Horvath Rita, Gorman Grainne, Chinnery Patrick F
Mitochondrial Research Group, School of Neuroscience, University of Newcastle upon Tyne, United Kingdom.
Neurotherapeutics. 2008 Oct;5(4):558-68. doi: 10.1016/j.nurt.2008.07.002.
Mitochondrial disorders are a heterogeneous group of diseases affecting different organs (brain, muscle, liver, and heart), and the severity of the disease is highly variable. The chronicity and heterogeneity, both clinically and genetically, means that many patients require surveillance follow-up over their lifetime, often involving multiple disciplines. Although our understanding of the genetic defects and their pathological impact underlying mitochondrial diseases has increased over the past decade, this has not been paralleled with regards to treatment. Currently, no definitive pharmacological treatment exists for patients with mitochondrial dysfunction, except for patients with primary deficiency of coenzyme Q10. Pharmacological and nonpharmacological treatments increasingly being investigated include ketogenic diet, exercise, and gene therapy. Management is aimed primarily at minimizing disability, preventing complications, and providing prognostic information and genetic counseling based on current best practice. Here, we evaluate therapies used previously and review current and future treatment modalities for both adults and children with mitochondrial disease.
线粒体疾病是一组异质性疾病,会影响不同器官(脑、肌肉、肝脏和心脏),疾病严重程度差异很大。临床和遗传方面的慢性和异质性意味着许多患者在其一生中都需要进行监测随访,通常涉及多个学科。尽管在过去十年中我们对线粒体疾病潜在的遗传缺陷及其病理影响的理解有所增加,但在治疗方面却没有相应进展。目前,除了辅酶Q10原发性缺乏的患者外,对于线粒体功能障碍患者尚无明确的药物治疗方法。越来越多正在研究的药物和非药物治疗方法包括生酮饮食、运动和基因治疗。管理主要旨在尽量减少残疾、预防并发症,并根据当前最佳实践提供预后信息和遗传咨询。在此,我们评估先前使用的治疗方法,并综述线粒体疾病成人和儿童患者当前及未来的治疗方式。