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Correlation study of Framingham risk score and vascular dementia: An observational study

Vascular dementia (VaD) is one of the most common forms of dementia, and second only to Alzheimer's disease. The purpose of this study was to evaluate the potential diagnostic value of Framingham risk score (FRS) in VaD by investigating the relationship among cardiovascular risks, FRS, and VaD....

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Autores principales: Li, Shan-Shan, Zheng, Jie, Mei, Bin, Wang, Han-Yao, Zheng, Miao, Zheng, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815664/
https://www.ncbi.nlm.nih.gov/pubmed/29390252
http://dx.doi.org/10.1097/MD.0000000000008387
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author Li, Shan-Shan
Zheng, Jie
Mei, Bin
Wang, Han-Yao
Zheng, Miao
Zheng, Kai
author_facet Li, Shan-Shan
Zheng, Jie
Mei, Bin
Wang, Han-Yao
Zheng, Miao
Zheng, Kai
author_sort Li, Shan-Shan
collection PubMed
description Vascular dementia (VaD) is one of the most common forms of dementia, and second only to Alzheimer's disease. The purpose of this study was to evaluate the potential diagnostic value of Framingham risk score (FRS) in VaD by investigating the relationship among cardiovascular risks, FRS, and VaD. Data were collected from patients (n = 130) at Tongji Hospital in Wuhan, China. They were divided into 2 groups, including the control group (n = 70) and the VaD group (n = 60). Statistical methods including t-test, logistic regression model, multiple linear regression model, and receiver-operating characteristic (ROC) curve were adopted for the assessment. A significant difference (all P < .05) was observed in systolic blood pressure (SBP), diastolic blood pressure (DBP), pulse pressure, total cholesterol (TC), homosysteine (HCY), glycosylated hemoglobin A1c (HbA1c), FRS, and cerebral white matter lesions (WMLs) between the 2 groups, even after adjusting for age (both P < .05). Age [odds ratio (OR) = 1.20; P = .002], FRS (OR = 1.55; P = .006), and WMLs (OR = 10.17; P = .011) were independent prognostic factors for VaD. The area under the ROC curve (AUC) of FRS for VaD diagnosis prediction was 0.830 (95% confidence interval, 95% CI: 0.730∼ 0.929). There was a significant difference in the AUC between WMLs and WMLs combined with FRS (0.788 (95% CI: 0.667 ∼ 0.880) versus 0.863 (95% CI: 0.754 ∼ 0.936, P = .049). Age, HbA1c, and FRS were negatively correlated with the mini-mental state examination (MMSE) scores (all P < .05) in the VaD group. Moreover, multiple stepwise linear regression analysis showed that the age and FRS were independent predictors of MMSE scores. FRS has a moderate predictive value for the VaD diagnosis, and also increases the risk of cognitive decline.
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spelling pubmed-58156642018-02-28 Correlation study of Framingham risk score and vascular dementia: An observational study Li, Shan-Shan Zheng, Jie Mei, Bin Wang, Han-Yao Zheng, Miao Zheng, Kai Medicine (Baltimore) 5300 Vascular dementia (VaD) is one of the most common forms of dementia, and second only to Alzheimer's disease. The purpose of this study was to evaluate the potential diagnostic value of Framingham risk score (FRS) in VaD by investigating the relationship among cardiovascular risks, FRS, and VaD. Data were collected from patients (n = 130) at Tongji Hospital in Wuhan, China. They were divided into 2 groups, including the control group (n = 70) and the VaD group (n = 60). Statistical methods including t-test, logistic regression model, multiple linear regression model, and receiver-operating characteristic (ROC) curve were adopted for the assessment. A significant difference (all P < .05) was observed in systolic blood pressure (SBP), diastolic blood pressure (DBP), pulse pressure, total cholesterol (TC), homosysteine (HCY), glycosylated hemoglobin A1c (HbA1c), FRS, and cerebral white matter lesions (WMLs) between the 2 groups, even after adjusting for age (both P < .05). Age [odds ratio (OR) = 1.20; P = .002], FRS (OR = 1.55; P = .006), and WMLs (OR = 10.17; P = .011) were independent prognostic factors for VaD. The area under the ROC curve (AUC) of FRS for VaD diagnosis prediction was 0.830 (95% confidence interval, 95% CI: 0.730∼ 0.929). There was a significant difference in the AUC between WMLs and WMLs combined with FRS (0.788 (95% CI: 0.667 ∼ 0.880) versus 0.863 (95% CI: 0.754 ∼ 0.936, P = .049). Age, HbA1c, and FRS were negatively correlated with the mini-mental state examination (MMSE) scores (all P < .05) in the VaD group. Moreover, multiple stepwise linear regression analysis showed that the age and FRS were independent predictors of MMSE scores. FRS has a moderate predictive value for the VaD diagnosis, and also increases the risk of cognitive decline. Wolters Kluwer Health 2017-12-15 /pmc/articles/PMC5815664/ /pubmed/29390252 http://dx.doi.org/10.1097/MD.0000000000008387 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 5300
Li, Shan-Shan
Zheng, Jie
Mei, Bin
Wang, Han-Yao
Zheng, Miao
Zheng, Kai
Correlation study of Framingham risk score and vascular dementia: An observational study
title Correlation study of Framingham risk score and vascular dementia: An observational study
title_full Correlation study of Framingham risk score and vascular dementia: An observational study
title_fullStr Correlation study of Framingham risk score and vascular dementia: An observational study
title_full_unstemmed Correlation study of Framingham risk score and vascular dementia: An observational study
title_short Correlation study of Framingham risk score and vascular dementia: An observational study
title_sort correlation study of framingham risk score and vascular dementia: an observational study
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815664/
https://www.ncbi.nlm.nih.gov/pubmed/29390252
http://dx.doi.org/10.1097/MD.0000000000008387
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