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Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns

BACKGROUND: Chemerin is a novel adipokine that plays a role in inflammation and atherosclerosis. Although there are several correlations between hypertension and the inflammatory system, there is still insufficient information about the relationship between blood pressure variability and inflammator...

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Autores principales: Meric, Murat, Soylu, Korhan, Avci, Bahattin, Yuksel, Serkan, Gulel, Okan, Yenercag, Mustafa, Coksevim, Metin, Uzun, Adem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010600/
https://www.ncbi.nlm.nih.gov/pubmed/24769499
http://dx.doi.org/10.12659/MSM.890784
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author Meric, Murat
Soylu, Korhan
Avci, Bahattin
Yuksel, Serkan
Gulel, Okan
Yenercag, Mustafa
Coksevim, Metin
Uzun, Adem
author_facet Meric, Murat
Soylu, Korhan
Avci, Bahattin
Yuksel, Serkan
Gulel, Okan
Yenercag, Mustafa
Coksevim, Metin
Uzun, Adem
author_sort Meric, Murat
collection PubMed
description BACKGROUND: Chemerin is a novel adipokine that plays a role in inflammation and atherosclerosis. Although there are several correlations between hypertension and the inflammatory system, there is still insufficient information about the relationship between blood pressure variability and inflammatory markers. In this study, we aimed to determine whether chemerin levels are elevated in non-dipper patients compared with dippers and healthy controls. MATERIAL/METHODS: This study was composed of a group of 90 patients: 60 hypertensive patients and 30 healthy control subjects (12 males, mean age 53.2±15.4 years). Ambulatory blood pressure monitoring devices (ABPM) were connected to all patients. Using data from the ABPM, hypertensive patients were divided into 2 groups: 30 dipper patients (12 males, mean age 52.5±15.1 years) and 30 non-dipper patients (11 males, mean age 54.6±13.0 years). Complete blood count and biochemistry were measured by standard methods and plasma chemerin concentrations were quantified by ELISA. RESULTS: Non-dipper patients demonstrated higher chemerin levels compared to dippers and normotensives (219.7±16.3 vs. 182.4±21.4 ng/ml; 219.7±16.3 vs. 85.4±38.1 ng/ml, respectively, p<0.001 for both comparisons). A receiver operating characteristic curve analysis revealed that the optimal cut-off value for chemerin to predict a non-dipping pattern was 201.4, with 90% sensitivity and 90% specificity. There was a positive correlation between chemerin levels and all ambulatory blood pressure values in all hypertensive patients. CONCLUSIONS: Chemerin, which plays a role in inflammation and atherosclerosis, was higher in non-dippers compared to dippers and normotensives. Additionally, chemerin shows positive correlations with blood pressure.
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spelling pubmed-40106002014-05-06 Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns Meric, Murat Soylu, Korhan Avci, Bahattin Yuksel, Serkan Gulel, Okan Yenercag, Mustafa Coksevim, Metin Uzun, Adem Med Sci Monit Clinical Research BACKGROUND: Chemerin is a novel adipokine that plays a role in inflammation and atherosclerosis. Although there are several correlations between hypertension and the inflammatory system, there is still insufficient information about the relationship between blood pressure variability and inflammatory markers. In this study, we aimed to determine whether chemerin levels are elevated in non-dipper patients compared with dippers and healthy controls. MATERIAL/METHODS: This study was composed of a group of 90 patients: 60 hypertensive patients and 30 healthy control subjects (12 males, mean age 53.2±15.4 years). Ambulatory blood pressure monitoring devices (ABPM) were connected to all patients. Using data from the ABPM, hypertensive patients were divided into 2 groups: 30 dipper patients (12 males, mean age 52.5±15.1 years) and 30 non-dipper patients (11 males, mean age 54.6±13.0 years). Complete blood count and biochemistry were measured by standard methods and plasma chemerin concentrations were quantified by ELISA. RESULTS: Non-dipper patients demonstrated higher chemerin levels compared to dippers and normotensives (219.7±16.3 vs. 182.4±21.4 ng/ml; 219.7±16.3 vs. 85.4±38.1 ng/ml, respectively, p<0.001 for both comparisons). A receiver operating characteristic curve analysis revealed that the optimal cut-off value for chemerin to predict a non-dipping pattern was 201.4, with 90% sensitivity and 90% specificity. There was a positive correlation between chemerin levels and all ambulatory blood pressure values in all hypertensive patients. CONCLUSIONS: Chemerin, which plays a role in inflammation and atherosclerosis, was higher in non-dippers compared to dippers and normotensives. Additionally, chemerin shows positive correlations with blood pressure. International Scientific Literature, Inc. 2014-04-28 /pmc/articles/PMC4010600/ /pubmed/24769499 http://dx.doi.org/10.12659/MSM.890784 Text en © Med Sci Monit, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Clinical Research
Meric, Murat
Soylu, Korhan
Avci, Bahattin
Yuksel, Serkan
Gulel, Okan
Yenercag, Mustafa
Coksevim, Metin
Uzun, Adem
Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
title Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
title_full Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
title_fullStr Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
title_full_unstemmed Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
title_short Evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
title_sort evaluation of plasma chemerin levels in patients with non-dipper blood pressure patterns
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010600/
https://www.ncbi.nlm.nih.gov/pubmed/24769499
http://dx.doi.org/10.12659/MSM.890784
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