Wolf Jacek, Drozdowski Jacek, Czechowicz Krzysztof, Winklewski Paweł J, Jassem Ewa, Kara Tomas, Somers Virend K, Narkiewicz Krzysztof
Department of Hypertension and Diabetology, Medical University of Gdańsk, Gdańsk, Poland; Department of Cardiovascular Diseases, International Clinical Research Center, St. Anne's University Hospital in Brno (FNUSA), Brno, Czech Republic.
Department of Pneumonology and Allergology, Medical University of Gdańsk, Gdańsk, Poland.
Int J Cardiol. 2016 Jan 1;202:67-72. doi: 10.1016/j.ijcard.2015.08.139. Epub 2015 Aug 21.
Beta1-receptor antagonists (BBs) are commonly administered in the treatment of cardiovascular disease (CVD). The reported benefits of BB use in CVD patients with concomitant obstructive sleep apnea (OSA) may be limited by their impact on apnea-induced bradycardias. Therefore the aim of the study was to test the influence of BBs on periapneic heart rate (HR) fluctuations in hypertensive patients with newly-detected and untreated OSA.
We studied 88 hypertensive patients (56 on BBs and 32 BB naive) with newly-diagnosed moderate-to-severe OSA who were free of major pulmonary comorbidities and did not require antiarrhythmic therapy. ECGs recorded during sleep were investigated for heart rate (HR) responses to apneas allowing to compare extreme HR accelerations and decelerations between the groups.
Average sleep-time HR was comparable in BB-naive (BB-) and BB-treated (BB+) patients. Direct comparisons showed that HR decelerations were also similar in the two subgroups (53.8±9.6 vs. 54.4±7.8 bpm; P=0.78, for BB- and BB+, respectively) however, BBs blunted the OSA-induced HR accelerations (82.3±12.2 vs. 74.3±10.0; P=0.003). After adjusting for baseline HR and magnitude of desaturations, HR decelerations were more evident in BB-naive group whereas tachycardic responses remained blunted in the BB+ group. The incidence of ectopies and conduction abnormalities were comparable across two groups.
Beta-blockers do not potentiate apnea-induced HR decelerations, attenuate apnea-induced increases in heart rate and do not influence incidence of ectopies and conduction abnormalities in patients with hypertension and moderate-to-severe, untreated OSA.
β1受体拮抗剂(BBs)常用于治疗心血管疾病(CVD)。在伴有阻塞性睡眠呼吸暂停(OSA)的CVD患者中,使用BBs的益处可能因其对呼吸暂停诱发的心动过缓的影响而受到限制。因此,本研究的目的是测试BBs对新发现且未经治疗的OSA高血压患者呼吸暂停期间心率(HR)波动的影响。
我们研究了88例新诊断为中度至重度OSA的高血压患者(56例使用BBs,32例未使用BBs),这些患者无主要肺部合并症且不需要抗心律失常治疗。对睡眠期间记录的心电图进行心率(HR)对呼吸暂停反应的研究,以比较两组之间的极端心率加速和减速情况。
未使用BBs(BB-)和使用BBs治疗(BB+)的患者平均睡眠时间心率相当。直接比较显示,两个亚组的心率减速也相似(分别为53.8±9.6和54.4±7.8次/分钟;P = 0.78),然而,BBs减弱了OSA诱发的心率加速(82.3±12.2和74.3±10.0;P = 0.003)。在调整基线心率和去饱和度幅度后,未使用BBs组的心率减速更明显,而BB+组的心动过速反应仍然减弱。两组异位心律和传导异常的发生率相当。
β受体阻滞剂不会增强呼吸暂停诱发的心率减速,减弱呼吸暂停诱发的心率增加,并且不影响高血压和中度至重度未经治疗的OSA患者的异位心律和传导异常发生率。