Fiandaca Massimo, Forsayeth John, Bankiewicz Krystof
Department of Neurological Surgery, Movement Disorder Research Program, University of California, Mission Center Building, San Francisco, CA 94103, USA.
Exp Neurol. 2008 Jan;209(1):51-7. doi: 10.1016/j.expneurol.2007.08.009. Epub 2007 Aug 24.
The incidence of Parkinson's disease (PD) increases greatly with age, and the baby-boomer population can expect to generate a large number of individuals with the disease, all of whom will have significantly increased medical care needs over periods of 20 years or more. This emerging healthcare burden to our society calls for accelerated efforts to understand this disease better and treat it more effectively. The growing interest in gene therapy grew out of a recognition that new medicines may be needed to combat the relentless progression of the disease in the face of conventional pharmaco-therapies and surgical interventions that have so far failed to offer more than palliative relief. The potential of gene therapy to alter dramatically the course of the disease lies very much with the challenge of converting a research tool into a medical option, a process that clearly requires a unique combination of rigor and flexibility. In this review, we examine the unique aspects of gene therapy that make its use in PD attractive, but also analyze the difficulties of employing a medicine that acts for the rest of the patient's life.
帕金森病(PD)的发病率随年龄增长大幅上升,婴儿潮一代预计会产生大量患该疾病的个体,所有这些人在20年或更长时间内的医疗需求将显著增加。这种给我们社会带来的新出现的医疗负担要求加快努力,以便更好地了解这种疾病并更有效地治疗它。对基因治疗兴趣的增加源于这样一种认识,即面对传统药物治疗和手术干预迄今未能提供超过姑息性缓解的情况,可能需要新的药物来对抗该疾病的持续进展。基因治疗有可能极大地改变疾病进程,这在很大程度上取决于将一种研究工具转化为一种医疗选择所面临的挑战,这一过程显然需要严谨性和灵活性的独特结合。在这篇综述中,我们研究了基因治疗在帕金森病中应用的独特之处,这些独特之处使其具有吸引力,但同时也分析了使用一种作用于患者余生的药物所面临的困难。