Effect of ezetimibe on low-density lipoprotein subtype distribution: results of a placebo-controlled, double-blind trial in patients treated by regular low-density lipoprotein apheresis and statins

被引:30
作者
Geiss, HC
Otto, C
Parhofer, KG
机构
[1] Univ Munich, Med Dept Grosshadern 2, D-81377 Munich, Germany
[2] Univ Mainz, Dept Med 1, D-55131 Mainz, Germany
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2006年 / 55卷 / 05期
关键词
D O I
10.1016/j.metabol.2005.11.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ezetimibe, a cholesterol absorption inhibitor, can be combined with statins to lower low-density lipoprotein (LDL) cholesterol. We have previously shown that ezetimibe can decrease LDL cholesterol by 16% even in patients treated by regular LDL apheresis and statins (Atherosclerosis. 2005;180:107-112). However, it is unclear whether ezetimibe decreases all LDL subfractions equally in patients with hypercholesterolemia. We therefore evaluated the effect of ezetimibe (5 weeks, 10 mg/d) on LDL subtype distribution in a placebo-controlled, double-blind randomized crossover study in 20 patients (age, 56 +/- 9 years; body mass index, 27.5 +/- 4 kg/m(2)) with severe hyperlipoproteinemia and coronary heart disease who are treated by statins and regular LDL apheresis. Both treatment periods (placebo and ezetimibe) were separated by a 5-week washout period. Low-density lipoprotein subtype distribution was determined at the end of each treatment period before apheresis by density gradient ultracentrifugation (LDL1, 1.020-1.024; LDL2, 1.025-1.029; LDL3, 1.030-1.034; LDL4, 1.035-1.040; LDL5, 1.041-1.047; LDL6, 1.048-1.057; LDL7, 1.058-1.066 g/mL). Overall, the LDL subtype distribution did not change significantly (large-buoyant LDL [LDL1 + LDL2], 17.2% +/- 6.4% vs 16.3% +/- 7.1%; intermediate LDL [LDL3 + LDL4], 49.3% +/- 4.5% vs 48.2% +/- 5.2%; small-dense LDL [LDL5 + LDL6 + LFL7] 33.5% +/- 8.0% vs 35.5% +/- 10% during placebo and ezetimibe treatments, respectively). With respect to the individual LDL subfractions, cholesterol was significantly (P < .05, Wilcoxon test) reduced by ezetimibe in LDL I to LDL5 with a somewhat more pronounced reduction in larger LDL (mean +/- SD, -20% +/- 28%, -17% +/- 32%, -14% +/- 25%, -13% +/- 27%, -11% +/- 21%, -7% +/- 21%, -4% +/- 19%; median, -28%, -12%, -18%, -16%, -4%, -4%, -2% for LDL subfractions 1-7, respectively). We therefore conclude that ezetimibe decreases cholesterol in nearly all LDL subfractions. Although this was established in patients concomitantly treated with statins and apheresis, this may also hold true in other clinically relevant situations. (c) 2006 Elsevier Inc. All rights.
引用
收藏
页码:599 / 604
页数:6
相关论文
共 33 条
[1]  
AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
[2]   ATHEROGENIC LIPOPROTEIN PHENOTYPE - A PROPOSED GENETIC-MARKER FOR CORONARY HEART-DISEASE RISK [J].
AUSTIN, MA ;
KING, MC ;
VRANIZAN, KM ;
KRAUSS, RM .
CIRCULATION, 1990, 82 (02) :495-506
[3]   Effect of ezetimibe coadministered with atorvastatin in 628 patients with primary hypercholesterolemia - A prospective, randomized, double-blind trial [J].
Ballantyne, CM ;
Houri, J ;
Notarbartolo, A ;
Melani, L ;
Lipka, LJ ;
Suresh, R ;
Sun, S ;
LeBeaut, AP ;
Sager, PT ;
Veltri, EP .
CIRCULATION, 2003, 107 (19) :2409-2415
[4]  
Berneis K, 2004, SWISS MED WKLY, V134, P720
[5]   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
[6]  
Chapman MJ, 1998, EUR HEART J, V19, pA24
[7]  
CHAPMAN MJ, 1981, J LIPID RES, V22, P339
[8]   Ezetimibe coadministered with simvastatin in patients with primary hypercholesterolemia [J].
Davidson, MH ;
McGarry, T ;
Bettis, R ;
Melani, L ;
Lipka, LJ ;
LeBeaut, AP ;
Suresh, R ;
Sun, S ;
Veltri, EP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 40 (12) :2125-2134
[9]   Efficacy and safety of a potent new selective cholesterol absorption inhibitor, Ezetimibe, in patients with primary hypercholesterolemia [J].
Dujovne, CA ;
Ettinger, MP ;
McNeer, JF ;
Lipka, LJ ;
LeBeaut, AP ;
Suresh, R ;
Yang, B ;
Veltri, EP .
AMERICAN JOURNAL OF CARDIOLOGY, 2002, 90 (10) :1092-1097
[10]   Efficacy and safety of the coadministration of ezetimibe with fenofibrate in patients with mixed hyperlipidaemia [J].
Farnier, M ;
Freeman, MW ;
Macdonell, G ;
Perevozskaya, I ;
Davies, MJ ;
Mitchel, YB ;
Gumbiner, B .
EUROPEAN HEART JOURNAL, 2005, 26 (09) :897-905