TY - JOUR
T1 - Alcohol consumption and risk of ventricular arrhythmias and sudden cardiac death
T2 - An observational study of 408,712 individuals
AU - Tu, Samuel J.
AU - Gallagher, Celine
AU - Elliott, Adrian D.
AU - Linz, Dominik
AU - Pitman, Bradley M.
AU - Hendriks, Jeroen M.L.
AU - Lau, Dennis H.
AU - Sanders, Prashanthan
AU - Wong, Christopher X.
N1 - Funding Information:
Funding Sources: This research has been conducted using the UK Biobank Resource under application number 62306. Dr Gallagher is supported by a Postdoctoral Fellowship from the University of Adelaide. Dr Elliott is supported by an Early Career Fellowship from the National Heart Foundation of Australia. Dr Linz is supported by the Beacon Research Fellowship from the University of Adelaide. Bradley M. Pitman is supported by a Postgraduate Scholarship from the Hospital Research Foundation. Dr Hendriks is supported by an Early Career Fellowship from the National Heart Foundation of Australia and the Derek Frewin Lectureship from the University of Adelaide. Dr Lau is supported by the Robert J. Craig Lectureship from the University of Adelaide. Dr Sanders is supported by a Practitioner Fellowship from the National Health and Medical Research Council of Australia and by the National Heart Foundation of Australia. Dr Wong is supported by a Mid-Career Fellowship from the Hospital Research Foundation and a Postdoctoral Fellowship from the National Heart Foundation of Australia.
Funding Information:
Funding Sources: This research has been conducted using the UK Biobank Resource under application number 62306. Dr Gallagher is supported by a Postdoctoral Fellowship from the University of Adelaide. Dr Elliott is supported by an Early Career Fellowship from the National Heart Foundation of Australia. Dr Linz is supported by the Beacon Research Fellowship from the University of Adelaide. Bradley M. Pitman is supported by a Postgraduate Scholarship from the Hospital Research Foundation. Dr Hendriks is supported by an Early Career Fellowship from the National Heart Foundation of Australia and the Derek Frewin Lectureship from the University of Adelaide. Dr Lau is supported by the Robert J. Craig Lectureship from the University of Adelaide. Dr Sanders is supported by a Practitioner Fellowship from the National Health and Medical Research Council of Australia and by the National Heart Foundation of Australia. Dr Wong is supported by a Mid-Career Fellowship from the Hospital Research Foundation and a Postdoctoral Fellowship from the National Heart Foundation of Australia. Disclosures: Dr Hendriks reports that the University of Adelaide has received on his behalf lecture and/or consulting fees from Medtronic and Pfizer/BMS. Dr Lau reports the University of Adelaide has received on his behalf lecture and/or consulting fees from Abbott Medical, Bayer, Biotronik, Boehringer Ingelheim, Medtronic, MicroPort, and Pfizer/BMS. Dr Sanders reports having served on the advisory board of Medtronic, Abbott Medical, Boston Scientific, CathRx, and PaceMate; reports that the University of Adelaide has received on his behalf lecture and/or consulting fees from Medtronic, Abbott Medical, and Boston Scientific; and reports that the University of Adelaide has received on his behalf research funding from Medtronic, Abbott Medical, Boston Scientific, and MicroPort. Dr Wong reports that the University of Adelaide has received on his behalf lecture, travel, and/or research funding from Abbott Medical, Bayer, Boehringer Ingelheim, Medtronic, Novartis, Servier, St. Jude Medical, and Vifor Pharma. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Publisher Copyright:
© 2021 Heart Rhythm Society
PY - 2022/2
Y1 - 2022/2
N2 - Background: Although previous studies have demonstrated a U-shaped relationship between alcohol and sudden cardiac death (SCD), there is a paucity of evidence on the role of alcohol specifically on incident ventricular arrhythmias (VAs). Objective: The purpose of this study was to characterize associations of total and beverage-specific alcohol consumption with incident VA and SCD using data from the UK Biobank. Methods: Alcohol consumption reported at baseline was calculated as UK standard drinks (8 g of alcohol) per week. Outcomes were assessed through hospitalization and death records. Alcohol consumption was modeled as restricted cubic splines in multivariate Cox regression models and corrected for regression dilution bias. Results: We studied 408,712 middle-aged individuals (52.1% female) over a median follow-up time of 11.5 years. A total of 1733 incident VA events and 2044 SCDs occurred. For incident VA, no clear association was seen with total alcohol consumption. Although consumption of greater amounts of spirits was associated with increased VA risk, no other significant beverage-specific associations were observed. For SCD, a U-shaped association was seen for total alcohol consumption, such that consumption of <26 drinks per week was associated with lowest risk. Consumption of greater amounts of beer, cider, and spirits was potentially associated with increasing SCD risk, whereas increasing red and white wine intake was associated with reduced risk. Conclusion: In this predominantly white cohort, no association of total alcohol consumption was observed with VA, whereas a U-shaped association was present for SCD. Additional studies utilizing accurately defined VA and SCD events are required to provide further insights into these contrasting findings.
AB - Background: Although previous studies have demonstrated a U-shaped relationship between alcohol and sudden cardiac death (SCD), there is a paucity of evidence on the role of alcohol specifically on incident ventricular arrhythmias (VAs). Objective: The purpose of this study was to characterize associations of total and beverage-specific alcohol consumption with incident VA and SCD using data from the UK Biobank. Methods: Alcohol consumption reported at baseline was calculated as UK standard drinks (8 g of alcohol) per week. Outcomes were assessed through hospitalization and death records. Alcohol consumption was modeled as restricted cubic splines in multivariate Cox regression models and corrected for regression dilution bias. Results: We studied 408,712 middle-aged individuals (52.1% female) over a median follow-up time of 11.5 years. A total of 1733 incident VA events and 2044 SCDs occurred. For incident VA, no clear association was seen with total alcohol consumption. Although consumption of greater amounts of spirits was associated with increased VA risk, no other significant beverage-specific associations were observed. For SCD, a U-shaped association was seen for total alcohol consumption, such that consumption of <26 drinks per week was associated with lowest risk. Consumption of greater amounts of beer, cider, and spirits was potentially associated with increasing SCD risk, whereas increasing red and white wine intake was associated with reduced risk. Conclusion: In this predominantly white cohort, no association of total alcohol consumption was observed with VA, whereas a U-shaped association was present for SCD. Additional studies utilizing accurately defined VA and SCD events are required to provide further insights into these contrasting findings.
KW - Alcohol
KW - Beer
KW - Cardiac arrest
KW - Spirits
KW - Sudden death
KW - Ventricular arrhythmia
KW - Wine
UR - http://www.scopus.com/inward/record.url?scp=85122838789&partnerID=8YFLogxK
U2 - 10.1016/j.hrthm.2021.09.040
DO - 10.1016/j.hrthm.2021.09.040
M3 - Article
C2 - 35101186
AN - SCOPUS:85122838789
SN - 1547-5271
VL - 19
SP - 177
EP - 184
JO - Heart Rhythm
JF - Heart Rhythm
IS - 2
ER -