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评估轻度认知障碍向阿尔茨海默病的进展:当前趋势和未来方向。

Assessing the progression of mild cognitive impairment to Alzheimer's disease: current trends and future directions.

机构信息

Department of Rehabilitation Medicine, Miller School of Medicine - University of Miami, P,O, Box 016960 (C-206), Miami, FL 33101, USA.

出版信息

Alzheimers Res Ther. 2010 Sep 29;2(5):28. doi: 10.1186/alzrt52.

Abstract

With the advent of advances in biomarker detection and neuropsychological measurement, prospects have improved for identifying and tracking the progression of Alzheimer's disease (AD) from its earliest stages through dementia. While new diagnostic techniques have exciting implications for initiating treatment earlier in the disease process, much work remains to be done to optimize the contributions of the expanding range of tools at the disposal of researchers and clinicians. The present paper examines recent work in cerebrospinal fluid biomarkers, magnetic resonance imaging, positron emission tomography, neuropsychological measures, and functional assessment. The strengths and weaknesses of current methodologies are explored and discussed. It is concluded that AD from its mild cognitive impairment state through dementia represents a continuous process, and that progression over time can best be accomplished by interval-level variables. Biomarkers that are most sensitive to early AD may not be the most optimal for monitoring longitudinal change, and it is likely that multivariate models incorporating cognitive measures, functional variables and biomarker data will be the most fruitful avenues for future research.

摘要

随着生物标志物检测和神经心理学测量技术的进步,人们有希望从疾病的早期阶段开始,识别和跟踪阿尔茨海默病(AD)的进展,并进行跟踪。虽然新的诊断技术为在疾病过程的早期开始治疗带来了令人兴奋的前景,但仍有许多工作要做,以优化研究人员和临床医生可利用的一系列工具的贡献。本文研究了最近在脑脊液生物标志物、磁共振成像、正电子发射断层扫描、神经心理学测量和功能评估方面的工作。探讨和讨论了当前方法的优缺点。结论是,从轻度认知障碍到痴呆,AD 代表了一个连续的过程,随着时间的推移,通过间隔变量可以最好地完成进展。对早期 AD 最敏感的生物标志物可能不是监测纵向变化的最佳选择,并且包含认知测量、功能变量和生物标志物数据的多变量模型可能是未来研究的最有成效的途径。

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