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Assessment of the relationship between endocan and obstructive sleep apnea severity

INTRODUCTION: Obstructive sleep apnea (OSA) and endothelial dysfunction are associated with cardiovascular risk factors and the development of atherosclerosis. Endocan is a marker of endothelial dysfunction, while obstructive sleep apnea is one of the causes of endothelial dysfunction. In this study...

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Autores principales: Pusuroglu, Hamdi, Somuncu, Umut, Bolat, Ismail, Akgul, Ozgur, Yıldırım, Hayriye Ak, Ozyilmaz, Sinem Ozbay, Ornek, Vesile, Surgit, Ozgur, Karakurt, Huseyin, Utkusavas, Ayfer, Alagic, Nermina, Yıldırım, Aydın
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667433/
https://www.ncbi.nlm.nih.gov/pubmed/33224333
http://dx.doi.org/10.5114/aoms.2020.97764
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author Pusuroglu, Hamdi
Somuncu, Umut
Bolat, Ismail
Akgul, Ozgur
Yıldırım, Hayriye Ak
Ozyilmaz, Sinem Ozbay
Ornek, Vesile
Surgit, Ozgur
Karakurt, Huseyin
Utkusavas, Ayfer
Alagic, Nermina
Yıldırım, Aydın
author_facet Pusuroglu, Hamdi
Somuncu, Umut
Bolat, Ismail
Akgul, Ozgur
Yıldırım, Hayriye Ak
Ozyilmaz, Sinem Ozbay
Ornek, Vesile
Surgit, Ozgur
Karakurt, Huseyin
Utkusavas, Ayfer
Alagic, Nermina
Yıldırım, Aydın
author_sort Pusuroglu, Hamdi
collection PubMed
description INTRODUCTION: Obstructive sleep apnea (OSA) and endothelial dysfunction are associated with cardiovascular risk factors and the development of atherosclerosis. Endocan is a marker of endothelial dysfunction, while obstructive sleep apnea is one of the causes of endothelial dysfunction. In this study, we investigated the relationship between endocan and obstructive sleep apnea severity. MATERIAL AND METHODS: A total of 179 patients with snoring complaints were included. All patients underwent polysomnography, and based on the results, the participations were allocated to the control group (n = 39) or to the obstructive sleep apnea group (n = 140). The OSA group was classified as having mild (apnea-hypopnea index (AHI) = 5–15; n = 43), moderate (AHI = 15–30; n = 42), or severe OSA (AHI > 30; n = 55). All participations had their endocan levels measured. RESULTS: Endocan levels in OSA patients were significantly higher than in the control group (11.8 (3.13–200) vs 3.13 (3.13–23) ng/ml, p < 0.001). Also, endocan levels were significantly higher in the severe OSA group than moderate and mild obstructive OSA (13.2 (3.13–200), 12.6 (3.13–200) and 8.44 (3.13–50.5) ng/ml, p = 0.015, respectively). Multiple logistic regression analysis showed that smoking, age and endocan levels were independent predictors of OSA severity (p = 0.024, p = 0.037, p = 0.004, respectively). CONCLUSIONS: Endocan seems to be a potential risk stratification marker in this patient population.
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spelling pubmed-76674332020-11-20 Assessment of the relationship between endocan and obstructive sleep apnea severity Pusuroglu, Hamdi Somuncu, Umut Bolat, Ismail Akgul, Ozgur Yıldırım, Hayriye Ak Ozyilmaz, Sinem Ozbay Ornek, Vesile Surgit, Ozgur Karakurt, Huseyin Utkusavas, Ayfer Alagic, Nermina Yıldırım, Aydın Arch Med Sci Clinical Research INTRODUCTION: Obstructive sleep apnea (OSA) and endothelial dysfunction are associated with cardiovascular risk factors and the development of atherosclerosis. Endocan is a marker of endothelial dysfunction, while obstructive sleep apnea is one of the causes of endothelial dysfunction. In this study, we investigated the relationship between endocan and obstructive sleep apnea severity. MATERIAL AND METHODS: A total of 179 patients with snoring complaints were included. All patients underwent polysomnography, and based on the results, the participations were allocated to the control group (n = 39) or to the obstructive sleep apnea group (n = 140). The OSA group was classified as having mild (apnea-hypopnea index (AHI) = 5–15; n = 43), moderate (AHI = 15–30; n = 42), or severe OSA (AHI > 30; n = 55). All participations had their endocan levels measured. RESULTS: Endocan levels in OSA patients were significantly higher than in the control group (11.8 (3.13–200) vs 3.13 (3.13–23) ng/ml, p < 0.001). Also, endocan levels were significantly higher in the severe OSA group than moderate and mild obstructive OSA (13.2 (3.13–200), 12.6 (3.13–200) and 8.44 (3.13–50.5) ng/ml, p = 0.015, respectively). Multiple logistic regression analysis showed that smoking, age and endocan levels were independent predictors of OSA severity (p = 0.024, p = 0.037, p = 0.004, respectively). CONCLUSIONS: Endocan seems to be a potential risk stratification marker in this patient population. Termedia Publishing House 2020-08-03 /pmc/articles/PMC7667433/ /pubmed/33224333 http://dx.doi.org/10.5114/aoms.2020.97764 Text en Copyright: © 2020 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
Pusuroglu, Hamdi
Somuncu, Umut
Bolat, Ismail
Akgul, Ozgur
Yıldırım, Hayriye Ak
Ozyilmaz, Sinem Ozbay
Ornek, Vesile
Surgit, Ozgur
Karakurt, Huseyin
Utkusavas, Ayfer
Alagic, Nermina
Yıldırım, Aydın
Assessment of the relationship between endocan and obstructive sleep apnea severity
title Assessment of the relationship between endocan and obstructive sleep apnea severity
title_full Assessment of the relationship between endocan and obstructive sleep apnea severity
title_fullStr Assessment of the relationship between endocan and obstructive sleep apnea severity
title_full_unstemmed Assessment of the relationship between endocan and obstructive sleep apnea severity
title_short Assessment of the relationship between endocan and obstructive sleep apnea severity
title_sort assessment of the relationship between endocan and obstructive sleep apnea severity
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667433/
https://www.ncbi.nlm.nih.gov/pubmed/33224333
http://dx.doi.org/10.5114/aoms.2020.97764
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