Key result
Moderate alcohol intake is linked to lower coagulatory factors, while heavy drinking impairs fibrinolysis.
Why the study?
Previous studies on the effect of alcohol consumption on hemostatic parameters have provided conflicting results regarding cardiovascular disease risk.
Does alcohol consumption alter hemostatic and fibrinolytic factors in adults free of cardiovascular disease?
Cross-Sectional (n=3,223)
Does alcohol consumption alter hemostatic and fibrinolytic factors in adults free of cardiovascular disease?
Light-to-moderate alcohol consumption is associated with a favorable profile of coagulatory factors, whereas higher intake impairs fibrinolytic potential, suggesting a complex dose-dependent effect on hemostasis.
Should not alter clinical alcohol guidance; leaves open whether hemostatic associations causally reduce cardiovascular events.
BACKGROUND: Moderate alcohol consumers have lower rates of cardiovascular disease than abstainers. One proposed mechanism is a beneficial effect on hemostatic parameters, but previous studies have provided conflicting results. METHODS AND RESULTS: We measured levels of fibrinogen, plasma viscosity, von Willebrand factor, factor VII, plasminogen activator inhibitor antigen-1, and tissue plasminogen activator antigen in a cross-sectional analysis of 3223 adults free of cardiovascular disease enrolled in the Framingham Offspring Study. We assessed their alcohol consumption with a standardized questionnaire. Light-to-moderate alcohol consumption was associated with lower levels of fibrinogen, plasma viscosity, von Willebrand factor, and factor VII. This association was most pronounced for consumers of 3 to 7 drinks weekly for viscosity and 7 to 21 drinks weekly for the other hemostatic measures. Alcohol intake of 7 to 21 drinks weekly or more was associated with impaired fibrinolytic potential, reflected by higher levels of plasminogen activator inhibitor antigen-1 and tissue plasminogen activator antigen. Wine drinkers had lower plasminogen activator inhibitor antigen-1 levels than other drinkers, particularly at 3 to 21 drinks weekly, but beverage type did not otherwise consistently affect the results. CONCLUSIONS: Light-to-moderate alcohol consumption is associated with lower levels of coagulatory factors, but higher intake is associated with impaired fibrinolytic potential. These findings are consistent with the hypothesis that a balance between hemostatic and fibrinolytic activity may contribute to the complex relation of alcohol use with coronary heart disease.
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Mukamal et al. (2001) conducted a cross-sectional in Healthy (free of cardiovascular disease) (n=3,223). Alcohol consumption vs. Abstainers or other drinking categories was evaluated on Levels of hemostatic factors (fibrinogen, plasma viscosity, von Willebrand factor, factor VII, plasminogen activator inhibitor antigen-1, and tissue plasminogen activator antigen). Light-to-moderate alcohol consumption (3 to 21 drinks weekly) was associated with lower coagulatory factors, while higher intake was associated with impaired fibrinolytic potential.
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