Cited by 119Lipoproteins and Cardiovascular HealthDiabetes, Cardiovascular Risks, and LipoproteinsCholesterol and Lipid Metabolism

Differential metabolic effects of pravastatin and simvastatin in hypercholesterolemic patients

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Koh, Kwang Kon, Quon, Michael J., Han, Seung Hwan, Lee, Yonghee, Kim, Soo Jin, Park, Jeong Beom, Shin, Eak Kyun·2009·Atherosclerosis

Abstract

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 QUICKI (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 QUICKI 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.

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Crossref · 10.1016/j.atherosclerosis.2008.09.021

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  • Prior studies by Koh et al. used the Quantitative Insulin-Sensitivity Check Index as a surrogate measure for insulin sensitivity, while Ohrvall et al. used the hyperinsulinemic-euglycemic clamp technique.

    “The 3 studies by Koh et al. (19,20,22) from 2008, 2009, and 2010 used the Quantitative Insulin-Sensitivity Check Index as a surrogate measure for insulin sensitivity, whereas the study by Ohrvall et al. (21) from 1995 used the hyperinsulinemic-euglycemic clamp technique.”

    From Simvastatin Effects on Skeletal Muscle (2013) · cites this paper as [19]

  • Statin treatment has been reported to impair insulin sensitivity and increase type 2 diabetes prevalence, with lipophilic statins having a stronger effect than hydrophilic statins.

    “Recently, it has been reported that statin treatment impairs insulin sensitivity and increases the prevalence of type 2 diabetes (19 -22); and it seems that lipophilic statins (i.e., simvastatin, atorvastatin, fluvastatin, lovastatin) have a more pronounced effect on insulin sensitivity compared with hydrophilic statins (i.e., pravastatin, rosuvastatin) (23).”

    From Simvastatin Effects on Skeletal Muscle (2013) · cites this paper as [19]

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References 46 · Cited by 119

Authors
Koh, K. K., Quon, M. J., Han, S. H., Lee, Y., Kim, S. J., Park, J. B., & Shin, E. K.
Affiliations
  • Gachon University (KR)
  • National Institutes of Health (US)
  • Ewha Womans University (KR)
Corresponding author
Koh, Kwang Kon
Venue
Atherosclerosis
Publisher
Elsevier BV
Published
2009-06
Volume
204
Issue
2
Pages
483-490
ISSN
0021-9150 (ISSN-L)
OpenAlex
W2035557600
Cited by
119
References
46
Citations by year
2026: 1 · 2024: 3 · 2023: 7 · 2022: 1 · 2021: 1 · 2020: 2 · 2019: 4 · 2018: 7 · 2017: 5 · 2016: 12 · 2015: 7 · 2014: 12 · 2013: 12 · 2012: 13
FWCI
11.24
Type
journal article
Language
en
Open access
Locations
  • Atherosclerosis (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Gachon University
  • National Institutes of Health
  • National Center for Complementary and Integrative Health (Z01AT000001)
Topics
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
  • Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
Keywords
simvastatin, pravastatin, statins, hypercholesterolemia, adiponectin, insulin resistance, QUICKI, leptin, lipoproteins, flow-mediated dilation, endothelial function, insulin levels, lipid-lowering therapy
MeSH terms
C-Reactive Protein, Double-Blind Method, Endothelium, Vascular, Female, Humans, Hypercholesterolemia, Insulin, Insulin Resistance, Lipoproteins, Male, Middle Aged, Vasodilation, Treatment Outcome, Pravastatin, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Simvastatin, Leptin, Adiponectin

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