Chen Meng-Hsiang, Chen Pei-Chin, Lu Cheng-Hsien, Chen Hsiu-Ling, Chao Yi-Ping, Li Shau-Hsuan, Chen Yi-Wen, Lin Wei-Che
Department of Diagnostic Radiology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan; Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Chang Gung University College of Medicine, Kaohsiung, Taiwan; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Oxid Med Cell Longev. 2017;2017:7371403. doi: 10.1155/2017/7371403. Epub 2017 Jan 23.
. Cardiovascular autonomic dysfunction is well known in Parkinson's disease (PD) presentation and it produces hypoperfusion of vital organs. The association between cardiovascular autonomic dysfunction and oxidative stress was examined in previous animal models. Oxidative stress and neuroinflammation were thought to have roles in PD pathogenesis. Owing to the relative low intrinsic antioxidative properties, brain white matter (WM) is vulnerable to the oxidative stress. This study is conducted to examine possible relationships by using a hypothesis-driven mediation model. . Twenty-nine patients with PD and 26 healthy controls participated in this study, with complete examinations of cardiac autonomic parameters, plasma DNA level, and WM integrity. A single-level three-variable mediation model was used to investigate the possible relationships. . The elevated serum oxidative stress biomarkers include plasma nuclear DNA and mitochondrial DNA, and poorer cardiac autonomic parameters and multiple regional microstructural WM changes are demonstrated. Further mediation analysis shows that plasma nuclear DNA served as the mediators between poorer baroreflex sensitivity and mean diffusivity changes in cingulum. . These results provide a possible pathophysiology for how the poor baroreflex sensitivity and higher oxidative stress adversely impacted the WM integrity. This model could provide us with a piece of the puzzle of the entire PD pathogenesis.
心血管自主神经功能障碍在帕金森病(PD)中很常见,它会导致重要器官灌注不足。先前的动物模型研究了心血管自主神经功能障碍与氧化应激之间的关联。氧化应激和神经炎症被认为在PD发病机制中起作用。由于脑白质(WM)相对较低的内在抗氧化特性,其易受氧化应激影响。本研究旨在通过使用假设驱动的中介模型来检验可能的关系。29例PD患者和26名健康对照参与了本研究,对心脏自主神经参数、血浆DNA水平和WM完整性进行了全面检查。采用单水平三变量中介模型来研究可能的关系。血清氧化应激生物标志物升高包括血浆核DNA和线粒体DNA,同时显示出较差的心脏自主神经参数和多个区域WM微观结构改变。进一步的中介分析表明,血浆核DNA在较差的压力反射敏感性与扣带回平均扩散率变化之间起中介作用。这些结果为压力反射敏感性差和较高氧化应激如何对WM完整性产生不利影响提供了一种可能的病理生理学机制。该模型可为我们提供整个PD发病机制的一部分线索。