Department of Neurology, University of Rochester Sleep Disorders Center, 2337 South Clinton Avenue, Rochester, NY, 14618, USA,
Curr Hypertens Rep. 2014 Jan;16(1):411. doi: 10.1007/s11906-013-0411-y.
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 [1-3].• 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 [25-27].• 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••, 38-42].
耐药性高血压、肥胖和阻塞性睡眠呼吸暂停(OSA),其发病率正在上升。大约每三个美国成年人中就有一个患有高血压,而这些人中相当一部分人患有难以治疗或耐药性高血压。肥胖和 OSA 是耐药性高血压的既定危险因素,这种病症预示着心血管风险显著增加。了解肥胖和 OSA 影响全身血压的各种机制对于更好地了解如何有效地治疗耐药性高血压患者至关重要。在这篇综述中,我们讨论了肥胖、OSA 和耐药性高血压之间的临床和病理生理关联。此外,我们还将探讨持续气道正压通气治疗(CPAP)和其他治疗干预措施对耐药性高血压患者血压控制的影响。
关键点
• 肥胖、阻塞性睡眠呼吸暂停和耐药性高血压是高发病症,其总体发病率呈上升趋势[1-3]。
• 肥胖和阻塞性睡眠呼吸暂停都是耐药性高血压发展的独立危险因素。
• OSA 的特征是上呼吸道塌陷的生理级联反应,这可能导致间歇性缺氧、高碳酸血症、显著的胸内负压增加和交感神经系统输出增加。
• 间歇性缺氧会导致内皮素系统的激活[17,18,19],从而导致耐药性高血压的发生。
• 间歇性缺氧会导致交感神经系统过度激活,这也可能导致耐药性高血压的发生[20,21]。
• OSA 导致肾上腺素能递质张力升高,这反过来可能导致耐药性高血压[25-27]。
• OSA 患者夜间收缩压“非杓型”的发生率更高,这是肾上腺素能递质张力增加的一个标志,这可能代表高血压靶器官疾病的一个危险因素[31,32]。
• 易发生液体蓄积的患者(包括肾病、心力衰竭和耐药性高血压)中 OSA 的患病率明显更高[33]。
• 日间使用压缩袜等干预措施减少日间下肢液体蓄积可以显著降低 OSA 的严重程度,尤其是在合并有耐药性高血压的患者中[35,36]。
• CPAP 治疗可以显著降低合并高血压和 OSA 的患者的血压。在合并耐药性高血压和 OSA 的患者中,治疗效果最为明显[16••,38-42]。