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Ayshat Yandieva

Moscow State University of Medicine and Dentistry of the Ministry of Healthcare, Russian Federation

Title: Effect of CPAP-treatment on the arterial stiffness and systemic inflammation in patients with metabolic syndrome and obstructive sleep apnea

Biography

Biography: Ayshat Yandieva

Abstract

Statement of the Problem:  The combination of metabolic syndrome (MetS) and obstructive sleep apnea (OSA) is characterized by a significant increase in cardiovascular risks. Some factors, such as systemic inflammation and arterial stiffening may mediate cardiovascular diseases in these patients. Arterial stiffness is widely accepted as early marker of atherosclerosis and cardiovascular outcomes. Systemic inflammation also plays an important role in the development of cardiovascular complications. The purpose of this study is to determine the effect of continuous positive airway pressure (CPAP) on arterial stiffness and plasma CRP levels in patients with MetS and OSA. Materials and methods: total of 74 patients with MetS and moderate-to-severe OSA were randomized to CPAP (n = 36) and non-CPAP (n = 38) treatment groups for 12 weeks to investigate the effects of CPAP-treatment on arterial stiffness and plasma CRP levels. Findings: Initially, there were no significant differences between the two groups for all the studied parameters. After 12 weeks of therapeutic CPAP, there was registered decrease in R/L-PWV (from 12,7±2,6 m/s to 11,1±3,4 m/s, p <0.05), CAVI (from 8,2±1,8 to 6,5 ±1,8, p <0.05), AIx (from 1,66±0,15 to 0,96±0,12, p<0,05), although change of ABI was not statistically significant. In non-CPAP patients, there was no reliable dynamic in parameters of arterial stiffness. Also, the CPAP-treatment patients presented lower circulating levels of CRP after 3 months of therapy: 6,17±0,52 mg/L vs. 8,32±0,44mg/L at the baseline (p<0,01). On the other hand, no significant differences were found in the control group of patients. Conclusions and significance: appropriate CPAP therapy in patients with MetS and OSA improves both vascular stiffness and chronic systemic inflammation, that leads to reducing general cardiovascular risks.