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. 2004 Feb;13(1):39-43.
doi: 10.1080/09629350410001664752.

Monocyte chemoattractant protein-1 in patients with peripheral arterial disease

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Monocyte chemoattractant protein-1 in patients with peripheral arterial disease

Jana Petrkova et al. Mediators Inflamm. 2004 Feb.

Abstract

Background: Chemokine-driven migration of inflammatory cells has been implicated in the pathogenesis of atherosclerotic conditions including peripheral arterial disease (PAD). Monocyte chemoattractant protein-1 (MCP-1) is elevated in patients with coronary artery disease and in hypertensive patients. This study therefore investigated MCP-1 in patients with PAD.

Methods: Serum MCP-1 was determined by enzyme-linked immunosorbent assay in 36 healthy, control subjects and in 19 patients with PAD. Statistical analysis utilised the Mann-Whitney test and Spearman correlation (p < 0.05).

Results: MCP-1 (pg/ml) was increased in patients compared with in controls (mean+/-standard error of the mean: PAD group, 748+/-60; control group, 459+/-27; p=0.0001). MCP-1 levels tended to decrease with progressing disease. From atherosclerosis risk factors, diabetes inclined to increase MCP-1 levels; hypertension had no effect. Serum MCP-1 correlated with cholesterol, triglycerides, low-density lipoprotein but not high-density lipoprotein.

Conclusion: Elevation of MCP-1 in the circulation of PAD patients shown in the present pilot study implicates this CC chemokine ligand 2 in inflammatory processes contributing to PAD clinical symptomatology. Further investigations are necessary to evaluate whether MCP-1 can be used as a potential marker of peripheral arterial disease follow-up and/or prognosis.

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References

    1. Nat Immunol. 2001 Feb;2(2):108-15 - PubMed
    1. Nat Immunol. 2001 Feb;2(2):95-101 - PubMed
    1. Biochem Biophys Res Commun. 2001 Jun 1;284(1):239-44 - PubMed
    1. Clin Exp Immunol. 2001 Jun;124(3):343-5 - PubMed
    1. Clin Exp Immunol. 2001 Jun;124(3):346-52 - PubMed

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