Tau pathology mediated the plasma biomarkers and cognitive function in patients with mild cognitive impairment

IF 3.9
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Abstract

Glial fibrillary acidic protein (GFAP) and neurofilament light (NfL) are putative non-amyloid biomarkers indicative of ongoing inflammatory and neurodegenerative disease processes. Hence, this study aimed to demonstrate the relationship between plasma biomarkers (GFAP and NfL) and 18F-AV-1451 tau PET images, and to explore their effects on cognitive function. Ninety-one participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database and 20 participants from the Shanghai Action of Prevention Dementia for the Elderly (SHAPE) cohort underwent plasma biomarker testing, 18F-AV-1451 tau PET scans and cognitive function assessments. Within the ADNI, there were 42 cognitively normal (CN) individuals and 49 with mild cognitive impairment (MCI). Similarly, in the SHAPE, we had 10 CN and 10 MCI participants. We calculated the standardized uptake value ratios (SUVRs) for the regions of interest (ROIs) in the 18F-AV-1451 PET scans. Using plasma biomarkers and regional SUVRs, we trained machine learning models to differentiate between MCI and CN subjects with ADNI database and validated in SHAPE.

Results showed that eight selected variables (including left amygdala SUVR, right amygdala SUVR, left entorhinal cortex SUVR, age, education, plasma NfL, plasma GFAP, plasma GFAP/ NfL) identified by LASSO could differentiate between the MCI and CN individuals, with AUC ranging from 0.783 to 0.926. Additionally, cognitive function was negatively associated with the plasma biomarkers and tau deposition in amygdala and left entorhinal cortex. Increased tau deposition in amygdala and left entorhinal cortex were related to increased plasma biomarkers. Moreover, tau pathology mediated the effect of plasma biomarkers level on the cognitive decline. The present study provides valuable insights into the association among plasma markers (GFAP and NfL), regional tau deposition and cognitive function. This study reports the mediation effect of brain regions tau deposition on the plasma biomarkers level and cognitive function, indicating the significance of tau pathology in the MCI patients.

Tau 病理学介导轻度认知障碍患者的血浆生物标志物和认知功能。
胶质纤维酸性蛋白(GFAP)和神经丝光(NfL)是指示炎症和神经退行性疾病过程的非淀粉样蛋白生物标记物。因此,本研究旨在证明血浆生物标志物(GFAP 和 NfL)与 18F-AV-1451 tau PET 图像之间的关系,并探讨它们对认知功能的影响。来自阿尔茨海默病神经影像学倡议(ADNI)数据库的91名参与者和来自上海预防老年痴呆行动(SHAPE)队列的20名参与者接受了血浆生物标志物检测、18F-AV-1451 tau PET扫描和认知功能评估。在 ADNI 中,有 42 人认知功能正常 (CN) ,49 人患有轻度认知功能障碍 (MCI)。同样,在SHAPE中,我们有10名认知正常(CN)和10名轻度认知障碍(MCI)患者。我们计算了 18F-AV-1451 PET 扫描感兴趣区(ROI)的标准化摄取值比(SUVR)。利用血浆生物标志物和区域 SUVR,我们通过 ADNI 数据库训练了机器学习模型来区分 MCI 和 CN 受试者,并在 SHAPE 中进行了验证。结果表明,LASSO识别的八个选定变量(包括左杏仁核SUVR、右杏仁核SUVR、左内皮层SUVR、年龄、教育程度、血浆NfL、血浆GFAP、血浆GFAP/ NfL)可以区分MCI和CN受试者,AUC在0.783到0.926之间。此外,认知功能与血浆生物标志物以及杏仁核和左侧内视网膜皮层的tau沉积呈负相关。杏仁核和左脑内皮层的tau沉积增加与血浆生物标志物增加有关。此外,tau病理学介导了血浆生物标志物水平对认知能力下降的影响。本研究就血浆标志物(GFAP和NfL)、区域性tau沉积和认知功能之间的关联提供了有价值的见解。本研究报告了脑区tau沉积对血浆生物标志物水平和认知功能的中介效应,表明了tau病理学在MCI患者中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental gerontology
Experimental gerontology Ageing, Biochemistry, Geriatrics and Gerontology
CiteScore
6.70
自引率
0.00%
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0
审稿时长
66 days
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