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本文引用的文献

1
Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.肌营养不良蛋白的缺失会破坏骨骼肌信号传导:钙离子、活性氧和一氧化氮在肌肉萎缩症发展中的作用。
Physiol Rev. 2016 Jan;96(1):253-305. doi: 10.1152/physrev.00007.2015.
2
Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains.肌营养不良蛋白及相关蛋白在运动、神经肌肉接头和大脑中的非机械作用。
Brain Sci. 2015 Jul 29;5(3):275-98. doi: 10.3390/brainsci5030275.
3
All-cause mortality and cardiovascular outcomes with prophylactic steroid therapy in Duchenne muscular dystrophy.预防性类固醇治疗杜氏肌营养不良症的全因死亡率和心血管结局。
J Am Coll Cardiol. 2013 Mar 5;61(9):948-54. doi: 10.1016/j.jacc.2012.12.008. Epub 2013 Jan 23.
4
DuchenneConnect Registry Report.杜兴氏肌营养不良症关联注册报告。
PLoS Curr. 2012 Feb 29;4:RRN1309. doi: 10.1371/currents.RRN1309.
5
Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years - four states, 2007.2007年四个州5至24岁男性中杜氏/贝克型肌营养不良症的患病率
MMWR Morb Mortal Wkly Rep. 2009 Oct 16;58(40):1119-22.
6
Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).杜氏肌营养不良症的延迟诊断:来自肌肉萎缩症监测、追踪与研究网络(MD STARnet)的数据。
J Pediatr. 2009 Sep;155(3):380-5. doi: 10.1016/j.jpeds.2009.02.007. Epub 2009 Apr 25.
7
Experience and strategy for the molecular testing of Duchenne muscular dystrophy.杜氏肌营养不良症分子检测的经验与策略
J Mol Diagn. 2005 Aug;7(3):317-26. doi: 10.1016/S1525-1578(10)60560-0.
8
Dystrophin: the protein product of the Duchenne muscular dystrophy locus.肌营养不良蛋白:杜氏肌营养不良基因座的蛋白质产物。
Cell. 1987 Dec 24;51(6):919-28. doi: 10.1016/0092-8674(87)90579-4.

来自母项目“肌肉萎缩症”认证杜兴氏肌营养不良症护理中心主任关于患者获得已批准疗法的集体声明。

Collective Statement Regarding Patient Access to Approved Therapies from the Center Directors of Parent Project Muscular Dystrophy's Certified Duchenne Care Centers.

作者信息

Ionita Cristian, Kinnett Kathi, Mathews Katherine

机构信息

Department of Pediatrics (Neurology), Yale University School of Medicine, New Haven, CT, USA.

Parent Project Muscular Dystrophy, MIddletown, OH, USA.

出版信息

PLoS Curr. 2018 Mar 15;10:ecurrents.md.4a12c57a46a24603cb3d36d7fe0668b6. doi: 10.1371/currents.md.4a12c57a46a24603cb3d36d7fe0668b6.

DOI:10.1371/currents.md.4a12c57a46a24603cb3d36d7fe0668b6
PMID:29623241
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5878098/
Abstract

The dystrophinopathies (Duchenne [DMD] and Becker muscular dystrophy) are progressive diseases that until recently had no specific treatments. New FDA pathways to drug approval in rare diseases have resulted in a dramatic increase in the number of treatment trials for DMD and recently, two approved drugs. Health insurance policies for DMD products have been constructed with limited input from neuromuscular specialists directly involved in patient care and without patient input. These policies often reflect a lack of understanding of the disease, clinical population or the treatment. To ensure that policy determinations reflect best clinical practice, we recommend insurers work with neuromuscular specialists with expertise in care for patients with dystrophinopathy, as well as patients and families, and prominent advocacy organizations, such as Parent Project Muscular Dystrophy, in developing policies.

摘要

肌营养不良症(杜氏肌营养不良症[DMD]和贝克肌营养不良症)是一种进行性疾病,直到最近都没有特效治疗方法。美国食品药品监督管理局(FDA)针对罕见病的新药审批途径,使得DMD治疗试验的数量大幅增加,最近还有两种药物获批。DMD产品的健康保险政策在制定时,直接参与患者护理的神经肌肉专家提供的意见有限,也没有患者的参与。这些政策往往反映出对该疾病、临床患者群体或治疗方法缺乏了解。为确保政策决定反映最佳临床实践,我们建议保险公司在制定政策时,与在肌营养不良症患者护理方面具有专业知识的神经肌肉专家、患者及其家属以及像肌肉萎缩症家长项目这样的知名倡导组织合作。