轻度认知障碍(MCI)在寻找其临床身份中的作用,对ne迪斯队列数据的评论

P. FélixBermejo
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引用次数: 1

摘要

老年人认知能力下降是一种众所周知的影响许多人的疾病。最早对这种临床现实的医学定义之一是克拉尔的“良性和恶性衰老性健忘”。在Kral之后,许多作者提出了老年人记忆障碍或认知衰退的其他实体:“年龄相关记忆障碍”、“年龄相关记忆衰退”、“年龄相关认知衰退”、轻度认知障碍(Mild cognitive impairment, MCI)和加拿大研究的“认知障碍非痴呆”(cognitive impairment Non-Dementia, CIND)。最近,DSM-V将老年人认知能力下降定义为“轻微神经认知障碍”。总的来说,MCI的引用次数远远超过MEDLINE中任何其他痴呆前状态(该医学数据库中有超过8000篇评论)。医学文献中的这种成功与其说是一种明确定义的临床疾病,不如说是一种争议的表达。事实上,近30年前,它在医学上的诞生,是作为一个排除痴呆症的研究实体。轻度认知障碍的理论定义非常明确(认知能力下降,痴呆风险增加);问题是对许多老年人认知能力下降的操作定义,随着时间的推移,已经产生了许多定义和亚型。综上所述,MCI被定义为认知能力下降(一个或多个认知领域,主要是记忆),患者的功能活动正常或接近正常,显然没有痴呆。根据受影响认知领域的类型和范围,MCI可分为遗忘型(仅受记忆影响)和非遗忘型(与记忆不同的另一认知领域如执行能力的缺陷)。这两种症状都可以单独或联合出现(仅健忘性轻度认知障碍,仅非健忘性轻度认知障碍,或健忘性或非健忘性加上其他认知领域受到影响)。这个实体有几个众所周知的特征。首先,它在老年人中很普遍,比痴呆状态(5-10%)更普遍(约10-15%)。显然,在这两种情况下,其流行率随所使用的业务定义和所研究的人口统计特征(年龄、性别和教育)而波动。其次,与认知正常的老年人相比,轻度认知障碍患者痴呆和死亡的风险更高。第三,它是一种不稳定的疾病,许多MCI病例不会发展为痴呆症,还有许多人在2-3年的时间内改变为正常的认知。第四,轻度认知损伤是一个异质性实体,有许多危险因素和病因;老年人的主要神经退行性疾病:阿尔茨海默病(AD)、帕金森病(PD)等并不总是痴呆前状态;脑血管疾病、抑郁症和老年合并症是许多MCI病例的基础。从流行病学的角度来看,在临床环境、基于人群的调查和试验研究三种不同的情况下对MCI的定义进行评论是很有趣的,因为在这三种情况下,MCI具有不同的特征和演变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Mild Cognitive Impairment (MCI) in Searching for its Clinical Identity,Comment of the NEDICES Cohort Data
Elderly cognitive decline is a well-known disorder that affects many people. One of the first medical definitions for this clinical reality was Kral’s “benign and malignant senescent forgetfulness”. After Kral, many authors proposed other entities of memory impairment or cognitive decline in the elderly: “Age-associated memory impairment”, “Agerelated memory decline”, “Ageing-associated cognitive decline”, Mild Cognitive Impairment (MCI) and “Cognitive Impairment Non-Dementia” (CIND) of the Canadian Study. And very recently, the DSM-V defined the elderly cognitive decline as a “Minor Neurocognitive Disorder”. By large, MCI had far more citations than any other predementia state in MEDLINE (more than 8,000 reviews in this medical database). This success in the medical literature is rather the expression of a controversy than a well-defined clinical disorder. In fact, its medical birth, near 30 years ago, was as a research entity that precludes dementia. The theoretical definition of MCI is quite clear (A cognitive decline with an increased dementia risk); the problem is the operational definition of this cognitive decline in many elderly that have produced, along the time many definitions and subtypes. In summary, MCI is defined as cognitive decline (of one or more cognitive domains, mainly memory) with normal or near normal functional activities of the patient, and obviously, no dementia. According to the type and extension of the affected cognitive domain, MCI has received several subtyping: Amnestic- only memory affected, non-amnestic- deficit in another cognitive domain different from the memory, such as executive capacities. Both of them could be shown alone or in combination (only amnestic MCI, only non-amnestic, or amnestic o non-amnestic plus other cognitive domain affected. There are several well-known characteristics of this entity. First, it is prevalent in the elderly, more prevalent (about 10-15%) that the dementia states (5-10%). Obviously, in both conditions, its prevalence oscillates with the operational definitions used and with the population demographic characteristics studied: age, sex and education. Second, MCI involves an increased risk of dementia and mortality in relation to the normal cognition elders. Third, it is an unstable disorder, many MCI cases do not evolve to dementia, and many others change to normal cognition in a period of 2-3 years. Fourth, MCI is a heterogeneous entity with many risk factors and aetiologies; it is not always the predementia state of the main neurodegenerative disorders of the elderly: Alzheimer disease (AD), Parkinson disease (PD) and others; cerebral vascular diseases, depression and elderly co-morbidities underpinning many MCI cases. From an epidemiological point of view, it is interesting to comment the MCI definition in three different scenarios: the clinical setting, the population-based surveys, and the trial studies because in these three scenarios, MCI had different characteristics and evolution.
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