TY - JOUR
T1 - Cardiometabolic changes after continuous positive airway pressure for obstructive sleep apnoea
T2 - a randomised sham-controlled study
AU - Hoyos, Camilla M.
AU - Killick, Roo
AU - Yee, Brendon J.
AU - Phillips, Craig L.
AU - Grunstein, Ronald R.
AU - Liu, Peter Y.
N1 - Corrigendum can be found in Thorax, 68, p. 879 , 2012.
http://dx.doi.org/10.1136/thoraxjnl-2011-201420corr1
PY - 2012
Y1 - 2012
N2 - Rationale and objectives: Impaired insulin sensitivity (ISx), increased visceral abdominal fat (VAF) and liver fat are all central components of the metabolic syndrome and characteristics of men with obstructive sleep apnoea (OSA). The reversibility of these observed changes with continuous positive airway pressure (CPAP) treatment in men with OSA has not been systematically studied in a randomised sham-controlled fashion. Methods: 65 men without diabetes who were CPAP naïve and had moderate to severe OSA (age=49±12 years, apnoea hypopnoea index (AHI)= 39.9±17.7 events/h, body mass index=31.3±5.2 kg/m2) were randomised to receive either real (n=34) or sham (n=31) CPAP for 12 weeks. At 12 weeks, all subjects received real CPAP for an additional 12 weeks. Measurements and main results: Main outcomes were the change at week 12 from baseline in VAF, ISx and liver fat. Other metabolic outcomes were changes in the disposition index, total fat, and blood leptin and adiponectin concentrations. The AHI was lower on CPAP compared with sham by 33 events/h (95% CI-43.9 to -22.2, p<0.0001) after 12 weeks. There were no between-group differences at 12 weeks in VAF (-13.0 cm 3, -42.4 to 16.2, p=0.37), ISx (-0.13 (min-1)(μU/ml)) -1, -0.40 to 0.14, p=0.33), liver fat (-0.5 cm3, -3.8 to 2.7, p=0.74) or any other cardiometabolic parameter. At 24 weeks, ISx (3.2×104 (min-1)(μU/ml))-1, 0.9×104 to 6.0×104, p=0.009), but not VAF (-1.4 cm3, -19.2 to 16.4, p=0.87) or liver fat (-0.2 Hounsfield units, -2.4 to 2.0, p=0.83) were improved compared with baseline in the whole study group. Conclusion: Reducing visceral adiposity in men with OSA cannot be achieved with CPAP alone and is likely to require weight-loss interventions. Longer-term effects of CPAP on other cardiometabolic markers such as ISx require further investigation to fully examine time dependencies. Trial Registration Number: ACTRN12608000301369.
AB - Rationale and objectives: Impaired insulin sensitivity (ISx), increased visceral abdominal fat (VAF) and liver fat are all central components of the metabolic syndrome and characteristics of men with obstructive sleep apnoea (OSA). The reversibility of these observed changes with continuous positive airway pressure (CPAP) treatment in men with OSA has not been systematically studied in a randomised sham-controlled fashion. Methods: 65 men without diabetes who were CPAP naïve and had moderate to severe OSA (age=49±12 years, apnoea hypopnoea index (AHI)= 39.9±17.7 events/h, body mass index=31.3±5.2 kg/m2) were randomised to receive either real (n=34) or sham (n=31) CPAP for 12 weeks. At 12 weeks, all subjects received real CPAP for an additional 12 weeks. Measurements and main results: Main outcomes were the change at week 12 from baseline in VAF, ISx and liver fat. Other metabolic outcomes were changes in the disposition index, total fat, and blood leptin and adiponectin concentrations. The AHI was lower on CPAP compared with sham by 33 events/h (95% CI-43.9 to -22.2, p<0.0001) after 12 weeks. There were no between-group differences at 12 weeks in VAF (-13.0 cm 3, -42.4 to 16.2, p=0.37), ISx (-0.13 (min-1)(μU/ml)) -1, -0.40 to 0.14, p=0.33), liver fat (-0.5 cm3, -3.8 to 2.7, p=0.74) or any other cardiometabolic parameter. At 24 weeks, ISx (3.2×104 (min-1)(μU/ml))-1, 0.9×104 to 6.0×104, p=0.009), but not VAF (-1.4 cm3, -19.2 to 16.4, p=0.87) or liver fat (-0.2 Hounsfield units, -2.4 to 2.0, p=0.83) were improved compared with baseline in the whole study group. Conclusion: Reducing visceral adiposity in men with OSA cannot be achieved with CPAP alone and is likely to require weight-loss interventions. Longer-term effects of CPAP on other cardiometabolic markers such as ISx require further investigation to fully examine time dependencies. Trial Registration Number: ACTRN12608000301369.
UR - http://www.scopus.com/inward/record.url?scp=85027925582&partnerID=8YFLogxK
UR - https://doi.org/10.1136/thoraxjnl-2011-201420corr1
U2 - 10.1136/thoraxjnl-2011-201420
DO - 10.1136/thoraxjnl-2011-201420
M3 - Article
C2 - 22561530
AN - SCOPUS:85027925582
SN - 0040-6376
VL - 67
SP - 1081
EP - 1089
JO - Thorax
JF - Thorax
IS - 12
ER -