Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
Int J Mol Sci. 2024 Jan 18;25(2):1173. doi: 10.3390/ijms25021173.
Alzheimer's disease (AD) is characterized by amyloid beta (Aβ) plaques and hyperphosphorylated tau in the brain. Aβ plaques precede cognitive impairments and can be detected through amyloid-positron emission tomography (PET) or in cerebrospinal fluid (CSF). Assessing the plasma Aβ42/Aβ40 ratio seems promising for non-invasive and cost-effective detection of brain Aβ accumulation. This approach involves some challenges, including the accuracy of blood-based biomarker measurements and the establishment of clear, standardized thresholds to categorize the risk of developing brain amyloid pathology. Plasma Aβ42/Aβ40 ratio was measured in 277 volunteers without dementia, 70 AD patients and 18 non-AD patients using single-molecule array. Patients ( = 88) and some volunteers ( = 66) were subject to evaluation of amyloid status by CSF Aβ quantification or PET analysis. Thresholds of plasma Aβ42/Aβ40 ratio were determined based on a Gaussian mixture model, a decision tree, and the Youden's index. The 0.0472 threshold, the one with the highest sensitivity, was retained for general population without dementia screening, and the 0.0450 threshold was retained for research and clinical trials recruitment, aiming to minimize the need for CSF or PET analyses to identify amyloid-positive individuals. These findings offer a promising step towards a cost-effective method for identifying individuals at risk of developing AD.
阿尔茨海默病(AD)的特征是大脑中存在淀粉样β(Aβ)斑块和过度磷酸化的 tau。Aβ 斑块先于认知障碍出现,可以通过淀粉样蛋白正电子发射断层扫描(PET)或脑脊液(CSF)检测到。评估血浆 Aβ42/Aβ40 比值似乎是一种有前途的方法,可以非侵入性且经济有效地检测大脑中 Aβ 的积累。这种方法存在一些挑战,包括血液生物标志物测量的准确性以及建立明确、标准化的阈值来分类发生脑淀粉样蛋白病理的风险。使用单分子阵列,对 277 名无痴呆的志愿者、70 名 AD 患者和 18 名非 AD 患者进行了血浆 Aβ42/Aβ40 比值测量。对患者(88 名)和一些志愿者(66 名)进行了 CSF Aβ 定量或 PET 分析评估淀粉样状态。根据高斯混合模型、决策树和 Youden 指数确定了血浆 Aβ42/Aβ40 比值的阈值。保留了具有最高灵敏度的 0.0472 阈值,用于无痴呆的一般人群筛查,保留了 0.0450 阈值,用于研究和临床试验招募,旨在尽量减少对 CSF 或 PET 分析的需求,以识别淀粉样蛋白阳性个体。这些发现为识别有患 AD 风险的个体提供了一个有前途的方法,具有成本效益。