Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease

Background. We investigated the level of soluble adhesion molecules in diabetic patients and the effect of the peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist rosiglitazone on plasma levels of adhesion molecules and an inflammation marker in type 2 diabetic patients with coronary arter...

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Main Authors: Guang Wang, Zhe Zhang, Jie Yu, Fuchun Zhang, Liyun He, Jinru Wei, Jieming Mao, Xian Wang
Format: Article
Language:English
Published: Wiley 2008-01-01
Series:PPAR Research
Online Access:http://dx.doi.org/10.1155/2008/548178
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author Guang Wang
Zhe Zhang
Jie Yu
Fuchun Zhang
Liyun He
Jinru Wei
Jieming Mao
Xian Wang
author_facet Guang Wang
Zhe Zhang
Jie Yu
Fuchun Zhang
Liyun He
Jinru Wei
Jieming Mao
Xian Wang
author_sort Guang Wang
collection DOAJ
description Background. We investigated the level of soluble adhesion molecules in diabetic patients and the effect of the peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist rosiglitazone on plasma levels of adhesion molecules and an inflammation marker in type 2 diabetic patients with coronary artery disease (CAD) after percutaneous coronary intervention (PCI). Methods. A total of 116 diabetic patients with CAD who had undergone PCI were randomized to receive rosiglitazone (4 mg/d) or not for 6 months. Plasma levels of soluble intercellular adhesion molecules (sICAM-1) and P-selectin (sP-selectin) were measured on ELISA. Results. After 6-month rosiglitazone treatment, plasma levels of sICAM-1 were lower than baseline and control group levels (370.4 (332.4–421.9) pg/mL versus 423.5 (327.4–500.3) pg/mL and 404.6 (345.2–483.4) pg/mL, P<.001). In addition, plasma levels of C-reactive protein were significantly reduced from baseline levels. However, plasma level of sP-selectin was not significantly lowered with rosiglitazone treatment than with control treatment after 6-month follow-up. Conclusions. Rosiglitazone reduces chronic inflammatory responses and improves levels of markers of endothelial dysfunction in patients with diabetes and CAD. PPAR-γ agonist may have a beneficial effect on the vascular endothelium through its anti-inflammatory mechanism and may be useful as therapy in patients undergoing PCI.
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spelling doaj-art-1a609ed85b504306bb9854e56989b8442025-02-03T01:10:23ZengWileyPPAR Research1687-47571687-47652008-01-01200810.1155/2008/548178548178Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery DiseaseGuang Wang0Zhe Zhang1Jie Yu2Fuchun Zhang3Liyun He4Jinru Wei5Jieming Mao6Xian Wang7Institute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaDepartment of Cardiovascular Surgery, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, ChinaBackground. We investigated the level of soluble adhesion molecules in diabetic patients and the effect of the peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist rosiglitazone on plasma levels of adhesion molecules and an inflammation marker in type 2 diabetic patients with coronary artery disease (CAD) after percutaneous coronary intervention (PCI). Methods. A total of 116 diabetic patients with CAD who had undergone PCI were randomized to receive rosiglitazone (4 mg/d) or not for 6 months. Plasma levels of soluble intercellular adhesion molecules (sICAM-1) and P-selectin (sP-selectin) were measured on ELISA. Results. After 6-month rosiglitazone treatment, plasma levels of sICAM-1 were lower than baseline and control group levels (370.4 (332.4–421.9) pg/mL versus 423.5 (327.4–500.3) pg/mL and 404.6 (345.2–483.4) pg/mL, P<.001). In addition, plasma levels of C-reactive protein were significantly reduced from baseline levels. However, plasma level of sP-selectin was not significantly lowered with rosiglitazone treatment than with control treatment after 6-month follow-up. Conclusions. Rosiglitazone reduces chronic inflammatory responses and improves levels of markers of endothelial dysfunction in patients with diabetes and CAD. PPAR-γ agonist may have a beneficial effect on the vascular endothelium through its anti-inflammatory mechanism and may be useful as therapy in patients undergoing PCI.http://dx.doi.org/10.1155/2008/548178
spellingShingle Guang Wang
Zhe Zhang
Jie Yu
Fuchun Zhang
Liyun He
Jinru Wei
Jieming Mao
Xian Wang
Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease
PPAR Research
title Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease
title_full Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease
title_fullStr Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease
title_full_unstemmed Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease
title_short Antidiabetic Rosiglitazone Reduces Soluble Intercellular Adhesion Molecule-1 Level in Type 2 Diabetic Patients with Coronary Artery Disease
title_sort antidiabetic rosiglitazone reduces soluble intercellular adhesion molecule 1 level in type 2 diabetic patients with coronary artery disease
url http://dx.doi.org/10.1155/2008/548178
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