{"title":"Mechanisms of U-Shaped Association between Alcohol Intake and the Risk of Sudden Cardiac Death","authors":"Karagueuzian Hs, Demirdjian L","doi":"10.16966/2379-769X.149","DOIUrl":null,"url":null,"abstract":"Large cohort epidemiological studies have shown a U-shaped association between the relative risk of Sudden Cardiac Death (SCD) and the dose of alcohol consumed across both genders. The mechanisms of this relationship, i.e., too little or too high promoting SCD while moderate doses providing protection, remain elusive. In this brief review, we provide plausible electrophysiological and biochemical mechanisms of the U-shaped association of the dose of alcohol and the risk of SCD. At moderate doses alcohol causes partial cellular uncoupling “paradoxically” improves the conduction at narrow ventricular conducting pathways (source) that adjoins a large tissue mass (sink) eliminating preexisting Unidirectional Conduction (UCB) (from source-to-sink) and preventing re-entry formation. In contrast, higher doses of alcohol by further increasing cellular uncoupling cause conduction block at multiple ventricular sites (wavebreaks) in isolated tissues and patterned monolayers of cardiac myocytes leading to the formation of multiple reentrant and non-reentrant wave fronts simulating fibrillation-like state. In the absence of alcohol, the vulnerable narrow conducting pathways remain unchanged promoting UCB (i.e., conduction block from source-to-sink block) increasing the risk of reentry formation. Re-entry leads to Ventricular Fibrillation (VF), a major cause of SCD. Our hypothesis of U-shaped association between alcohol dose and SCD is based on the preponderance of clinical epidemiological data and on basic experimental studies using intact animal hearts and patterned monolayers of cardiac myocytes with vulnerable narrow strands of conducting pathways (source) abutting to a large tissue mass (sink). in 12 ounces of regular beer (~5% per volume alcohol), in five ounces of wine (~12% per volume alcohol) and 1.5 ounces of spirits (~40% alcohol). Therefore, up to 15 g/day is considered “light-to-moderate,” and greater than 30 g/day is considered “high” [3,4]. The potential benefits of light-to-moderate doses of alcohol consumption, however, has not received universal acceptance. A recent systematic review of epidemiological data by The Global Burden of Disease Study by Alcohol Collaborators challenged the health benefits of light-to-moderate levels of alcohol consumption. This meta-analysis concluded that the level of alcohol consumption that minimized harm “across all health outcomes particularly the risk of cancer, was zero” [10]. This seeming controversy stems from the fact that certain diseases like Atrial Fibrillation (AF), stroke, [11] hypertension, heart failure, cardiomyopathy, cancer, and liver disease do not manifest any benefit from alcohol, [5,12,13] while other diseases do. The potential mechanisms of the observed benefits of low-to-moderate alcohol consumption in CAD and SCD remain undefined because the observed epidemiologic data are associative and not causative, providing no mechanistic insight by which alcohol causes it’s beneficial or its ill effects. Since the questions that motivate Introduction It has long been recognized that acute alcohol intoxication can cause death from accidents or violence and that long-term misuse can increase the incidence of certain kinds of cancer and multi-organ diseases affecting the heart and the liver. According to a 2014 report prepared by the World Health Organization, Global Status Report on Alcohol and Health, an alcohol attributable death occurs every 10 seconds. Yet, increasing evidence suggests that regular consumption of light-to-moderate amounts of alcohol (i.e., one to one and one half standard units) can reduce the risk of Ischemic Heart Disease (IHD) and Sudden Cardiac Death (SCD) [1-6]. These same studies uniformly reported that higher doses of chronic alcohol consumption (>3 standard units) cancel the beneficial cardiac effects of the lower doses of alcohol, promoting Coronary Artery Disease (CAD), SCD, cardiomyopathy, hypertension, and heart failure [7,8]. Cardiac and multi-organ diseases induced by chronic higher doses (>3 units) of alcohol consumption result in an average of 22 years of reduction in life expectancy compared to the general population [9]. According to the National Institute on Alcohol Abuse and Alcoholism, one U.S. “standard” drink contains ~15 grams of pure alcohol, which is found http://dx.doi.org/10.16966/2379-769X.149","PeriodicalId":91746,"journal":{"name":"Journal of heart health","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of heart health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.16966/2379-769X.149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Large cohort epidemiological studies have shown a U-shaped association between the relative risk of Sudden Cardiac Death (SCD) and the dose of alcohol consumed across both genders. The mechanisms of this relationship, i.e., too little or too high promoting SCD while moderate doses providing protection, remain elusive. In this brief review, we provide plausible electrophysiological and biochemical mechanisms of the U-shaped association of the dose of alcohol and the risk of SCD. At moderate doses alcohol causes partial cellular uncoupling “paradoxically” improves the conduction at narrow ventricular conducting pathways (source) that adjoins a large tissue mass (sink) eliminating preexisting Unidirectional Conduction (UCB) (from source-to-sink) and preventing re-entry formation. In contrast, higher doses of alcohol by further increasing cellular uncoupling cause conduction block at multiple ventricular sites (wavebreaks) in isolated tissues and patterned monolayers of cardiac myocytes leading to the formation of multiple reentrant and non-reentrant wave fronts simulating fibrillation-like state. In the absence of alcohol, the vulnerable narrow conducting pathways remain unchanged promoting UCB (i.e., conduction block from source-to-sink block) increasing the risk of reentry formation. Re-entry leads to Ventricular Fibrillation (VF), a major cause of SCD. Our hypothesis of U-shaped association between alcohol dose and SCD is based on the preponderance of clinical epidemiological data and on basic experimental studies using intact animal hearts and patterned monolayers of cardiac myocytes with vulnerable narrow strands of conducting pathways (source) abutting to a large tissue mass (sink). in 12 ounces of regular beer (~5% per volume alcohol), in five ounces of wine (~12% per volume alcohol) and 1.5 ounces of spirits (~40% alcohol). Therefore, up to 15 g/day is considered “light-to-moderate,” and greater than 30 g/day is considered “high” [3,4]. The potential benefits of light-to-moderate doses of alcohol consumption, however, has not received universal acceptance. A recent systematic review of epidemiological data by The Global Burden of Disease Study by Alcohol Collaborators challenged the health benefits of light-to-moderate levels of alcohol consumption. This meta-analysis concluded that the level of alcohol consumption that minimized harm “across all health outcomes particularly the risk of cancer, was zero” [10]. This seeming controversy stems from the fact that certain diseases like Atrial Fibrillation (AF), stroke, [11] hypertension, heart failure, cardiomyopathy, cancer, and liver disease do not manifest any benefit from alcohol, [5,12,13] while other diseases do. The potential mechanisms of the observed benefits of low-to-moderate alcohol consumption in CAD and SCD remain undefined because the observed epidemiologic data are associative and not causative, providing no mechanistic insight by which alcohol causes it’s beneficial or its ill effects. Since the questions that motivate Introduction It has long been recognized that acute alcohol intoxication can cause death from accidents or violence and that long-term misuse can increase the incidence of certain kinds of cancer and multi-organ diseases affecting the heart and the liver. According to a 2014 report prepared by the World Health Organization, Global Status Report on Alcohol and Health, an alcohol attributable death occurs every 10 seconds. Yet, increasing evidence suggests that regular consumption of light-to-moderate amounts of alcohol (i.e., one to one and one half standard units) can reduce the risk of Ischemic Heart Disease (IHD) and Sudden Cardiac Death (SCD) [1-6]. These same studies uniformly reported that higher doses of chronic alcohol consumption (>3 standard units) cancel the beneficial cardiac effects of the lower doses of alcohol, promoting Coronary Artery Disease (CAD), SCD, cardiomyopathy, hypertension, and heart failure [7,8]. Cardiac and multi-organ diseases induced by chronic higher doses (>3 units) of alcohol consumption result in an average of 22 years of reduction in life expectancy compared to the general population [9]. According to the National Institute on Alcohol Abuse and Alcoholism, one U.S. “standard” drink contains ~15 grams of pure alcohol, which is found http://dx.doi.org/10.16966/2379-769X.149