Moderate alcohol intake and lower risk of coronary heart disease: meta-analysis of effects on lipids and haemostatic factors

被引:1032
作者
Rimm, EB [1 ]
Williams, P
Fosher, K
Criqui, M
Stampfer, MJ
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[3] Univ Calif San Diego, San Diego Sch Med & Family & Prevent Med, La Jolla, CA 92093 USA
来源
BMJ-BRITISH MEDICAL JOURNAL | 1999年 / 319卷 / 7224期
关键词
D O I
10.1136/bmj.319.7224.1523
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective To summarise quantitatively the association between moderate alcohol intake and biological markers of risk of coronary heart disease and to predict how these changes would lower the risk. Design Meta-analysis of all experimental studies that assessed the effects of moderate alcohol intake on concentrations of high density lipoprotein cholesterol, apolipoprotein A I, fibrinogen, triglycerides, and other biological markers previously found to be associated with risk of coronary heart disease. Participants Men and woman free of previous chronic disease and who were not dependent on alcohol. Studies were included in which biomarkers were assessed before and after participants consumed up to 100 g of alcohol a dal: Interventions Alcohol as ethanol, beer, wine, or spirits. Main outcome measures Changes in concentrations of high density lipoprotein cholesterol, apolipoprotein A I, Lp(a) lipoprotein, triglycerides, tissue type plasminogen activator activity, tissue type plasminogen activator antigen, insulin, and glucose after consuming an experimental dose of alcohol for 1 to 9 weeks; a shelter period was accepted for studies of change in concentrations of fibrinogen, factor VIT, von Willebrand factor, tissue type plasminogen activator activity and tissue type plasminogen activator antigen. Results 61 data records were abstracted from 42 eligible studies with information on change in biological markers of risk of coronary heart disease. An experimental dose of 30 g of ethanol a day increased concentrations of high density lipoprotein cholesterol by 3.99 mg/dl (95% confidence interval 3.25 to 4.73), apolipoprotein A I by 8.82 mg/dl (7.79 to 9.86), and triglyceride by 5.69 mg/dl (2.49 to 8.89). Several haemostatic factors related to a thrombolytic profile were modestly affected by alcohol. On the basis of published associations between these biomarkers and risk of coronary heart disease 30 g of alcohol a day would cause an estimated reduction of 24.7% in risk of coronary heart disease. Conclusions Alcohol intake is causally related to lower risk of coronary heart disease through changes in lipids and. haemostatic factors.
引用
收藏
页码:1523 / 1528D
页数:10
相关论文
共 115 条
[1]
[Anonymous], STAT SCI
[2]
[Anonymous], 1989, REC DIET ALL
[3]
A PROSPECTIVE-STUDY OF NUTRITIONAL FACTORS AND HYPERTENSION AMONG UNITED-STATES MEN [J].
ASCHERIO, A ;
RIMM, EB ;
GIOVANNUCCI, EL ;
COLDITZ, GA ;
ROSNER, B ;
WILLETT, WC ;
SACKS, F ;
STAMPFER, MJ .
CIRCULATION, 1992, 86 (05) :1475-1484
[4]
PREPRANDIAL DRINKING AND PLASMA-LIPIDS IN MAN [J].
BARBORIAK, JJ ;
HOGAN, WJ .
ATHEROSCLEROSIS, 1976, 24 (1-2) :323-325
[5]
ALTERATIONS OF LIPID-METABOLISM IN HEALTHY VOLUNTEERS DURING LONG-TERM ETHANOL INTAKE [J].
BELFRAGE, P ;
BERG, B ;
HAGERSTRAND, I ;
NILSSONEHLE, P ;
TORNQVIST, H ;
WIEBE, T .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1977, 7 (02) :127-131
[6]
Belfrage P, 1973, Acta Med Scand Suppl, V552, P1
[7]
BERG B, 1973, ACTA MED SCAND, P13
[8]
TIME COURSE, MAGNITUDE AND NATURE OF THE CHANGES INDUCED IN HDL BY MODERATE ALCOHOL INTAKE IN YOUNG NON-DRINKING MALES [J].
BERTIERE, MC ;
BETOULLE, D ;
APFELBAUM, M ;
GIRARDGLOBA, A .
ATHEROSCLEROSIS, 1986, 61 (01) :7-14
[9]
Association of alcohol consumption with HDL subpopulations defined by apolipoprotein A-I and apolipoprotein A-II content [J].
Branchi, A ;
Rovellini, A ;
Tomella, C ;
Sciariada, L ;
Torri, A ;
Molgora, M ;
Sommariva, D .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 1997, 51 (06) :362-365
[10]
ALCOHOL AND HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL - A RANDOMIZED CONTROLLED TRIAL [J].
BURR, ML ;
FEHILY, AM ;
BUTLAND, BK ;
BOLTON, CH ;
EASTHAM, RD .
BRITISH JOURNAL OF NUTRITION, 1986, 56 (01) :81-86