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Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets

Obesity is a dramatically increasing disease, accompanied with comorbidities such as cardiovascular disease and obstructive sleep apnea syndrome (OSAS). Both obesity and OSAS per se are associated with systemic inflammation. However, the multifactorial impact of obesity, OSAS, and its concomitant di...

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Autores principales: Meyhöfer, Svenja, Steffen, Armin, Plötze-Martin, Kirstin, Lange, Christian, Marquardt, Jens-Uwe, Bruchhage, Karl-Ludwig, Meyhöfer, Sebastian M., Pries, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563442/
https://www.ncbi.nlm.nih.gov/pubmed/36921085
http://dx.doi.org/10.4049/immunohorizons.2300009
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author Meyhöfer, Svenja
Steffen, Armin
Plötze-Martin, Kirstin
Lange, Christian
Marquardt, Jens-Uwe
Bruchhage, Karl-Ludwig
Meyhöfer, Sebastian M.
Pries, Ralph
author_facet Meyhöfer, Svenja
Steffen, Armin
Plötze-Martin, Kirstin
Lange, Christian
Marquardt, Jens-Uwe
Bruchhage, Karl-Ludwig
Meyhöfer, Sebastian M.
Pries, Ralph
author_sort Meyhöfer, Svenja
collection PubMed
description Obesity is a dramatically increasing disease, accompanied with comorbidities such as cardiovascular disease and obstructive sleep apnea syndrome (OSAS). Both obesity and OSAS per se are associated with systemic inflammation. However, the multifactorial impact of obesity, OSAS, and its concomitant diseases on the immunological characteristics of circulating monocytes has not yet been fully resolved. Monocyte subsets of 82 patients with obesity were analyzed in whole blood measurements in terms of the CD14/CD16 cell surface expression patterns and different monocytic adhesion molecules using flow cytometry. Plasma levels of adipokines adiponectin and leptin of all patients were evaluated and correlated with accompanying cellular and clinical values. Whole blood measurements revealed a significant overall redistribution of CD14/CD16 monocyte subsets in patients with obesity. Monocytic adhesion molecules CD11a, CD11b, and CX3CR1 were significantly elevated. The observed alterations significantly correlated with plasma leptin levels and diabetes status as crucial amplifying factors. The additive impact of obesity, diabetes, and OSAS on the immunological balance of peripheral blood monocytes requires a coordinated regimen in terms of therapeutic treatment, respiratory support, and weight loss to improve the systemic immunity in these patients.
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spelling pubmed-105634422023-10-23 Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets Meyhöfer, Svenja Steffen, Armin Plötze-Martin, Kirstin Lange, Christian Marquardt, Jens-Uwe Bruchhage, Karl-Ludwig Meyhöfer, Sebastian M. Pries, Ralph Immunohorizons Clinical and Translational Immunology Obesity is a dramatically increasing disease, accompanied with comorbidities such as cardiovascular disease and obstructive sleep apnea syndrome (OSAS). Both obesity and OSAS per se are associated with systemic inflammation. However, the multifactorial impact of obesity, OSAS, and its concomitant diseases on the immunological characteristics of circulating monocytes has not yet been fully resolved. Monocyte subsets of 82 patients with obesity were analyzed in whole blood measurements in terms of the CD14/CD16 cell surface expression patterns and different monocytic adhesion molecules using flow cytometry. Plasma levels of adipokines adiponectin and leptin of all patients were evaluated and correlated with accompanying cellular and clinical values. Whole blood measurements revealed a significant overall redistribution of CD14/CD16 monocyte subsets in patients with obesity. Monocytic adhesion molecules CD11a, CD11b, and CX3CR1 were significantly elevated. The observed alterations significantly correlated with plasma leptin levels and diabetes status as crucial amplifying factors. The additive impact of obesity, diabetes, and OSAS on the immunological balance of peripheral blood monocytes requires a coordinated regimen in terms of therapeutic treatment, respiratory support, and weight loss to improve the systemic immunity in these patients. AAI 2023-03-15 /pmc/articles/PMC10563442/ /pubmed/36921085 http://dx.doi.org/10.4049/immunohorizons.2300009 Text en Copyright © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the CC BY 4.0 Unported license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical and Translational Immunology
Meyhöfer, Svenja
Steffen, Armin
Plötze-Martin, Kirstin
Lange, Christian
Marquardt, Jens-Uwe
Bruchhage, Karl-Ludwig
Meyhöfer, Sebastian M.
Pries, Ralph
Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets
title Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets
title_full Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets
title_fullStr Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets
title_full_unstemmed Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets
title_short Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets
title_sort plasma leptin levels, obstructive sleep apnea syndrome, and diabetes are associated with obesity-related alterations of peripheral blood monocyte subsets
topic Clinical and Translational Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563442/
https://www.ncbi.nlm.nih.gov/pubmed/36921085
http://dx.doi.org/10.4049/immunohorizons.2300009
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