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脑脊液生物标志物在临床诊断的阿尔茨海默病和非阿尔茨海默病性痴呆中的增量价值。

Incremental Value of CSF Biomarkers in Clinically Diagnosed AD and Non-AD Dementia.

作者信息

Oudart Jean-Baptiste, Djerada Zoubir, Nonnonhou Vignon, Badr Sarah, Bertholon Laurie-Anne, Dammak Anis, Jaidi Yacine, Novella Jean-Luc, Pallet Nicolas, Gillery Philippe, Mahmoudi Rachid

机构信息

Laboratory of Biochemistry and Molecular Biology, Faculty of Medicine, University of Reims Champagne-Ardenne, SFR CAP-Santé (FED 4231), Reims, France.

CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire - MEDyC, Reims, France.

出版信息

Front Neurol. 2020 Jun 25;11:560. doi: 10.3389/fneur.2020.00560. eCollection 2020.

Abstract

Cerebrospinal fluid (CSF) biomarkers are used to diagnose Alzheimer disease (AD), especially in atypical clinical presentations. No consensus currently exists regarding cut-off values. This study aimed, firstly, to define optimal cut-off values for CSF biomarkers, and secondly, to investigate the most relevant diagnostic strategy for AD based on CSF biomarker combinations. A total of 380 patients were prospectively included: 140 with AD, 240 with various neurological diagnoses (non-AD). CSF biomarkers were measured using ELISA. Univariate and multivariate analyses were performed using random forest and logistic regression approaches. Univariate receiver operating curve curves analysis of T-Tau, P-Tau, Aβ, Aβ concentrations, and Aβ/Aβ ratio levels showed AD cut-off values of ≥355, ≥57, ≤706, ≥10,854, and ≤0.059 ng/L, respectively. Multivariate analysis using random forest and logistic regression found that the algorithm based on P-Tau, Aβ concentrations and Aβ/Aβ ratio yielded the best discrimination between AD and non-AD populations. The cross-validation technique of the final model showed a mean accuracy of 0.85 and a mean AUC of 0.89. This study confirms that the Aβ/Aβ ratio was more useful than the Aβ concentration in discriminating AD from non-AD populations in daily practice. These results indicate that the Aβ/Aβ ratio should be assessed in all cases, independently of Aβ concentrations.

摘要

脑脊液(CSF)生物标志物用于诊断阿尔茨海默病(AD),尤其是在非典型临床表现中。目前关于临界值尚无共识。本研究旨在,首先,确定CSF生物标志物的最佳临界值,其次,基于CSF生物标志物组合研究AD最相关的诊断策略。前瞻性纳入了总共380例患者:140例AD患者,240例患有各种神经系统疾病诊断(非AD)。使用酶联免疫吸附测定法(ELISA)测量CSF生物标志物。使用随机森林和逻辑回归方法进行单变量和多变量分析。对总tau蛋白(T-Tau)、磷酸化tau蛋白(P-Tau)、淀粉样蛋白β42(Aβ42)、淀粉样蛋白β40(Aβ40)浓度以及Aβ42/Aβ40比值水平进行单变量受试者操作特征曲线分析,显示AD的临界值分别为≥355、≥57、≤706、≥10,854和≤0.059 ng/L。使用随机森林和逻辑回归的多变量分析发现,基于P-Tau、Aβ42浓度和Aβ42/Aβ40比值的算法在AD和非AD人群之间产生了最佳区分。最终模型的交叉验证技术显示平均准确率为0.85,平均曲线下面积(AUC)为0.89。本研究证实,在日常实践中,Aβ42/Aβ40比值在区分AD和非AD人群方面比Aβ42浓度更有用。这些结果表明,在所有病例中都应评估Aβ42/Aβ40比值,而与Aβ42浓度无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c4c/7330115/494ff402c613/fneur-11-00560-g0001.jpg

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