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Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease

Both morning hypertension (MH) and nocturnal hypertension (NH) are associated with severe target organ damage in patients with chronic kidney disease (CKD). However, the isolated or combined effects of MH and NH on target organ damage are less well‐defined. A cross‐sectional study was conducted amon...

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Autores principales: Li, Xue, Ke, Jianting, Chen, Xiaoqiu, Yin, Mengmeng, Lou, Tanqi, Zhang, Jun, Peng, Hui, Wang, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8678691/
https://www.ncbi.nlm.nih.gov/pubmed/33682307
http://dx.doi.org/10.1111/jch.14234
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author Li, Xue
Ke, Jianting
Chen, Xiaoqiu
Yin, Mengmeng
Lou, Tanqi
Zhang, Jun
Peng, Hui
Wang, Cheng
author_facet Li, Xue
Ke, Jianting
Chen, Xiaoqiu
Yin, Mengmeng
Lou, Tanqi
Zhang, Jun
Peng, Hui
Wang, Cheng
author_sort Li, Xue
collection PubMed
description Both morning hypertension (MH) and nocturnal hypertension (NH) are associated with severe target organ damage in patients with chronic kidney disease (CKD). However, the isolated or combined effects of MH and NH on target organ damage are less well‐defined. A cross‐sectional study was conducted among 2386 non‐dialysis CKD patients with ambulatory blood pressure monitoring. The authors categorized patients into four groups based on the presence or absence of MH and NH. Multivariate logistic analyses were used to evaluate the correlation between hypertension subtypes and target organ damage, including left ventricular hypertrophy (LVH), abnormal carotid intima‐media thickness (CIMT), low estimated glomerular filtration rate (eGFR), and albuminuria. The percentages of isolated MH, isolated NH, and combined MH and NH were 2.3%, 24.0%, and 49.3%, respectively. Compared to patients without MH and NH, isolated MH was only related to low eGFR (2.26 [95% confidence interval: 1.00–5.09]) and albuminuria (2.17 [95% CI: 1.03–4.54]). Meanwhile, combined MH and NH group compared to the group without MH and NH had a higher risk of LVH (2.87 [95% CI: 2.01–4.09]), abnormal CIMT (2.01 [95% CI: 1.47–2.75]), low eGFR (3.18 [95% CI: 2.23–4.54]), and albuminuria (1.79 [95% CI: 1.33–2.40]), even in patients without daytime hypertension. The risk of cardiovascular and renal damage was also observed in the isolated NH group. In conclusion, morning hypertension is associated with kidney dysfunction and has combined effects with nocturnal hypertension on cardiovascular damage in chronic kidney disease patients.
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spelling pubmed-86786912021-12-23 Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease Li, Xue Ke, Jianting Chen, Xiaoqiu Yin, Mengmeng Lou, Tanqi Zhang, Jun Peng, Hui Wang, Cheng J Clin Hypertens (Greenwich) Ambulatory Blood Pressure Both morning hypertension (MH) and nocturnal hypertension (NH) are associated with severe target organ damage in patients with chronic kidney disease (CKD). However, the isolated or combined effects of MH and NH on target organ damage are less well‐defined. A cross‐sectional study was conducted among 2386 non‐dialysis CKD patients with ambulatory blood pressure monitoring. The authors categorized patients into four groups based on the presence or absence of MH and NH. Multivariate logistic analyses were used to evaluate the correlation between hypertension subtypes and target organ damage, including left ventricular hypertrophy (LVH), abnormal carotid intima‐media thickness (CIMT), low estimated glomerular filtration rate (eGFR), and albuminuria. The percentages of isolated MH, isolated NH, and combined MH and NH were 2.3%, 24.0%, and 49.3%, respectively. Compared to patients without MH and NH, isolated MH was only related to low eGFR (2.26 [95% confidence interval: 1.00–5.09]) and albuminuria (2.17 [95% CI: 1.03–4.54]). Meanwhile, combined MH and NH group compared to the group without MH and NH had a higher risk of LVH (2.87 [95% CI: 2.01–4.09]), abnormal CIMT (2.01 [95% CI: 1.47–2.75]), low eGFR (3.18 [95% CI: 2.23–4.54]), and albuminuria (1.79 [95% CI: 1.33–2.40]), even in patients without daytime hypertension. The risk of cardiovascular and renal damage was also observed in the isolated NH group. In conclusion, morning hypertension is associated with kidney dysfunction and has combined effects with nocturnal hypertension on cardiovascular damage in chronic kidney disease patients. John Wiley and Sons Inc. 2021-03-07 /pmc/articles/PMC8678691/ /pubmed/33682307 http://dx.doi.org/10.1111/jch.14234 Text en © 2021 The Authors. The Journal of Clinical Hypertension published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Ambulatory Blood Pressure
Li, Xue
Ke, Jianting
Chen, Xiaoqiu
Yin, Mengmeng
Lou, Tanqi
Zhang, Jun
Peng, Hui
Wang, Cheng
Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
title Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
title_full Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
title_fullStr Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
title_full_unstemmed Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
title_short Different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
title_sort different effects of morning and nocturnal hypertension on target organ damage in chronic kidney disease
topic Ambulatory Blood Pressure
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8678691/
https://www.ncbi.nlm.nih.gov/pubmed/33682307
http://dx.doi.org/10.1111/jch.14234
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