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SPECT 分子影像学在家族性帕金森病中的应用。

SPECT Molecular Imaging in Familial Parkinson's Disease.

机构信息

Department of Clinical Neuroscience, Centre for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.

Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", Neuroscience Section, University of Salerno, Salerno, Italy.

出版信息

Int Rev Neurobiol. 2018;142:225-260. doi: 10.1016/bs.irn.2018.09.004. Epub 2018 Oct 30.

Abstract

Dopamine transporter (DAT) imaging with single-photon emission computed tomography (SPECT) is a diagnostic tool to study the integrity of the dopaminergic system in patients with parkinsonism and uncertain diagnosis. DAT SPECT enables to detect the presence of nigrostriatal deficit even in the early or pre-symptomatic stages of the disease and to quantify the DAT loss with the progression of nigrostriatal degeneration. For these reasons, DAT SPECT has been also used as a tool to study genetic conditions that are associated with parkinsonism in order to examine the degree and patterns of dopaminergic deficits that are present in at risk subjects and in affected patients carrying the mutations. Studies included subjects with sporadic mutations of common genes associated with Parkinson's disease (PD) and families with both affected patients and asymptomatic carriers. For obvious reasons, the majority of the studies have included a limited number of subjects. Therefore, because of the heterogeneity and the size of the cohorts examined, in many cases the findings can be merely descriptive and general conclusions on the patterns of dopaminergic deficit in different genetic conditions need to take into account some exceptions.

摘要

使用单光子发射计算机断层扫描 (SPECT) 进行多巴胺转运体 (DAT) 成像,是一种用于研究帕金森病患者和不确定诊断患者多巴胺能系统完整性的诊断工具。DAT SPECT 能够检测到即使在疾病的早期或亚临床阶段也存在黑质纹状体缺陷,并随着黑质纹状体变性的进展来量化 DAT 损失。由于这些原因,DAT SPECT 也被用作研究与帕金森病相关的遗传条件的工具,以检查有风险的受试者和携带突变的受影响患者中存在的多巴胺能缺陷的程度和模式。研究包括患有常见与帕金森病 (PD) 相关基因的散发性突变的受试者和既有受影响患者又有无症状携带者的家族。由于显而易见的原因,大多数研究纳入的受试者数量有限。因此,由于所检查队列的异质性和大小,在许多情况下,研究结果可能只是描述性的,并且需要考虑到一些例外情况,才能得出关于不同遗传条件下多巴胺能缺陷模式的一般结论。

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