Mild cognitive impairment: a concept in evolution

被引:1110
作者
Petersen, R. C. [1 ]
Caracciolo, B. [2 ,3 ,4 ]
Brayne, C. [5 ]
Gauthier, S. [6 ]
Jelic, V. [3 ,7 ]
Fratiglioni, L. [2 ,3 ,8 ]
机构
[1] Mayo Clin, Coll Med, Dept Neurol, Mayo Alzheimers Dis Res Ctr, Rochester, MN 55905 USA
[2] Karolinska Inst, Aging Res Ctr, Dept Neurobiol Care Sci & Soc, S-10401 Stockholm, Sweden
[3] Stockholm Univ, S-10691 Stockholm, Sweden
[4] Stockholm Univ, Stress Res Inst, S-10691 Stockholm, Sweden
[5] Univ Cambridge, Cambridge Inst Publ Hlth, Cambridge, England
[6] Douglas Mental Hlth Res Inst, McGill Ctr Studies Aging, Montreal, PQ, Canada
[7] Karolinska Inst, Div Clin Geriatr, Dept Neurobiol Care Sci & Soc, S-10401 Stockholm, Sweden
[8] Stockholm Gerontol Res Ctr, Stockholm, Sweden
关键词
Alzheimer's disease; dementia; memory impairment; mild cognitive impairment; VASCULAR RISK-FACTORS; ALZHEIMERS-DISEASE; CARDIOVASCULAR HEALTH; CEREBROSPINAL-FLUID; GENERAL-POPULATION; DEMENTIA RISK; NO DEMENTIA; VITAMIN-E; PROGRESSION; PREVALENCE;
D O I
10.1111/joim.12190
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The construct of mild cognitive impairment (MCI) has evolved over the past 10years since the publication of the new MCI definition at the Key Symposium in 2003, but the core criteria have remained unchanged. The construct has been extensively used worldwide, both in clinical and in research settings, to define the grey area between intact cognitive functioning and clinical dementia. A rich set of data regarding occurrence, risk factors and progression of MCI has been generated. Discrepancies between studies can be mostly explained by differences in the operationalization of the criteria, differences in the setting where the criteria have been applied, selection of subjects and length of follow-up in longitudinal studies. Major controversial issues that remain to be further explored are algorithmic versus clinical classification, reliability of clinical judgment, temporal changes in cognitive performances and predictivity of putative biomarkers. Some suggestions to further develop the MCI construct include the tailoring of the clinical criteria to specific populations and to specific contexts. The addition of biomarkers to the clinical phenotypes is promising but requires deeper investigation. Translation of findings from the specialty clinic to the population setting, although challenging, will enhance uniformity of outcomes. More longitudinal population-based studies on cognitive ageing and MCI need to be performed to clarify all these issues.
引用
收藏
页码:214 / 228
页数:15
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