PREDICTION OF THE THERAPEUTIC RESPONSE TO SIMVASTATIN BY PRETREATMENT LIPID CONCENTRATIONS IN 2082 SUBJECTS

被引:3
作者
MISEREZ, AR
ROSSI, FA
KELLER, U
机构
[1] UNIV BASEL HOSP, DEPT INTERNAL MED, CH-4031 BASEL, SWITZERLAND
[2] BRUNNER & HESS SOFTWARE STAT ANAL, ZURICH, SWITZERLAND
关键词
HYPERCHOLESTEROLEMIA; SIMVASTATIN; LOW DENSITY LIPOPROTEIN; HIGH DENSITY LIPOPROTEIN; TRIGLYCERIDES; HMG-COA-REDUCTASE INHIBITORS; ADVERSE EFFECTS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
2082 hypercholesterolemic subjects were treated with simvastatin for 12 weeks. In 530 patients the dose was increased after 6 weeks from 10 to 20 mg because of persistently high cholesterol concentrations. Total cholesterol (TC) in the 1552 patients taking 10 mg fell by 1.61 mmol.l(-1) (18.4%), LDL cholesterol (LDLC) by 1.53 mmol.l(-1) (25.2%), and triglycerides (TG) by 0.13 mmol.l(-1) (5.5%); HDL cholesterol (HDLC) significantly increased by 0.05 mmol.l(-1) (3.6%). In the 530 patients taking 20mg TC fell by 1.89 mmol.l(-1) (19.9%), LDLC by 1.78 mmol.l(-1) (26.0%), and TG by 0.13 mmol.l(-1) (5.5%); HDLC increased by 0.05 mmol.l(-1) (3.7%). The reductions in TC, LDLC, and TG were positively correlated and the increase in HDLC negatively correlated with their respective baseline values. There were independent significant correlations of the fall in LDLC with sex (MANOVA), baseline TG, and adherence to a lipid-lowering diet. The falls in TG significantly correlated with baseline fructosamine concentrations and dietary adherence. There were 571 adverse events in 16.6% of the patients but no case of myopathy. These results show that simvastatin is usually well tolerated and that its effects on TC and LDLC depend on their baseline concentrations.
引用
收藏
页码:107 / 114
页数:8
相关论文
共 38 条
[1]  
ARMBRUSTER DA, 1987, CLIN CHEM, V33, P2153
[2]   INHIBITORS OF HYDROXYMETHYLGLUTARYL COENZYME-A REDUCTASE FOR TREATING HYPERCHOLESTEROLEMIA [J].
BARTH, JD ;
KRUISBRINK, OAE ;
VANDIJK, AL .
BRITISH MEDICAL JOURNAL, 1990, 301 (6753) :669-669
[3]   LONG-TERM CLINICAL TOLERANCE OF LOVASTATIN AND SIMVASTATIN [J].
BILHEIMER, DW .
CARDIOLOGY, 1990, 77 :58-65
[4]   EXPANDED CLINICAL-EVALUATION OF LOVASTATIN (EXCEL) STUDY RESULTS .1. EFFICACY IN MODIFYING PLASMA-LIPOPROTEINS AND ADVERSE EVENT PROFILE IN 8245 PATIENTS WITH MODERATE HYPERCHOLESTEROLEMIA [J].
BRADFORD, RH ;
SHEAR, CL ;
CHREMOS, AN ;
DUJOVNE, C ;
DOWNTON, M ;
FRANKLIN, FA ;
GOULD, AL ;
HESNEY, M ;
HIGGINS, J ;
HURLEY, DP ;
LANGENDORFER, A ;
NASH, DT ;
POOL, JL ;
SCHNAPER, H .
ARCHIVES OF INTERNAL MEDICINE, 1991, 151 (01) :43-49
[5]  
BROCARD JJ, 1991, SCHWEIZ MED WSCHR, V121, P977
[6]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[7]  
BRUCKERT E, 1992, CLIN CHEM, V38, P1698
[8]  
CLEEMAN JI, 1988, ARCH INTERN MED, V148, P36, DOI 10.1001/archinte.148.1.36
[9]   SIMVASTATIN BUT NOT PRAVASTATIN INHIBITS THE PROLIFERATION OF RAT AORTA MYOCYTES [J].
CORSINI, A ;
RAITERI, M ;
SOMA, M ;
FUMAGALLI, R ;
PAOLETTI, R .
PHARMACOLOGICAL RESEARCH, 1991, 23 (02) :173-180
[10]   COMPARISON OF DIFFERENT HMG-COA REDUCTASE INHIBITORS [J].
DITSCHUNEIT, HH ;
KUHN, K ;
DITSCHUNEIT, H .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1991, 40 :S27-S32