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Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia

Amnestic mild cognitive impairment (MCI) is a prodromal stage of dementia, with a higher incidence of these patients progressing to Alzheimer’s disease (AD) than normal aging people. A biomarker for the early detection and prediction for this progression is important. We recruited MCI subjects in th...

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Autores principales: Tien, Yi-Ting, Lee, Wei-Ju, Liao, Yi-Chu, Wang, Wen-Fu, Jhang, Kai-Ming, Wang, Shuu-Jiun, Fuh, Jong-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904474/
https://www.ncbi.nlm.nih.gov/pubmed/31822765
http://dx.doi.org/10.1038/s41598-019-55318-0
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author Tien, Yi-Ting
Lee, Wei-Ju
Liao, Yi-Chu
Wang, Wen-Fu
Jhang, Kai-Ming
Wang, Shuu-Jiun
Fuh, Jong-Ling
author_facet Tien, Yi-Ting
Lee, Wei-Ju
Liao, Yi-Chu
Wang, Wen-Fu
Jhang, Kai-Ming
Wang, Shuu-Jiun
Fuh, Jong-Ling
author_sort Tien, Yi-Ting
collection PubMed
description Amnestic mild cognitive impairment (MCI) is a prodromal stage of dementia, with a higher incidence of these patients progressing to Alzheimer’s disease (AD) than normal aging people. A biomarker for the early detection and prediction for this progression is important. We recruited MCI subjects in three teaching hospitals and conducted longitudinal follow-up for 5 years at one-year intervals. Cognitively healthy controls were recruited for comparisom at baseline. Plasma transthyretin (TTR) levels were measured by ELISA. Survival analysis with time to AD conversion as an outcome variable was calculated with the multivariable Cox proportional hazards models using TTR as a continuous variable with adjustment for other covariates and bootstrapping resampling analysis. In total, 184 MCI subjects and 40 sex- and age-matched controls were recruited at baseline. At baseline, MCI patients had higher TTR levels compared with the control group. During the longitudinal follow-ups, 135 MCI patients (73.4%) completed follow-up at least once. The TTR level was an independent predictor for MCI conversion to AD when using TTR as a continuous variable (p = 0.023, 95% CI 1.001–1.007). In addition, in MCI converters, the TTR level at the point when they converted to AD was significantly lower than that at baseline (328.6 ± 66.5 vs. 381.9 ± 77.6 ug/ml, p < 0.001). Our study demonstrates the temporal relationship between the plasma TTR level and the conversion from MCI to AD.
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spelling pubmed-69044742019-12-13 Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia Tien, Yi-Ting Lee, Wei-Ju Liao, Yi-Chu Wang, Wen-Fu Jhang, Kai-Ming Wang, Shuu-Jiun Fuh, Jong-Ling Sci Rep Article Amnestic mild cognitive impairment (MCI) is a prodromal stage of dementia, with a higher incidence of these patients progressing to Alzheimer’s disease (AD) than normal aging people. A biomarker for the early detection and prediction for this progression is important. We recruited MCI subjects in three teaching hospitals and conducted longitudinal follow-up for 5 years at one-year intervals. Cognitively healthy controls were recruited for comparisom at baseline. Plasma transthyretin (TTR) levels were measured by ELISA. Survival analysis with time to AD conversion as an outcome variable was calculated with the multivariable Cox proportional hazards models using TTR as a continuous variable with adjustment for other covariates and bootstrapping resampling analysis. In total, 184 MCI subjects and 40 sex- and age-matched controls were recruited at baseline. At baseline, MCI patients had higher TTR levels compared with the control group. During the longitudinal follow-ups, 135 MCI patients (73.4%) completed follow-up at least once. The TTR level was an independent predictor for MCI conversion to AD when using TTR as a continuous variable (p = 0.023, 95% CI 1.001–1.007). In addition, in MCI converters, the TTR level at the point when they converted to AD was significantly lower than that at baseline (328.6 ± 66.5 vs. 381.9 ± 77.6 ug/ml, p < 0.001). Our study demonstrates the temporal relationship between the plasma TTR level and the conversion from MCI to AD. Nature Publishing Group UK 2019-12-10 /pmc/articles/PMC6904474/ /pubmed/31822765 http://dx.doi.org/10.1038/s41598-019-55318-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tien, Yi-Ting
Lee, Wei-Ju
Liao, Yi-Chu
Wang, Wen-Fu
Jhang, Kai-Ming
Wang, Shuu-Jiun
Fuh, Jong-Ling
Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia
title Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia
title_full Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia
title_fullStr Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia
title_full_unstemmed Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia
title_short Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia
title_sort plasma transthyretin as a predictor of amnestic mild cognitive impairment conversion to dementia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904474/
https://www.ncbi.nlm.nih.gov/pubmed/31822765
http://dx.doi.org/10.1038/s41598-019-55318-0
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