Abstract
BACKGROUND: Whether the efficacy of continuous positive airway pressure (CPAP) therapy differs by duration in patients with obstructive sleep apnoea (OSA) and type 2 diabetes mellitus (T2DM) is unclear. This study aimed to evaluate the effects of CPAP therapy duration on these patients. METHODS: We conducted a systematic review and meta-analysis of randomised controlled trials (RCTs) published up to 27 December 2024. We searched MEDLINE, EMBASE and the Cochrane Library for studies on patients with OSA and T2DM treated with CPAP. Outcomes of interest were haemoglobin A1c (HbA1c), fasting blood glucose (FBG), mean blood glucose (MBG), Homeostasis Model of Assessment of Insulin Resistance Index (HOMA-IR), body mass index (BMI) and Epworth Sleepiness Scale (ESS) score. Two reviewers independently screened studies, extracted data and assessed the risk of bias using the Cochrane risk of bias tool 2 tool. Data were synthesised using a random-effects model based on heterogeneity, and results were expressed as mean differences (MDs) with 95% CIs. RESULTS: 14 studies enrolling 1273 participants were included in the meta-analysis. The included trials were categorised into short-term (<12 weeks), medium-term (12-<24 weeks) and long-term (≥24 weeks) based on the duration of the CPAP intervention. Analysis showed that long-term CPAP intervention was associated with a significant reduction in HOMA-IR levels (MD -1.67; 95% CI -2.57 to -0.77). CPAP was associated with increases in BMI levels after medium-term (MD 0.31 kg/m(2); 95% CI 0.06 to 0.57) and long-term (MD 0.74 kg/m(2); 95% CI 0.20 to 1.27) intervention. Similarly, ESS levels showed a significant reduction after medium-term (MD -1.45; 95% CI -2.84 to -0.06) and long-term (MD -1.79; 95% CI -3.45 to -0.13) CPAP intervention. The duration of CPAP intervention did not significantly affect changes in FBG, MBG or HbA1c levels. CONCLUSION: Evidence from multiple RCTs indicates that the efficacy of CPAP therapy varies with treatment duration in patients with OSA and T2DM, showing benefits for insulin resistance and sleepiness with longer use but no significant effect on key glycaemic markers. TRIAL REGISTRATION NUMBER: The study protocol was prospectively registered with PROSPERO (https://www.crd.york.ac.uk/) (registration number: CRD42025633203).