Differential metabolic effects of pravastatin and simvastatin in hypercholesterolemic patients

被引:99
作者
Koh, Kwang Kon [1 ]
Quon, Michael J. [2 ]
Han, Seung Hwan
Lee, Yonghee [3 ]
Kim, Soo Jin
Park, Jeong Beorn
Shin, Eak Kyun
机构
[1] Gachon Univ, Vasc Med & Atherosclerosis Unit, Gil Med Ctr, Inchon 405760, South Korea
[2] NIH, Diabet Unit, NCCAM, Bethesda, MD 20892 USA
[3] Ewha Womans Univ, Dept Stat, Seoul, South Korea
关键词
Statins; Adipocytokines; Insulin resistance; Endothelial function; C-REACTIVE PROTEIN; ASSESSING INSULIN SENSITIVITY; SCOTLAND CORONARY PREVENTION; DEPENDENT DIABETES-MELLITUS; RANDOMIZED CONTROLLED-TRIAL; HYPERTENSIVE PATIENTS; THERAPEUTIC INTERVENTIONS; ENDOTHELIAL DYSFUNCTION; CARDIOVASCULAR-DISEASE; ADIPONECTIN LEVELS;
D O I
10.1016/j.atherosclerosis.2008.09.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Lipophilic and hydrophilic statins have different effects on adiponectin and insulin resistance in experimental studies and different effects on the rate of onset of new diabetes in large scale clinical studies. Therefore, we hypothesized that simvastatin and pravastatin may have differential metabolic effects in hypercholesterolemic patients. Methods: This was a randomized, single-blind, placebo-controlled, parallel study. Age, gender, and body mass index were matched. Forty-three patients were given placebo, simvastatin 20mg. or pravastatin 40 mg, respectively once daily for 2 months. Results: Simvastatin and pravastatin therapy significantly changed lipoprotein levels and improved flow-mediated dilation after 2 months when compared with baseline (P<0.001) or placebo treatment (P<0.001 by ANOVA). Simvastatin therapy significantly increased insulin levels (mean % changes; 127%, P=0.014) and decreased plasma adiponectin levels (10%, P=0.012) and insulin sensitivity as assessed by QUICK1 (6%, P=0.007) when compared with baseline. By contrast, pravastatin therapy did not significantly change insulin levels (-3%, P=0.437) but significantly increased plasma adiponectin levels (9%, P=0.011) and insulin sensitivity (6%, P=0.008) when compared with baseline. In addition, these effects of simvastatin were significant when compared with pravastatin (P<0.001 for insulin levels by ANOVA on Ranks, P<0.001 for adiponectin and P= 0.001 for QUICK1 by ANOVA). When compared with baseline, simvastatin significantly increased plasma leptin levels (35%, P=0.028), but pravastatin did not (1%, P=0.822). Conclusions: Despite causing comparable changes in lipoprotein and endothelium-dependent dilation, simvastatin and pravastatin therapy had differential metabolic effects in hypercholesterolemic patients that may be clinically relevant. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:483 / 490
页数:8
相关论文
共 50 条
[31]   Differential effects of simvastatin and atorvastatin on high-density lipoprotein cholesterol and apolipoprotein A-I are consistent across hypercholesterolemic patient subgroups [J].
Davidson, MH ;
Ose, L ;
Frohlich, J ;
Scott, RS ;
Dujovne, CA ;
Escobar, ID ;
Bertolami, MC ;
Cihon, F ;
MacCubbin, DL ;
Mercuri, M .
CLINICAL CARDIOLOGY, 2003, 26 (11) :509-514
[32]   Effects of diet and simvastatin on fatty acid composition in hypercholesterolemic men -: A randomized controlled trial [J].
Jula, A ;
Marniemi, J ;
Rönnemaa, T ;
Virtanen, A ;
Huupponen, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (09) :1952-1959
[33]   Effects of combining simvastatin with rosiglitazone on inflammation, oxidant stress and ambulatory blood pressure in patients with the metabolic syndrome: the SIROCO study [J].
Lazich, I. ;
Sarafidis, P. ;
de Guzman, E. ;
Patel, A. ;
Oliva, R. ;
Bakris, G. .
DIABETES OBESITY & METABOLISM, 2012, 14 (02) :181-186
[34]   Differential effects of pravastatin on the pharmacokinetics of paroxetine in normal and diabetic rats [J].
Li, Feng ;
Ling, Zhao-li ;
Wang, Zhong-jian ;
Zhong, Ze-yu ;
Shu, Nan ;
Zhang, Mian ;
Liu, Can ;
Liu, Li ;
Liu, Xiao-dong .
XENOBIOTICA, 2017, 47 (01) :20-30
[35]   Effects of Pravastatin and Atorvastatin on HDL Cholesterol and Glucose Metabolism in Patients with Dyslipidemia and Glucose Intolerance: The PRAT Study [J].
Sasaki, Jun ;
Otonari, Takatoshi ;
Uchida, Yasufumi ;
Ikeda, Yoshihiko ;
Biro, Sadatoshi ;
Kono, Suminori .
JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS, 2013, 20 (04) :368-379
[36]   Vascular effects of simvastatin combined with ramipril in hypercholesterolemic patients with coronary artery disease, compared with simvastatin alone: a randomized, double-blind, placebo-controlled, crossover study [J].
Koh, KK ;
Son, JW ;
Ahn, JY ;
Jin, DK ;
Kim, HS ;
Kim, DS ;
Han, SH ;
Chung, WJ ;
Park, GS ;
Shin, EK .
ATHEROSCLEROSIS, 2004, 177 (01) :147-153
[37]   Amlodipine improves endothelial function and metabolic parameters in patients with hypertension [J].
Koh, Kwang Kon ;
Han, Seung Hwan ;
Ahn, Jeong Yeal ;
Chung, Wook-Jin ;
Lee, Yonghee ;
Shin, Eak Kyun .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2009, 133 (01) :23-31
[38]   Comparison of rosuvastatin with atorvastatin, simvastatin and pravastatin in achieving cholesterol goals and improving plasma lipids in hypercholesterolaemic patients with or without the metabolic syndrome in the MERCURY I trial. (vol 7, pg 430, 2004) [J].
Stender, S ;
Schuster, H ;
Barter, P ;
Watkins, C ;
Kallend, D .
DIABETES OBESITY & METABOLISM, 2005, 7 (04) :460-460
[39]   Pravastatin Versus Simvastatin for Prevention of Contrast-Induced Nephropathy [J].
Munoz, Monica A. ;
Maxwell, Pamela R. ;
Green, Kay ;
Hughes, Darrel W. ;
Talbert, Robert L. .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS, 2011, 16 (3-4) :376-379
[40]   Lipid-altering efficacy of the ezetimibe/simvastatin single tablet versus rosuvastatin in hypercholesterolemic patients [J].
Catapano, Alberico L. ;
Davidson, Michael H. ;
Ballantyne, Christie M. ;
Brady, William E. ;
Gazzara, Russell A. ;
Tomassini, Joanne E. ;
Tershakovec, Andrew M. .
CURRENT MEDICAL RESEARCH AND OPINION, 2006, 22 (10) :2041-2053