Clinical Neurocardiology Section, Clinical Neurosciences Program, Division of Intramural Research, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Clinical Neurocardiology Section, Clinical Neurosciences Program, Division of Intramural Research, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Parkinsonism Relat Disord. 2018 Jul;52:90-93. doi: 10.1016/j.parkreldis.2017.10.003. Epub 2017 Oct 5.
By the time a person develops the motor manifestations of Parkinson's disease (PD), substantial loss of nigrostriatal dopamine neurons has already occurred. There is great interest in identifying biomarkers that can detect pre-clinical PD. Braak's neuropathological staging concept imputes early autonomic involvement. Here we report results from a small prospective cohort study about the utility of neuroimaging evidence of cardiac sympathetic denervation in predicting PD among individuals with multiple PD risk factors.
Subjects provided information about family history of PD, olfactory dysfunction, dream enactment behavior, and orthostatic hypotension at a protocol-specific website. From this pool, 27 people with at least 3 risk factors confirmed underwent cardiac F-dopamine positron emission tomographic scanning and were followed for at least 3 years. Interventricular septal and left ventricular free wall concentrations of F-dopamine-derived radioactivity were measured.
Of the 27 subjects, 4 were diagnosed with PD within the 3-year follow-up period (Pre-Clinical PD group); 23 risk-matched (mean 3.2 risk factors) subjects remained disease-free (No-PD group). Compared to the No-PD group, the Pre-Clinical PD group had lower initial values for septal and free wall concentrations of F-dopamine-derived radioactivity (p = 0.0248, 0.0129). All 4 Pre-Clinical PD subjects had evidence of decreased cardiac sympathetic innervation in the interventricular septum or left ventricular free wall, in contrast with 3 of 23 (13%) No-PD subjects (p = 0.0020 by Fisher's exact test).
People with multiple PD risk factors and diagnosed with PD within 3 years have evidence of antecedent cardiac sympathetic denervation. The findings fit with Braak's staging concept.
当一个人出现帕金森病(PD)的运动表现时,黑质纹状体多巴胺神经元已经发生了大量的损失。人们非常感兴趣的是确定可以检测临床前 PD 的生物标志物。Braak 的神经病理学分期概念推测早期自主神经受累。在这里,我们报告了一项小型前瞻性队列研究的结果,该研究探讨了心脏去交感神经支配的神经影像学证据在预测具有多种 PD 风险因素的个体 PD 中的作用。
受试者在特定方案的网站上提供有关 PD 家族史、嗅觉功能障碍、梦境行为和直立性低血压的信息。从这个群体中,有 27 名至少有 3 个危险因素的人接受了心脏 F-多巴胺正电子发射断层扫描,并至少随访了 3 年。测量了 F-多巴胺衍生放射性物质的室间隔和左心室游离壁浓度。
在 27 名受试者中,有 4 人在 3 年随访期间被诊断为 PD(临床前 PD 组);23 名风险匹配(平均 3.2 个危险因素)的受试者保持无病状态(无 PD 组)。与无 PD 组相比,临床前 PD 组 F-多巴胺衍生放射性物质的室间隔和游离壁浓度初始值较低(p=0.0248,0.0129)。与无 PD 组的 3 名受试者(13%)相比,所有 4 名临床前 PD 受试者的室间隔或左心室游离壁均存在心脏去交感神经支配减少的证据(Fisher 确切检验,p=0.0020)。
具有多种 PD 风险因素并在 3 年内被诊断为 PD 的人有前驱性心脏去交感神经支配的证据。这些发现符合 Braak 的分期概念。