临床荟萃 ›› 2021, Vol. 36 ›› Issue (1): 16-20.doi: 10.3969/j.issn.1004-583X.2021.01.003

• 论著 • 上一篇    下一篇

血清淀粉样蛋白A、高敏C反应蛋白、一氧化氮与稳定型冠心病不良心血管事件的关系

任玲, 江珊()   

  1. 锦州医科大学锦州市中心医院 研究生培养基地 心血管内科, 辽宁 锦州 121000
  • 收稿日期:2020-07-04 出版日期:2021-01-20 发布日期:2021-01-16
  • 通讯作者: 江珊 E-mail:Jiangshan_j@163.com

Relationship between serum amyloid A, high sensitive C-reactive protein, nitric oxide and adverse cardiovascular events in patients with stable coronary heart disease

Ren Ling, Jiang Shan()   

  1. Department of Cardiovascular Medicine, Graduate Training Base of Jinzhou Central Hospital, Jinzhou Medical University, Jinzhou 121000, China
  • Received:2020-07-04 Online:2021-01-20 Published:2021-01-16
  • Contact: Jiang Shan E-mail:Jiangshan_j@163.com

摘要:

目的 探讨血清淀粉样蛋白A、高敏C反应蛋白、一氧化氮水平与稳定型冠心病不良心血管事件的关系。方法 回顾性选择稳定型冠心病患者161例,并根据1年的随访结果分为A组(发生不良心血管事件,78例)和B组(未发生不良心血管事件,83例),收集分析患者临床资料,分析稳定型冠心病发生不良心血管事件危险因素,观察血清淀粉样蛋白A、高敏C反应蛋白、一氧化氮对稳定型冠心病发生不良心血管事件预测价值。结果 A组糖尿病、高血压发病率明显高于B组(P<0.05)。A组血清淀粉样蛋白A、高敏C反应蛋白明显大于B组,一氧化氮小于B组(P<0.05)。Logistic回归分析结果显示,糖尿病、高血压、血清淀粉样蛋白A、高敏C反应蛋白、一氧化氮是稳定型冠心病发生心血管不良事件的危险因素。血清淀粉样蛋白A、高敏C反应蛋白、一氧化氮预测稳定型冠心病患者发生心血管不良事件的AUC分别为0.603、0.633、0.706,特异度分别为为0.634、0.651、0.680,敏感度分别为0.673、0.665、0.673,联合预测稳定型冠心病患者发生心血管不良事件AUC为0.744,特异度为0.716,敏感度为0.773。结论 血清淀粉样蛋白A、高敏C反应蛋白高表达、一氧化氮低表达是稳定型冠心病患者发生心血管不良事件的危险因素,且三者联合预测稳定型冠心病患者发生心血管不良事件的价值较高具有一定的临床价值。

关键词: 冠心病, 血清淀粉样蛋白A, C反应蛋白质, 一氧化氮, 心血管不良事件

Abstract:

Objective To investigate the relationship between serum amyloid A(SAA), high-sensitivity C-reactive protein(hs-CRP), nitric oxide(NO) and adverse cardiovascular events(ACE) in patients with stable coronary heart disease(CHD).Methods 161 patients with stable CHD were selected retrospectively, and were divided into group A (78 cases with ACE) and group B (83 cases without adverse cardiovascular events) based on one-year follow-up results.The clinical data of the patients were collected, the risk factors of ACE in stable CHD were analyzed, and the predictive value of SAA, hs-CRP and NO for ACE in stable CHD was observed.Results The incidence of diabetes and hypertension in group A was significantly higher than that in group B (P<0.05). SAA and hs-CRP in group A were significantly higher than those in group B, and NO was lower than that in group B (P<0.05). Logistic regression analysis showed that diabetes mellitus, hypertension, SAA, hs-CRP, NO were the risk factors of ACE in stable CHD. ROC curve showing the AUC of SAA, hs-CRP and NO in the diagnosis of ACE in patients with stable CHD was 0.603, 0.633 and 0.706 respectively, the specificity was 0.634, 0.651 and 0.680 respectively, the sensitivity was 0.673, 0.665 and 0.673 respectively, the AUC of the three combined diagnosis of cardiovascular adverse events in patients with stable CHD was 0.744, the specificity was 0.716 and the sensitivity was 0.773. Conclusion High expression of SAA, high expression of hs-CRP and low expression of NO are the risk factors of ACE in patients with stable CHD, and the combination of the three factors has a high clinical value in predicting ACE in patients with stable CHD.

Key words: coronary disease, serum amyloid A, C-reactive protein, nitric oxide, cardiovascular adverse events

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