Effect of ω-3 fatty acids and simvastatin on hemostatic risk factors and postprandial hyperlipemia in patients with combined hyperlipemia

被引:80
作者
Nordoy, A
Bonaa, KH
Sandset, PM
Hansen, JB
Nilsen, H
机构
[1] Univ Tromso, Dept Med, Inst Clin Med, Tromso, Norway
[2] Univ Tromso, Inst Community Med, Tromso, Norway
[3] Univ Oslo, Ulleval Hosp, Dept Med, Oslo, Norway
关键词
combined hyperlipemia; postprandial hyperlipemia; hemostatic risk factors;
D O I
10.1161/01.ATV.20.1.259
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with combined hyperlipemia have lipid abnormalities associated with an increased tendency to develop atherosclerosis and thrombosis. This tendency may be accelerated during postprandial hyperlipemia, In the present double-blind parallel study, 41 patients with combined hyperlipemia and serum triacylglycerols between 2.0 and 15.0 mmol/L and serum total cholesterol >5.3 mmol/L at the end of a 3-month dietary run-in period were treated with simvastatin at 20 mg/d for at least 10 weeks; patients were then randomized into 2 groups receiving simvastatin + omega-3 fatty acids at 3.36 g/d or placebo (corn oil) for an additional 5 weeks. Hemostatic variables that have been associated with increased thrombotic tendency were evaluated with subjects in the fasting state and during postprandial hyperlipemia before and after combined treatment. Supplementation of omega-3 fatty acid reduced tissue factor pathway inhibitor antigen (P<0.05) in the fasting state, reduced the degree of postprandial hyperlipemia (P<0.005), and reduced activated factor VII concentration appearing during postprandial hyperlipemia, In conclusion, omega-3 fatty acids given in addition to simvastatin to patients with combined hyperlipemia reduced the free tissue factor pathway inhibitor fraction in the fasting state and inhibited the activation of factor VII occurring during postprandial lipemia, thus representing a potential beneficial effect on the hemostatic risk profile in this patient group.
引用
收藏
页码:259 / 265
页数:7
相关论文
共 44 条
[31]   ACTIVATION OF FACTOR-IX BY REACTION-PRODUCT OF TISSUE FACTOR AND FACTOR-VII-ADDITIONAL PATHWAY FOR INITIATING BLOOD-COAGULATION [J].
OSTERUD, B ;
RAPAPORT, SI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5260-5264
[32]  
PATSCH JR, 1983, P NATL ACAD SCI-BIOL, V80, P1449, DOI 10.1073/pnas.80.5.1449
[33]   RELATION OF TRIGLYCERIDE-METABOLISM AND CORONARY-ARTERY DISEASE - STUDIES IN THE POSTPRANDIAL STATE [J].
PATSCH, JR ;
MIESENBOCK, G ;
HOPFERWIESER, T ;
MUHLBERGER, V ;
KNAPP, E ;
DUNN, JK ;
GOTTO, AM ;
PATSCH, W .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (11) :1336-1345
[34]   A novel specific immunoassay for plasma two-chain factor VIIa: Investigation of FVIIa levels in normal individuals and in patients with acute coronary syndromes [J].
Philippou, H ;
Adami, A ;
Amersey, RA ;
Stubbs, PJ ;
Lane, DA .
BLOOD, 1997, 89 (03) :767-775
[35]  
RUDDOCK V, 1994, Q J MED, V87, P403
[36]   THE EFFECTS OF SATURATED FAT AND N-6 POLYUNSATURATED FAT ON POSTPRANDIAL LIPEMIA AND HEMOSTATIC ACTIVITY [J].
SALOMAA, V ;
RASI, V ;
PEKKANEN, J ;
JAUHIAINEN, M ;
VAHTERA, E ;
PIETINEN, P ;
KORHONEN, H ;
KUULASMAA, K ;
EHNHOLM, C .
ATHEROSCLEROSIS, 1993, 103 (01) :1-11
[37]   TREATMENT WITH HYDROXYMETHYLGLUTARYL-COENZYME-A REDUCTASE INHIBITORS IN HYPERCHOLESTEROLEMIA INDUCES CHANGES IN THE COMPONENTS OF THE EXTRINSIC COAGULATION SYSTEM [J].
SANDSET, PM ;
LUND, H ;
NORSETH, J ;
ABILDGAARD, U ;
OSE, L .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (01) :138-145
[38]  
SANDSET PM, 1991, HAEMOSTASIS, V21, P219
[39]   CHROMOGENIC SUBSTRATE ASSAY OF EXTRINSIC PATHWAY INHIBITOR (EPI) - LEVELS IN THE NORMAL POPULATION AND RELATION TO CHOLESTEROL [J].
SANDSET, PM ;
LARSEN, ML ;
ABILDGAARD, U ;
LINDAHL, AK ;
ODEGAARD, OR .
BLOOD COAGULATION & FIBRINOLYSIS, 1991, 2 (03) :425-433
[40]  
SAS, 1990, SAS STAT US GUID