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用于帕金森病中多巴胺能功能障碍和微结构退化的早期检测的杂交 PET-MRI。

Hybrid PET-MRI for early detection of dopaminergic dysfunction and microstructural degradation involved in Parkinson's disease.

机构信息

Department of Radiology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.

Department of Radiology, Nanjing Second Hospital, Nanjing University of Chinese Medicine, Nanjing, China.

出版信息

Commun Biol. 2021 Oct 7;4(1):1162. doi: 10.1038/s42003-021-02705-x.

Abstract

Dopamine depletion and microstructural degradation underlie the neurodegenerative processes in Parkinson's disease (PD). To explore early alterations and underlying associations of dopamine and microstructure in PD patients utilizing the hybrid positron emission tomography (PET)-magnetic resonance imaging (MRI). Twenty-five PD patients in early stages and twenty-four matched healthy controls underwent hybrid F-fluorodopa (DOPA) PET-diffusion tensor imaging (DTI) scanning. The striatal standardized uptake value ratio (SUVR), DTI maps (fractional anisotropy, FA; mean diffusivity, MD) in subcortical grey matter, and deterministic tractography of the nigrostriatal pathway were processed. Values in more affected (MA) side, less affected (LA) side and mean were analysed. Correlations and mediations among PET, DTI and clinical characteristics were further analysed. PD groups exhibited asymmetric pattern of dopaminergic dysfunction in putamen, impaired integrity in the microstructures (nigral FA, putaminal MD, and FA of nigrostriatal projection). On MA side, significant associations between DTI metrics (nigral FA, putaminal MD, and FA of nigrostriatal projection) and motor performance were significantly mediated by putaminal SUVR, respectively. Early asymmetric disruptions in putaminal dopamine concentrations and nigrostriatal pathway microstructure were detected using hybrid PET-MRI. The findings further implied that molecular degeneration mediates the modulation of microstructural disorganization on motor dysfunction in the early stages of PD.

摘要

多巴胺耗竭和微观结构退化是帕金森病 (PD) 神经退行性过程的基础。利用正电子发射断层扫描 (PET)-磁共振成像 (MRI) 技术探索 PD 患者多巴胺和微观结构的早期改变及其潜在关联。25 名早期 PD 患者和 24 名匹配的健康对照者接受了 F-氟多巴 (DOPA) PET-弥散张量成像 (DTI) 扫描。处理纹状体标准化摄取值比 (SUVR)、亚皮质灰质的 DTI 图谱(各向异性分数,FA;平均弥散度,MD)和黑质纹状体通路的确定性追踪。分析了更受影响(MA)侧、受影响较少(LA)侧和平均值。进一步分析了 PET、DTI 和临床特征之间的相关性和中介作用。PD 组在壳核中表现出多巴胺能功能障碍的不对称模式,微观结构受损(黑质 FA、壳核 MD 和黑质纹状体投射的 FA)。在 MA 侧,DTI 指标(黑质 FA、壳核 MD 和黑质纹状体投射的 FA)与运动表现之间存在显著关联,这些关联分别由壳核 SUVR 显著介导。使用混合 PET-MRI 检测到早期壳核多巴胺浓度和黑质纹状体通路微观结构的不对称破坏。这些发现进一步表明,分子退化调节了 PD 早期运动功能障碍的微观结构紊乱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28bc/8497575/c3340ce4ccd5/42003_2021_2705_Fig1_HTML.jpg

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