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特发性快速眼动睡眠行为障碍患者早期黑质纹状体神经退行性变的临床标志物。

Clinical markers of early nigrostriatal neurodegeneration in idiopathic rapid eye movement sleep behavior disorder.

机构信息

Hans-Berger Department of Neurology, University Hospital Jena, Germany.

出版信息

Sleep Med. 2013 Nov;14(11):1064-70. doi: 10.1016/j.sleep.2013.06.008. Epub 2013 Aug 13.

Abstract

BACKGROUND

Rapid eye movement sleep behavior disorder (RBD) is an early feature in α synucleinopathies and may precede other clinical manifestations of disease for several years. Olfactory dysfunction and mild motor abnormalities (MMAs) are highly prevalent in prodromal α synucleinopathies such as RBD and are suspected to be predictive neurodegenerative markers. Because both markers also are highly prevalent in the healthy elderly population, the discriminative value to detect an early neurodegenerative process is unclear.

METHODS

We examined 28 patients with idiopathic RBD (iRBD) without manifest neurodegenerative disease to determine diagnostic accuracy of MMAs and olfactory dysfunction in identifying patients with early nigrostriatal degeneration in transcranial sonography (TCS) and (123)I-2β-carbomethoxy-3β-(4-iodophenyl)-N-(3-fluoropropyl)-nortropane single-photon emission computed tomography ((123)I-FP-CIT-SPECT).

RESULTS

Sixty-three percent of our participants showed MMAs which were strongly associated with abnormal TCS and (123)I-FP-CIT-SPECT findings. The discriminative value in detecting participants with early nigrostriatal degeneration was excellent (area under the receiver operating characteristic [ROC] curve, 0.84 [P≤.003] for TCS and 0.79 [P≤.066] for (123)I-FP-CIT-SPECT). Olfactory dysfunction was present in 78% of iRBD participants, but it was not linked with neuroimaging abnormalities or MMAs. Olfactory dysfunction did not discriminate participants with early nigrostriatal degeneration (area under the ROC curve, 0.54 [P≤.747] for TCS and 0.31 [P≤.225] for (123)I-FP-CIT-SPECT). Early RBD manifestation but no demographic (e.g., age, gender) or clinical characteristics of RBD (e.g., duration, severity of RBD) were associated with neuroimaging abnormalities in TCS and (123)I-FP-CIT-SPECT.

CONCLUSIONS

Unlike olfactory dysfunction, MMAs discriminate patients with early nigrostriatal degeneration in iRBD. Early RBD manifestation seems to be an additional risk factor which aggravates neurodegenerative risk.

摘要

背景

快速眼动睡眠行为障碍(RBD)是α-突触核蛋白病的早期特征,可能在疾病的其他临床表现出现前数年就出现。嗅觉功能障碍和轻度运动异常(MMAs)在 RBD 等前驱期α-突触核蛋白病中非常普遍,被怀疑是具有预测性的神经退行性标记物。由于这两种标志物在健康老年人中也非常普遍,因此尚不清楚其用于检测早期神经退行性过程的区分价值。

方法

我们检查了 28 名无明显神经退行性疾病的特发性 RBD(iRBD)患者,以确定 MMAs 和嗅觉功能障碍在经颅超声(TCS)和(123)I-2β- 碳甲氧基-3β-(4-碘苯基)-N-(3-氟丙基)-去甲托烷单光子发射计算机断层扫描((123)I-FP-CIT-SPECT)中识别早期黑质纹状体变性患者的诊断准确性。

结果

我们的参与者中有 63%表现出 MMAs,这些 MMAs与异常的 TCS 和(123)I-FP-CIT-SPECT 发现强烈相关。在检测有早期黑质纹状体变性的参与者方面,该标志物具有出色的区分价值(受试者工作特征曲线下面积,TCS 为 0.84[P≤.003],(123)I-FP-CIT-SPECT 为 0.79[P≤.066])。78%的 iRBD 患者存在嗅觉功能障碍,但与神经影像学异常或 MMAs 无关。嗅觉功能障碍不能区分有早期黑质纹状体变性的参与者(TCS 的受试者工作特征曲线下面积为 0.54[P≤.747],(123)I-FP-CIT-SPECT 的为 0.31[P≤.225])。早期 RBD 表现,而不是人口统计学(如年龄、性别)或 RBD 的临床特征(如 RBD 的持续时间、严重程度)与 TCS 和(123)I-FP-CIT-SPECT 中的神经影像学异常相关。

结论

与嗅觉功能障碍不同,MMAs 可区分 iRBD 中早期黑质纹状体变性的患者。早期 RBD 表现似乎是加重神经退行性风险的另一个危险因素。

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