Dino Ferrari Centre, Neuroscience Section, Department of Pathophysiology and Transplantation (DEPT), Neurology Unit, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Via Francesco Sforza 35, 20122, Milan, Italy.
Mol Neurobiol. 2018 Aug;55(8):6307-6318. doi: 10.1007/s12035-017-0831-9. Epub 2018 Jan 2.
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by the degeneration of lower motor neurons (MNs) in the spinal cord and brain stem, which results in relentless muscle weakness and wasting, leading to premature death due to respiratory complications. The identification of the specific mutations in the survival motor neuron 1 (SMN1) gene that causes SMA has led to the development of experimental therapeutic strategies to increase SMN protein expression, including antisense oligonucleotides, small molecules, and gene therapy, which have so far shown promising results. The timing of therapeutic intervention is crucial since most of the degeneration in MNs occurs in the first months of life in patients with SMA type 1, which is the most severe and common form of SMA. Nevertheless, a precise temporal window for therapeutic intervention has not yet been identified. Evidence from in vivo studies in mice and large animals suggested that early therapeutic intervention for SMA correlated with better motor performance, longer survival, and, occasionally, rescue of the pathological phenotype. Indeed, the need to compensate for the loss of SMN protein function seemed to diminish during adulthood (even though repair ability after nerve injury remained impaired), suggesting the possibility of tapering the therapy administration late in the disease course. Moreover, recent clinical trials on children afflicted with SMA type 1 have shown a more rapid achievement of motor milestones and diminished disease severity when therapy was administered at an early age and earlier in the disease course. Finally, these results highlight the importance of newborn screening for SMA to facilitate early diagnosis and present the patient with available treatments while they are still in the presymptomatic stage.
脊髓性肌萎缩症(SMA)是一种常染色体隐性神经肌肉疾病,其特征是脊髓和脑干中的运动神经元(MNs)进行性退化,导致肌肉无力和萎缩,最终因呼吸并发症导致过早死亡。对导致 SMA 的生存运动神经元 1(SMN1)基因的特定突变的鉴定,导致了增加 SMN 蛋白表达的实验性治疗策略的发展,包括反义寡核苷酸、小分子和基因治疗,迄今为止已显示出有希望的结果。治疗干预的时机至关重要,因为大多数 MN 退化发生在 SMA 1 型患者生命的前几个月,这是最严重和最常见的 SMA 形式。然而,尚未确定治疗干预的精确时间窗口。来自小鼠和大型动物体内研究的证据表明,SMA 的早期治疗干预与更好的运动表现、更长的生存时间以及偶尔恢复病理表型相关。事实上,在成年期似乎需要补偿 SMN 蛋白功能的丧失(尽管神经损伤后的修复能力仍然受损),这表明在疾病过程的后期可能需要减少治疗药物的剂量。此外,最近对患有 SMA 1 型的儿童进行的临床试验表明,当治疗在早期和疾病早期进行时,运动里程碑的实现更快,疾病严重程度降低。最后,这些结果强调了对 SMA 进行新生儿筛查的重要性,以促进早期诊断,并在患者仍处于无症状阶段时提供可用的治疗方法。