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Atrial remodeling in obstructive sleep apnea: Implications for atrial fibrillation

机译:阻塞性睡眠呼吸暂停中的心房重塑:对心房颤动的影响

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Background: There is a known association between obstructive sleep apnea (OSA) and atrial fibrillation (AF); however, how OSA affects the atrial myocardium is not well described. Objective: To determine whether patients with OSA have an abnormal atrial substrate. Methods: Forty patients undergoing ablation of paroxysmal AF and in sinus rhythm (20 with OSA [apneahypopnea index < 15] and 20 reference patients with no OSA [apneahypopnea index < 15] by polysomnography) were studied. Multipolar catheters were positioned at the lateral right atrium (RA), coronary sinus, crista terminalis, and RA septum to determine the effective refractory period at 5 sites, conduction time along linear catheters at the RA and the coronary sinus, conduction at the crista terminalis, and sinus node function (corrected sinus node recovery time). Biatrial electroanatomic maps were created to determine the voltage, conduction, and distribution of complex electrograms (duration < 50 ms). Results: The groups had no differences in the prevalence of established risk factors for AF. Patients with OSA had the following compared with those without OSA: no difference in effective refractory period (P =.9), prolonged conduction times along the coronary sinus and RA (P =.02), greater number (P =.003) and duration (P =.03) of complex electrograms along the crista terminalis, longer P-wave duration (P =.01), longer corrected sinus node recovery time (P =.02), lower atrial voltage (RA, P <.001; left atrium, P <.001), slower atrial conduction velocity (RA, P =.001; left atrium, P =.02), and more widespread complex electrograms in both atria (RA, P =.02; left atrium, P =.01). Conclusion: OSA is associated with significant atrial remodeling characterized by atrial enlargement, reduction in voltage, site-specific and widespread conduction abnormalities, and longer sinus node recovery. These features may in part explain the association between OSA and AF.
机译:背景:阻塞性睡眠呼吸暂停(OSA)和心房颤动(AF)之间存在已知的关联;但是,OSA如何影响心肌心肌。目的:确定OSA患者是否具有异常心房底物。方法:研究了40名接受阵发性AF和窦性节奏消融的患者(20例使用OSA [apneahypopopnea指数<15],并研究了20例没有OSA的参考患者[apneahypopopnea index <15]。将多极导管定位在右侧右侧(RA),冠状窦,Crista末端和RA隔垫片,以确定5个位置的有效耐火周期,沿RA的线性导管和冠状窦在Crista末端传导,在Crista末端传导,和窦淋巴结函数(校正后的鼻窦节点恢复时间)。创建了双胞胎电工图,以确定复杂电图的电压,传导和分布(持续时间<50 ms)。结果:这些小组在已建立的AF风险因素的患病率上没有差异。与没有OSA的患者相比,OSA患者的有效耐火周期没有差异(p = .9),沿冠状窦和RA延长传导时间(P = .02),数量更大(P = .003)和沿Crista末端的复合电图的持续时间(p = .03),较长的p波持续时间(p = .01),更长的校正后窦淋巴结恢复时间(p = .02),较低的心房电压(ra,p <.001) ;左心房,p <.001),较慢的心房传导速度(RA,p = .001;左心房,p = .02),并且在两个心房中都有更多广泛的复杂电图(RA,p = .02;左心房,左心房, p = .01)。结论:OSA与显着的心房重塑有关,其特征是心房增大,电压降低,位点特异性和广泛传导异常以及较长的鼻窦节点恢复。这些功能可能部分解释了OSA和AF之间的关联。

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