Chen Ying-Tsung, Orimo Satoshi, Wei Cheng-Yu, Hung Guang-Uei, Yang Shieh-Yueh, Chiu Pai-Yi
Department of Psychiatry, Show Chwan Memorial Hospital, Changhua, Taiwan.
Department of Psychiatry, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan.
Front Aging Neurosci. 2022 May 19;14:920591. doi: 10.3389/fnagi.2022.920591. eCollection 2022.
An abnormal increase of α-synuclein in the brain is the hallmark of dementia with Lewy bodies (DLB). However, the diagnostic power of plasma α-synuclein in DLB is not yet confirmed. Parkinsonism is highly associated with and is one of the core clinical features of DLB. We studied plasma α-synuclein and developed a novel tool that combined plasma α-synuclein level and Motor Dysfunction Questionnaire (MDQ), namely Synuclein Motor Dysfunction Composite Scale (SMDCS), for the clinical discrimination of DLB from Alzheimer's disease (AD).
This cross-sectional study analyzed participants' demographical data, plasma α-synuclein level, MDQ, structured clinical history questionnaire, neuropsychological and motor function tests, and neuroimaging studies. The power of plasma α-synuclein level, MDQ, and SMDCS for discriminating DLB from non-demented controls (NC) or AD were compared.
Overall, 121 participants diagnosed as 58 DLB, 31 AD, and 31 NC were enrolled. Patients with DLB had significantly higher mean plasma α-synuclein level (0.24 ± 0.32 pg/ml) compared to the NC group (0.08 ± 0.05 pg/ml) and the AD group (0.08 ± 0.05 pg/ml). The DLB group demonstrated higher MDQ (2.95 ± 1.60) compared to the NC (0.42 ± 0.98) or AD (0.44 ± 0.99) groups. The sensitivity/specificity of plasma α-synuclein level, MDQ, and SMDCS for differentiating DLB from non-DLB were 0.80/0.64, 0.83/0.89, and 0.88/0.93, respectively.
Both plasma α-synuclein and MDQ were significantly higher in patients with DLB compared to the NC or AD groups. The novel SMDCS, significantly improved accuracy for the clinical differentiation of DLB from AD or NC.
大脑中α-突触核蛋白异常增加是路易体痴呆(DLB)的标志。然而,血浆α-突触核蛋白在DLB中的诊断价值尚未得到证实。帕金森综合征与DLB高度相关,是DLB的核心临床特征之一。我们研究了血浆α-突触核蛋白,并开发了一种新工具,将血浆α-突触核蛋白水平与运动功能障碍问卷(MDQ)相结合,即突触核蛋白运动功能障碍综合量表(SMDCS),用于临床鉴别DLB与阿尔茨海默病(AD)。
这项横断面研究分析了参与者的人口统计学数据、血浆α-突触核蛋白水平、MDQ、结构化临床病史问卷、神经心理学和运动功能测试以及神经影像学研究。比较了血浆α-突触核蛋白水平、MDQ和SMDCS区分DLB与非痴呆对照(NC)或AD的能力。
总共纳入了121名参与者,其中58名诊断为DLB,31名诊断为AD,31名诊断为NC。与NC组(0.08±0.05 pg/ml)和AD组(0.08±0.05 pg/ml)相比,DLB患者的平均血浆α-突触核蛋白水平显著更高(0.24±0.32 pg/ml)。与NC组(0.42±0.98)或AD组(0.44±0.99)相比,DLB组的MDQ更高(2.95±1.60)。血浆α-突触核蛋白水平、MDQ和SMDCS区分DLB与非DLB的敏感性/特异性分别为0.80/0.64、0.83/0.89和0.88/0.93。
与NC组或AD组相比,DLB患者的血浆α-突触核蛋白和MDQ均显著更高。新的SMDCS显著提高了临床鉴别DLB与AD或NC的准确性。