Mori-Yoshimura Madoka, Nishino Ichizo
Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry.
Brain Nerve. 2015 Sep;67(9):1115-23. doi: 10.11477/mf.1416200269.
Distal myopathy with rimmed vacuoles or GNE myopathy, is an early adult-onset myopathy with slow progression that preferentially affects the tibialis anterior muscle. Severely affected patients show marked limb muscle atrophy together with respiratory dysfunction. The disease is caused by a mutation in the GNE gene that catalyzes two rate-limiting reactions in cytosolic sialic acid synthesis. Oral treatment with sialic acid metabolite prevents muscle atrophy and weakness in a mouse GNE myopathy model and a global Phase III study is currently underway. In addition, a global patient registry of neuromuscular cases is widely accepted as a useful tool to obtain epidemiological data and bolster patient recruitment for further development of this treatment strategy.
伴有镶边空泡的远端肌病或GNE肌病,是一种成年早期发病的肌病,进展缓慢,优先累及胫前肌。严重受累患者表现出明显的肢体肌肉萎缩以及呼吸功能障碍。该疾病由GNE基因突变引起,GNE基因催化胞质唾液酸合成中的两个限速反应。在小鼠GNE肌病模型中,唾液酸代谢物的口服治疗可预防肌肉萎缩和无力,目前一项全球III期研究正在进行。此外,一个全球神经肌肉病例患者登记处被广泛认为是获取流行病学数据和促进患者招募以进一步开发这种治疗策略的有用工具。