open access

Vol 65, No 4 (2014)
Original paper
Submitted: 2014-08-29
Accepted: 2014-08-29
Published online: 2014-08-29
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The effect of short-term combined treatment with simvastatin and ezetimibe on circulating adipokine levels in patients with isolated hypercholesterolemia

Robert Krysiak, Witold Żmuda, Bogdan Marek, Bogusław Okopień
DOI: 10.5603/EP.2014.0037
·
Endokrynol Pol 2014;65(4):275-280.

open access

Vol 65, No 4 (2014)
Original Paper
Submitted: 2014-08-29
Accepted: 2014-08-29
Published online: 2014-08-29

Abstract

Introduction: Although several studies have assessed plasma adipokines in patients treated with hypolipidemic agents, these studies have provided contrasting results.

Material and methods: This study included 19 high-risk patients with elevated total and LDL cholesterol levels treated with simvastatin (40 mg daily) and ezetimibe (10 mg daily). Plasma levels of leptin, adiponectin, visfatin, tumour necrosis factor-α, free fatty acids as well as C-reactive protein were measured before and after 30 days of treatment. High-risk hypercholesterolemic patients were compared with 17 age-, sex- and weight-matched healthy subjects who did not receive any treatment.

Results: Compared to the healthy subjects, hypercholesterolemic patients exhibited lower plasma levels of adiponectin, as well as higher plasma levels of the remaining adipokines. Administration of simvastatin and ezetimibe for 30 days reduced plasma levels of leptin, visfatin, TNF-α, as well as increased plasma levels of adiponectin. The treatment also reduced free fatty acids and C-reactive protein.

Conclusions: High-risk hypercholesterolemic patients with elevated cholesterol levels are characterised by abnormal production of adipose tissue hormones. Short-term treatment with simvastatin and ezetimibe partially restores adipokine production and inhibits low-grade inflammation. (Endokrynol Pol 2014; 65 (4): 275–280)

Abstract

Introduction: Although several studies have assessed plasma adipokines in patients treated with hypolipidemic agents, these studies have provided contrasting results.

Material and methods: This study included 19 high-risk patients with elevated total and LDL cholesterol levels treated with simvastatin (40 mg daily) and ezetimibe (10 mg daily). Plasma levels of leptin, adiponectin, visfatin, tumour necrosis factor-α, free fatty acids as well as C-reactive protein were measured before and after 30 days of treatment. High-risk hypercholesterolemic patients were compared with 17 age-, sex- and weight-matched healthy subjects who did not receive any treatment.

Results: Compared to the healthy subjects, hypercholesterolemic patients exhibited lower plasma levels of adiponectin, as well as higher plasma levels of the remaining adipokines. Administration of simvastatin and ezetimibe for 30 days reduced plasma levels of leptin, visfatin, TNF-α, as well as increased plasma levels of adiponectin. The treatment also reduced free fatty acids and C-reactive protein.

Conclusions: High-risk hypercholesterolemic patients with elevated cholesterol levels are characterised by abnormal production of adipose tissue hormones. Short-term treatment with simvastatin and ezetimibe partially restores adipokine production and inhibits low-grade inflammation. (Endokrynol Pol 2014; 65 (4): 275–280)

Get Citation

Keywords

simvastatin; ezetimibe; hypercholesterolemia; leptin; adiponectin; visfatin; tumour necrosis factor α (TNF-α)

About this article
Title

The effect of short-term combined treatment with simvastatin and ezetimibe on circulating adipokine levels in patients with isolated hypercholesterolemia

Journal

Endokrynologia Polska

Issue

Vol 65, No 4 (2014)

Article type

Original paper

Pages

275-280

Published online

2014-08-29

Page views

1564

Article views/downloads

1900

DOI

10.5603/EP.2014.0037

Bibliographic record

Endokrynol Pol 2014;65(4):275-280.

Keywords

simvastatin
ezetimibe
hypercholesterolemia
leptin
adiponectin
visfatin
tumour necrosis factor α (TNF-α)

Authors

Robert Krysiak
Witold Żmuda
Bogdan Marek
Bogusław Okopień

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