Eckert Thomas, Tang Chengke, Eidelberg David
Center for Neurosciences, Feinstein Institute for Medical Research, North Shore-Long Island Jewish Health System, Manhasset, NY 11030, USA.
Lancet Neurol. 2007 Oct;6(10):926-32. doi: 10.1016/S1474-4422(07)70245-4.
Clinical research into Parkinson's disease has focused increasingly on the development of interventions that slow the neurodegeneration underlying this disorder. These investigations have stimulated interest in finding objective biomarkers that show changes in the rate of disease progression with treatment. Through radiotracer-based imaging of nigrostriatal dopaminergic function, a specific class of biomarkers to monitor the progression of Parkinson's disease has been identified, and these biomarkers were used in the clinical trials of drugs with the potential to modify the course of the disease. However, in some of these studies there was discordance between the imaging outcome measures and blinded clinical ratings of disease severity. Research is underway to identify and validate alternative ways to image brain metabolism, through which the efficacy of new therapies for Parkinson's disease and related disorders can be assessed.
During recent years, spatial covariance analysis has been used with (18)F-fluorodeoxyglucose PET to detect abnormal patterns of brain metabolism in patients with neurodegenerative disorders. Rapid, automated, voxel-based algorithms have been used with metabolic imaging to quantify the activity of disease-specific networks. This approach has helped to characterise the unique metabolic patterns associated with the motor and cognitive features of Parkinson's disease. The results of several studies have shown correction of abnormal motor, but not cognitive, network activity by treatment with dopaminergic therapy and deep brain stimulation. The authors of a longitudinal imaging study of early-stage Parkinson's disease reported substantial differences in the development of these metabolic networks over a follow-up of 4 years. WHERE NEXT?: Developments in network imaging have provided the basis for several new applications of metabolic imaging in the study of Parkinson's disease. A washout study is currently underway to determine the long-duration effects of dopaminergic therapy on the network activity related to Parkinson's disease, which will be useful to plan future trials of disease-modifying drugs. Network approaches are also being applied to the study of atypical parkinsonian syndromes. The characterisation of specific patterns associated with atypical parkinsonian syndromes and classic Parkinson's disease will be the basis for a fully automated imaging-based procedure for early differential diagnosis. Efforts are underway to quantify the networks related to Parkinson's disease with less invasive imaging methods. Assessments of network activity with perfusion-weighted MRI show excellent concordance with measurements done with established radiotracer techniques. This approach will ultimately enable the assessment of abnormal network activity in people who are genetically at risk of Parkinson's disease.
帕金森病的临床研究越来越多地聚焦于开发减缓该疾病潜在神经退行性变的干预措施。这些研究激发了人们寻找客观生物标志物的兴趣,这些生物标志物能够显示疾病进展速率随治疗的变化情况。通过基于放射性示踪剂的黑质纹状体多巴胺能功能成像,已确定了一类用于监测帕金森病进展的特定生物标志物,并且这些生物标志物被用于有可能改变疾病进程的药物的临床试验中。然而,在其中一些研究中,成像结果测量与疾病严重程度的盲法临床评分之间存在不一致。目前正在开展研究,以确定和验证对脑代谢进行成像的替代方法,借此可评估帕金森病及相关疾病新疗法的疗效。
近年来,空间协方差分析已与(18)F - 氟脱氧葡萄糖正电子发射断层扫描(PET)结合使用,以检测神经退行性疾病患者脑代谢的异常模式。基于体素的快速、自动化算法已用于代谢成像,以量化疾病特异性网络的活动。这种方法有助于刻画与帕金森病运动和认知特征相关的独特代谢模式。多项研究结果表明,多巴胺能疗法和深部脑刺激治疗可纠正异常的运动网络活动,但不能纠正认知网络活动。一项早期帕金森病纵向成像研究的作者报告称,在4年的随访中,这些代谢网络的发展存在显著差异。
网络成像的发展为代谢成像在帕金森病研究中的多项新应用奠定了基础。目前正在进行一项洗脱研究,以确定多巴胺能疗法对与帕金森病相关的网络活动的长期影响,这将有助于规划未来疾病修饰药物的试验。网络方法也正在应用于非典型帕金森综合征的研究。刻画与非典型帕金森综合征和经典帕金森病相关的特定模式,将成为基于成像的早期鉴别诊断全自动程序的基础。目前正在努力用侵入性较小的成像方法量化与帕金森病相关的网络。灌注加权磁共振成像对网络活动的评估与既定放射性示踪剂技术的测量结果显示出极好的一致性。这种方法最终将能够评估有帕金森病遗传风险人群的异常网络活动。