首页> 外文期刊>Journal of Alzheimer's disease: JAD >Using cerebrospinal fluid marker profiles in clinical diagnosis of dementia with lewy bodies, Parkinson's disease, and Alzheimer's disease
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Using cerebrospinal fluid marker profiles in clinical diagnosis of dementia with lewy bodies, Parkinson's disease, and Alzheimer's disease

机译:使用脑脊液标记物谱在路易体痴呆,帕金森氏病和阿尔茨海默氏病的临床诊断中

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Background: Dementia with Lewy bodies (DLB) is difficult to differentiate from other neuro-degenerative diseases. Patients are often mistaken to suffer from Parkinson's disease (PD) or Alzheimer's disease (AD) because of the overlapping clinical appearances concerning cognition and movement. Objective: We investigated the possibility for a valid differential diagnosis using cerebrospinal fluid (CSF) biomarkers. Methods: In the context of a large retrospective study, we analyzed data of patients suffering from degenerative, ischemic, or inflammatory CNS (central nervous system) diseases and identified those with DLB (n = 34), PD (n = 37), and AD (n = 47) for further analyses. Results: We detected abnormalities in the CSF profiles of those patients with DLB while using a combination of decreased amyloid-β (Aβ)42 and increased tau levels. By stratification of data by disease severity, we observed a high sensitivity of this combination especially in the subgroup of patients with advanced stages, while the sensitivity in early forms was lower. In addition, with clinical deterioration, the abnormalities in the CSF profile became more pronounced. Conclusion: We conclude that DLB can be distinguished from PD, in spite of both being synucleinopathies, by CSF profiles using neurodegenerative marker analysis. The pathophysiology of increased tau and decreased Aβ levels in those conditions has to be elucidated further, since both proteins are known to be involved in the pathogenesis of AD, but no clear explanation has been postulated for DLB yet.
机译:背景:路易体痴呆(DLB)很难与其他神经退行性疾病区分开。由于与认知和运动有关的临床表现重叠,患者常常被误认为患有帕金森氏病(PD)或阿尔茨海默氏病(AD)。目的:我们调查了使用脑脊液(CSF)生物标志物进行有效鉴别诊断的可能性。方法:在一项大型回顾性研究的背景下,我们分析了患有退行性,缺血性或炎性CNS(中枢神经系统)疾病的患者的数据,并确定了患有DLB(n = 34),PD(n = 37)和AD(n = 47)进行进一步分析。结果:我们结合使用降低的淀粉样蛋白-β(Aβ)42和增加的tau水平,检测了这些DLB患者的CSF谱异常。通过按疾病严重程度对数据进行分层,我们观察到这种组合的敏感性较高,尤其是在晚期患者亚组中,而早期形式的敏感性较低。另外,随着临床恶化,CSF谱中的异常变得更加明显。结论:我们得出结论,尽管两者都是突触核病,但通过使用神经变性标记物分析的CSF谱图,可以将DLB与PD区别开来。由于已知两种蛋白都参与了AD的发病机理,因此必须进一步阐明tau升高和Aβ降低的病理生理机制,但目前尚无关于DLB的明确解释。

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