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Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly

The association of hemodynamics with cognitive impairment and white matter lesions (WMLs) has come to the foreground in recent years. Six hundred eighty-nine elderly participants aged ≥60 years were eligible enrolled. After an average of 5.4 years follow-up, there was a significant decline in Mini-M...

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Autores principales: Zhang, Hua, Liu, Hongxia, Dong, Yuanli, Wang, Juan, Zhao, Yingxin, Cui, Yi, Chai, Qiang, Liu, Zhendong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834267/
https://www.ncbi.nlm.nih.gov/pubmed/29541422
http://dx.doi.org/10.18632/oncotarget.23191
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author Zhang, Hua
Liu, Hongxia
Dong, Yuanli
Wang, Juan
Zhao, Yingxin
Cui, Yi
Chai, Qiang
Liu, Zhendong
author_facet Zhang, Hua
Liu, Hongxia
Dong, Yuanli
Wang, Juan
Zhao, Yingxin
Cui, Yi
Chai, Qiang
Liu, Zhendong
author_sort Zhang, Hua
collection PubMed
description The association of hemodynamics with cognitive impairment and white matter lesions (WMLs) has come to the foreground in recent years. Six hundred eighty-nine elderly participants aged ≥60 years were eligible enrolled. After an average of 5.4 years follow-up, there was a significant decline in Mini-Mental State Examination (MMSE) scores and increases in total white matter hyperintensities (WMH), periventricular (P)WMH, and deep (D)WMH (P < 0.001). The participants were grouped by the tertiles of carotid mean wall shear stress (WSS). The decline in MMSE scores and the increases in total WMH, PWMH, and DWMH decreased from the lowest group to the highest group. There were significant differences between each group comparison (all P <0.05). Mean WSS was an independent and significant factor for the changes in MMSE scores, total WMH, PWMH, and DWMH after adjustment for confounders (P <0.001). The risk of developing cognitive impairment was higher in the lowest (hazard ratio: 2.753; 95% CI: 1.945 to 3.895; P < 0.001) and intermediate (hazard ratio: 1.531; 95% CI: 1.084 to 2.162; P = 0.015) groups than in the highest group after adjustment for confounders. Similar associations were yielded between peak WSS and the changes in MMSE scores, total WMH, PWMH, and DWMH. Our results indicated that carotid WSS is an independent factor for the progression of cognitive impairment and WMLs in the elderly. Low WSS significantly deteriorates the progression of cognitive impairment and WMLs.
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spelling pubmed-58342672018-03-14 Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly Zhang, Hua Liu, Hongxia Dong, Yuanli Wang, Juan Zhao, Yingxin Cui, Yi Chai, Qiang Liu, Zhendong Oncotarget Clinical Research Paper The association of hemodynamics with cognitive impairment and white matter lesions (WMLs) has come to the foreground in recent years. Six hundred eighty-nine elderly participants aged ≥60 years were eligible enrolled. After an average of 5.4 years follow-up, there was a significant decline in Mini-Mental State Examination (MMSE) scores and increases in total white matter hyperintensities (WMH), periventricular (P)WMH, and deep (D)WMH (P < 0.001). The participants were grouped by the tertiles of carotid mean wall shear stress (WSS). The decline in MMSE scores and the increases in total WMH, PWMH, and DWMH decreased from the lowest group to the highest group. There were significant differences between each group comparison (all P <0.05). Mean WSS was an independent and significant factor for the changes in MMSE scores, total WMH, PWMH, and DWMH after adjustment for confounders (P <0.001). The risk of developing cognitive impairment was higher in the lowest (hazard ratio: 2.753; 95% CI: 1.945 to 3.895; P < 0.001) and intermediate (hazard ratio: 1.531; 95% CI: 1.084 to 2.162; P = 0.015) groups than in the highest group after adjustment for confounders. Similar associations were yielded between peak WSS and the changes in MMSE scores, total WMH, PWMH, and DWMH. Our results indicated that carotid WSS is an independent factor for the progression of cognitive impairment and WMLs in the elderly. Low WSS significantly deteriorates the progression of cognitive impairment and WMLs. Impact Journals LLC 2017-12-12 /pmc/articles/PMC5834267/ /pubmed/29541422 http://dx.doi.org/10.18632/oncotarget.23191 Text en Copyright: © 2018 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Zhang, Hua
Liu, Hongxia
Dong, Yuanli
Wang, Juan
Zhao, Yingxin
Cui, Yi
Chai, Qiang
Liu, Zhendong
Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
title Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
title_full Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
title_fullStr Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
title_full_unstemmed Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
title_short Low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
title_sort low carotid wall shear stress independently accelerates the progression of cognitive impairment and white matter lesions in the elderly
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834267/
https://www.ncbi.nlm.nih.gov/pubmed/29541422
http://dx.doi.org/10.18632/oncotarget.23191
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