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Effect of atorvastatin (10 mg/day) on glucose metabolism in patients with the metabolic syndrome.
Am J Cardiol. 2006 Jul 01; 98(1):66-9.AJ

Abstract

Large interventional studies have shown that statins may reduce the incidence of type 2 diabetes mellitus. However, it is uncertain whether short-term statin therapy can affect insulin sensitivity in patients with the metabolic syndrome. We evaluated the effect of atorvastatin (10 mg/day) in 10 insulin-resistant subjects (age 40 +/- 12 years, body mass index 33.6 +/- 5.2 kg/m(2), triglycerides 2.84 +/- 1.99 mmol/L [249 +/- 175 mg/dl], glucose 6.06 +/- 0.67 mmol/L [109 +/- 12 mg/dl)] using the homeostasis model assessment (HOMA) index (parameter of insulin resistance derived from fasting glucose and fasting insulin concentrations; 5.7 +/- 2.6) in a randomized placebo-controlled, double-blind, crossover study. Subjects were randomized to receive placebo or atorvastatin, each given for 6 weeks separated by a 6-week wash-out period. At the beginning and end of each treatment phase, the patients underwent an oral glucose tolerance test, a 72-hour continuous glucose measurement, and a detailed lipid determination, including a standardized fat tolerance test. Compared with placebo, atorvastatin resulted in a significant (p = 0.05) reduction in the HOMA index (-21%), fasting C-peptides (-18%), glucose (area under the curve during the oral glucose tolerance test, -7%), and a borderline (p = 0.08) reduction of insulin (-18%). The parameters derived from the continuous 72-hour glucose monitoring did not change. A significant reduction also occurred in the total and low-density lipoprotein cholesterol concentrations, although the fasting and postprandial triglyceride concentrations did not change significantly. However, we found a significant correlation between atorvastatin-induced changes in the HOMA and baseline HOMA and between the atorvastatin-induced changes in triglycerides and insulin concentrations. The free-fatty acid, interleukin-6, and high sensitivity C-reactive protein concentrations did not change. Our data indicated that in insulin-resistant, nondiabetic subjects, 6 weeks of atorvastatin (10 mg/day) resulted in significant improvement in insulin sensitivity.

Authors+Show Affiliations

Department of Internal Medicine II, Klinikum Grosshadern, Ludwig-Maximilians University, Munich, Germany.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Randomized Controlled Trial

Language

eng

PubMed ID

16784923

Citation

Huptas, Sebastian, et al. "Effect of Atorvastatin (10 Mg/day) On Glucose Metabolism in Patients With the Metabolic Syndrome." The American Journal of Cardiology, vol. 98, no. 1, 2006, pp. 66-9.
Huptas S, Geiss HC, Otto C, et al. Effect of atorvastatin (10 mg/day) on glucose metabolism in patients with the metabolic syndrome. Am J Cardiol. 2006;98(1):66-9.
Huptas, S., Geiss, H. C., Otto, C., & Parhofer, K. G. (2006). Effect of atorvastatin (10 mg/day) on glucose metabolism in patients with the metabolic syndrome. The American Journal of Cardiology, 98(1), 66-9.
Huptas S, et al. Effect of Atorvastatin (10 Mg/day) On Glucose Metabolism in Patients With the Metabolic Syndrome. Am J Cardiol. 2006 Jul 1;98(1):66-9. PubMed PMID: 16784923.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Effect of atorvastatin (10 mg/day) on glucose metabolism in patients with the metabolic syndrome. AU - Huptas,Sebastian, AU - Geiss,Hans-Christian, AU - Otto,Carsten, AU - Parhofer,Klaus Georg, Y1 - 2006/05/04/ PY - 2005/07/27/received PY - 2006/01/17/revised PY - 2006/01/17/accepted PY - 2006/6/21/pubmed PY - 2006/8/4/medline PY - 2006/6/21/entrez SP - 66 EP - 9 JF - The American journal of cardiology JO - Am J Cardiol VL - 98 IS - 1 N2 - Large interventional studies have shown that statins may reduce the incidence of type 2 diabetes mellitus. However, it is uncertain whether short-term statin therapy can affect insulin sensitivity in patients with the metabolic syndrome. We evaluated the effect of atorvastatin (10 mg/day) in 10 insulin-resistant subjects (age 40 +/- 12 years, body mass index 33.6 +/- 5.2 kg/m(2), triglycerides 2.84 +/- 1.99 mmol/L [249 +/- 175 mg/dl], glucose 6.06 +/- 0.67 mmol/L [109 +/- 12 mg/dl)] using the homeostasis model assessment (HOMA) index (parameter of insulin resistance derived from fasting glucose and fasting insulin concentrations; 5.7 +/- 2.6) in a randomized placebo-controlled, double-blind, crossover study. Subjects were randomized to receive placebo or atorvastatin, each given for 6 weeks separated by a 6-week wash-out period. At the beginning and end of each treatment phase, the patients underwent an oral glucose tolerance test, a 72-hour continuous glucose measurement, and a detailed lipid determination, including a standardized fat tolerance test. Compared with placebo, atorvastatin resulted in a significant (p = 0.05) reduction in the HOMA index (-21%), fasting C-peptides (-18%), glucose (area under the curve during the oral glucose tolerance test, -7%), and a borderline (p = 0.08) reduction of insulin (-18%). The parameters derived from the continuous 72-hour glucose monitoring did not change. A significant reduction also occurred in the total and low-density lipoprotein cholesterol concentrations, although the fasting and postprandial triglyceride concentrations did not change significantly. However, we found a significant correlation between atorvastatin-induced changes in the HOMA and baseline HOMA and between the atorvastatin-induced changes in triglycerides and insulin concentrations. The free-fatty acid, interleukin-6, and high sensitivity C-reactive protein concentrations did not change. Our data indicated that in insulin-resistant, nondiabetic subjects, 6 weeks of atorvastatin (10 mg/day) resulted in significant improvement in insulin sensitivity. SN - 0002-9149 UR - https://www.unboundmedicine.com/medline/citation/16784923/Effect_of_atorvastatin__10_mg/day__on_glucose_metabolism_in_patients_with_the_metabolic_syndrome_ DB - PRIME DP - Unbound Medicine ER -