Department of Physiology, University of Louisville, Louisville, KY, USA.
Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.
Cardiovasc Toxicol. 2021 Feb;21(2):169-178. doi: 10.1007/s12012-020-09610-5. Epub 2020 Oct 12.
Smoking is associated with cardiac arrhythmia, stroke, heart failure, and sudden cardiac arrest, all of which may derive from increased sympathetic influence on cardiac conduction system and altered ventricular repolarization. However, knowledge of the effects of smoking on supraventricular conduction, and the role of the sympathetic nervous system in them, remains incomplete. Participants with intermediate-high cardiovascular disease risk were measured for urinary catecholamines and cotinine, and 12-lead electrocardiograms (ECGs) were measured for atrial and atrioventricular conduction times, including P duration, PR interval, and PR segment (lead II), which were analyzed for associations with cotinine by generalized linear models. Statistical mediation analyses were then used to test whether any significant associations between cotinine and atrioventricular conduction were mediated by catecholamines. ECG endpoints and urinary metabolites were included from a total of 136 participants in sinus rhythm. Atrial and atrioventricular conduction did not significantly differ between smokers (n = 53) and non-smokers (n = 83). Unadjusted and model-adjusted linear regressions revealed cotinine significantly and inversely associated with PR interval and PR segment, but not P duration. Dopamine, norepinephrine, and epinephrine all inversely associated with PR interval, whereas only dopamine was also inversely associated with PR segment (p < 0.05). Dopamine and norepinephrine (but not epinephrine) also associated positively with cotinine. Dopamine mediated the relationship between cotinine and PR interval, as well as the relationship between cotinine and PR segment. Smoking is associated with accelerated atrioventricular conduction and elevated urinary dopamine and norepinephrine. Smoking may accelerate atrioventricular nodal conduction via increased dopamine production.
吸烟与心律失常、中风、心力衰竭和心源性猝死有关,所有这些都可能源于心脏传导系统交感神经影响增加和心室复极改变。然而,关于吸烟对窦上性传导的影响以及交感神经系统在其中的作用,人们的认识仍然不完整。对具有中高度心血管疾病风险的参与者进行尿儿茶酚胺和可替宁检测,并对 12 导联心电图(ECG)进行心房和房室传导时间测量,包括 P 波持续时间、PR 间期和 PR 段(导联 II),并通过广义线性模型分析可替宁与它们的相关性。然后,使用统计中介分析来测试可替宁与房室传导之间的任何显著相关性是否通过儿茶酚胺介导。来自窦性节律的总共 136 名参与者的 ECG 终点和尿代谢物都包含在内。吸烟者(n=53)和不吸烟者(n=83)之间的心房和房室传导没有显著差异。未调整和模型调整的线性回归显示,可替宁与 PR 间期和 PR 段呈显著负相关,但与 P 波持续时间无关。多巴胺、去甲肾上腺素和肾上腺素均与 PR 间期呈负相关,而只有多巴胺与 PR 段也呈负相关(p<0.05)。多巴胺和去甲肾上腺素(但不是肾上腺素)也与可替宁呈正相关。多巴胺介导了可替宁与 PR 间期之间的关系,以及可替宁与 PR 段之间的关系。吸烟与房室结传导加速和尿液多巴胺和去甲肾上腺素升高有关。吸烟可能通过增加多巴胺的产生来加速房室结的传导。