Effect of simvastatin and/or pioglitazone on insulin resistance, insulin secretion, adiponectin, and proinsulin levels in nondiabetic patients at cardiovascular risk -: the PIOSTAT study

被引:69
作者
Forst, Thomas
Pfuetzner, Andreas
Luebben, Georg
Weber, Matthias
Marx, Nikolaus
Karagiannis, Efstrathios
Koehler, Carsta
Baurecht, Werner
Hollberg, Cloth
Hanefeld, Markolf
机构
[1] Inst Clin Res & Dev, Dept Med, D-55116 Mainz, Germany
[2] Univ Mainz, Dept Endocrinol, D-55130 Mainz, Germany
[3] TAKEDA Pharma GMBH Med, D-52066 Aachen, Germany
[4] Univ Ulm, Dept Cardiol, D-89081 Ulm, Germany
[5] TUD, GWT, D-01307 Dresden, Germany
[6] Acromion, D-50226 Frechen, Germany
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2007年 / 56卷 / 04期
关键词
D O I
10.1016/j.metabol.2006.11.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the effect of pioglitazone in comparison with and in combination with simvastatin on insulin resistance, plasma adiponectin, postprandial plasma glucose, insulin, and intact proinsulin levels in a nondiabetic population at cardiovascular risk. One hundred twenty-five nondiabetic patients at cardiovascular risk were randomized to pioglitazone (PTO), pioglilazone and simvastatin (PIO/SIM), or simvastatin (SIM) treatments. Blood samples were taken for the measurement of adiponectin and lipid levels. In addition, an oral glucose load with the measurements of glucose, insulin, and intact proinsulin levels was performed. Adiponectin levels increased from 14.0 +/- 8.2 to 27.6 +/- 14.5 mu g/mL (P < .0001) during PTO treatment and from 11.7 +/- 10.0 to 26.7 +/- 15.7 mu g/mL (P < .0001) during PIO/SIM treatment. A decrease in adiponectin levels from 15.5 +/- 12.7 to 11.6 +/- 7.0 mu g/mL (P < .05) was observed during SIM treatment. Although fasting intact proinsulin levels remained unchanged, the increase in postprandial intact proinsulin levels could be reduced from 29.5 +/- 21.4 to 22.1 +/- 17.5 mu mol/L (P < .01) during PTO treatment and from 24.3 +/- 27.4 to 21.1 +/- 16.5 mmol/L (P < .05) during PTO/SIM treatment. Lipid parameters improved during SIM treatment but not during PTO treatment. Combined treatment with PIO/SIM was superior in improving overall cardiovascular risk profile than every single drug. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:491 / 496
页数:6
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