Predictors of Clinical Progression of Subjective Memory Impairment in Elderly Subjects: Data from the Clinical Research Centers for Dementia of South Korea (CREDOS)

被引:25
作者
Hong, Yun Jeong [1 ]
Yoon, Bora [6 ]
Shim, Yong S. [4 ]
Kim, Seon-Ok [2 ]
Kim, Hwa Jung [3 ]
Choi, Seong Hye [8 ]
Jeong, Jee Hyang [5 ]
Yoon, Soo Jin [7 ]
Yang, Dong Won [4 ]
Lee, Jae-Hong [1 ]
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Clin Epidemiol & Biostat, Seoul, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Prevent Med, Seoul, South Korea
[4] Catholic Univ Korea, Dept Neurol, Seoul 137701, South Korea
[5] Ewha Womans Univ, Dept Neurol, Sch Med, Seoul, South Korea
[6] Konyang Univ, Coll Med, Dept Neurol, Taejon, South Korea
[7] Eulji Univ, Sch Med, Dept Neurol, Taejon, South Korea
[8] Inha Univ, Sch Med, Dept Neurol, Inchon, South Korea
关键词
Subjective memory impairment; Mild cognitive impairment; Alzheimer's disease; Progression; Predictors; WHITE-MATTER HYPERINTENSITIES; MILD COGNITIVE IMPAIRMENT; ALZHEIMERS-DISEASE; COMPLAINTS; DECLINE;
D O I
10.1159/000430807
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background/Aims: The aims of this study were to determine baseline factors related to the progression of subjective memory impairment (SMI) in elderly subjects and to develop a new modeling scale to predict progression. Methods: Elderly subjects with SMI were recruited from the nationwide Clinical Research Centers for Dementia of South Korea (CREDOS) multicenter cohort and divided into two groups: (1) progressed to mild cognitive impairment or Alzheimer's disease or (2) stable without progression. Baseline clinical characteristics were compared between the groups, and the most relevant predictors of progression were assessed. A new modeling scale combining the predictors was developed. Results: In total, 129 subjects with SMI were analyzed. The follow-up duration was 0.5-4.7 years, and the median time to event was 3.64 years. The progressing group (n = 29) differed from the stable group (n = 100) in terms of baseline age, apolipoprotein E4 (APOE4) status, and some cognitive domains. Older age, a lower Mini-Mental State Examination recall score, APOE4 carrier, and a lower verbal delayed recall score were the most relevant predictors of progression, and a new modeling scale with these 4 predictors provided a better explanation of progression. Conclusion: SMI subjects with a higher risk of progression can be identified using a new modeling scale and might need further evaluations and more frequent follow-up. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:158 / 165
页数:8
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