Evidence map›Paper›PMID 37807780›Full record

ArticleJournal of Alzheimer's disease : JAD2023

Development of a Cognitive Composite for Preclinical Alzheimer's Disease in Korean Older Adults.

Minjae Kim, Dahyun Yi, Min Soo Byun, Hyejin Ahn, Joon Hyung Jung, Nayeong Kong, Yoonyoung Chang, Hyeji Choi, Jungmin Choi, Kyungtae Kim and 3 more

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

13 authors.

Minjae KimDepartment of Psychiatry, Soonchunhyang University Seoul Hospital, Seoul, Korea.
Dahyun YiMedical Research Center, Institute of Human Behavioral Medicine, Seoul National University, Seoul, Korea.
Min Soo ByunDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Hyejin AhnDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Joon Hyung JungDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Nayeong KongDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Yoonyoung ChangDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Hyeji ChoiDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Jungmin ChoiDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Kyungtae KimDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Gijung JungDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Dong Young LeeMedical Research Center, Institute of Human Behavioral Medicine, Seoul National University, Seoul, Korea.
KBASE Research Group

Funding

KBASE2: Korean Brain Aging Study, Longitudinal Endophenotypes and Systems BiologyU01AG072177 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LEE, DONG YOUNG, NHO, KWANGSIK TIMOTHY · 2021 to 2025
$11.2M
NIA NIH HHS U01 AG072177
6 · The paper itself

Abstract

backgroundAs tracking subtle cognitive declines in the preclinical stage of Alzheimer's disease (AD) is difficult with traditional individual outcome measures, need for cognitive composite for preclinical AD is widely recognized.

objectiveWe aimed to develop culturally appropriate cognitive composite that sensitively identifies subtle cognitive decline of preclinical AD in Korean older adults.

methodsA total 225 cognitively normal elderly individuals from the Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer's Disease, were included. Tests of episodic memory, orientation, and executive function were carefully selected through review of previously established composites. Three candidate composites including Consortium to Establish a Registry for Alzheimer's Disease Word list recall (WLR), Logical memory (LM) II, and Mini-Mental status examination (MMSE) in common, and Letter fluency test (LF), category fluency test, or Stroop color and word test, were selected.

resultsStudent t-tests demonstrated that only the composite composed of WLR, LM II, MMSE, and LF (Composite 1) showed a significant difference in score decline over two-year follow-up period between Aβ positive and negative group (p = 0.03). Linear mixed model analyses also showed that the Aβ x time interaction effect was significant only for Composite 1 (p = 0.025). Based on the results, Composite 1 was chosen as the final cognitive composite for preclinical Alzheimer's disease (CPAD).

conclusionsCPAD can be used to assess subtle cognitive decline of preclinical AD in clinical research settings, especially in Korean older adults. It also may be used for monitoring progression or treatment benefits in clinical practices.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAmyloid beta-PeptidesCognitionDisease ProgressionHumansNeuropsychological TestsRepublic of KoreaAmyloid beta-PeptidesAlzheimer’s diseasecognitive compositecognitively normalpreclinical Alzheimer’s disease

Identifiers

PMID37807780
PMCPMC10657668

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.