In Brief Neuropsychological Assessment, Amnestic Mild Cognitive Impairment (MCI) Is associated with Cerebrospinal Fluid Biomarkers for Cognitive Decline in Contrast to the Prevailing NIA-AA MCI Criterion

被引:5
作者
Hessen, Erik [1 ,2 ]
Kirsebom, Bjorn-Eivind [3 ,4 ]
Eriksson, Cecilia Magdalena [1 ,2 ,5 ]
Eliassen, Carl Fredrik [1 ,2 ]
Nakling, Arne Exner [6 ]
Brathen, Geir [7 ,8 ]
Waterloo, Knut K. [3 ,4 ]
Aarsland, Dag [1 ,9 ,10 ]
Fladby, Tormod [1 ,11 ]
机构
[1] Akershus Univ Hosp, Dept Neurol, PB 1000, N-1478 Lorenskog, Norway
[2] Univ Oslo, Inst Psychol, Oslo, Norway
[3] Univ Hosp North Norway, Dept Neurol, Tromso, Norway
[4] UiT Arctic Univ Norway, Fac Hlth Sci, Dept Psychol, Tromso, Norway
[5] Akershus Univ Hosp, Dept Geriatr Psychiat, Lorenskog, Norway
[6] Betanien Hosp, Bergen, Norway
[7] Norwegian Univ Sci & Technol, Fac Med & Heath Sci, Dept Neuromed & Movement Sci, Trondheim, Norway
[8] Univ Hosp Trondheim, Dept Neurol & Clin Neurophysiol, Trondheim, Norway
[9] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Old Age Psychiat, London, England
[10] Stavanger Univ Hosp, Ctr Age Related Dis, Stavanger, Norway
[11] Univ Oslo, Inst Clin Med, Campus Ahus, Oslo, Norway
关键词
Alzheimer's disease; amnestic MCI; brief neuropsychological assessment; cerebrospinal fluid biomarkers; mild cognitive impairment; NIA-AA MCI criterion; NIA-AA stage 2; ALZHEIMERS-DISEASE; FOLLOW-UP; SCORES; PREVALENCE; FRAMEWORK; DEMENTIA; SUBTYPES; MEMORY;
D O I
10.3233/JAD-180964
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: In the care of persons with cognitive problems, it is important to use a valid mild cognitive impairment (MCI) criterion that discriminates well between normal and pathological aging. Objective: To find the brief neuropsychological screening criterion that best correlates with cerebrospinal fluid (CSF) biomarkers for cognitive decline and dementia in persons seeking help for cognitive problems. Methods: 452 consecutively recruited patients (age 40-80 years) from memory-clinics in the Norwegian national multicentre longitudinal study Dementia Disease Initiation were included. CSF data as well as full data from brief neuropsychological screening were available for all patients. Results: Amnestic MCI, including at least one memory test below T-score 40, outperformed the conventional US National Institute on Aging-Alzheimer's Association (NIA-AA) MCI criterion. Only amnestic MCI was significantly associated with biomarker pattern of NIA-AA stage 2 (low CSF A beta(42) concentrations and elevated tau) in multivariate regression analysis. Conclusions: The finding that amnestic MCI based on brief neuropsychological assessment is significantly associated with CSF biomarkers for cognitive decline and Alzheimer's disease is in accordance with longitudinal studies that find memory impairment; both in itself and especially in combination with other cognitive deficit to constitute a risk factor for subsequent cognitive decline and dementia. The prevalence of pathological biomarkers for Alzheimer's disease is common in the elderly and the clinical significance of present findings depend on longitudinal validation.
引用
收藏
页码:715 / 723
页数:9
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