Division of Pediatric Pulmonary, Massachusetts General Hospital for Children, Harvard Medical School, Boston, MA, USA.
Division of Pulmonology Pediatric Pulmonary, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
J Neuromuscul Dis. 2018;5(1):47-58. doi: 10.3233/JND-170272.
Duchenne muscular dystrophy (DMD) is a rare, degenerative, X-linked genetic disease that results in progressive muscle loss and premature death, most commonly from respiratory or cardiac failure. DMD is primarily caused by whole exon deletions, resulting in a shift of the dystrophin mRNA reading frame that prevents production of functional dystrophin protein. Eteplirsen, a phosphorodiamidate morpholino oligomer (PMO), is designed to skip exon 51, restore the reading frame, and induce production of internally shortened dystrophin in patients with mutations amenable to such treatment.
Describe lung function assessed throughout eteplirsen studies 201/202.
Studies 201/202 included 12 patients treated with eteplirsen over 5 years. Pulmonary function tests included forced vital capacity (FVC), maximum expiratory pressure (MEP), and maximum inspiratory pressure (MIP). With no long-term placebo control, FVC results were compared with data from the United Dystrophinopathy Project (UDP). MIP and MEP were compared to published natural history.
Age-adjusted mixed-model repeated-measures analysis showed decreases of 2.3% and 2.6% annually for FVC% p and MEP% p, and an annual increase of 0.6% for MIP% p for the eteplirsen-treated cohort. Data from the UDP demonstrated a 4.1% decline in FVC% p. The published natural history reports annual declines of at least 2.7% and 3.8% for MEP% p and MIP% p, respectively, in patients with DMD.
With eteplirsen treatment, deterioration of respiratory muscle function based on FVC% p was half of that seen in the UDP; MEP% p and MIP% p compared favorably with natural history.
杜氏肌营养不良症(DMD)是一种罕见的、进行性的、X 连锁的遗传性疾病,导致肌肉逐渐丧失和过早死亡,最常见的原因是呼吸或心力衰竭。DMD 主要由整个外显子缺失引起,导致肌营养不良蛋白 mRNA 阅读框架移位,从而阻止功能性肌营养不良蛋白的产生。Eteplirsen 是一种磷酰胺二酯吗啉寡聚物(PMO),旨在跳过外显子 51,恢复阅读框架,并诱导对这种治疗有反应的突变患者产生内部缩短的肌营养不良蛋白。
描述在 eteplirsen 研究 201/202 中评估的肺功能。
研究 201/202 包括 12 名接受 eteplirsen 治疗超过 5 年的患者。肺功能测试包括用力肺活量(FVC)、最大呼气压力(MEP)和最大吸气压力(MIP)。由于没有长期安慰剂对照,因此将 FVC 结果与美国肌营养不良症项目(UDP)的数据进行比较。MIP 和 MEP 与已发表的自然病史进行了比较。
年龄调整的混合模型重复测量分析显示,eteplirsen 治疗组的 FVC%p 和 MEP%p 每年分别下降 2.3%和 2.6%,MIP%p 每年增加 0.6%。UDP 数据显示 FVC%p 下降了 4.1%。已发表的自然病史报告显示,DMD 患者的 MEP%p 和 MIP%p 每年分别至少下降 2.7%和 3.8%。
用 eteplirsen 治疗,基于 FVC%p 的呼吸肌功能恶化程度是 UDP 所见的一半;MEP%p 和 MIP%p 与自然病史相比表现良好。