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持续气道正压通气对未控制的高血压合并阻塞性睡眠呼吸暂停患者中心和外周血压的影响:随机对照MORPHEOS临床试验

Effects of Continuous Positive Airway Pressure on Central and Peripheral Blood Pressure in Patients with Uncontrolled Hypertension and Obstructive Sleep Apnea: The Randomized Controlled MORPHEOS Clinical Trial.

作者信息

Lorenzi-Filho Geraldo, Cruz Fernanda C S G, Queiróz Daniel B C, Vieira Marcelo Luiz C, Pedrosa Rodrigo P, Couto Patriota Tarcya L G, Righi Camila G, Martinez Denis, da Silva Geruza A, Silva Giovanio V, Pio-Abreu Andrea, Cabrini Mayara L, Giampá Sara Q C, Dórea Egidio L, Lotufo Paulo A, Benseñor Isabela M, Bortolotto Luiz A, Fuchs Flávio D, Drager Luciano F

机构信息

Laboratorio do Sono, Disciplina de Pneumologia, Instituto do Coracao.

Setor de Ecocardiografia, and.

出版信息

Ann Am Thorac Soc. 2025 May;22(5):757-767. doi: 10.1513/AnnalsATS.202407-688OC.

Abstract

Previous studies evaluating the effect of continuous positive airway pressure (CPAP) on blood pressure (BP) among patients with obstructive sleep apnea (OSA) showed variable results. Moreover, several studies recruited patients with normal or controlled BP, and compliance with antihypertensive drug treatment was not monitored. In addition, very few studies investigated central BP in this scenario. To evaluate whether OSA treatment is able to reduce central and peripheral BP in patients with uncontrolled hypertension (HTN) despite well-documented use of antihypertensive treatment. MORPHEOS is a multicenter randomized controlled trial designed to evaluate the effects of CPAP or placebo (nasal dilator strips [NDSs]) for 6 months in patients with moderate to severe OSA and uncontrolled HTN on office BP, ambulatory BP monitoring (ABPM), and central BP (coprimary endpoints). Uncontrolled HTN was defined by at least one abnormal parameter on ABPM after 1 month and ⩾80% adherence to medication based on a pill count. Pill counts, adherence to CPAP or NDS, and office BP were determined once per week in the first month and monthly thereafter. A total of 123 patients completed the study (NDS,  = 64; CPAP,  = 59). The two groups were similar at baseline. Adherence to NDS (⩾80%) and CPAP (⩾4 hours per night) were 98.3% and 81.7%, respectively. Compared with NDSs, office systolic BP (Δ = -10 ± 16 mm Hg;  < 0.001) and diastolic BP (Δ = -7 ± 12 mm Hg;  = 0.001) were reduced significantly in the CPAP group. Despite the BP-lowering effect of CPAP not reaching statistical significance for the ABPM parameters, the rate of 24-hour ABPM control (<130/80 mm Hg) was higher in the CPAP group than in the NDS group (40.7% vs. 20%;  = 0.024). Central diastolic BP was reduced significantly (Δ = -6 ± 9 mm Hg; adjusted  = 0.029). CPAP improves the rates of BP control in patients with OSA and uncontrolled HTN with regular use of medications. Clinical trial registered with www.clinicaltrials.gov (NCT02270658).

摘要

以往评估持续气道正压通气(CPAP)对阻塞性睡眠呼吸暂停(OSA)患者血压(BP)影响的研究结果不一。此外,一些研究纳入了血压正常或得到控制的患者,且未监测其抗高血压药物治疗的依从性。此外,在这种情况下很少有研究调查中心血压。为了评估OSA治疗是否能够降低尽管有充分记录的抗高血压治疗但仍患有未控制高血压(HTN)患者的中心血压和外周血压。MORPHEOS是一项多中心随机对照试验,旨在评估CPAP或安慰剂(鼻扩张条[NDS])对中度至重度OSA和未控制HTN患者进行6个月治疗对诊室血压、动态血压监测(ABPM)和中心血压(共同主要终点)的影响。未控制的HTN定义为1个月后ABPM至少有一项异常参数且基于药丸计数的药物依从性⩾80%。在第一个月每周测定一次药丸计数、CPAP或NDS的依从性以及诊室血压,此后每月测定一次。共有123名患者完成了研究(NDS组=64例;CPAP组=59例)。两组在基线时相似。NDS的依从性(⩾80%)和CPAP的依从性(每晚⩾4小时)分别为98.3%和81.7%。与NDS相比,CPAP组诊室收缩压(Δ=-10±16mmHg;P<0.001)和舒张压(Δ=-7±12mmHg;P=0.001)显著降低。尽管CPAP对ABPM参数的降压效果未达到统计学显著性,但CPAP组24小时ABPM控制率(<130/80mmHg)高于NDS组(40.7%对20%;P=0.024)。中心舒张压显著降低(Δ=-6±9mmHg;校正P=0.029)。经常使用药物的情况下,CPAP可提高OSA和未控制HTN患者的血压控制率。临床试验已在www.clinicaltrials.gov注册(NCT02270658)。

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