血清MFAP4、FBN1水平与慢性心力衰竭病人心肌纤维化的关系

    Study on the relationship between the serum levels of MFAP4 and FBN1 and myocardial fibrosis in patients with chronic heart failure

    • 摘要:
      目的: 分析血清微纤维相关蛋白4(microfibrillation-associated protein 4,MFAP4)、原纤维蛋白1(fibrillar protein 1, FBN1)水平与慢性心力衰竭病人心肌纤维化的关系。
      方法: 选取慢性心力衰竭病人146例作为观察组,另选取同期健康体检者146名为对照组。采用ELISA法检测2组血清MFAP4、FBN1水平;采用放射免疫法检测心肌纤维化指标层粘连蛋白(LN)、Ⅲ型前胶原(PCⅢ)、透明质酸(HA)水平。分析血清MFAP4、FBN1、心肌纤维化指标间的相关性及MFAP4、FBN1对慢性心力衰竭病人心肌纤维化的诊断价值。
      结果: 观察组血清MFAP4、FBN1和LN、PCⅢ、HA水平均明显高于对照组(P < 0.01)。Pearson相关分析显示,观察组病人血清MFAP4与FBN1水平呈明显正相关关系(P < 0.01),且二者均与LN、PCⅢ、HA水平呈明显正相关关系(P < 0.01);logistic回归分析显示,MFAP4、FBN1和LN、PCⅢ、HA均为慢性心力衰竭的独立危险因素(P < 0.01)。观察组中,预后不良病人血清MFAP4和FBN1水平均明显高于预后良好病人(P < 0.01)。ROC曲线分析显示,MFAP4、FBN1诊断慢性心力衰竭病人心肌纤维化的AUC分别为0.814、0.831,二者联合诊断慢性心力衰竭病人心肌纤维化的AUC为0.881,优于单独诊断(P < 0.05)。
      结论: MFAP4、FBN1表达与慢性心力衰竭病人心肌纤维化密切相关,二者高表达可能促进慢性心力衰竭病人心肌纤维化,是慢性心力衰竭心肌纤维化的危险因素。

       

      Abstract:
      Objective To explore the relationship between the serum levels of microfibrillar associated protein 4 (MFAP4), fibrillin-1 (FBN1) and myocardial fibrosis in patients with chronic heart failure (CHF).
      Methods A total of 146 patients with CHF were selected as the observation group, and 146 healthy subjects were set as the control group at the same time. The serum levels of MFAP4 and FBN1 were detected by ELISA, and the levels of LN, PCⅢ and HA were detected by radioimmunoassay. The correlation between the serum levels of MFAP4, FBN1 and myocardial fibrosis indexes, and diagnostic value of MFAP4 and FBN1 in patients with CHF were analyzed.
      Results The serum levels of MFAP4, FBN1, LN, PCⅢ and HA in the observation group were significantly higher than those in control group (P < 0.01). The results of pearson correlation analysis showed that the serum levels of MFAP4 were significantly positively correlated with FBN1 (P < 0.01), and both were significantly positively correlated with LN, PCⅢ and HA levels in the observation group (P < 0.01). The results of logistic regression analysis showed that the MFAP4, FBN1 and LN, PCⅢ and HA were the independent risk factors of chronic heart failure (P < 0.01). In the observation group, the serum levels of MFAP4 and FBN1 in patients with poor prognosis were significantly higher than those in patients with good prognosis (P < 0.01). The results of ROC curve analysis showed that the AUC of MFAP4 and FBN1 in diagnosing myocardial fibrosis in patients with chronic heart failure were 0.814 and 0.831, respectively, and the AUC of MFAP4 and FBN1 in diagnosing myocardial fibrosis in patients with chronic heart failure was 0.881, which was better than that of single diagnosis (P < 0.05).
      Conclusions The expressions of MFAP4 and FBN1 are closely related to the myocardial fibrosis in patients with CHF. The high expression of both may promote the myocardial fibrosis in patients with CHF, and is a risk factor for myocardial fibrosis in CHF.

       

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