CONFERENCE PROCEEDING
Effects of smoking cessation on HDL
functionality
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Department of Cardiology, School of Medicine, Fukuoka
University, Fukuoka, Japan
Publication date: 2019-10-12
Corresponding author
Emi Kawachi
Department of Cardiology, School of Medicine, Fukuoka
University, Fukuoka, Japan
Tob. Induc. Dis. 2019;17(Suppl 1):A42
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ABSTRACT
Objective:
Cigarette smoking is positively correlated with the morbidity
of cardiovascular diseases (CVD). It was reported that
reduced high density lipoprotein (HDL) functionality is one
of the causes of CVD. In this study, we hypothesized that
smoking cessation could lead to improved HDL functions,
and evaluated the cholesterol efflux capacity, antioxidative
capacity of HDL in participants before and after smoking
cessation.
Methods:
Thirty-two Japanese adult smokers aged were enrolled
for treatment at the Smoking Cessation Clinic of Fukuoka
University Hospital. Participants either received varenicline
for 12 weeks or wore a transdermal nicotine patch on
their chest for 8 weeks. Successful smoking cessation
was identified by both a self-assessment report and
the end-expiratory carbon monoxide (CO) concentration
(under 8ppm). Plasma lipid profiles, plasma and HDL
malondialdehyde (MDA) levels, HDL subfractions as
analyzed by capillary isotachophoresis, cholesterol efflux
capacity and antioxidative capacity of HDL were measured
before and after this intervention.
Results:
After smoking cessation, HDL-C, apoA-I levels and HDL
subfractions did not significantly change. Nevertheless,
cholesterol efflux capacity and the antioxidative capacity of
HDL were significantly improved in the successful smoking
cessation group. The extent of the changes in cholesterol
efflux capacity and antioxidative capacity of HDL correlated
with those in the end-expiratory CO concentration and
MDA in HDL, respectively.
Conclusions:
Our findings indicate that cigarette smoking impairs HDL
function and smoking cessation restores it. This may be
one of the mechanisms by which smoking cessation has
beneficial effects against CVD.
CITATIONS (1):
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