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The Role of Obesity and Obstructive Sleep Apnea in the Pathogenesis and Treatment of Resistant Hypertension
Authors:Jonathan A Marcus  Aravind Pothineni  Carolina Z Marcus  John D Bisognano
Institution:1. Department of Neurology, University of Rochester Sleep Disorders Center, 2337 South Clinton Avenue, Rochester, NY, 14618, USA
2. Department of Internal Medicine and Pediatrics, University of Rochester Medical Center, 400 Red Creek Drive, Suite 110, Rochester, NY, 14623, USA
3. Cardiology Division, Department of Internal Medicine, University of Rochester Medical Center, Rochester, NY, USA
4. University of Rochester Medical Center/School of Medicine and Dentistry, 601 Elmwood Ave, Box 679-7, Rochester, NY, 14642, USA
Abstract:The incidence of resistant hypertension, obesity, and obstructive sleep apnea (OSA), three highly prevalent conditions in the United States, is rising. Approximately one in three adults in the US has hypertension, and a significant proportion of these individuals have hypertension that is difficult to treat, or resistant. Obesity and OSA are well-established risk factors for resistant hypertension, a condition that portends significant cardiovascular risk. Awareness of the various mechanisms by which obesity and OSA impact systemic blood pressure is essential to better understand how best to effectively care for patients with resistant hypertension. In this review, we discuss the clinical and pathophysiologic associations between obesity, OSA, and resistant hypertension. Furthermore, we will explore the effect of continuous positive airway pressure therapy (CPAP) and other therapeutic interventions on blood pressure control in patients with resistant hypertension. Key Points ? Obesity, obstructive sleep apnea, and resistant hypertension are highly prevalent conditions, with increasing overall incidence 13]. ? Both obesity and obstructive sleep apnea are independent risk factors for the development of resistant hypertension. ? OSA is characterized by a physiologic cascade of collapse of the upper airway, which can lead to intermittent hypoxia, hypercapnia, significant negative intra-thoracic pressure, and increased SNS output. ? Intermittent hypoxia leads to activation of the endothelin system 17, 18, 19?], which can lead to the development of resistant hypertension. ? Intermittent hypoxia can lead to the over activation of the SNS, which can also contribute to the development of resistant hypertension 20, 21]. ? OSA leads to state of elevated adrenergic tone, which in turn may contribute to resistant hypertension 2527]. ? OSA patients have a higher incidence of “non-dipping” of nocturnal systolic blood pressure, a marker of increased adrenergic tone. This potentially represents a risk factor for hypertensive end organ disease 31, 32]. ? The prevalence of OSA is significantly higher in patients predisposed to fluid accumulation: including kidney disease, heart failure and resistant hypertension 33]. ? Interventions (such as the daytime use of compression stocking) which reduce daytime lower extremity fluid accumulation can significantly reduce the severity of OSA, particularly in patients with comorbid resistant hypertension 35, 36]. ? CPAP therapy can significantly reduce blood pressure in patients with comorbid hypertension and OSA. The treatment effect is most pronounced in those with resistant hypertension and OSA 16??, 3842].
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