Elsevier

Sleep Medicine Clinics

Volume 11, Issue 3, September 2016, Pages 273-286
Sleep Medicine Clinics

Consequences of Obstructive Sleep Apnea: Cardiovascular Risk of Obstructive Sleep Apnea and Whether Continuous Positive Airway Pressure Reduces that Risk

https://doi.org/10.1016/j.jsmc.2016.05.002Get rights and content

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Key points

  • Obstructive sleep apnea (OSA) is associated with unique perturbations that include intermittent hypoxia, sympathetic activation, and oxidative stress.

  • OSA is a cause of hypertension, and can worsen the outcome of coronary artery disease, atrial fibrillation, and stroke.

  • Treatment of OSA can improve the outcomes of all cardiovascular disorders.

  • Expedited approaches to identification and treatment of OSA are important interventions in the management of cardiovascular disease.

Overview of sleep-disordered breathing

The term sleep-disordered breathing (SDB) encompasses all respiratory disorders of sleep and includes both OSA and central sleep apnea (CSA). SDB is defined by the presence of 5 or more respiratory events (apneas or hypopneas) per 1 hour of sleep; that is, an apnea-hypopnea index (AHI) of 5 or more events per hour. The SDB is classified as OSA if more than half of the events are classified as obstructive and CSA if more than half of the events are central. Determination of the obstructive or

Mechanism of cardiovascular disease in obstructive sleep apnea

Extensive work in the past 3 decades has greatly expanded the understanding of the mechanism of CVD in patients with OSA. Several pathways have been identified as important for the development of CVD in OSA. These pathways may provide targets for therapeutic interventions in the near future.

Systemic Hypertension and Obstructive Sleep Apnea: A Critical Causative Relationship

Systemic hypertension deserves special attention as the most common CVD leading to a significant portion of CVD-linked mortality in developed societies.55 Systemic hypertension is the best-established cardiovascular consequence of OSA. Mounting evidence from experimental, observational, and clinical trials over the past 3 decades has established OSA as a modifiable risk factor for systemic hypertension.

The earliest compelling description of a dose-response relationship between OSA and systemic

Summary

As discussed in this article, significant evidence has shown a pathophysiologic link between OSA/SDB and CVD/VED. In addition, emerging clinical trial data have shown a relationship between OSA/SDB and a variety of CVD states. Potential treatment benefits of SDB on CVD risk in certain patient populations have also been shown. However, a clear demonstration of a direct causal pathway from SDB to CVD is lacking with most CVDs and large, multicenter, double-blinded, randomized controlled trials

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    Disclosure Statement: R. Khayat received research grant support from Philips Respironics; A. Pleister has no disclosures.

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