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DOI 10.1155/2014/165742

Медицинская библиотека · Mediators of inflammation · 2014

Elevated plasma IL-37, IL-18, and IL-18BP concentrations in patients with acute coronary syndrome.

Ji Qingwei, Zeng Qiutang, Huang Ying, Shi Ying, Lin Yingzhong, Lu Zhengde, Meng Kai, Wu Bangwei, Yu Kunwu, Chai Meng, Liu Yuyang, Zhou Yujie

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

More recently, evidence showed that the novel anti-inflammatory cytokine interleukin- (IL-) 37 was expressed in the foam-like cells of atherosclerotic coronary and carotid artery plaques, suggesting that IL-37 is involved in atherosclerosis-related diseases. However, the plasma levels of IL-37 in patients with acute coronary syndrome (ACS, including unstable angina pectoris and acute myocardial infarction) have yet to be investigated.

METHODS

Plasma IL-37, IL-18, and IL-18BP levels were measured in 50 patients with stable angina pectoris (SAP), 75 patients with unstable angina pectoris (UAP), 67 patients with acute myocardial infarction (AMI), and 65 control patients.

RESULTS

The plasma IL-37, IL-18, and IL-18BP levels were significantly increased in ACS patients compared to SAP and control patients. A correlation analysis showed that the plasma biomarker levels were positively correlated with each other and with the levels of C-reactive protein (CRP), N-terminal probrain natriuretic peptide (NT-proBNP), and left ventricular end-diastolic dimension (LVEDD) but negatively correlated with left ventricular ejection fraction (LVEF). Furthermore, the plasma IL-37, IL-18, and IL-18BP had no correlation with the severity of the coronary artery stenosis.

CONCLUSIONS

The results indicate that the plasma IL-37 levels are associated with the onset of ACS.

Для цитирования: Ji Qingwei, Zeng Qiutang, Huang Ying, Shi Ying, Lin Yingzhong, Lu Zhengde, Meng Kai, Wu Bangwei, Yu Kunwu, Chai Meng, Liu Yuyang, Zhou Yujie. Elevated plasma IL-37, IL-18, and IL-18BP concentrations in patients with acute coronary syndrome.. Mediators of inflammation. 2014. DOI: 10.1155/2014/165742.

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