Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
UK Dementia Research Institute at UCL, London, United Kingdom.
Mov Disord. 2022 Jul;37(7):1495-1504. doi: 10.1002/mds.28994. Epub 2022 Mar 23.
Alzheimer's disease (AD) co-pathology is common in dementia with Lewy bodies and is associated with increased decline. Plasma pTau181 is a blood-based biomarker that can detect AD co-pathology.
We investigated whether pTau181 was associated with cognitive decline in mild cognitive impairment with Lewy bodies (MCI-LB) and MCI with AD (MCI-AD).
We assessed plasma pTau181 using a single-molecule array (Simoa) immunoassay at baseline and follow-up in a longitudinal cohort of MCI-LB, MCI-AD, and controls.
One hundred forty-six subjects (56 probable MCI-LB, 22 possible MCI-LB, 44 MCI-AD, and 24 controls) were reviewed for up to 5.7 years. Probable MCI-LB had significantly higher pTau181 (22.2% mean increase) compared with controls and significantly lower (24.4% mean decrease) levels compared with MCI-AD. Receiver operating characteristic analyses of pTau181 in discriminating probable MCI-LB from controls showed an area under the curve (AUC) of 0.68 (83% specificity, 57% sensitivity); for discriminating MCI-AD from healthy controls, AUC was 0.8 (83.3% specificity, 72.7% sensitivity). pTau181 concentration was less useful in discriminating between probable MCI-LB and MCI-AD: AUC of 0.64 (71.4% specificity, 52.3% sensitivity). There was an association between pTau181 and cognitive decline in MCI-AD but not in MCI-LB. In a subset with repeat samples there was a nonsignificant 3% increase per follow-up year in plasma pTau181. The rate of change in pTau181 was not significantly different in different diagnostic subgroups.
pTau181 was not associated with an increased decline assessed using either baseline or repeat pTau181. pTau181 partially discriminated probable MCI-LB from controls and MCI-AD from controls but was not useful in distinguishing probable MCI-LB from MCI-AD. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
阿尔茨海默病(AD)共病在路易体痴呆中很常见,与认知能力下降有关。血浆 pTau181 是一种基于血液的生物标志物,可以检测 AD 共病。
我们研究了 pTau181 是否与路易体痴呆的轻度认知障碍(MCI-LB)和 AD 性 MCI(MCI-AD)的认知能力下降有关。
我们使用单分子阵列(Simoa)免疫测定法在 MCI-LB、MCI-AD 和对照组的纵向队列中在基线和随访时评估血浆 pTau181。
146 名受试者(56 例可能的 MCI-LB、22 例可能的 MCI-LB、44 例 MCI-AD 和 24 例对照)接受了长达 5.7 年的随访。与对照组相比,可能的 MCI-LB 的 pTau181 显著升高(平均增加 22.2%),与 MCI-AD 相比,pTau181 水平显著降低(平均降低 24.4%)。使用 pTau181 区分可能的 MCI-LB 与对照组的受试者工作特征分析显示曲线下面积(AUC)为 0.68(特异性 83%,敏感性 57%);区分 MCI-AD 与健康对照组的 AUC 为 0.8(特异性 83.3%,敏感性 72.7%)。pTau181 浓度在区分可能的 MCI-LB 与 MCI-AD 方面的作用不大:AUC 为 0.64(特异性 71.4%,敏感性 52.3%)。在具有重复样本的亚组中,血浆 pTau181 每年增加 3%。pTau181 的变化率在不同的诊断亚组中没有显著差异。
pTau181 与使用基线或重复 pTau181 评估的认知能力下降无关。pTau181 部分区分了可能的 MCI-LB 与对照组和 MCI-AD 与对照组,但在区分可能的 MCI-LB 与 MCI-AD 方面没有用处。© 2022 作者。运动障碍协会代表国际帕金森病和运动障碍协会由 Wiley 期刊出版公司出版。