血清CTRP9与LTBP-2对老年慢性心力衰竭患者不良心血管事件的预测价值

    Predictive value of serum CTRP9 and LTBP-2 for adverse cardiovascular events in elderly patients with chronic heart failure

    • 摘要:
      目的 探究血清补体C1q肿瘤坏死因子相关蛋白9(CTRP9)与潜在转化生长因子β结合蛋白2(LTBP-2)对老年慢性心力衰竭(CHF)患者发生主要不良心血管事件(MACE)的预测价值。
      方法 选取2020年8月~2021年10月在青岛大学附属心血管病医院收治的150例经检查确诊的老年CHF患者作为研究对象,对患者进行12个月随访,45例患者发生MACE作为MACE组,105例患者未发生MACE为无MACE组。比较MACE组与无MACE组患者血清CTRP9、LTBP-2水平。ROC曲线分析CTRP9、LTBP-2对老年CHF患者发生MACE的预测价值。Logistic回归分析影响老年CHF患者发生MACE的因素。
      结果 与无MACE组相比,MACE组LVEDD、LVESD、BNP水平升高,LVEF水平降低(均P<0.01)。血清LTBP-2水平升高,CTRP9水平降低(均P<0.01)。ROC分析显示血清CTRP9水平评估MACE发生的AUC是0.772,截断值为137.50 μg/L,灵敏度为73.30%,特异度为66.70%;LTBP-2水平评估MACE发生的AUC是0.771,截断值为20.02 μg/L,灵敏度为71.10%,特异度为61.90%,二者联合检测的灵敏度为84.40%,特异度为80.00%,AUC为0.889(95%CI: 0.838~0.940)。多因素Logistic回归分析显示,LTBP-2是影响患者发生MACE的危险因素,CTRP9为保护因素(均P<0.01)。
      结论 血清CTRP9和LTBP-2对评估老年CHF患者MACE的发生有一定的诊断价值。

       

      Abstract:
      AIM  To explore the predictive value of serum complement C1q tumor necrosis factor related protein 9 (CTRP9) and potential transforming growth factor β binding protein 2 (LTBP-2) for major adverse cardiovascular events (MACE) in elderly patients with chronic heart failure (CHF).
      METHODS 150 elderly CHF patients diagnosed through examination and admitted to the Affiliated Cardiovascular Hospital of Qingdao University from August 2020 to October 2021 were selected as the study subjects. The patients were followed up for 12 months, with 45 patients in the MACE group and 105 patients in the non MACE group. Compare the serum levels of CTRP9 and LTBP-2 between the MACE group and the non MACE group patients. The predictive value of ROC curve analysis of CTRP9 and LTBP-2 for MACE in elderly CHF patients. Logistic regression analysis of factors affecting the occurrence of MACE in elderly CHF patients.
      RESULTS Compared with the non MACE group, the MACE group had higher levels of LVEDD, LVESD, BNP, and lower levels of LVEF (all P<0.01). The serum LTBP-2 level increased, while the CTRP9 level decreased (both P<0.01). ROC analysis showed that the AUC for evaluating MACE occurrence based on serum CTRP9 levels was 0.772, with a cutoff value of 137.50 μg/L, sensitivity of 73.30%, specificity of 66.70%; The AUC of MACE assessed by LTBP-2 level is 0.771, with a cutoff value of 20.02 μg/L, sensitivity is 71.10%, specificity is 61.90%. The sensitivity of the combined detection of the two is 84.40%, specificity is 80.00%, and AUC is 0.889 (95% CI: 0.838~0.940). Multivariate logistic regression analysis showed that LTBP-2 was a risk factor for MACE in patients, while CTRP9 was a protective factor (all P<0.01).
      CONCLUSION Serum CTRP9 and LTBP-2 have certain diagnostic value in evaluating the occurrence of MACE in elderly CHF patients.

       

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