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快速进展性痴呆的新型诊断和预后评估方法:基于淀粉样蛋白/ tau蛋白/神经退行性变(ATN)框架的指标

Novel diagnostic and prognostic approach for rapidly progressive dementias: Indicators based on amyloid/tau/neurodegeneration (ATN) framework.

作者信息

Cheng Yuan, Chen Shu-Fen, Zhang Ya-Ru, Guo Yu, Wu Kai-Min, Huang Yu-Yuan, Aerqin Qiaolifan, Kuo Kevin, Li Hong-Qi, Chen Shi-Dong, Liu Wei-Shi, Dong Qiang, Yu Jin-Tai

机构信息

State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Department of Neurology and Institute of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

National Center for Neurological Disorders, Shanghai, China.

出版信息

CNS Neurosci Ther. 2024 Jul;30(7):e14857. doi: 10.1111/cns.14857.

Abstract

AIMS

Apply established cerebrospinal fluid (CSF) and serum biomarkers and novel combined indicators based on the amyloid/tau/neurodegeneration (ATN) framework to improve diagnostic and prognostic power in patients with rapidly progressive dementias (RPDs).

METHODS

CSF and serum biomarkers of Alzheimer's disease (AD) common neuropathology including Aβ42, Aβ40, p-Tau, and t-Tau were measured in cognitively normal (CN) controls (n = 33) and three RPD groups with rapidly progressive AD (rpAD, n = 23), autoimmune encephalitis (AE, n = 25), and Creutzfeldt-Jakob disease (CJD, n = 28). Logistic regression and multiple linear regression were used for producing combined indicators and prognostic assessment, respectively, including A&T, A&N, T&N, A&T&N, etc. RESULTS: Combined diagnostic indicator with A&T&N had the potential for differentiating AE from other types of RPDs, identifying 62.51% and 75% of AE subjects based on CSF and serum samples, respectively, compared to 39.13% and 37.5% when using autoantibodies. CSF t-Tau was associated with survival in the CJD group (adjusted R-Square = 0.16, p = 0.02), and its prognosis value improved when using combined predictors based on the ATN framework (adjusted R-Square = 0.273, p = 0.014).

CONCLUSION

Combined indicators based on the ATN framework provide a novel perspective for establishing biomarkers for early recognition of RPDs due to treatment-responsive causes.

摘要

目的

应用已确立的脑脊液(CSF)和血清生物标志物以及基于淀粉样蛋白/ tau /神经变性(ATN)框架的新型联合指标,以提高快速进展性痴呆(RPD)患者的诊断和预后能力。

方法

在认知正常(CN)对照(n = 33)和三个RPD组中测量阿尔茨海默病(AD)常见神经病理学的CSF和血清生物标志物,包括Aβ42、Aβ40、p-Tau和t-Tau,这三个RPD组分别为快速进展性AD(rpAD,n = 23)、自身免疫性脑炎(AE,n = 25)和克雅氏病(CJD,n = 28)。分别使用逻辑回归和多元线性回归来生成联合指标和预后评估,包括A&T、A&N、T&N、A&T&N等。结果:A&T&N联合诊断指标有区分AE与其他类型RPD的潜力,基于CSF和血清样本分别识别出62.51%和75%的AE受试者,而使用自身抗体时分别为39.13%和37.5%。CSF t-Tau与CJD组的生存相关(调整后R方 = 0.16,p = 0.02),当使用基于ATN框架的联合预测指标时其预后价值有所提高(调整后R方 = 0.273,p = 0.014)。

结论

基于ATN框架的联合指标为建立生物标志物以早期识别由治疗反应性原因导致的RPD提供了新视角。

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