Pyle Angela, Anugrha Haidyan, Kurzawa-Akanbi Marzena, Yarnall Alison, Burn David, Hudson Gavin
Mitochondrial Research Group, Institute of Genetic Medicine, University of Newcastle Upon Tyne, UK.
Insitutute of Neuroscience, University of Newcastle Upon Tyne, UK.
Neurobiol Aging. 2016 Feb;38:216.e7-216.e10. doi: 10.1016/j.neurobiolaging.2015.10.033. Epub 2015 Nov 5.
Like any organ, the brain is susceptible to the march of time and a reduction in mitochondrial biogenesis is a hallmark of the aging process. In the largest investigation of mitochondrial copy number in Parkinson's disease (PD) to date and by using multiple tissues, we demonstrate that reduced Parkinson DNA (mitochondrial DNA mtDNA) copy number is a biomarker for the etiology of PD. We used established methods of mtDNA quantification to assess the copy number of mtDNA in n = 363 peripheral blood samples, n = 151 substantia nigra pars compacta tissue samples and n = 120 frontal cortex tissue samples from community-based PD cases fulfilling UK-PD Society brain bank criteria for the diagnosis of PD. Accepting technical limitations, our data show that PD patients suffer a significant reduction in mtDNA copy number in both peripheral blood and the vulnerable substantia nigra pars compacta when compared to matched controls. Our study indicates that reduced mtDNA copy number is restricted to the affected brain tissue, but is also reflected in the peripheral blood, suggesting that mtDNA copy number may be a viable diagnostic predictor of PD.
与任何器官一样,大脑也容易受到时间的影响,线粒体生物合成减少是衰老过程的一个标志。在迄今为止对帕金森病(PD)中线粒体拷贝数进行的最大规模研究中,我们使用了多种组织,证明帕金森病DNA(线粒体DNA,mtDNA)拷贝数减少是PD病因的一个生物标志物。我们使用既定的mtDNA定量方法,评估了符合英国帕金森病协会脑库PD诊断标准的社区PD病例的n = 363份外周血样本、n = 151份黑质致密部组织样本和n = 120份额叶皮质组织样本中的mtDNA拷贝数。尽管存在技术局限性,但我们的数据显示,与匹配的对照组相比,PD患者外周血和易损的黑质致密部中的mtDNA拷贝数均显著减少。我们的研究表明,mtDNA拷贝数减少不仅局限于受影响的脑组织,在外周血中也有体现,这表明mtDNA拷贝数可能是一种可行的PD诊断预测指标。