood biomarkers associated with consistent nerve conduction studies.

摘要

遗传性神经病的治疗主要依赖于症状治疗。近年来,对神经病潜在致病机制的深入了解使得能够开发改善病情的疗法。在此,我们系统回顾了过去五年该领域出现的疗法。基于临床上用于诊断遗传性神经病的基因面板,创建了一份以周围神经病为临床特征的疾病更新列表。通过作者对已发表数据的分析扩展了该列表,并由两位专家进行了验证。对患有我们列表中一种疾病的人类患者的研究进行全面检索,得到了28项将神经病作为主要或次要结局进行评估的研究。尽管使用各种量表和评分系统使得比较困难,但该分析确定了存在已批准疗法的与神经病相关的疾病。一个重要发现是,仅在少数病例中评估了神经病的症状和/或生物标志物。因此,未来试验中对神经病治疗效果的进一步研究必须采用客观、一致的方法,如可穿戴技术、运动单位指标、MRI或超声成像,或使用与一致的神经传导研究相关的血液生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2e8/10305260/3b2aa2a21e61/pharmaceutics-15-01626-g001.jpg

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