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Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort
BACKGROUND AND PURPOSE: Patients with mild cognitive impairment (MCI) and their caregivers are concerned with the likelihood and time course of progression to dementia. This study was performed to identify the clinical predictors of the MCI progression in a Korean registry, and investigated the effe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Dementia Association
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427964/ https://www.ncbi.nlm.nih.gov/pubmed/30906345 http://dx.doi.org/10.12779/dnd.2016.15.3.68 |
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author | Shim, Yong S. Yang, Dong Won Yoon, Bora Lee, Yunhwan Hong, Chang Hyung Seo, Sang Won Yoon, Soo Jin Jeong, Jee Hyang Park, Moon Ho Choi, Seong Hye Kim, Seong Yoon |
author_facet | Shim, Yong S. Yang, Dong Won Yoon, Bora Lee, Yunhwan Hong, Chang Hyung Seo, Sang Won Yoon, Soo Jin Jeong, Jee Hyang Park, Moon Ho Choi, Seong Hye Kim, Seong Yoon |
author_sort | Shim, Yong S. |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Patients with mild cognitive impairment (MCI) and their caregivers are concerned with the likelihood and time course of progression to dementia. This study was performed to identify the clinical predictors of the MCI progression in a Korean registry, and investigated the effects of medications without evidence, frequently prescribed in clinical practice. METHODS: Using a Korean cohort that included older adults with MCI who completed at least one follow-up visit, clinical characteristics and total medical expenses including prescribed medications were compared between two groups: progressed to dementia or not. Cox proportional hazards regression analysis was conducted. RESULTS: During the mean 1.42±0.72 years, 215 (27.63%) of 778 participants progressed to dementia. The best predictors were age [hazard ratio (HR), 1.036; 95% confidence interval (CI), 1.006–1.067; p=0.018], apolipoprotein ε4 allele (HR, 2.247; 95% CI, 1.512–3.337; p<0.001), Clinical Dementia Rating scale-sum of boxes scores (HR, 1.367; 95% CI, 1.143–1.636; p=0.001), Instrumental Activities of Daily Living scores (HR, 1.035; 95% CI, 1.003–1.067; p=0.029), and lower Mini-Mental State Examination scores (HR, 0.892; 95% CI, 0.839–0.949; p<0.001). Total medical expenses were not different. CONCLUSIONS: Our data are in accordance with previous reports about clinical predictors for the progression from MCI to dementia. Total medical expenses were not different between groups with and without progression. |
format | Online Article Text |
id | pubmed-6427964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Dementia Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-64279642019-03-22 Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort Shim, Yong S. Yang, Dong Won Yoon, Bora Lee, Yunhwan Hong, Chang Hyung Seo, Sang Won Yoon, Soo Jin Jeong, Jee Hyang Park, Moon Ho Choi, Seong Hye Kim, Seong Yoon Dement Neurocogn Disord Original Article BACKGROUND AND PURPOSE: Patients with mild cognitive impairment (MCI) and their caregivers are concerned with the likelihood and time course of progression to dementia. This study was performed to identify the clinical predictors of the MCI progression in a Korean registry, and investigated the effects of medications without evidence, frequently prescribed in clinical practice. METHODS: Using a Korean cohort that included older adults with MCI who completed at least one follow-up visit, clinical characteristics and total medical expenses including prescribed medications were compared between two groups: progressed to dementia or not. Cox proportional hazards regression analysis was conducted. RESULTS: During the mean 1.42±0.72 years, 215 (27.63%) of 778 participants progressed to dementia. The best predictors were age [hazard ratio (HR), 1.036; 95% confidence interval (CI), 1.006–1.067; p=0.018], apolipoprotein ε4 allele (HR, 2.247; 95% CI, 1.512–3.337; p<0.001), Clinical Dementia Rating scale-sum of boxes scores (HR, 1.367; 95% CI, 1.143–1.636; p=0.001), Instrumental Activities of Daily Living scores (HR, 1.035; 95% CI, 1.003–1.067; p=0.029), and lower Mini-Mental State Examination scores (HR, 0.892; 95% CI, 0.839–0.949; p<0.001). Total medical expenses were not different. CONCLUSIONS: Our data are in accordance with previous reports about clinical predictors for the progression from MCI to dementia. Total medical expenses were not different between groups with and without progression. Korean Dementia Association 2016-09 2016-10-18 /pmc/articles/PMC6427964/ /pubmed/30906345 http://dx.doi.org/10.12779/dnd.2016.15.3.68 Text en © 2016 Korean Dementia Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Shim, Yong S. Yang, Dong Won Yoon, Bora Lee, Yunhwan Hong, Chang Hyung Seo, Sang Won Yoon, Soo Jin Jeong, Jee Hyang Park, Moon Ho Choi, Seong Hye Kim, Seong Yoon Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort |
title | Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort |
title_full | Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort |
title_fullStr | Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort |
title_full_unstemmed | Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort |
title_short | Clinical Predictors for Mild Cognitive Impairment Progression in a Korean Cohort |
title_sort | clinical predictors for mild cognitive impairment progression in a korean cohort |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427964/ https://www.ncbi.nlm.nih.gov/pubmed/30906345 http://dx.doi.org/10.12779/dnd.2016.15.3.68 |
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