Cognitive Phenotypes of Older Adults with Subjective Cognitive Decline and Amnestic Mild Cognitive Impairment: The Czech Brain Aging Study

被引:13
|
作者
Jester, Dylan J. [1 ]
Andel, Ross [1 ,2 ,3 ,4 ]
Cechova, Katerina [2 ,3 ,4 ]
Laczo, Jan [2 ,3 ,4 ]
Lerch, Ondrej [2 ,3 ,4 ]
Markova, Hana [2 ,3 ,4 ]
Nikolai, Tomas [2 ,3 ,4 ]
Vyhnalek, Martin [2 ,3 ,4 ]
Hort, Jakub [2 ,3 ,4 ]
机构
[1] Univ S Florida, Sch Aging Studies, 13301 Bruce B Downs Blvd,MHC 1318, Tampa, FL 33612 USA
[2] Charles Univ Prague, Fac Med 2, Dept Neurol, Memory Clin, Prague 15006, Czech Republic
[3] Motol Univ Hosp, Prague 15006, Czech Republic
[4] St Annes Univ Hosp Brno, Int Clin Res Ctr, Brno 65691, Czech Republic
关键词
Subjective cognitive complaints; Mild cognitive impairment; Transition to dementia; Machine learning; Neuropsychological performance; Prospective cohort study; ALZHEIMERS-DISEASE; MEMORY COMPLAINTS; NORMATIVE DATA; DEMENTIA; PROGRESSION; HETEROGENEITY; VERSION; CLASSIFICATION; PREDICTOR; FRAMEWORK;
D O I
10.1017/S1355617720001046
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To compare cognitive phenotypes of participants with subjective cognitive decline (SCD) and amnestic mild cognitive impairment (aMCI), estimate progression to MCI/dementia by phenotype and assess classification error with machine learning. Method: Dataset consisted of 163 participants with SCD and 282 participants with aMCI from the Czech Brain Aging Study. Cognitive assessment included the Uniform Data Set battery and additional tests to ascertain executive function, language, immediate and delayed memory, visuospatial skills, and processing speed. Latent profile analyses were used to develop cognitive profiles, and Cox proportional hazards models were used to estimate risk of progression. Random forest machine learning algorithms reported cognitive phenotype classification error. Results: Latent profile analysis identified three phenotypes for SCD, with one phenotype performing worse across all domains but not progressing more quickly to MCI/dementia after controlling for age, sex, and education. Three aMCI phenotypes were characterized by mild deficits, memory and language impairment (dysnomic aMCI), and severe multi-domain aMCI (i.e., deficits across all domains). A dose-response relationship between baseline level of impairment and subsequent risk of progression to dementia was evident for aMCI profiles after controlling for age, sex, and education. Machine learning more easily classified participants with aMCI in comparison to SCD (8% vs. 21% misclassified). Conclusions: Cognitive performance follows distinct patterns, especially within aMCI. The patterns map onto risk of progression to dementia.
引用
收藏
页码:329 / 342
页数:14
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