Department of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Clinical Development Medical Affairs, Roche Diagnostic Solutions, Roche Diagnostics GmbH, Penzberg, Germany.
Alzheimers Res Ther. 2022 Apr 26;14(1):60. doi: 10.1186/s13195-022-01003-w.
Cerebrospinal fluid (CSF) analysis for detecting amyloid positivity may be as reliable as positron emission tomography (PET). We evaluated the performance of the amyloid beta (Aβ)42/40 ratio for predicting amyloid positivity by PET, compared with Aβ42 alone, and phosphorylated tau 181 (pTau181)/Aβ42 and total tau (tTau)/Aβ42 ratios, using fully automated CSF immunoassays (Roche Diagnostics International Ltd, Rotkreuz, Switzerland) in a heterogeneous cohort of patients with a range of cognitive disorders reflecting the typical population of a memory clinic.
CSF samples from 103 patients with known amyloid PET status (PET positive = 54; PET negative = 49) were retrospectively selected from one site in Germany; 71 patients were undergoing treatment for mild cognitive impairment (n = 44) or mild-to-moderate dementia (n = 27) due to Alzheimer's disease (AD), and 32 patients were undergoing treatment for non-AD-related cognitive disorders. Aβ42, pTau181, and tTau concentrations were measured in CSF samples using the respective Elecsys CSF immunoassays modified for use on the cobas e 411 analyzer; Aβ40 concentrations were measured using a non-commercially available robust prototype assay. Sensitivities/specificities for amyloid positivity cut-offs (Youden-derived and pre-defined) were calculated, and receiver operating characteristic analyses determined area under the curve (AUC) versus amyloid PET status. Limitations include a small sample size, use of a pre-analytical protocol not in accordance with the Elecsys CSF immunoassay method sheets, and the lack of a pre-defined cut-off for Aβ42/40.
Point estimates for sensitivity and specificity of CSF biomarkers and biomarker ratios versus amyloid PET were 0.93 and 0.57 for Aβ42, 0.96 and 0.69 for pTau181/Aβ42, 0.92 and 0.69 for tTau/Aβ42, and 0.94 and 0.82 for Aβ42/40. For AUCs, point estimates (95% confidence intervals) versus amyloid PET were 0.78 (0.68-0.88) for Aβ42, 0.88 (0.81-0.95) for pTau181/Aβ42, 0.87 (0.80-0.95) for tTau/Aβ42, and 0.90 (0.83-0.97) for Aβ42/40.
CSF Aβ42/40 ratio can predict PET amyloid positivity with high accuracy in patients with a range of cognitive disorders when evaluating Aβ pathology independent of tau and neurodegeneration for research purposes. The performance of Aβ42/40 was comparable with pTau181/Aβ42 and tTau/Aβ42 used in clinical practice and better than Aβ42 alone.
脑脊液(CSF)分析检测淀粉样蛋白阳性的可靠性可能与正电子发射断层扫描(PET)相当。我们使用罗氏诊断国际有限公司(Roche Diagnostics International Ltd)的全自动 CSF 免疫分析(瑞士 Rotkreuz),评估了 Aβ42/40 比值在预测 PET 阳性中的表现,与 Aβ42 单独使用相比,还评估了 Aβ42/40 比值与磷酸化 tau181(pTau181)/Aβ42 和总 tau(tTau)/Aβ42 比值的表现,该比值用于反映记忆诊所典型人群的认知障碍范围的异质队列患者。
从德国一个地点回顾性选择了 103 名已知有淀粉样蛋白 PET 状态的患者的 CSF 样本(PET 阳性=54;PET 阴性=49);71 名患者因阿尔茨海默病(AD)而接受轻度认知障碍(n=44)或轻度至中度痴呆(n=27)的治疗,32 名患者因非 AD 相关认知障碍而接受治疗。使用各自经改良后适用于 cobas e 411 分析仪的 Elecsys CSF 免疫分析,在 CSF 样本中测量 Aβ42、pTau181 和 tTau 浓度;使用非商业上可用的稳健原型测定法测量 Aβ40 浓度。计算了针对淀粉样蛋白阳性的截止值(Youden 推导和预定义)的灵敏度/特异性,并通过接收者操作特征分析确定了曲线下面积(AUC)与淀粉样蛋白 PET 状态的关系。局限性包括样本量小、使用不符合 Elecsys CSF 免疫分析方法表的预分析方案以及缺乏预定义的 Aβ42/40 截止值。
CSF 生物标志物和生物标志物比值与淀粉样蛋白 PET 的灵敏度和特异性的点估计值分别为 Aβ42 为 0.93 和 0.57,pTau181/Aβ42 为 0.96 和 0.69,tTau/Aβ42 为 0.92 和 0.69,Aβ42/40 为 0.94 和 0.82。对于 AUC,针对淀粉样蛋白 PET 的点估计值(95%置信区间)分别为 Aβ42 为 0.78(0.68-0.88),pTau181/Aβ42 为 0.88(0.81-0.95),tTau/Aβ42 为 0.87(0.80-0.95),Aβ42/40 为 0.90(0.83-0.97)。
当独立于 tau 和神经退行性变评估 Aβ 病理学以用于研究目的时,CSF Aβ42/40 比值可以在患有各种认知障碍的患者中以高精度预测 PET 淀粉样蛋白阳性。Aβ42/40 的表现与临床实践中使用的 pTau181/Aβ42 和 tTau/Aβ42 相当,优于 Aβ42 单独使用。