Perlman Susan L
Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
J Child Neurol. 2012 Sep;27(9):1217-22. doi: 10.1177/0883073812453872.
There are now 21 agents or classes of therapeutic agents in the Friedreich ataxia research pipeline (http://www.curefa.org/pipeline.html) that have been developed in the 15 years since the discovery of the frataxin gene, with the ongoing characterization of its mutations and the resulting molecular pathology. Twenty-four studies are currently posted on ClinicalTrials.gov. Twenty-seven works discussing the results of clinical trials in Friedreich ataxia have been published. In 2010, 42 public (National Institutes of Health) and private (Friedreich Ataxia Research Alliance, Muscular Dystrophy Association, and National Ataxia Foundation) grants were funded for translational and clinical research in Friedreich ataxia. Millions of dollars from public, private, and industry-based initiatives have been dedicated to research in Friedreich ataxia therapeutics. Despite this vigorous international effort, there is as yet no proven disease-modifying therapy for Friedreich ataxia.
自发现frataxin基因后的15年里,目前在弗里德赖希共济失调研究进程中(http://www.curefa.org/pipeline.html)已有21种治疗药物或药物类别,同时其突变及由此产生的分子病理学也在持续得到鉴定。目前在ClinicalTrials.gov上公布了24项研究。已发表了27篇讨论弗里德赖希共济失调临床试验结果的论文。2010年,为弗里德赖希共济失调的转化研究和临床研究提供了42项公共(美国国立卫生研究院)和私人(弗里德赖希共济失调研究联盟、肌肉萎缩症协会和全国共济失调基金会)资助。来自公共、私人和行业倡议的数百万美元已投入到弗里德赖希共济失调治疗研究中。尽管有这种积极的国际努力,但目前仍没有经证实的针对弗里德赖希共济失调的疾病改善疗法。