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线粒体肌病的管理进展

Advances in Management of Mitochondrial Myopathies.

作者信息

Bangeas Athanasios, Poulidou Vasiliki, Liampas Ioannis, Marogianni Chrysa, Aloizou Athina-Maria, Tsouris Zisis, Sgantzos Markos, Arnaoutoglou Marianthi, Bogdanos Dimitrios P, Dardiotis Efthimios, Siokas Vasileios

机构信息

Department of Neurology, Laboratory of Neurogenetics, University Hospital of Larissa, Faculty of Medicine, School of Health Sciences, University of Thessaly, 41100 Larissa, Greece.

First Department of Neurology, AHEPA University Hospital, Aristotle University of Thessaloniki, Stilponos Kyriakidi 1, 54636 Thessaloniki, Greece.

出版信息

Int J Mol Sci. 2025 Jun 5;26(11):5411. doi: 10.3390/ijms26115411.

Abstract

Mitochondria, the energy factories of human organisms, can be the cause of a variety of genetic disorders called mitochondrial myopathies. Mitochondrial diseases arise from genetic alterations in either mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) and can manifest with great heterogeneity, leading to multiorgan dysfunction. The purpose of this article is to concisely review the pathophysiology, genetics and main clinical features of mitochondrial myopathies, focusing mainly on the treatment and management of these disorders. Currently, a particular treatment for mitochondrial myopathies does not exist, while the available guidelines concerning management are based on experts' opinions. The therapeutic options currently applied largely aim at symptom relief and amelioration of patients' quality of life. The most commonly used regimens involve the administration of vitamins and cofactors, although hard evidence regarding their true benefit for patients is still lacking. Recent studies have demonstrated promising results for elamipretide; however, phase III clinical trials are still ongoing. Regarding patient management, a multidisciplinary approach with the collaboration of different specialties is required. Further clinical trials for the already applied treatment options, as well as on novel experimental therapies, are of utmost importance in order to improve patients' outcomes.

摘要

线粒体作为人类机体的能量工厂,可能是多种被称为线粒体肌病的遗传疾病的病因。线粒体疾病源于线粒体DNA(mtDNA)或核DNA(nDNA)的基因改变,且表现出极大的异质性,会导致多器官功能障碍。本文旨在简要回顾线粒体肌病的病理生理学、遗传学及主要临床特征,重点关注这些疾病的治疗与管理。目前,尚无针对线粒体肌病的特效治疗方法,现有的管理指南基于专家意见。当前应用的治疗选择主要旨在缓解症状并改善患者生活质量。最常用的治疗方案包括给予维生素和辅助因子,不过仍缺乏关于其对患者真正益处的确凿证据。近期研究已证实艾拉米肽有令人期待的结果;然而,III期临床试验仍在进行中。在患者管理方面,需要不同专业协作的多学科方法。对已应用的治疗选择以及新型实验性疗法开展进一步临床试验,对于改善患者预后至关重要。

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