Laboratoire de Biochimie Protéomique Clinique (LBPC-PPC), Univ Montpellier, CHU Montpellier, INM INSERM, Hôpital St Eloi, IRMB 80 av A Fliche, 34295, Montpellier, France.
Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
J Neural Transm (Vienna). 2022 Feb;129(2):231-237. doi: 10.1007/s00702-022-02474-9. Epub 2022 Feb 15.
Blood biomarkers represent a major advance for improving the management, diagnosis, and monitoring of Alzheimer's disease (AD). However, their context of use in relation to routine cerebrospinal fluid (CSF) analysis for the quantification of amyloid peptides and tau proteins remains to be determined.
We studied in two independent cohorts, the performance of blood biomarkers in detecting "nonpathological" (A-/T-/N-), amyloid (A+) or neurodegenerative (T+ /N+) CSF profiles.
Plasma Aβ/Aβ ratio and phosphorylated tau (p-tau(181)) were independent and complementary predictors of the different CSF profile and in particular of the nonpathological (A-/T-/N-) profile with a sensitivity and specificity close to 85%. These performances and the corresponding biomarker thresholds were significantly different from those related to AD detection.
The use of blood biomarkers to identify patients who may benefit from secondary CSF testing represents an attractive stratification strategy in the clinical management of patients visiting memory clinics. This could reduce the need for lumbar puncture and foreshadow the use of blood testing on larger populations.
血液生物标志物代表了改善阿尔茨海默病(AD)管理、诊断和监测的重大进展。然而,它们在常规脑脊液(CSF)分析中用于定量检测淀粉样肽和tau 蛋白的使用情况仍有待确定。
我们在两个独立的队列中研究了血液生物标志物在检测“非病理”(A-/T-/N-)、淀粉样(A+)或神经退行性(T+ / N+)CSF 谱中的性能。
血浆 Aβ/Aβ 比值和磷酸化 tau(p-tau(181))是不同 CSF 图谱的独立且互补的预测因子,尤其是非病理(A-/T-/N-)图谱,其灵敏度和特异性接近 85%。这些性能和相应的生物标志物阈值与 AD 检测相关的性能和阈值有显著差异。
使用血液生物标志物来识别可能受益于二级 CSF 检测的患者,这代表了对就诊于记忆诊所的患者进行临床管理的一种有吸引力的分层策略。这可以减少腰椎穿刺的需求,并预示着更大人群的血液检测的使用。