Effect of low-dose alcohol use versus abstention on apolipoproteins A-I and B

Richard D. Moore, Craig R. Smith, Peter O. Kwiterovich, Thomas A. Pearson

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

An inverse association between low to moderate alcohol consumption and coronary heart disease has been demonstrated in epidemiologic studies of diverse design. An attempt was made to determine if this association might be due to an effect of alcohol on apolipoproteins A-I and B and to determine if low-dose alcohol intake might have a potentially protective effect by this mechanism in persons at increased risk for coronary heart disease. To address this, an eight-week prospective randomized clinical trial of abstention versus low-dose alcohol consumption, defined as one beverage per day, was conducted in white men, aged 21 to 60 years, most of whom were patients of a preventive cardiology program. Apolipoprotein A-I levels had a mean increase of 9 mg/dl in the 28 participants who drank alcohol compared with a mean decline of 5 mg/dl in the 28 participants who abstained (p <0.005). This association was independent of other cardiovascular risk factors. Low-density lipoprotein (LDL)-B levels had a mean increase of 7 mg/dl in both arms of the trial (NS). However, the ratio of apolipoprotein A-I to LDL-B increased by 4 percent in the drinkers and decreased 10 percent in the abstainers (p <0.03). No significant changes in mean levels of total high-density lipoprotein (HDL)-, HDL2-, or HDL3-cholesterol were observed with this low dose of alcohol. This effect on apolipoprotein A-I suggests a possible mechanism by which low-dose alcohol may lower the risk of coronary heart disease.

Original languageEnglish (US)
Pages (from-to)884-890
Number of pages7
JournalThe American journal of medicine
Volume84
Issue number5
DOIs
StatePublished - May 1988

ASJC Scopus subject areas

  • General Medicine

Fingerprint

Dive into the research topics of 'Effect of low-dose alcohol use versus abstention on apolipoproteins A-I and B'. Together they form a unique fingerprint.

Cite this