Department of Psychiatry and Psychotherapy, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.
Department of Psychiatry and Psychotherapy, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany,
Dement Geriatr Cogn Disord. 2022;51(2):182-192. doi: 10.1159/000524390. Epub 2022 May 3.
Several recent research studies show high performance of blood biomarkers to identify Alzheimer's disease also in the pre-dementia mild cognitive impairment (MCI) stage, but data from the routine clinical care memory clinic setting are needed.
We examined plasma samples of 144 memory clinic patients, including dementia of Alzheimer type (DAT, n = 54), MCI (n = 57), and subjective cognitive decline (SCD, n = 33), who either presented as self-referrals or were referred by general practitioners or neurologists or psychiatrists. The plasma biomarkers, amyloid-beta42 (Aß42), amyloid-beta40 (Aß40), phospho-Tau181 (pTau181), total-tau (tTau), and neurofilament light (NFL), as well as different ratios, were measured using the ultrasensitive single molecule array (Simoa) immunoassay technology. Statistical analysis including Kruskal-Wallis test, linear regression, and receiver operating characteristics analyses was performed.
Of the single markers, we observed statistically significant group effects of pTau181 (H(2) = 34.43, p < 0.001) and NFL (H(2) = 27.66, p < 0.001). All individual group comparisons of pTau181 were significant, while the contrast of SCD versus MCI for NFL was not significant. In addition, the ratios of Aß42/Aß40 (H(2) = 7.50, p = 0.02) and pTau181/Aß42 (H(2) = 25.26, p < 0.001) showed significant group effects with significant difference between all groups for pTau181/Aß42 and an SCD versus MCI difference for Aß42/Aß40. PTau181 showed the highest area under the curve of 0.85 for the discrimination of SCD and DAT with a sensitivity of 80% and a specificity of 79% at a cut-off of 12.2 pg/mL. Age influenced Aß42, Aß40, and NFL concentrations.
Plasma pTau181 and NFL, as well as the ratios Aß42/Aß40 and pTau181/Aß42, are biomarkers, which can differentiate diagnostic groups in a memory clinic setting outside of research studies.
最近的几项研究表明,血液生物标志物在识别阿尔茨海默病方面具有很高的性能,甚至在轻度认知障碍(MCI)的痴呆前阶段也有很好的效果,但需要在常规临床护理的记忆诊所环境中获得数据。
我们检测了 144 名记忆诊所患者的血浆样本,包括阿尔茨海默病型痴呆(DAT,n = 54)、MCI(n = 57)和主观认知下降(SCD,n = 33),他们要么是自我转诊,要么是由全科医生、神经科医生或精神科医生转诊。使用超灵敏单分子阵列(Simoa)免疫分析技术测量血浆生物标志物β淀粉样蛋白 42(Aβ42)、β淀粉样蛋白 40(Aβ40)、磷酸化 Tau181(pTau181)、总 Tau(tTau)和神经丝轻链(NFL)以及不同的比值。进行了包括 Kruskal-Wallis 检验、线性回归和接收者操作特征分析在内的统计分析。
在单个标志物中,我们观察到 pTau181(H(2)= 34.43,p < 0.001)和 NFL(H(2)= 27.66,p < 0.001)的组间有统计学意义。pTau181 的所有个体组间比较均有统计学意义,而 NFL 中 SCD 与 MCI 的对比则无统计学意义。此外,Aβ42/Aβ40 的比值(H(2)= 7.50,p = 0.02)和 pTau181/Aβ42 的比值(H(2)= 25.26,p < 0.001)显示出有统计学意义的组间效应,所有组间的 pTau181/Aβ42 差异均有统计学意义,Aβ42/Aβ40 的 SCD 与 MCI 差异也有统计学意义。pTau181 对 SCD 和 DAT 的鉴别诊断曲线下面积最高,为 0.85,其灵敏度为 80%,特异性为 79%,截断值为 12.2pg/ml。年龄影响 Aβ42、Aβ40 和 NFL 浓度。
在研究之外的记忆诊所环境中,血浆 pTau181 和 NFL 以及 Aβ42/Aβ40 和 pTau181/Aβ42 的比值是可以区分诊断组的生物标志物。