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正常衰老、轻度认知障碍和阿尔茨海默病的多模态鉴别及认知衰退预测

Multimodal Discrimination between Normal Aging, Mild Cognitive Impairment and Alzheimer's Disease and Prediction of Cognitive Decline.

作者信息

Bauer Corinna M, Cabral Howard J, Killiany Ronald J

机构信息

Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA.

Department of Biostatistics, Boston University School of Public Health, Boston, MA 02118, USA.

出版信息

Diagnostics (Basel). 2018 Feb 6;8(1):14. doi: 10.3390/diagnostics8010014.

Abstract

Alzheimer's Disease (AD) and mild cognitive impairment (MCI) are associated with widespread changes in brain structure and function, as indicated by magnetic resonance imaging (MRI) morphometry and 18-fluorodeoxyglucose position emission tomography (FDG PET) metabolism. Nevertheless, the ability to differentiate between AD, MCI and normal aging groups can be difficult. Thus, the goal of this study was to identify the combination of cerebrospinal fluid (CSF) biomarkers, MRI morphometry, FDG PET metabolism and neuropsychological test scores to that best differentiate between a sample of normal aging subjects and those with MCI and AD from the Alzheimer's Disease Neuroimaging Initiative. The secondary goal was to determine the neuroimaging variables from MRI, FDG PET and CSF biomarkers that can predict future cognitive decline within each group. To achieve these aims, a series of multivariate stepwise logistic and linear regression models were generated. Combining all neuroimaging modalities and cognitive test scores significantly improved the index of discrimination, especially at the earliest stages of the disease, whereas MRI gray matter morphometry variables best predicted future cognitive decline compared to other neuroimaging variables. Overall these findings demonstrate that a multimodal approach using MRI morphometry, FDG PET metabolism, neuropsychological test scores and CSF biomarkers may provide significantly better discrimination than any modality alone.

摘要

阿尔茨海默病(AD)和轻度认知障碍(MCI)与脑结构和功能的广泛变化相关,磁共振成像(MRI)形态学和18-氟脱氧葡萄糖正电子发射断层扫描(FDG PET)代谢已表明了这一点。然而,区分AD、MCI和正常衰老组可能存在困难。因此,本研究的目的是确定脑脊液(CSF)生物标志物、MRI形态学、FDG PET代谢和神经心理学测试分数的组合,以最佳地区分正常衰老受试者样本与来自阿尔茨海默病神经影像倡议组织的MCI和AD患者。次要目标是确定来自MRI、FDG PET和CSF生物标志物的神经影像变量,这些变量可预测每组未来的认知衰退。为实现这些目标,生成了一系列多元逐步逻辑回归和线性回归模型。结合所有神经影像模态和认知测试分数可显著提高鉴别指数,尤其是在疾病的最早阶段,而与其他神经影像变量相比,MRI灰质形态学变量最能预测未来的认知衰退。总体而言,这些发现表明,使用MRI形态学、FDG PET代谢、神经心理学测试分数和CSF生物标志物的多模态方法可能比任何单一模态提供显著更好的鉴别效果。

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