Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities

Systemic inflammation is important in obstructive sleep apnea (OSA) pathophysiology and its comorbidity. We aimed to assess the levels of inflammatory biomarkers in a large sample of OSA patients and to investigate any correlation between these biomarkers with clinical and polysomnographic (PSG) par...

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Main Authors: Izolde Bouloukaki, Charalampos Mermigkis, Nikolaos Tzanakis, Eleftherios Kallergis, Violeta Moniaki, Eleni Mauroudi, Sophia E. Schiza
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2017/4573756
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author Izolde Bouloukaki
Charalampos Mermigkis
Nikolaos Tzanakis
Eleftherios Kallergis
Violeta Moniaki
Eleni Mauroudi
Sophia E. Schiza
author_facet Izolde Bouloukaki
Charalampos Mermigkis
Nikolaos Tzanakis
Eleftherios Kallergis
Violeta Moniaki
Eleni Mauroudi
Sophia E. Schiza
author_sort Izolde Bouloukaki
collection DOAJ
description Systemic inflammation is important in obstructive sleep apnea (OSA) pathophysiology and its comorbidity. We aimed to assess the levels of inflammatory biomarkers in a large sample of OSA patients and to investigate any correlation between these biomarkers with clinical and polysomnographic (PSG) parameters. This was a cross-sectional study in which 2983 patients who had undergone a polysomnography for OSA diagnosis were recruited. Patients with known comorbidities were excluded. Included patients (n=1053) were grouped according to apnea-hypopnea index (AHI) as mild, moderate, and severe. Patients with AHI < 5 served as controls. Demographics, PSG data, and levels of high-sensitivity C-reactive protein (hs-CRP), fibrinogen, erythrocyte sedimentation rate (ESR), and uric acid (UA) were measured and compared between groups. A significant difference was found between groups in hs-CRP, fibrinogen, and UA. All biomarkers were independently associated with OSA severity and gender (p<0.05). Females had increased levels of hs-CRP, fibrinogen, and ESR (p<0.001) compared to men. In contrast, UA levels were higher in men (p<0.001). Our results suggest that inflammatory markers significantly increase in patients with OSA without known comorbidities and correlate with OSA severity. These findings may have important implications regarding OSA diagnosis, monitoring, treatment, and prognosis. This trial is registered with ClinicalTrials.gov number NCT03070769.
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spelling doaj-art-026aa8fc62214b33850d858d5e660f3a2025-02-03T01:12:18ZengWileyMediators of Inflammation0962-93511466-18612017-01-01201710.1155/2017/45737564573756Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without ComorbiditiesIzolde Bouloukaki0Charalampos Mermigkis1Nikolaos Tzanakis2Eleftherios Kallergis3Violeta Moniaki4Eleni Mauroudi5Sophia E. Schiza6Sleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, GreeceSystemic inflammation is important in obstructive sleep apnea (OSA) pathophysiology and its comorbidity. We aimed to assess the levels of inflammatory biomarkers in a large sample of OSA patients and to investigate any correlation between these biomarkers with clinical and polysomnographic (PSG) parameters. This was a cross-sectional study in which 2983 patients who had undergone a polysomnography for OSA diagnosis were recruited. Patients with known comorbidities were excluded. Included patients (n=1053) were grouped according to apnea-hypopnea index (AHI) as mild, moderate, and severe. Patients with AHI < 5 served as controls. Demographics, PSG data, and levels of high-sensitivity C-reactive protein (hs-CRP), fibrinogen, erythrocyte sedimentation rate (ESR), and uric acid (UA) were measured and compared between groups. A significant difference was found between groups in hs-CRP, fibrinogen, and UA. All biomarkers were independently associated with OSA severity and gender (p<0.05). Females had increased levels of hs-CRP, fibrinogen, and ESR (p<0.001) compared to men. In contrast, UA levels were higher in men (p<0.001). Our results suggest that inflammatory markers significantly increase in patients with OSA without known comorbidities and correlate with OSA severity. These findings may have important implications regarding OSA diagnosis, monitoring, treatment, and prognosis. This trial is registered with ClinicalTrials.gov number NCT03070769.http://dx.doi.org/10.1155/2017/4573756
spellingShingle Izolde Bouloukaki
Charalampos Mermigkis
Nikolaos Tzanakis
Eleftherios Kallergis
Violeta Moniaki
Eleni Mauroudi
Sophia E. Schiza
Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities
Mediators of Inflammation
title Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities
title_full Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities
title_fullStr Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities
title_full_unstemmed Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities
title_short Evaluation of Inflammatory Markers in a Large Sample of Obstructive Sleep Apnea Patients without Comorbidities
title_sort evaluation of inflammatory markers in a large sample of obstructive sleep apnea patients without comorbidities
url http://dx.doi.org/10.1155/2017/4573756
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