Correction of intermittent hypoxia reduces inflammation in obese subjects with obstructive sleep apnea

JCI Insight. 2017 Sep 7;2(17):e94379. doi: 10.1172/jci.insight.94379.

Abstract

Background: In obese subjects with obstructive sleep apnea (OSA), chronic intermittent hypoxia (CIH) may be linked to systemic and adipose tissue inflammation.

Methods: We obtained abdominal subcutaneous adipose tissue biopsies from OSA and non-OSA obese (BMI > 35) subjects at baseline and after 24 weeks (T1) of weight-loss intervention plus continuous positive airway pressure (c-PAP) or weight-loss intervention alone, respectively. OSA subjects were grouped according to good (therapeutic) or poor (subtherapeutic) adherence to c-PAP.

Results: At baseline, anthropometric and metabolic parameters, serum cytokines, and adipose tissue mRNA levels of obesity-associated chemokines and inflammatory markers were not different in OSA and non-OSA subjects. At T1, body weight was significantly reduced in all groups. Serum concentrations of IL-2, IL-4, IL-6, MCP-1, PDGFβ, and VEGFα were reduced by therapeutic c-PAP in OSA subjects and remained unaltered in non-OSA and subtherapeutic c-PAP groups. Similarly, adipose tissue mRNA levels of macrophage-specific (CD68, CD36) and ER stress (ATF4, CHOP, ERO-1) gene markers, as well as of IL-6, PDGFβ, and VEGFα, were decreased only in the therapeutic c-PAP group.

Conclusion: CIH does not represent an additional factor increasing systemic and adipose tissue inflammation in morbid obesity. However, in subjects with OSA, an effective c-PAP therapy improves systemic and obesity-associated inflammatory markers.

Funding: Ministero dell'Università e della Ricerca and Progetti di Rilevante Interesse Nazionale.

Keywords: Adipose tissue; Cytokines; Metabolism; Pulmonology; hypoxia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdomen
  • Adult
  • Biomarkers / metabolism
  • Body Mass Index
  • Continuous Positive Airway Pressure
  • Cytokines / blood
  • Cytokines / genetics
  • Endoplasmic Reticulum Stress / genetics
  • Female
  • Humans
  • Hypoxia / therapy*
  • Inflammation / complications
  • Inflammation / prevention & control*
  • Inflammation Mediators / metabolism
  • Male
  • Middle Aged
  • Obesity / complications*
  • Proto-Oncogene Proteins c-sis / blood
  • RNA, Messenger / genetics
  • Sleep Apnea, Obstructive / complications
  • Sleep Apnea, Obstructive / etiology*
  • Sleep Apnea, Obstructive / therapy
  • Subcutaneous Fat / pathology
  • Vascular Endothelial Growth Factor A / blood
  • Weight Loss

Substances

  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Proto-Oncogene Proteins c-sis
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A