TY - JOUR
T1 - The Relationship of Alcohol Consumption and HDL Metabolism in the Multiethnic Dallas Heart Study
AU - Badia, Rohit R.
AU - Pradhan, Roma V.
AU - Ayers, Colby R.
AU - Chandra, Alvin
AU - Rohatgi, Anand
N1 - Funding Information:
None. The views expressed in this manuscript are those of the authors and do not necessarily represent the views of the National Heart, Lung, and Blood Institute; the National Institutes of Health; or the U.S. Department of Health and Human Services. Supported by the Donald W. Reynolds Foundation (Las Vegas, NV), and by United States Public Health Service General Clinical Research Center (USPHS GCRC) grant #M01-RR00633 from National Institutes of Health/National Center for Research Resources-Clinical Research. A. Rohatgi: supported by NIH/NHLBI R01HL136724 and NIH/NHLBI K24HL146838. NMR particle data provided by LabCorp (previously LipoScience); Raleigh, NC. This research was supported by contracts HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168 and N01-HC-95169 from the National Heart, Lung, and Blood Institute, and by grants UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420 from the National Center for Advancing Translational Sciences (NCATS).
Funding Information:
Supported by the Donald W. Reynolds Foundation (Las Vegas, NV), and by United States Public Health Service General Clinical Research Center (USPHS GCRC) grant #M01- RR00633 from National Institutes of Health/National Center for Research Resources-Clinical Research .
Funding Information:
This research was supported by contracts HHSN268201500003I , N01-HC-95159, N01-HC- 95160 , N01-HC- 95161 , N01-HC- 95162 , N01-HC- 95163 , N01-HC- 95164 , N01-HC- 95165 , N01-HC- 95166 , N01-HC- 95167 , N01-HC-95168 and N01-HC-95169 from the National Heart, Lung, and Blood Institute, and by grants UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420 from the National Center for Advancing Translational Sciences (NCATS).
Publisher Copyright:
© 2022
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background: Small studies have suggested that moderate alcohol consumption increases HDL cholesterol (HDL-C) levels and cholesterol efflux capacity (CEC), a main anti-atherosclerotic HDL function. Objectives: This study aimed to understand the degree to which alcohol intake is associated with various HDL markers in a large, multiethnic population cohort, the Dallas Heart Study (DHS), and whether alcohol modifies the link between HDL markers and atherosclerotic cardiovascular disease (ASCVD). Methods: Participants of the DHS were included if they had self-reported alcohol intake and CEC measurements (N=2,919). Alcohol intake was analyzed continuously (grams/week) and as an ordered categorical variable (never, past, light, moderate, heavy, and binge drinkers). HDL-C, CEC, HDL particle number (HDL-P), HDL particle size (HDL-size), and ApoA-I were the primary HDL measures. Results: After adjustment for confounding variables, increasing continuous measure of alcohol intake was associated with increased levels of all HDL markers. Moreover, as compared to moderate drinkers, light drinkers had decreased levels of the HDL markers. Conclusion: In a large, multiethnic cohort, increased alcohol intake was associated with increased levels of multiple markers of HDL metabolism. However, the association of HDL markers with ASCVD risk as modified by alcohol consumption is unable to be determined in this low-risk cohort.
AB - Background: Small studies have suggested that moderate alcohol consumption increases HDL cholesterol (HDL-C) levels and cholesterol efflux capacity (CEC), a main anti-atherosclerotic HDL function. Objectives: This study aimed to understand the degree to which alcohol intake is associated with various HDL markers in a large, multiethnic population cohort, the Dallas Heart Study (DHS), and whether alcohol modifies the link between HDL markers and atherosclerotic cardiovascular disease (ASCVD). Methods: Participants of the DHS were included if they had self-reported alcohol intake and CEC measurements (N=2,919). Alcohol intake was analyzed continuously (grams/week) and as an ordered categorical variable (never, past, light, moderate, heavy, and binge drinkers). HDL-C, CEC, HDL particle number (HDL-P), HDL particle size (HDL-size), and ApoA-I were the primary HDL measures. Results: After adjustment for confounding variables, increasing continuous measure of alcohol intake was associated with increased levels of all HDL markers. Moreover, as compared to moderate drinkers, light drinkers had decreased levels of the HDL markers. Conclusion: In a large, multiethnic cohort, increased alcohol intake was associated with increased levels of multiple markers of HDL metabolism. However, the association of HDL markers with ASCVD risk as modified by alcohol consumption is unable to be determined in this low-risk cohort.
KW - Alcohol
KW - Cardiovascular disease
KW - Cholesterol efflux
KW - Dallas Heart Study
KW - HDL markers
KW - Humans
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U2 - 10.1016/j.jacl.2022.10.008
DO - 10.1016/j.jacl.2022.10.008
M3 - Article
C2 - 36464598
AN - SCOPUS:85143290464
SN - 1933-2874
VL - 17
SP - 124
EP - 130
JO - Journal of Clinical Lipidology
JF - Journal of Clinical Lipidology
IS - 1
ER -