Qin Wei, Li Fangyu, Jia Longfei, Wang Qi, Li Ying, Wei Yiping, Li Yan, Jin Hongmei, Jia Jianping
Innovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
Beijing Key Laboratory of Geriatric Cognitive Disorders, Capital Medical University, Beijing, China.
Front Aging Neurosci. 2022 Jun 13;14:900773. doi: 10.3389/fnagi.2022.900773. eCollection 2022.
There is an urgent need for cost-effective, easy-to-measure biomarkers to identify subjects who will develop Alzheimer's disease (AD), especially at the pre-symptomatic stage. This stage can be determined in autosomal dominant AD (ADAD) which offers the opportunity to observe the dynamic biomarker changes during the life-course of AD stages. This study aimed to investigate serum biomarkers during different AD stages and potential novel protein biomarkers of presymptomatic AD.
In the first stage, 32 individuals [20 mutation carriers including 10 with AD, and 10 with mild cognitive impairment (MCI), and 12 healthy controls] from ADAD families were analyzed. All subjects underwent a complete clinical evaluation and a comprehensive neuropsychological battery. Serum samples were collected from all subjects, and antibody arrays were used to analyze 170 proteins in these samples. The most promising biomarkers were identified during this screening and were then measured in serum samples of 12 subjects with pre-MCI and 20 controls.
The serum levels of 13 proteins were significantly different in patients with AD or MCI compared to controls. Of the 13 proteins, cathepsin D, immunoglobulin E, epidermal growth factor receptor (EGFR), matrix metalloproteinase-9 (MMP-9), von Willebrand factor (vWF), haptoglobin, and phosphorylated Tau-181 (p-Tau181) correlated with all cognitive measures ( = -0.69-0.76). The areas under the receiver operating characteristic curve of these seven proteins were 0.71-0.93 for the classification of AD and 0.57-0.95 for the classification of MCI. Higher levels of p-Tau181 were found in the serum of pre-MCI subjects than in the serum of controls. The p-Tau181 serum level might detect AD before symptoms occur (area under the curve 0.85, sensitivity 75%, specificity 81.67%).
A total of 13 serum proteins showed significant differences between subjects with AD and MCI and healthy controls. The p-Tau181 serum level might be a broadly available and cost-effective biomarker to identify individuals with preclinical AD and assess the severity of AD.
迫切需要具有成本效益且易于测量的生物标志物,以识别将发展为阿尔茨海默病(AD)的个体,尤其是在症状前阶段。这一阶段可在常染色体显性AD(ADAD)中确定,它为观察AD病程中生物标志物的动态变化提供了机会。本研究旨在调查不同AD阶段的血清生物标志物以及症状前AD潜在的新型蛋白质生物标志物。
在第一阶段,对来自ADAD家族的32名个体[20名突变携带者,包括10名患有AD的个体、10名患有轻度认知障碍(MCI)的个体以及12名健康对照]进行了分析。所有受试者均接受了全面的临床评估和综合神经心理测试。从所有受试者中采集血清样本,并使用抗体阵列分析这些样本中的170种蛋白质。在此次筛查中确定了最有前景的生物标志物,随后在12名轻度认知障碍前期(pre-MCI)受试者和20名对照的血清样本中对其进行测量。
与对照组相比,AD或MCI患者血清中13种蛋白质的水平存在显著差异。在这13种蛋白质中,组织蛋白酶D、免疫球蛋白E、表皮生长因子受体(EGFR)、基质金属蛋白酶-9(MMP-9)、血管性血友病因子(vWF)、触珠蛋白和磷酸化Tau-181(p-Tau181)与所有认知指标相关(r = -0.69 - 0.76)。这七种蛋白质的受试者工作特征曲线下面积在AD分类中为0.71 - 0.93,在MCI分类中为0.57 - 0.95。在pre-MCI受试者血清中发现的p-Tau181水平高于对照组血清中的水平。p-Tau181血清水平可能在症状出现前检测到AD(曲线下面积0.85,敏感性75%,特异性81.67%)。
共有13种血清蛋白质在AD、MCI受试者与健康对照之间表现出显著差异。p-Tau181血清水平可能是一种广泛可用且具有成本效益的生物标志物,用于识别临床前AD个体并评估AD的严重程度。