Plasma pre β-HDL formation is decreased by atorvastatin treatment in type 2 diabetes mellitus: Role of phospholipid transfer protein

被引:19
作者
Dallinga-Thie, G. M. [1 ]
van Tol, A. [2 ,3 ]
Dullaart, R. P. F. [3 ]
机构
[1] Acad Med Ctr Amsterdam, Lab Expt Vasc Med G1 113, Amsterdam, Netherlands
[2] Erasmus Univ, Dept Cell Biol & Genet, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Endocrinol, NL-9713 AV Groningen, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2009年 / 1791卷 / 08期
关键词
Atorvastatin; High density lipoprotein; Triglyceride; Phospholipid transfer protein; Cholesteryl ester transfer protein; Pre-beta HDL; HIGH-DENSITY-LIPOPROTEIN; ESTER TRANSFER PROTEIN; INTIMA-MEDIA THICKNESS; HEART-DISEASE; SUBPOPULATION PROFILE; CHOLESTEROL EFFLUX; PARTICLE-SIZE; ATHEROSCLEROSIS; ROSUVASTATIN; METABOLISM;
D O I
10.1016/j.bbalip.2009.03.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atorvastatin lowers plasma phospholipid transfer protein (PLTP) activity, which stimulates pre-beta-HDL, generation in vitro. We determined the effect of atorvastatin on pre-beta-HDL formation and its relation with PLTP activity in type 2 diabetes. Methods: Plasma pre-beta-HDL formation as well as plasma apo A-I, LpA, LpAI: All, cholesteryl ester transfer protein (CETP) and PLTP activity were measured before and after 30 weeks treatment in 40 patients randomized to atorvastatin 80 mg daily and 41 placebo receiving patients. Pre-beta HDL formation was measured by crossed immunoelectrophoresis under conditions of lecithin:cholesterol acyltransferase (LCAT) inhibition. Results: Plasma pre-beta-HDL formation, triglycerides, LDL cholesterol, PLTP activity, and CETP decreased after statin treatment (all P<0.001 vs placebo), whereas HDL cholesterol increased (P < 0.005). Plasma apo A-I, LpAI and LpAI:AII remained unchanged compared to placebo. In all patients combined, the changes in pre-beta-HDL formation were independently related to the decrease in plasma triglycerides (beta = 0.31; P = 0.006) and PLTP activity (beta = 0.23: P = 0.038), without a contribution of CETP. In the atorvastatin treated patients, the decrease in pre-beta-HDL formation tended to be related to the decrease in PLTP activity (beta = 0.30, P = 0.061) after controlling for decreases in triglycerides (beta = 0.22, P = 0.22). Conclusion: High dose atorvastatin decreases the capacity of plasma to generate pre-beta-HDL particles in type 2 diabetic patients, probably via lowering of plasma PUP activity and triglycerides. This could contribute to an improvement in the atherogenic lipoprotein profile. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:714 / 718
页数:5
相关论文
共 31 条
[1]   Comparison of the effects of high doses of rosuvastatin versus atorvastatin on the subpopulations of high-density lipoproteins [J].
Asztalos, Bela F. ;
Le Maulf, Florence ;
Dallal, Gerald E. ;
Stein, Evan ;
Jones, Peter H. ;
Horvath, Katalin V. ;
McTaggart, Fergus ;
Schaefer, Ernst J. .
AMERICAN JOURNAL OF CARDIOLOGY, 2007, 99 (05) :681-685
[2]   High-density lipoprotein subpopulation profile and coronary heart disease prevalence in male participants of the Framingham Offspring Study [J].
Asztalos, BF ;
Cupples, LA ;
Demissie, S ;
Horvath, KV ;
Cox, CE ;
Batista, MC ;
Schaefer, EJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (11) :2181-2187
[3]   Effects of atorvastatin on the HDL subpopulation profile of coronary heart disease patients [J].
Asztalos, BF ;
Horvath, KV ;
McNamara, JR ;
Roheim, PS ;
Rubinstein, JJ ;
Schaefer, EJ .
JOURNAL OF LIPID RESEARCH, 2002, 43 (10) :1701-1707
[4]   Value of high-density lipoprotein (HDL) subpopulations in predicting recurrent cardiovascular events in the Veterans Affairs HDL Intervention Trial [J].
Asztalos, BF ;
Collins, D ;
Cupples, LA ;
Demissie, S ;
Horvath, KV ;
Bloomfield, HE ;
Robins, SJ ;
Schaefer, EJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2185-2191
[5]   Change in α1 HDL concentration predicts progression in coronary artery stenosis [J].
Asztalos, BF ;
Batista, M ;
Horvath, KV ;
Cox, CE ;
Dallal, GE ;
Morse, JS ;
Brown, GB ;
Schaefer, EJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (05) :847-852
[6]  
Berkplanken I, 2001, DIABETES CARE, V24, P1335
[7]   EARLY INCORPORATION OF CELL-DERIVED CHOLESTEROL INTO PRE-BETA-MIGRATING HIGH-DENSITY LIPOPROTEIN [J].
CASTRO, GR ;
FIELDING, CJ .
BIOCHEMISTRY, 1988, 27 (01) :25-29
[8]   Plasma phospholipid transfer protein activity is decreased in type 2diabetes during treatment with atorvastatin - A role for apolipoprotein E? [J].
Dallinga-Thie, GM ;
van Tol, A ;
Hattori, H ;
Rensen, PCN ;
Sijbrands, EJG .
DIABETES, 2006, 55 (05) :1491-1496
[9]   Increased cholesterol efflux from cultured fibroblasts to plasma from hypertriglyceridemic type 2 diabetic patients:: Roles of pre β-HDL, phospholipid transfer protein and cholesterol esterification [J].
de Vries, R. ;
Groen, A. K. ;
Perton, F. G. ;
Dallinga-Thie, G. M. ;
van Wijland, M. J. A. ;
Dikkeschei, L. D. ;
Wolffenbuttel, B. H. R. ;
van Tol, A. ;
Dullaart, R. P. F. .
ATHEROSCLEROSIS, 2008, 196 (02) :733-741
[10]   Cellular cholesterol efflux to plasma from moderately hypercholesterolaemic type 1 diabetic patients is enhanced, and is unaffected by simvastatin treatment [J].
de Vries, R ;
Kerstens, MN ;
Sluiter, WJ ;
Groen, AK ;
van Tol, A ;
Dullaart, RPF .
DIABETOLOGIA, 2005, 48 (06) :1105-1113