The effect of atorvastatin on serum lipids, lipoproteins and NMR spectroscopy defined lipoprotein subclasses in type 2 diabetic patients with ischaemic heart disease

被引:77
作者
Soedamah-Muthu, SS
Colhoun, HM
Thomason, MJ
Betteridge, DJ
Durrington, PN
Hitman, GA
Fuller, JH
Julier, K
Mackness, MI
Neil, HAW
机构
[1] Royal Free & UCL, Sch Med, London, England
[2] Univ Coll & Middlesex Sch Med, London, England
[3] Univ Manchester, Manchester Royal Infirm, Dept Med, Manchester M13 9WL, Lancs, England
[4] Univ London, Barts & London Queen Marys Sch Med & Dent, London, England
[5] Univ Oxford, Oxford, England
关键词
lipoprotein subclasses; HMG-CoA reductase inhibitors; diabetes; NMR spectroscopy;
D O I
10.1016/S0021-9150(02)00428-8
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
The effect of statin therapy on subclasses of LDL, VLDL and HDL lipoproteins is unclear. We compared changes in serum lipids, apolipoproteins and nuclear magnetic resonance (NMR) spectroscopy measured lipoprotein subclass concentration and average particle size over a minimum 6 months treatment period of atorvastatin 10 mg vs. placebo in 122 men and women. All subjects had type 2 diabetes and a modest dyslipidaemia (mean LDL-cholesterol 3.2 mmol/l and median triglycerides 1.8 mmol/l) and had a previous myocardial infarction. Compared with placebo, atorvastatin therapy was associated with a greater decrease in medium VLDL (median within person change -13.4 vs. -5.9 nmol/l, P < 0.001 adjusted for baseline level), small VLDL (median change 17.8 vs. -8.1 nmol/l, P = 0.002), large LDL (mean within person change -167.9 vs. -48.6 nmol/l, P < 0.00 1) and medium LDL (median within person change -101.8 vs. -22.3 nmol/l, P = 0.017). Atorvastatin therapy was also associated with a greater increase in large HDL than placebo (median change 1.40 vs. 0.80 mumol/l, P = 0.02) and there was little change in small HDL so that average HDL particle size increased significantly with atorvastatin (P = 0.04). In addition to reducing levels of (enzymatically measured) triglyceride, LDL-cholesterol and apolipoprotein B in diabetic patients, atorvastatin significantly reduces NMR measured medium and small VLDL and large and medium LDL, and increases large HDL. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:243 / 255
页数:13
相关论文
共 54 条
[1]
AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
[2]
Efficacy and safety of a new HMG-CoA reductase inhibitor, atorvastatin, in patients with hypertriglyceridemia [J].
BakkerArkema, RG ;
Davidson, MH ;
Goldstein, RJ ;
Davignon, J ;
Isaacsohn, JL ;
Weiss, SR ;
Keilson, LM ;
Brown, WV ;
Miller, VT ;
Shurzinske, LJ ;
Black, DM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (02) :128-133
[3]
COMPARISON OF GEMFIBROZIL VERSUS SIMVASTATIN IN FAMILIAL COMBINED HYPERLIPIDEMIA AND EFFECTS ON APOLIPOPROTEIN-B-CONTAINING LIPOPROTEINS, LOW-DENSITY-LIPOPROTEIN SUBFRACTION PROFILE, AND LOW-DENSITY-LIPOPROTEIN OXIDIZABILITY [J].
BREDIE, SJH ;
DEBRUIN, TWA ;
DEMACKER, PNM ;
KASTELEIN, JJP ;
STALENHOEF, AFH .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (05) :348-353
[4]
Low-density lipoprotein size, pravastatin treatment, and coronary events [J].
Campos, H ;
Moye, LA ;
Glasser, SP ;
Stampfer, MJ ;
Sacks, FM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (12) :1468-1474
[5]
EFFECTS OF PRAVASTATIN ON APOLIPOPROTEIN-SPECIFIC HIGH-DENSITY-LIPOPROTEIN SUBPOPULATIONS AND LOW-DENSITY-LIPOPROTEIN SUBCLASS PHENOTYPES IN PATIENTS WITH PRIMARY HYPERCHOLESTEROLEMIA [J].
CHEUNG, MC ;
AUSTIN, MA ;
MOULIN, P ;
WOLF, AC ;
CRYER, D ;
KNOPP, RH .
ATHEROSCLEROSIS, 1993, 102 (01) :107-119
[6]
DEGRAAF J, 1993, NETH J MED, V43, P254
[7]
Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels - Results of AFCAPS/TexCAPS [J].
Downs, JR ;
Clearfield, M ;
Weis, S ;
Whitney, E ;
Shapiro, DR ;
Beere, PA ;
Langendorfer, A ;
Stein, EA ;
Kruyer, W ;
Gotto, AM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (20) :1615-1622
[8]
RELATION OF THE LEVEL OF HIGH-DENSITY-LIPOPROTEIN SUBFRACTIONS TO THE PRESENCE AND EXTENT OF CORONARY-ARTERY DISEASE [J].
DREXEL, H ;
AMANN, FW ;
RENTSCH, K ;
NEUENSCHWANDER, C ;
LUETHY, A ;
KHAN, SI ;
FOLLATH, F .
AMERICAN JOURNAL OF CARDIOLOGY, 1992, 70 (04) :436-440
[9]
PRAVASTATIN EFFECTIVELY LOWERS LDL CHOLESTEROL IN FAMILIAL COMBINED HYPERLIPIDEMIA WITHOUT CHANGING LDL SUBCLASS PATTERN [J].
FRANCESCHINI, G ;
CASSINOTTI, M ;
VECCHIO, G ;
GIANFRANCESCHI, G ;
PAZZUCCONI, F ;
MURAKAMI, T ;
SIRTORI, M ;
DACQUARICA, AL ;
SIRTORI, CR .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (10) :1569-1575
[10]
Relation of lipoprotein subclasses as measured by proton nuclear magnetic resonance spectroscopy to coronary artery disease [J].
Freedman, DS ;
Otvos, JD ;
Jeyarajah, EJ ;
Barboriak, JJ ;
Anderson, AJ ;
Walker, JA .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (07) :1046-1053