4.6 Article

The balance of serum matrix metalloproteinase-8 and its tissue inhibitor in acute coronary syndrome and its recurrence

期刊

INTERNATIONAL JOURNAL OF CARDIOLOGY
卷 167, 期 2, 页码 362-368

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2011.12.095

关键词

Acute coronary syndrome; Acute myocardial infarction; Unstable angina pectoris; Inflammation; Matrix metalloproteinase-8; Tissue inhibitor of metalloproteinases-1

资金

  1. Lund University, Lund University Hospital
  2. Helsinki University Central Hospital Foundation (EVO)
  3. Academy of Finland [210722, 130408, 110340, 217554, 130043]
  4. Paulo Foundation
  5. Finnish Dental Society Apollonia
  6. Sigrid Juselius Foundation
  7. Academy of Finland (AKA) [130408, 210722, 217554, 130043, 110340, 210722, 130043, 217554, 130408, 110340] Funding Source: Academy of Finland (AKA)

向作者/读者索取更多资源

Background: Matrix metalloproteinase-8 (MMP-8) is involved in the breakdown of the extracellular matrix increasing the vulnerability of atherosclerotic lesions. We analysed the diagnostic value of serum MMP-8 and tissue inhibitor of metalloproteinase-1 (TIMP-1) concentrations in acute coronary syndrome (ACS) and their prognostic value in ACS recurrence. Methods: The population comprised 343 patients with ACS [including 108 unstable angina pectoris and 235 acute myocardial infarctions (AMI)] and 326 healthy controls. Additionally, 157 (45.8%) patients were resampled during the recovery. The ACS patients were followed up for 6 years. Results: MMP-8, TIMP-1, and their molar ratio distinguished the cases from the controls; C-statistic of the multivariate model (95% CI, p-value) including the MMP-8/TIMP-1 ratio regarding its discriminating ability for AMI was 0.922 (0.893-0.950, p < 0.001). After the acute phase of ACS, median MMP-8 and TIMP-1 concentrations decreased (p < 0.001) by 34.5 and 28.7%, respectively, but ended up on a different level than those found in the controls. In the follow-up, acute phase and recovery period TIMP-1 concentrations associated with cardiovascular death with hazard ratios 4.31 (2.00-9.26, p < 0.001) and 4.69 (1.10-20.01, p = 0.037), respectively. Conclusions: The increase of serum MMP-8 and TIMP-1 concentrations may reflect plaque instability and tissue damage. TIMP-1 concentrations are associated with poor outcome in patients with ACS. The findings may have practical implications in both diagnostics and therapeutics. (c) 2011 Elsevier Ireland Ltd. All rights reserved.

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