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Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy

OBJECTIVES: Human immunodeficiency virus (HIV) and antiretroviral therapy (ART) are associated with renal disease and increased cardiovascular risk. The relationship between HIV and ambulatory blood pressure (ABP) non-dipping status, a risk factor for cardiovascular events and target-organ damage, h...

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Autores principales: Borkum, Megan, Alfred, Athlet, Wearne, Nicola, Rayner, Brian, Dave, Joel A, Levitt, Naomi S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Clinics Cardive Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170173/
https://www.ncbi.nlm.nih.gov/pubmed/25192297
http://dx.doi.org/10.5830/CVJA-2014-029
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author Borkum, Megan
Alfred, Athlet
Wearne, Nicola
Rayner, Brian
Dave, Joel A
Levitt, Naomi S
author_facet Borkum, Megan
Alfred, Athlet
Wearne, Nicola
Rayner, Brian
Dave, Joel A
Levitt, Naomi S
author_sort Borkum, Megan
collection PubMed
description OBJECTIVES: Human immunodeficiency virus (HIV) and antiretroviral therapy (ART) are associated with renal disease and increased cardiovascular risk. The relationship between HIV and ambulatory blood pressure (ABP) non-dipping status, a risk factor for cardiovascular events and target-organ damage, has never been assessed in South Africa. Study objectives were to establish the prevalence of chronic kidney disease, and assess the ABP profile in asymptomatic HIV-positive clinic out-patients. METHODS: This was a prospective cohort study. Office blood pressure (BP), urinary microalbumin–creatinine ratio, urine dipsticks, serum creatinine and estimated glomerular filtration rate (eGFR) were measured at baseline and six months after ART initiation. A subset of HIV-positive subjects and an HIV-negative control group underwent 24-hour ABP monitoring. RESULTS: No patient had an eGFR < 60 ml/min, three patients (4.7%) had microalbuminuria and one had macroalbuminuria. Mean office systolic BP was 111 ± 14 mmHg at baseline and increased by 5 mmHg to 116 ± 14 mmHg (p = 0.05) at six months. This increase was not confirmed by ABP monitoring. In the HIV-positive and -negative patients, the prevalences of non-dipping were 80 and 52.9%, respectively (p = 0.05, odds ratio = 3.56, 95% CI: 0.96–13.13). No relationship between dipping status and ART usage was found. CONCLUSION: The prevalence of chronic kidney disease (CKD) was lower than anticipated. HIV infection was associated with an ambulatory non-dipping status, which suggests an underlying dysregulation of the cardiovascular system. In the short term, ART does not seem to improve loss of circadian rhythm.
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spelling pubmed-41701732015-04-10 Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy Borkum, Megan Alfred, Athlet Wearne, Nicola Rayner, Brian Dave, Joel A Levitt, Naomi S Cardiovasc J Afr Cardiovascular Topics OBJECTIVES: Human immunodeficiency virus (HIV) and antiretroviral therapy (ART) are associated with renal disease and increased cardiovascular risk. The relationship between HIV and ambulatory blood pressure (ABP) non-dipping status, a risk factor for cardiovascular events and target-organ damage, has never been assessed in South Africa. Study objectives were to establish the prevalence of chronic kidney disease, and assess the ABP profile in asymptomatic HIV-positive clinic out-patients. METHODS: This was a prospective cohort study. Office blood pressure (BP), urinary microalbumin–creatinine ratio, urine dipsticks, serum creatinine and estimated glomerular filtration rate (eGFR) were measured at baseline and six months after ART initiation. A subset of HIV-positive subjects and an HIV-negative control group underwent 24-hour ABP monitoring. RESULTS: No patient had an eGFR < 60 ml/min, three patients (4.7%) had microalbuminuria and one had macroalbuminuria. Mean office systolic BP was 111 ± 14 mmHg at baseline and increased by 5 mmHg to 116 ± 14 mmHg (p = 0.05) at six months. This increase was not confirmed by ABP monitoring. In the HIV-positive and -negative patients, the prevalences of non-dipping were 80 and 52.9%, respectively (p = 0.05, odds ratio = 3.56, 95% CI: 0.96–13.13). No relationship between dipping status and ART usage was found. CONCLUSION: The prevalence of chronic kidney disease (CKD) was lower than anticipated. HIV infection was associated with an ambulatory non-dipping status, which suggests an underlying dysregulation of the cardiovascular system. In the short term, ART does not seem to improve loss of circadian rhythm. Clinics Cardive Publishing 2014 /pmc/articles/PMC4170173/ /pubmed/25192297 http://dx.doi.org/10.5830/CVJA-2014-029 Text en Copyright © 2010 Clinics Cardive Publishing http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cardiovascular Topics
Borkum, Megan
Alfred, Athlet
Wearne, Nicola
Rayner, Brian
Dave, Joel A
Levitt, Naomi S
Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy
title Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy
title_full Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy
title_fullStr Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy
title_full_unstemmed Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy
title_short Ambulatory blood pressure profiles in a subset of HIV-positive patients pre and post antiretroviral therapy
title_sort ambulatory blood pressure profiles in a subset of hiv-positive patients pre and post antiretroviral therapy
topic Cardiovascular Topics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170173/
https://www.ncbi.nlm.nih.gov/pubmed/25192297
http://dx.doi.org/10.5830/CVJA-2014-029
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