Marcus Gregory M, Dukes Jonathan W, Vittinghoff Eric, Nah Gregory, Badhwar Nitish, Moss Joshua D, Lee Randall J, Lee Byron K, Tseng Zian H, Walters Tomos E, Vedantham Vasanth, Gladstone Rachel, Fan Shannon, Lee Emily, Fang Christina, Ogomori Kelsey, Hue Trisha, Olgin Jeffrey E, Scheinman Melvin M, Hsia Henry, Ramchandani Vijay A, Gerstenfeld Edward P
Division of Cardiology, University of California-San Francisco, San Francisco, California, USA.
Cardiology Associates Medical Group Inc., Ventura, California, USA.
JACC Clin Electrophysiol. 2021 May;7(5):662-670. doi: 10.1016/j.jacep.2020.11.026. Epub 2021 Jan 27.
This study sought to identify acute changes in human atrial electrophysiology during alcohol exposure.
The mechanism by which a discrete episode of atrial fibrillation (AF) occurs remains unknown. Alcohol appears to increase the risk for AF, providing an opportunity to study electrophysiologic effects that may render the heart prone to arrhythmia.
In this randomized, double-blinded, placebo-controlled trial, intravenous alcohol titrated to 0.08% blood alcohol concentration was compared with a volume and osmolarity-matched, masked, placebo in patients undergoing AF ablation procedures. Right, left, and pulmonary vein atrial effective refractory periods (AERPs) and conduction times were measured pre- and post-infusion. Isoproterenol infusions and burst atrial pacing were used to assess AF inducibility.
Of 100 participants (50 in each group), placebo recipients were more likely to be diabetic (22% vs. 4%; p = 0.007) and to have undergone a prior AF ablation (36% vs. 22%; p = 0.005). Pulmonary vein AERPs decreased an average of 12 ms (95% confidence interval: 1 to 22 ms; p = 0.026) in the alcohol group, with no change in the placebo group (p = 0.98). Whereas no statistically significant differences in continuously assessed AERPs were observed, the proportion of AERP sites tested that decreased with alcohol (median: 0.5; interquartile range: 0.6 to 0.6) was larger than with placebo (median: 0.4; interquartile range: 0.2 to 0.6; p = 0.0043). No statistically significant differences in conduction times or in the proportion with inducible AF were observed.
Acute exposure to alcohol reduces AERP, particularly in the pulmonary veins. These data demonstrate a direct mechanistic link between alcohol, a common lifestyle exposure, and immediate proarrhythmic effects in human atria. (How Alcohol Induces Atrial Tachyarrhythmias Study [HOLIDAY]; NCT01996943).
本研究旨在确定酒精暴露期间人类心房电生理学的急性变化。
孤立性房颤(AF)发作的机制尚不清楚。酒精似乎会增加房颤风险,这为研究可能使心脏易患心律失常的电生理效应提供了机会。
在这项随机、双盲、安慰剂对照试验中,将静脉输注酒精使血酒精浓度达到0.08%的情况与在接受房颤消融手术的患者中输注体积和渗透压匹配的、隐蔽的安慰剂进行比较。在输注前后测量右心房、左心房和肺静脉心房有效不应期(AERPs)及传导时间。使用异丙肾上腺素输注和心房猝发起搏来评估房颤的诱发率。
100名参与者(每组50名)中,安慰剂组患者更可能患有糖尿病(22%对4%;p = 0.007)且曾接受过房颤消融术(36%对22%;p = 0.005)。酒精组肺静脉AERPs平均降低12毫秒(95%置信区间:1至22毫秒;p = 0.026),而安慰剂组无变化(p = 0.98)。虽然在连续评估的AERPs中未观察到统计学上的显著差异,但经酒精处理后AERP检测部位减少的比例(中位数:0.5;四分位间距:0.6至0.6)大于安慰剂组(中位数:0.4;四分位间距:0.2至0.6;p = 0.0043)。在传导时间或可诱发房颤的比例方面未观察到统计学上的显著差异。
急性酒精暴露会降低AERP,尤其是在肺静脉。这些数据表明,酒精这种常见的生活方式暴露与人类心房立即出现的促心律失常效应之间存在直接的机制联系。(酒精如何诱发房性快速性心律失常研究[HOLIDAY];NCT01996943)