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Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease.

Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease. Research Abstract Details 

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  • Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease. Abstract Text:

    norihito inamiNorihito Inami,shosaku nomuraShosaku Nomura,takayuki shimazuTakayuki Shimazu,kenichi manabeKenichi Manabe,yutaka kimuraYutaka Kimura,toshiji iwasakaToshiji Iwasaka,norihito inamiNorihito Inami,shosaku nomuraShosaku Nomura,takayuki shimazuTakayuki Shimazu,kenichi manabeKenichi Manabe,yutaka kimuraYutaka Kimura,toshiji iwasakaToshiji Iwasaka,

    BACKGROUND: Some factors play pathogenic roles in the development of restenosis after percutaneous coronary intervention (PCI). We measured and compared the ratio of elevated levels of monocytic chemotactic peptide-1 (MCP-1), regulated on activation normally T-cell expressed and secreted (RANTES), soluble (s) P-selectin, sE-selectin and adiponectin after PCI. METHODS: Plasma levels of chemokines and soluble markers were measured before and 30 days after PCI in 96 patients (69 males and 27 females, aged 63 +/- 9 years) who underwent PCI and who had repeated angiograms at a 6-month follow-up. In addition, we carried out the basic study of the tissue factor expression on monocytic cell line (THP-1) by MCP-1. RESULTS: Restenosis occurred in 33 (34.4%) patients. A significant and time-dependent increase in MCP-1 was observed in the restenosis group. However, there were no significant differences in RANTES, sP-selectin, and sE-selectin levels with or without restenosis. Adiponectin levels in patients with coronary artery disease were significantly lower than levels in normal controls. However, adiponectin levels were no different at baseline between patients with or without restenosis. MCP-1 did not induce the expression of tissue factor on THP-1. However, the recombinant sCD40 ligand-induced expression of tissue factor on THP-1 was enhanced by the addition of MCP-1. CONCLUSION: These findings suggest that restenosis development after PCI in patients with coronary artery disease may involve the participation of MCP-1 after PCI, and adiponectin incompletely prevent this MCP-1-dependent restenosis.

    Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease. Publishing Authors By Initials

    n inamiN Inami,s nomuraS Nomura,t shimazuT Shimazu,k manabeK Manabe,y kimuraY Kimura,t iwasakaT Iwasaka,n inamiN Inami,s nomuraS Nomura,t shimazuT Shimazu,k manabeK Manabe,y kimuraY Kimura,t iwasakaT Iwasaka,

    For similar abstracts research abstracts see: abstracts research

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    Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of thrombosis and thrombolysis

    VOLUME: 24

    Page Numbers: 267-73

    Journal Abbreviation: J. Thromb. Thrombolysis

    ISSN: 0929-5305

    DAY: 8

    MONTH: 05

    YEAR: 2007

    Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease. Information

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    LANGUAGE: eng

    NlmUniqueID: 9502018

    Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease. Keywords Mesh Terms:

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    Grant and Affiliation Information for Adiponectin incompletely prevent MCP-1-dependent restenosis after percutaneous coronary intervention in patients with coronary artery disease.

    AFFILIATION: Second Department of Internal Medicine, Kansai Medical University, Moriguchi, Osaka, Japan.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: J Thromb Thrombolysis

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