Lopez Oscar L
Continuum (Minneap Minn). 2013 Apr;19(2 Dementia):411-24. doi: 10.1212/01.CON.0000429175.29601.97.
The term mild cognitive impairment (MCI) is used to describe older subjects with demonstrable cognitive impairment who have not crossed the threshold for dementia. Because patients with MCI have an increased risk of developing dementia, especially Alzheimer disease (AD), there is significant interest in the clinical characterization of these subjects and in understanding the pathophysiology of the transition from MCI to AD.
The MCI syndrome, as an expression of an incipient disorder that may lead to dementia, is extremely heterogeneous and may coexist with systemic, neurologic, or psychiatric disorders that can cause cognitive deficits. Recent clinical criteria were designed to take into account the different forms of clinical presentation of the syndrome, and introduced the possible contribution of biomarkers to the clinical diagnosis. Bedside diagnosis of MCI can be difficult, since patients who report having cognitive problems may have normal scores in global cognitive scales or in brief neuropsychological instruments.
This article presents the evolution of the clinical concept of MCI, the operationalization of its current definitions, the development of biomarkers that can help to identify an underlying neurodegenerative process as the etiology of the syndrome, and its proposed treatments.
术语“轻度认知障碍(MCI)”用于描述有明显认知障碍但未达到痴呆阈值的老年受试者。由于MCI患者患痴呆症的风险增加,尤其是阿尔茨海默病(AD),因此人们对这些受试者的临床特征以及理解从MCI向AD转变的病理生理学有着浓厚兴趣。
MCI综合征作为一种可能导致痴呆的初期疾病表现,极其异质性,可能与可引起认知缺陷的全身性、神经或精神疾病共存。最近的临床标准旨在考虑该综合征不同形式的临床表现,并引入生物标志物对临床诊断的可能贡献。MCI的床边诊断可能困难,因为报告有认知问题的患者在整体认知量表或简短神经心理测试中得分可能正常。
本文介绍了MCI临床概念的演变、其当前定义的实施、有助于识别作为该综合征病因的潜在神经退行性过程的生物标志物的发展以及其推荐治疗方法。