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Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans

Obstructive sleep apnea (OSA) has been related to elevation of inflammatory cytokines and development of insulin resistance in morbidly obese (MO) subjects. However, it is still unclear whether the systemic concentration of anti-inflammatory mediators is also affected in MO subjects directly related...

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Autores principales: Leon-Cabrera, Sonia, Arana-Lechuga, Yoaly, Esqueda-León, Enrique, Terán-Pérez, Guadalupe, Gonzalez-Chavez, Antonio, Escobedo, Galileo, Velázquez Moctezuma, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402489/
https://www.ncbi.nlm.nih.gov/pubmed/25944984
http://dx.doi.org/10.1155/2015/493409
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author Leon-Cabrera, Sonia
Arana-Lechuga, Yoaly
Esqueda-León, Enrique
Terán-Pérez, Guadalupe
Gonzalez-Chavez, Antonio
Escobedo, Galileo
Velázquez Moctezuma, Javier
author_facet Leon-Cabrera, Sonia
Arana-Lechuga, Yoaly
Esqueda-León, Enrique
Terán-Pérez, Guadalupe
Gonzalez-Chavez, Antonio
Escobedo, Galileo
Velázquez Moctezuma, Javier
author_sort Leon-Cabrera, Sonia
collection PubMed
description Obstructive sleep apnea (OSA) has been related to elevation of inflammatory cytokines and development of insulin resistance in morbidly obese (MO) subjects. However, it is still unclear whether the systemic concentration of anti-inflammatory mediators is also affected in MO subjects directly related to the severity of OSA and level of insulin resistance. Normal weight and MO subjects were subjected to overnight polysomnography in order to establish the severity of OSA, according to the apnea-hypopnea index (AHI). Blood samples were obtained for estimation of total cholesterol and triglycerides, insulin, glucose, insulin resistance, tumor necrosis factor alpha (TNF-α), interleukin 12 (IL12), and interleukin 10 (IL-10). Serum levels of IL-10 were significantly lower in MO subjects with OSA than in MO and control individuals without OSA. Besides being inversely associated with serum TNF-α and IL-12, decreased IL-10 levels were significantly related to increased AHI, hyperinsulinemia, and insulin resistance. Serum IL-10 is significantly reduced in morbidly obese subjects with severe OSA while also showing a clear relationship with a state of hyperinsulinemia and insulin resistance probably regardless of obesity in the present sample. It may be of potential clinical interest to identify the stimulatory mechanisms of IL-10 in obese individuals with OSA.
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spelling pubmed-44024892015-05-05 Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans Leon-Cabrera, Sonia Arana-Lechuga, Yoaly Esqueda-León, Enrique Terán-Pérez, Guadalupe Gonzalez-Chavez, Antonio Escobedo, Galileo Velázquez Moctezuma, Javier Mediators Inflamm Research Article Obstructive sleep apnea (OSA) has been related to elevation of inflammatory cytokines and development of insulin resistance in morbidly obese (MO) subjects. However, it is still unclear whether the systemic concentration of anti-inflammatory mediators is also affected in MO subjects directly related to the severity of OSA and level of insulin resistance. Normal weight and MO subjects were subjected to overnight polysomnography in order to establish the severity of OSA, according to the apnea-hypopnea index (AHI). Blood samples were obtained for estimation of total cholesterol and triglycerides, insulin, glucose, insulin resistance, tumor necrosis factor alpha (TNF-α), interleukin 12 (IL12), and interleukin 10 (IL-10). Serum levels of IL-10 were significantly lower in MO subjects with OSA than in MO and control individuals without OSA. Besides being inversely associated with serum TNF-α and IL-12, decreased IL-10 levels were significantly related to increased AHI, hyperinsulinemia, and insulin resistance. Serum IL-10 is significantly reduced in morbidly obese subjects with severe OSA while also showing a clear relationship with a state of hyperinsulinemia and insulin resistance probably regardless of obesity in the present sample. It may be of potential clinical interest to identify the stimulatory mechanisms of IL-10 in obese individuals with OSA. Hindawi Publishing Corporation 2015 2015-04-06 /pmc/articles/PMC4402489/ /pubmed/25944984 http://dx.doi.org/10.1155/2015/493409 Text en Copyright © 2015 Sonia Leon-Cabrera et al. https://creativecommons.org/licenses/by/3.0/ 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
Leon-Cabrera, Sonia
Arana-Lechuga, Yoaly
Esqueda-León, Enrique
Terán-Pérez, Guadalupe
Gonzalez-Chavez, Antonio
Escobedo, Galileo
Velázquez Moctezuma, Javier
Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans
title Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans
title_full Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans
title_fullStr Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans
title_full_unstemmed Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans
title_short Reduced Systemic Levels of IL-10 Are Associated with the Severity of Obstructive Sleep Apnea and Insulin Resistance in Morbidly Obese Humans
title_sort reduced systemic levels of il-10 are associated with the severity of obstructive sleep apnea and insulin resistance in morbidly obese humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402489/
https://www.ncbi.nlm.nih.gov/pubmed/25944984
http://dx.doi.org/10.1155/2015/493409
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