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Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia

INTRODUCTION: Dyslipidemia combined with hypertension increases the risk of cardiovascular disease (CVD). The current study aimed to investigate the association of dipping and non-dipping hypertension with CVD in patients with dyslipidemia. MATERIAL AND METHODS: A total of 243 documented dyslipidemi...

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Autores principales: Dai, Siping, Huang, Bo, Zou, Yunliang, Liu, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425204/
https://www.ncbi.nlm.nih.gov/pubmed/30899285
http://dx.doi.org/10.5114/aoms.2018.72609
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author Dai, Siping
Huang, Bo
Zou, Yunliang
Liu, Yan
author_facet Dai, Siping
Huang, Bo
Zou, Yunliang
Liu, Yan
author_sort Dai, Siping
collection PubMed
description INTRODUCTION: Dyslipidemia combined with hypertension increases the risk of cardiovascular disease (CVD). The current study aimed to investigate the association of dipping and non-dipping hypertension with CVD in patients with dyslipidemia. MATERIAL AND METHODS: A total of 243 documented dyslipidemia patients with hypertension were enrolled. Clinical characteristics and clinic and 24-hour blood pressure (BP) parameters were compared between dipping and non-dipping groups based on 24-hour ambulatory blood pressure monitoring. Logistic regression analysis was performed to evaluate the association of dipping and non-dipping hypertension with CVD. RESULTS: Compared to the dipping group, patients in the non-dipping group were older, more likely to be male and smokers, had higher serum creatinine levels, and were more likely to have chronic kidney disease and CVD (p < 0.05 for all comparisons). No significant between-group differences in clinic systolic and diastolic BP (SBP and DBP) were observed. However, compared to the dipping group, 24-hour SBP, nighttime SBP and DBP, and night-day ratio of SBP and DBP were all significantly higher in the non-dipping group (p < 0.05 for all comparisons). In the dipping group, only night-day ratio of SBP was significantly associated with CVD, with an odds ratio (OR) of 1.09 (95% confidence interval (CI) of 1.02–1.34). In the non-dipping group, both night-day ratio of SBP and DBP were significantly associated with CVD, with an OR of 1.72 (95% CI: 1.33–2.06) and 1.23 (95% CI: 1.05–1.66), respectively. CONCLUSIONS: In patients with dyslipidemia, non-dipping hypertension is more closely related to CVD compared to dipping hypertension.
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spelling pubmed-64252042019-03-21 Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia Dai, Siping Huang, Bo Zou, Yunliang Liu, Yan Arch Med Sci Clinical Research INTRODUCTION: Dyslipidemia combined with hypertension increases the risk of cardiovascular disease (CVD). The current study aimed to investigate the association of dipping and non-dipping hypertension with CVD in patients with dyslipidemia. MATERIAL AND METHODS: A total of 243 documented dyslipidemia patients with hypertension were enrolled. Clinical characteristics and clinic and 24-hour blood pressure (BP) parameters were compared between dipping and non-dipping groups based on 24-hour ambulatory blood pressure monitoring. Logistic regression analysis was performed to evaluate the association of dipping and non-dipping hypertension with CVD. RESULTS: Compared to the dipping group, patients in the non-dipping group were older, more likely to be male and smokers, had higher serum creatinine levels, and were more likely to have chronic kidney disease and CVD (p < 0.05 for all comparisons). No significant between-group differences in clinic systolic and diastolic BP (SBP and DBP) were observed. However, compared to the dipping group, 24-hour SBP, nighttime SBP and DBP, and night-day ratio of SBP and DBP were all significantly higher in the non-dipping group (p < 0.05 for all comparisons). In the dipping group, only night-day ratio of SBP was significantly associated with CVD, with an odds ratio (OR) of 1.09 (95% confidence interval (CI) of 1.02–1.34). In the non-dipping group, both night-day ratio of SBP and DBP were significantly associated with CVD, with an OR of 1.72 (95% CI: 1.33–2.06) and 1.23 (95% CI: 1.05–1.66), respectively. CONCLUSIONS: In patients with dyslipidemia, non-dipping hypertension is more closely related to CVD compared to dipping hypertension. Termedia Publishing House 2018-01-05 2019-03 /pmc/articles/PMC6425204/ /pubmed/30899285 http://dx.doi.org/10.5114/aoms.2018.72609 Text en Copyright: © 2018 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Dai, Siping
Huang, Bo
Zou, Yunliang
Liu, Yan
Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
title Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
title_full Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
title_fullStr Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
title_full_unstemmed Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
title_short Associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
title_sort associations of dipping and non-dipping hypertension with cardiovascular diseases in patients with dyslipidemia
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425204/
https://www.ncbi.nlm.nih.gov/pubmed/30899285
http://dx.doi.org/10.5114/aoms.2018.72609
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