6533b7d6fe1ef96bd1265ce8

RESEARCH PRODUCT

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

subject

description

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 (PIO), pioglitazone 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 μg/mL (P < .0001) during PIO treatment and from 11.7 ± 10.0 to 26.7 ± 15.7 μg/mL (P < .0001) during PIO/SIM treatment. A decrease in adiponectin levels from 15.5 ± 12.7 to 11.6 ± 7.0 μg/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 pmol/L (P < .01) during PIO treatment and from 24.3 ± 27.4 to 21.1 ± 16.5 mmol/L (P < .05) during PIO/SIM treatment. Lipid parameters improved during SIM treatment but not during PIO treatment. Combined treatment with PIO/SIM was superior in improving overall cardiovascular risk profile than every single drug.