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与FKRP基因相关的R9型肢带型肌营养不良症:现状与治疗前景

[Limb-Girdle Muscular Dystrophy type R9 linked to the FKRP gene: state of the art and therapeutic perspectives].

作者信息

Villar Quiles Rocío Nur, Richard Isabelle, Bouchet-Seraphin Céline, Stojkovic Tanya

机构信息

Centre de Référence des maladies neuromusculaires Nord/Est/Île-de-France, APHP, Groupe Hospitalier Pitié-Salpêtrière, Sorbonne Université, Paris, France.

Généthon, 91000 Évry, France. - Université Paris-Saclay, Université d'Évry, Inserm, Généthon, unité de recherche Integrare, UMR_S951, 91000 Évry, France.

出版信息

Med Sci (Paris). 2020 Dec;36 Hors série n° 2:28-33. doi: 10.1051/medsci/2020239. Epub 2021 Jan 11.

Abstract

Mutations in the FKRP gene encoding the fukutin-related protein (FKRP) cause a wide spectrum of myopathies, ranging from severe forms of congenital muscular dystrophies associated with structural abnormalities of the central nervous system, to exertional myalgia or asymptomatic hyperCKemia, and to a form of limb girdle muscular dystrophy, LGMD-R9, (ex-LGMD-2I). LGMD-R9 is characterized by a proximal girdle deficit predominantly in the lower limbs to start with, with respiratory and cardiac damage that may affect the vital prognosis. Serum CK levels are markedly elevated and, on muscle biopsy, is detected a dystrophic formula associated with a reduction in the glycosylation of α-dystroglycan by immunostains and immunoblotting. Muscle MRI typically shows damage to proximal muscles (iliopsoas, adductors, gluteus maximus, quadriceps) with relative preservation of the muscles of the anterior compartment of the thighs (gracilis and sartorius). Genetic analysis, by specific sequencing of the FKRP gene or of a panel grouping together all the genes involved in the glycosylation of α-dystroglycan, or a larger panel of genes, generally confirms the diagnosis, the most frequent mutation being the missense p.(Leu276Ile). Currently, treatment of LGMD-R9 is symptomatic, requiring a multidisciplinary approach. A prospective study of the natural history of the disease is currently underway in Europe (GNT-015-FKRP). New therapeutic approaches are envisaged, such as gene therapy mediated by vectors derived from the adeno-associated virus (AAV). This is effective in animal models, allowing correction of defects in the glycosylation of alpha-dystroglycan and an increase in its binding capacity to the extracellular matrix. At the same time, preclinical studies have shown, in an animal model, the efficacy of ribitol, an alcohol pentose found in natural compounds, which has led to a phase I trial whose clinical development is underway.

摘要

编码福金相关蛋白(FKRP)的FKRP基因突变会导致多种肌病,范围从与中枢神经系统结构异常相关的严重先天性肌营养不良,到运动性肌痛或无症状高肌酸激酶血症,再到一种肢带型肌营养不良症,即LGMD-R9(原LGMD-2I)。LGMD-R9的特征是最初主要在下肢出现近端带肌无力,伴有可能影响生命预后的呼吸和心脏损害。血清肌酸激酶水平显著升高,肌肉活检时,通过免疫染色和免疫印迹检测到与α- dystroglycan糖基化减少相关的营养不良模式。肌肉磁共振成像(MRI)通常显示近端肌肉(髂腰肌、内收肌、臀大肌、股四头肌)受损,而大腿前侧肌群(股薄肌和缝匠肌)相对保留。通过对FKRP基因或一组包含所有参与α- dystroglycan糖基化的基因,或更大的基因组合进行特定测序的基因分析,通常可以确诊,最常见的突变是错义突变p.(Leu276Ile)。目前,LGMD-R9的治疗是对症治疗,需要多学科方法。欧洲目前正在进行一项关于该疾病自然史的前瞻性研究(GNT-015-FKRP)。设想了新的治疗方法,如由腺相关病毒(AAV)衍生载体介导的基因治疗。这在动物模型中是有效的,能够纠正α- dystroglycan糖基化缺陷并增加其与细胞外基质的结合能力。同时,临床前研究在动物模型中显示了天然化合物中发现的戊糖醇核糖醇的疗效,这已导致一项正在进行临床开发的I期试验。

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