The effects of different alcoholic drinks on lipids, insulin and haemostatic and inflammatory markers in older men

被引:53
作者
Wannamethee, SG
Lowe, GDO
Shaper, G
Whincup, PH
Rumley, A
Walker, M
Lennon, L
机构
[1] UCL Royal Free & Univ Coll Med Sch, Dept Primary Care & Populat Sci, London NW3 2PF, England
[2] Univ Glasgow, Royal Infirm, Dept Med, Glasgow, Lanark, Scotland
[3] St Georges Med Sch Hosp, Dept Publ Hlth Sci, London, England
关键词
alcohol intake; haemostasis; insulin; lipids;
D O I
10.1160/TH03-04-0221
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Light to moderate drinking is associated with lower risk of coronary heart (CHD) than non-drinkers. We have examined the relationships between total alcohol intake and type of alcoholic beverage and several potential biological mechanisms. We carried out the study in 3158 men aged 60-79 years drawn from general practices in 24 British towns with no history of myocardial infarction, stroke or diabetes and who were not on warfarin. Total alcohol consumption showed a significant positive dose-response relationship with high density lipoprotein cholesterol (HDL-C), coagulation factor IX, haematocrit, blood viscosity, and tissue plasminogen (t-PA) antigen, and an inverse dose-response relationship with insulin, fibrinogen, von Wille- brand factor (vWF) and triglycerides after adjustment for possible confounders. Total alcohol consumption showed weak associations with plasma viscosity and fibrin D-dimer, and no association with factors VII,VIII, or C-reactive protein (CRP). Wine was specifically associated with lower CRP, plasma viscosity, factor VIII and triglycerides. The findings are consistent with the suggestion that HDL-C in particular but also insulin and haemostatic factors may contribute to the beneficial effect of light to moderate drinking on risk of CHD. Wine has effects that may confer greater protection than other alcoholic beverages.
引用
收藏
页码:1080 / 1087
页数:8
相关论文
共 36 条
[1]  
ANDERSEN L, 1993, CLIN CHEM, V39, P578
[2]   Alcoholic beverage preference, diet, and health habits in the UNC Alumni Heart Study [J].
Barefoot, JC ;
Gronbæk, M ;
Feaganes, JR ;
McPherson, RS ;
Williams, RB ;
Siegler, IC .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 76 (02) :466-472
[3]   Haematocrit, viscosity, erythrocyte sedimentation rate: meta-analyses of prospective studies of coronary heart disease [J].
Danesh, J ;
Collins, R ;
Peto, R ;
Lowe, GDO .
EUROPEAN HEART JOURNAL, 2000, 21 (07) :515-520
[4]   Association of fibrinogen, C-reactive protein, albumin, or leukocyte count with coronary heart disease - Meta-analyses of prospective studies [J].
Danesh, J ;
Collins, R ;
Appleby, P ;
Peto, R .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (18) :1477-1482
[5]   Meta-analysis of wine and beer consumption in relation to vascular risk [J].
Di Castelnuovo, A ;
Rotondo, S ;
Iacoviello, L ;
Donati, MB ;
de Gaetano, G .
CIRCULATION, 2002, 105 (24) :2836-2844
[6]   Biochemical measures in a population-based study: effect of fasting duration and time of day [J].
Emberson, JR ;
Whincup, PH ;
Walker, M ;
Thomas, M ;
Alberti, KGMM .
ANNALS OF CLINICAL BIOCHEMISTRY, 2002, 39 :493-501
[7]   Type of alcoholic beverage and risk of myocardial infarction [J].
Gaziano, JM ;
Hennekens, CH ;
Godfried, SL ;
Sesso, HD ;
Glynn, RJ ;
Breslow, JL ;
Buring, JE .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 83 (01) :52-57
[8]   MODERATE ALCOHOL INTAKE, INCREASED LEVELS OF HIGH-DENSITY-LIPOPROTEIN AND ITS SUBFRACTIONS, AND DECREASED RISK OF MYOCARDIAL-INFARCTION [J].
GAZIANO, JM ;
BURING, JE ;
BRESLOW, JL ;
GOLDHABER, SZ ;
ROSNER, B ;
VANDENBURGH, M ;
WILLETT, W ;
HENNEKENS, CH .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (25) :1829-1834
[9]  
Goldberg IJ, 2001, CIRCULATION, V103, P472
[10]   Effect of alcohol consumption on systemic markers of inflammation [J].
Imhof, A ;
Froehlich, M ;
Brenner, H ;
Boeing, H ;
Pepys, MB ;
Koenig, W .
LANCET, 2001, 357 (9258) :763-767