Free Content The effect of short-term withdrawal from continuous positive airway pressure therapy on sympathetic activity and markers of vascular inflammation in subjects with obstructive sleep apnoea

Authors: PHILLIPS, CRAIG L.; YANG, QIAO; WILLIAMS, ANDREW1; ROTH, MICHAEL2; YEE, BRENDON J.; HEDNER, JAN A.; BEREND, NORBERT2; GRUNSTEIN, RONALD R.

Source: Journal of Sleep Research, Volume 16, Number 2, June 2007 , pp. 217-225(9)

Publisher: Blackwell Publishing

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Abstract:

Summary

Obstructive sleep apnoea (OSA) is commonly associated with cardiovascular disease and sympathetic activation. However, it is unclear whether this association is independent of obesity and to what extent treatment with nasal continuous positive airway pressure (CPAP) alleviates the vascular inflammation that underpins cardiovascular disease. We therefore evaluated whether short-term withdrawal from CPAP therapy in subjects with moderate-severe OSA would result in increased levels of sympathetic activity and circulating inflammatory cytokines independent of weight. Vascular inflammatory markers (hsCRP, hsIL-6 and hsTNF-α) were assessed in 20 subjects after one and seven nights of withdrawal from CPAP together with the hypoxia-responsive angiogenic marker VEGF and urinary catecholamines. Compared with baseline on CPAP, withdrawal from therapy resulted in an immediate return of OSA with an increase in RDI to 26.7 ± 5.2 and 39.0 ± 5.9 events per hour after one and seven nights without CPAP, respectively (both P <0.0001). This was accompanied by a concomitant rise in daytime urinary noradrenaline (P <0.0001) after seven nights CPAP withdrawal that was positively associated with the severity of hypoxaemia. In contrast, withdrawal from CPAP therapy was not accompanied by any change in measured cytokines or VEGF (all P >0.1). In conclusion, 1 week of CPAP withdrawal was associated with a return of OSA and a marked increase in sympathetic activity without a concomitant elevation of vascular inflammatory markers.

Keywords: inflammatory cytokines; obesity; sleep apnoea

Document Type: Research article

DOI: 10.1111/j.1365-2869.2007.00589.x

Affiliations: 1: Department of Clinical Immunology, Royal Prince Alfred Hospital, Sydney, Australia 2: Woolcock Institute of Medical Research, University of Sydney, Sydney, Australia

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