Oxford Parkinson's Disease Centre, Oxford, United Kingdom.
Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Ann Clin Transl Neurol. 2020 Jan;7(1):26-35. doi: 10.1002/acn3.50962. Epub 2019 Dec 9.
Rapid eye movement sleep behavior disorder (RBD) patients have a high risk of developing a Parkinsonian disorder, offering an opportunity for neuroprotective intervention. Predicting near-term conversion, however, remains a challenge. Dopamine transporter imaging, while informative, is expensive and not widely available. Here, we investigate the utility of susceptibility-weighted MRI (SWI) to detect abnormalities of the substantia nigra in RBD, and explore their association with striatal dopaminergic deficits.
SWI of the substantia nigra was performed in 46 RBD patients, 27 Parkinson's patients, and 32 control subjects. Dorsal nigral hyperintensity (DNH) was scored by two blinded raters, and separately quantified using a semiautomated process. Forty-two RBD patients were also imaged with I-ioflupane single-photon emission computed tomography (DaT SPECT/CT).
Consensus visual DNH classification was possible in 87% of participants. 27.5% of RBD patients had lost DNH, compared with 7.7% of control subjects and 96% of Parkinson's patients. RBD patients lacking DNH had significantly lower putamen dopaminergic SPECT/CT activity compared to RBD patients with DNH present (specific uptake ratios 1.89 vs. 2.33, P = 0.002). The mean quantified DNH signal intensity declined in a stepwise pattern, with RBD patients having lower intensity than controls (0.837 vs. 0.877, P = 0.01) but higher than PD patients (0.837 vs. 0.765, P < 0.001).
Over one quarter of RBD patients have abnormal substantia nigra SWI reminiscent of Parkinson's, which is associated with a greater dopaminergic deficit. This modality may help enrich neuroprotective trials with early converters.
快速眼动睡眠行为障碍(RBD)患者发生帕金森病的风险很高,这为神经保护干预提供了机会。然而,预测近期的转化仍然是一个挑战。多巴胺转运蛋白成像虽然信息丰富,但价格昂贵且尚未广泛应用。在这里,我们研究了磁共振敏感加权成像(SWI)检测 RBD 患者黑质异常的效用,并探讨了其与纹状体多巴胺能缺陷的关系。
对 46 例 RBD 患者、27 例帕金森病患者和 32 例对照组进行了 SWI 检查。两名盲法评分者对背侧黑质高信号(DNH)进行评分,并分别使用半自动处理方法进行定量。42 例 RBD 患者还进行了碘-[123I]-β-单-C 乙基-丙基异睛(I-ioflupane)单光子发射计算机断层扫描(DaT SPECT/CT)。
87%的参与者可以进行共识视觉 DNH 分类。27.5%的 RBD 患者出现 DNH 缺失,而对照组和帕金森病患者分别为 7.7%和 96%。与存在 DNH 的 RBD 患者相比,缺乏 DNH 的 RBD 患者纹状体 DaT SPECT/CT 活性显著降低(特异性摄取比值 1.89 与 2.33,P=0.002)。DNH 信号强度呈逐步下降模式,RBD 患者的强度低于对照组(0.837 与 0.877,P=0.01),但高于帕金森病患者(0.837 与 0.765,P<0.001)。
超过四分之一的 RBD 患者的黑质 SWI 异常,类似于帕金森病,这与更大的多巴胺能缺陷有关。这种方式可能有助于用早期转化者丰富神经保护试验。