| Literature DB >> 28966076 |
Matthew Light1, Karen McCowen2, Atul Malhotra3, Omar A Mesarwi4.
Abstract
Obstructive sleep apnea (OSA) is common, and many cross-sectional and longitudinal studies have established OSA as an independent risk factor for the development of a variety of adverse metabolic disease states, including hypertension, insulin resistance, type 2 diabetes, nonalcoholic fatty liver disease, dyslipidemia, and atherosclerosis. Nasal continuous positive airway pressure (CPAP) has long been the mainstay of therapy for OSA, but definitive studies demonstrating the efficacy of CPAP in improving metabolic outcomes, or in reducing incident disease burden, are lacking; moreover, CPAP has variable rates of adherence. Therefore, the future of OSA management, particularly with respect to limiting OSA-related metabolic dysfunction, likely lies in a coming wave of alternative approaches to endophenotyping OSA patients, personalized care, and defining and targeting mechanisms of OSA-induced adverse health outcomes.Entities:
Keywords: Hyperglycemia; Obesity; Sleep apnea endophenotypes; Sleep disordered breathing
Mesh:
Year: 2017 PMID: 28966076 PMCID: PMC5874161 DOI: 10.1016/j.metabol.2017.09.004
Source DB: PubMed Journal: Metabolism ISSN: 0026-0495 Impact factor: 8.694