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Pentoxifylline decreases serum level of adhesion molecules in atherosclerosis patients
Amir Hooshang Mohammadpour1,2, Homa Falsoleiman3, Jamal Shamsara2
1Dept. of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Science, Mashhad, Iran.
Insights
Pentoxifylline (PTX) significantly reduced adhesion molecules in coronary artery disease (CAD) patients. This pilot study suggests PTX may be a beneficial treatment for managing inflammation in CAD.
Area of Science:
- Cardiovascular Medicine
- Inflammation Research
- Pharmacology
Background:
- Inflammation plays a key role in the development and progression of atherosclerotic disease.
- Biomarkers such as monocyte chemoattractant protein 1 (MCP-1), IL-18, and adhesion molecules correlate with atherosclerosis severity and cardiovascular event risk.
- Previous animal studies indicate pentoxifylline (PTX) can reduce these inflammatory factors.
Purpose of the Study:
- To evaluate the effect of pentoxifylline (PTX) on inflammatory biomarkers in patients with coronary artery disease (CAD).
- To assess PTX's impact on serum levels of MCP-1, IL-18, ICAM-1, and VCAM-1 in CAD patients.
Main Methods:
- A double-blind, randomized pilot clinical study involving 40 patients with documented CAD.
- Patients received either PTX (400 mg three times daily) or a placebo for 2 months.
- Serum concentrations of MCP-1, IL-18, ICAM-1, and VCAM-1 were measured using enzyme-linked immunosorbent assay before and after the intervention.
Main Results:
- Serum levels of intercellular adhesion molecule 1 (ICAM-1) and vascular cell adhesion molecule 1 (VCAM-1) were significantly decreased after two months of PTX treatment (P<0.05).
Conclusions:
- Pentoxifylline administration in CAD patients significantly reduces levels of adhesion molecules.
- These findings suggest PTX may have a role in managing inflammation associated with coronary artery disease.
Background:
Inflammation is involved in development, progression, and complications of atherosclerotic disease. Clinical studies have indicated that the level of monocyte chemoattractant protein 1 (MCP-1), IL-18, and adhesion molecules correlates with the severity of atherosclerosis and can predict future cardiovascular events. Experimental studies have shown pentoxifylline (PTX) reduces these factors in animal models. The purpose of the present pilot study was to evaluate effect of PTX on a group of inflammatory biomarkers in patients with coronary artery disease (CAD).
Methods:
Forty patients with angiographically documented CAD, who fulfilled inclusion and exclusion criteria, were entered in the double-blind, randomized, pilot clinical study. The patients were randomly given PTX (400 mg three times daily) or placebo (3 tab/day) for 2 months. Serum concentrations of MCP-1, IL-18, intercellular adhesion Molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) were measured before and at the end of intervention by enzyme-linked immunosorbant assay.
Results:
Our study showed that the serum levels of ICAM-1 and VCAM-1 was decreased in the study population after two-month treatment (P<0.05).
Conclusion:
Based on the results of our pilot study, administration of PTX in CAD patients significantly decreases adhesion molecules levels.
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