Pedro Pesini, PhD. Vía Hispanidad 21, 50009 Zaragoza, Spain; Telephone number: +34 976 796 562; Fax: (+34) 976 217 802; Email:
J Prev Alzheimers Dis. 2019;6(1):34-41. doi: 10.14283/jpad.2018.41.
Easily accessible biomarkers are needed for the early identification of individuals at risk of developing Alzheimer's disease (AD) in large population screening strategies.
This study evaluated the potential of plasma β-amyloid (Aβ) biomarkers in identifying early stages of AD and predicting cognitive decline over the following two years.
Total plasma Aβ42/40 ratio (TP42/40) was determined in 83 cognitively normal individuals (CN) and 145 subjects with amnestic mild cognitive impairment (a-MCI) stratified by an FDG-PET AD-risk pattern.
Significant lower TP42/40 ratio was found in a-MCI patients compared to CN. Moreover, a-MCIs with a high-risk FDG-PET pattern for AD showed even lower plasma ratio levels. Low TP42/40 at baseline increased the risk of progression to dementia by 70%. Furthermore, TP42/40 was inversely associated with neocortical amyloid deposition (measured with PiB-PET) and was concordant with the AD biomarker profile in cerebrospinal fluid (CSF).
TP42/40 demonstrated value in the identification of individuals suffering a-MCI, in the prediction of progression to dementia, and in the detection of underlying AD pathology revealed by FDG-PET, Amyloid-PET and CSF biomarkers, being, thus, consistently associated with all the well-established indicators of AD.
在大规模人群筛查策略中,需要易于获取的生物标志物来早期识别有患阿尔茨海默病(AD)风险的个体。
本研究评估了血浆β-淀粉样蛋白(Aβ)生物标志物在识别 AD 早期阶段和预测随后两年认知能力下降方面的潜力。
在 83 名认知正常个体(CN)和 145 名有遗忘型轻度认知障碍(a-MCI)的受试者中,测定总血浆 Aβ42/40 比值(TP42/40),并根据 FDG-PET AD 风险模式进行分层。
与 CN 相比,a-MCI 患者的 TP42/40 比值明显降低。此外,具有 AD 高风险 FDG-PET 模式的 a-MCI 患者的血浆比值水平甚至更低。基线时低 TP42/40 使进展为痴呆的风险增加了 70%。此外,TP42/40 与新皮质淀粉样蛋白沉积(用 PiB-PET 测量)呈负相关,与脑脊液(CSF)中的 AD 生物标志物谱一致。
TP42/40 在识别患有 a-MCI 的个体、预测向痴呆进展以及检测 FDG-PET、淀粉样蛋白-PET 和 CSF 生物标志物揭示的潜在 AD 病理方面具有价值,因此与所有公认的 AD 指标一致。