Effects of obstructive sleep apnea on circulating ICAM-1, IL-8, and MCP-1

Department of Geriatric Medicine, Graduate School of Medicine, University of Tokyo, Tokyo1 13-8655, Japan Obstructive sleep apnea syndrome (OSAS) is one of the most important risk factors of cardiovascular disorders. In the treatment of OSAS, nasal continuous positive airway pressure (nCPAP) has bee...

Full description

Saved in:
Bibliographic Details
Published inJournal of applied physiology (1985) Vol. 94; no. 1; pp. 179 - 184
Main Authors Ohga, Eijiro, Tomita, Tetsuji, Wada, Hiroo, Yamamoto, Hiroshi, Nagase, Takahide, Ouchi, Yasuyoshi
Format Journal Article
LanguageEnglish
Published Bethesda, MD Am Physiological Soc 01.01.2003
American Physiological Society
Subjects
Online AccessGet full text
ISSN8750-7587
1522-1601
DOI10.1152/japplphysiol.00177.2002

Cover

More Information
Summary:Department of Geriatric Medicine, Graduate School of Medicine, University of Tokyo, Tokyo1 13-8655, Japan Obstructive sleep apnea syndrome (OSAS) is one of the most important risk factors of cardiovascular disorders. In the treatment of OSAS, nasal continuous positive airway pressure (nCPAP) has been widely used and found to be effective. In the present study, we hypothesized that the hypoxic stress caused by obstructive sleep apnea would increase circulating intercellular adhesion molecule-1 (ICAM-1), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1) in untreated OSAS patients compared with an age-matched control group. In addition, we hypothesized that nCPAP may decrease OSAS-induced hypoxic stress and mediators. To examine these hypotheses, we measured circulating ICAM-1 and IL-8 before and after nCPAP therapy in OSAS patients. We observed that nCPAP decreased apnea, desaturation, and the circulating ICAM-1 and IL-8 levels in OSAS patients. The circulating levels of ICAM-1, IL-8, and MCP-1 in untreated OSAS patients were significantly greater than those in the controls. These observations suggest that nCPAP therapy could reduce OSAS-induced hypoxia and generation of inflammatory mediators. Treatment of OSAS using nCPAP can be, therefore, a potential approach to decrease risk of the progression of OSAS-associated disorders. cytokines; cardiovascular disorders; ischemic heart disease; desaturation magnitude; hypoxic stress; intracellular adhesion molecule-1; monocyte chemoattractant protein-1; interleukin-8
Bibliography:SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
ISSN:8750-7587
1522-1601
DOI:10.1152/japplphysiol.00177.2002