Key result
Patients with stable angina pectoris demonstrated significantly higher IL-8-stimulated neutrophil release of MMP-9 compared to healthy controls, despite having similar plasma MMP-9 levels.
Case-Control (n=91)
No
Leukocyte-derived MMP-9 and TIMP-1 are significantly altered in patients with stable angina pectoris despite normal plasma levels, suggesting leukocytes are more prone to release and produce MMP-9 in symptomatic CAD.
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Altered neutrophil MMP-9 release in stable angina may reflect leukocyte dysregulation; hypothesis-generating and should not yet change practice.
OBJECTIVE: There is a growing interest for matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in plasma as novel biomarkers in coronary artery disease (CAD). We aimed to identify the sources of MMP-8, MMP-9, TIMP-1 and TIMP-2 among peripheral blood cells and further explore whether gene expression or protein release was altered in patients with stable angina pectoris (SA). METHODS: In total, plasma MMP-9 was measured in 44 SA patients and 47 healthy controls. From 10 patients and 10 controls, peripheral blood mononuclear cells (PBMC) and neutrophils were isolated and stimulated ex vivo. MMPs, TIMPs and myeloperoxidase were measured in plasma and supernatants by ELISA. The corresponding gene expression was measured by real-time PCR. RESULTS: Neutrophils were the dominant source of MMP-8 and MMP-9. Upon moderate stimulation with IL-8, the neutrophil release of MMP-9 was higher in the SA patients compared with controls (p<0.05). In PBMC, the TIMP-1 and MMP-9 mRNA expression was higher in SA patients compared with controls, p<0.01 and 0.05, respectively. There were no differences in plasma levels between patients and controls except for TIMP-2, which was lower in patients, p<0.01. CONCLUSION: Measurements of MMPs and TIMPs in plasma may be of limited use. Despite similar plasma levels in SA patients and controls, the leukocyte-derived MMP-9 and TIMP-1 are significantly altered in patients. The findings indicate that the leukocytes are more prone to release and produce MMP-9 in symptomatic and angiographically verified CAD-a phenomenon that may have clinical implications in the course of disease.
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Jönsson et al. (2011) conducted a case-control in Stable Angina Pectoris (n=91). Stable Angina Pectoris vs. Healthy controls was evaluated on IL-8-induced neutrophil release of MMP-9 (ng/ml) (p=<0.05). Patients with stable angina pectoris demonstrated significantly higher IL-8-stimulated neutrophil release of MMP-9 compared to healthy controls, despite having similar plasma MMP-9 levels.
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