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Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS

OBJECTIVE: The present study was planned to examine the relationships between obstructive sleep apnea syndrome (OSAS) and the newly revealed adipokines adropin and adiponectin concentrations that display significant metabolic and cardiovascular functions and the levels of proinflammatory cytokine le...

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Autores principales: Celikhisar, Hakan, Ilkhan, Gulay Dasdemir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225856/
https://www.ncbi.nlm.nih.gov/pubmed/32454912
http://dx.doi.org/10.1155/2020/2571283
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author Celikhisar, Hakan
Ilkhan, Gulay Dasdemir
author_facet Celikhisar, Hakan
Ilkhan, Gulay Dasdemir
author_sort Celikhisar, Hakan
collection PubMed
description OBJECTIVE: The present study was planned to examine the relationships between obstructive sleep apnea syndrome (OSAS) and the newly revealed adipokines adropin and adiponectin concentrations that display significant metabolic and cardiovascular functions and the levels of proinflammatory cytokine levels. METHOD: A total of 166 overweight and obese male patients with a body mass index (BMI) >27 kg/m(2) were included in the study. Among study participants, 84 were recently diagnosed with OSAS by polysomnography with an apnea-hypopnea index (AHI) ≥5, and 82 were nonapneic with normal polysomnography (AHI<5) findings. The serum adropin and adiponectin levels of all cases were analyzed via the enzyme-linked immunosorbent assay method. Serum interleukin-1 (IL-1) beta and tumor necrotizing factor-alpha (TNF-alpha) levels were determined using Luminex cytokine multiplex analyses. RESULTS: The mean age of the OSAS patients was 50.9 ± 5.7 years and BMI was 32.4 ± 6.0 kg/m(2), and there was no statistically significant difference determined with the control group (49.3 ± 5.8 years and 30.6 ± 5, 6 kg/m(2)) (p > 0.05). There were no statistically significant differences between the OSAS and control groups concerning total cholesterol, triglyceride, low-density lipoprotein (LDL), high-density lipoprotein (HDL), and glucose levels. Adiponectin was lower in the OSAS group at a statistically significant level in comparison with the control group and was related at a statistically significant level to OSAS intensity. Adropin concentration was determined to be higher in the OSAS group at a statistically significant level in comparison with the control group. CONCLUSION: The results of our study suggest that increased adropin concentration may be an indicator of endothelium dysfunction in OSAS patients. Serum adropin and adiponectin levels may be new bioindicators used for diagnosis and risk assessment in OSAS patients.
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spelling pubmed-72258562020-05-23 Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS Celikhisar, Hakan Ilkhan, Gulay Dasdemir Can Respir J Research Article OBJECTIVE: The present study was planned to examine the relationships between obstructive sleep apnea syndrome (OSAS) and the newly revealed adipokines adropin and adiponectin concentrations that display significant metabolic and cardiovascular functions and the levels of proinflammatory cytokine levels. METHOD: A total of 166 overweight and obese male patients with a body mass index (BMI) >27 kg/m(2) were included in the study. Among study participants, 84 were recently diagnosed with OSAS by polysomnography with an apnea-hypopnea index (AHI) ≥5, and 82 were nonapneic with normal polysomnography (AHI<5) findings. The serum adropin and adiponectin levels of all cases were analyzed via the enzyme-linked immunosorbent assay method. Serum interleukin-1 (IL-1) beta and tumor necrotizing factor-alpha (TNF-alpha) levels were determined using Luminex cytokine multiplex analyses. RESULTS: The mean age of the OSAS patients was 50.9 ± 5.7 years and BMI was 32.4 ± 6.0 kg/m(2), and there was no statistically significant difference determined with the control group (49.3 ± 5.8 years and 30.6 ± 5, 6 kg/m(2)) (p > 0.05). There were no statistically significant differences between the OSAS and control groups concerning total cholesterol, triglyceride, low-density lipoprotein (LDL), high-density lipoprotein (HDL), and glucose levels. Adiponectin was lower in the OSAS group at a statistically significant level in comparison with the control group and was related at a statistically significant level to OSAS intensity. Adropin concentration was determined to be higher in the OSAS group at a statistically significant level in comparison with the control group. CONCLUSION: The results of our study suggest that increased adropin concentration may be an indicator of endothelium dysfunction in OSAS patients. Serum adropin and adiponectin levels may be new bioindicators used for diagnosis and risk assessment in OSAS patients. Hindawi 2020-05-04 /pmc/articles/PMC7225856/ /pubmed/32454912 http://dx.doi.org/10.1155/2020/2571283 Text en Copyright © 2020 Hakan Celikhisar and Gulay Dasdemir Ilkhan. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Celikhisar, Hakan
Ilkhan, Gulay Dasdemir
Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS
title Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS
title_full Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS
title_fullStr Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS
title_full_unstemmed Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS
title_short Alterations in Serum Adropin, Adiponectin, and Proinflammatory Cytokine Levels in OSAS
title_sort alterations in serum adropin, adiponectin, and proinflammatory cytokine levels in osas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225856/
https://www.ncbi.nlm.nih.gov/pubmed/32454912
http://dx.doi.org/10.1155/2020/2571283
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