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轻度认知障碍患者进展为可能的阿尔茨海默病型痴呆的预测因素。

Predictors of conversion to dementia of probable Alzheimer type in patients with mild cognitive impairment.

作者信息

Modrego Pedro J

机构信息

Neurology Department, Miguel Servet University Hospital, Zaragoza, Spain.

出版信息

Curr Alzheimer Res. 2006 Apr;3(2):161-70. doi: 10.2174/156720506776383103.

Abstract

BACKGROUND

Mild Cognitive Impairment is a common condition defined as transitional state between normality and dementia of Alzheimer type. Clinically is characterized by subjective and objective memory loss beyond the expected for age and educational level, although a broad range of cognitive inefficiencies may appear, with preservation of daily living activities. Approximately half the patients convert to dementia within 3 years. Since no all patients convert to dementia it is essential to find reliable predictors so as to start the appropriate treatment as soon as possible.

METHOD

Extensive Medline-based search for articles dealing with predictors of conversion to dementia in Mild Cognitive Impairment (MCI).

RESULTS

There is a substantial body of literature dealing with predictors of dementia in patients with MCI. These predictors range from a simple delayed recall task on Mini-Mental to sophisticated radiological techniques and CSF biomarkers. Comprehensive neuropsychological tests rarely surpass 70% sensitivity and specificity. The presence of the APOE epsilon 4 allele has been associated with increased risk of conversion but the sensitivity is quite low. CSF biochemical markers are being developed with encouraging results. beta-amyloid 42 protein is usually lower in converters than in people with stable cognitive status and tau protein is higher. The sensitivity is substantial but specificity is so far low. An epitope of tau protein (P231) looks more specific of Alzheimer's disease and therefore a promising biomarker. In the blood, high beta-amyloid protein levels indicate risk of conversion but only a few studies have been published. Hippocampal or entorhinal atrophy on MRI is one of the most used radiological markers of conversion but quantification of atrophy is not simple as it is subject to artifacts and anatomic variations. Proton Magnetic Resonance Spectroscopy (MRS) and Positron Emission Tomography (PET) are emerging as the most promising predictive tools. The highest degree of accuracy (>90%) has been achieved by means of PET plus either memory performance or APOE4 genotype. However, the samples of the published studies are mostly small, and these instruments are not widely available.

CONCLUSIONS

There is no enough evidence to recommend specific techniques for predictions. Until an accurate marker is developed, a combined use of cognitive tests, APOE genotype, and a neuroradiological technique is probably the best option for prediction purposes depending on availability and experience.

摘要

背景

轻度认知障碍是一种常见病症,被定义为正常状态与阿尔茨海默病型痴呆之间的过渡状态。临床上其特征为超出年龄和教育水平预期的主观和客观记忆丧失,尽管可能会出现广泛的认知效率低下情况,但日常生活活动能力仍得以保留。约半数患者会在3年内转变为痴呆。由于并非所有患者都会转变为痴呆,因此找到可靠的预测指标以便尽早开始适当治疗至关重要。

方法

基于Medline广泛检索关于轻度认知障碍(MCI)向痴呆转变的预测指标的文章。

结果

有大量文献涉及MCI患者痴呆的预测指标。这些预测指标范围从简易精神状态检查中的简单延迟回忆任务到复杂的放射学技术和脑脊液生物标志物。全面的神经心理学测试的敏感性和特异性很少超过70%。APOEε4等位基因的存在与转变风险增加相关,但敏感性相当低。脑脊液生化标志物正在研发,结果令人鼓舞。β淀粉样蛋白42在转变者中通常低于认知状态稳定者,而tau蛋白则较高。敏感性较高,但目前特异性较低。tau蛋白的一个表位(P231)似乎对阿尔茨海默病更具特异性,因此是一种有前景的生物标志物。在血液中,高β淀粉样蛋白水平表明有转变风险,但仅有少数研究发表。MRI上的海马或内嗅皮质萎缩是最常用的转变放射学标志物之一,但萎缩的量化并不简单,因为它受伪影和解剖变异影响。质子磁共振波谱(MRS)和正电子发射断层扫描(PET)正成为最有前景的预测工具。通过PET结合记忆表现或APOE4基因型已实现最高程度的准确性(>90%)。然而,已发表研究的样本大多较小,且这些仪器并不广泛可用。

结论

没有足够证据推荐用于预测的特定技术。在开发出准确标志物之前,根据可获得性和经验,联合使用认知测试、APOE基因型和神经放射学技术可能是预测的最佳选择。

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