血清微小RNA-182-5p、微小RNA-31-5p联合预测溃疡性结肠炎预后的价值

Value of combined prediction of prognosis in ulcerative colitis by serum microRNA-182-5p and microRNA-31-5p

  • 摘要:
    目的 探讨血清微小RNA-182-5p(miR-182-5p)、微小RNA-31-5p(miR-31-5p)联合预测溃疡性结肠炎(UC)患者预后的价值。
    方法 选取112例UC患者作为研究对象(观察组)。根据Mayo评分将患者分为A组(轻度, n=39)、B组(中度, n=45)和C组(重度, n=28)。另择同期体检健康者70例为对照组。采用逆转录定量聚合酶链反应法测定血清miR-182-5p、miR-31-5p的表达水平。采用Logistic回归分析法筛选UC患者预后不良的影响因素。采用受试者工作特征(ROC)曲线分析血清miR-182-5p、miR-31-5p水平预测患者预后不良的临床价值。
    结果 观察组血清miR-182-5p表达水平低于对照组, miR-31-5p表达水平高于对照组,差异有统计学意义(P < 0.05)。UC患者病情越严重,血清miR-182-5p表达水平越低,血清miR-31-5p表达水平越高(P < 0.05)。预后不良患者的血清miR-182-5p表达水平低于预后良好患者, miR-31-5p水平高于预后良好患者,差异有统计学意义(P < 0.05)。血清miR-31-5p表达水平升高(OR=3.153)、miR-182-5p水平降低(OR=0.695)是UC患者预后不良的危险因素(P < 0.05)。血清miR-182-5p、miR-31-5p单独预测UC患者预后不良的曲线下面积(AUC)分别为0.723、0.811, 二者联合预测的AUC为0.913, 灵敏度为94.12%, 特异度为85.90%。血清miR-182-5p、miR-31-5p联合预测优于其单独预测(P < 0.05)。
    结论 UC患者病情越加重,血清miR-182-5p表达水平越低, miR-31-5p表达水平越高。

     

    Abstract:
    Objective To investigate the value of combined prediction of prognosis in patients with ulcerative colitis (UC) by serum microRNA-182-5p (miR-182-5p) and microRNA-31-5p (miR-31-5p).
    Methods A total of 112 UC patients were selected as the study subjects (observation group). According to the Mayo score, they were divided into Group A (mild, n=39), Group B (moderate, n=45) and Group C (severe, n=28). Additionally, 70 healthy individuals undergoing physical examinations during the same period were selected as control group. The expression levels of serum miR-182-5p and miR-31-5p were measured using reverse transcription quantitative polymerase chain reaction. Logistic regression analysis was employed to screen influencing factors for poor prognosis in UC patients. The clinical value of serum miR-182-5p and miR-31-5p levels in predicting poor prognosis in patients was analyzed using the receiver operating characteristic (ROC) curve.
    Results The expression level of serum miR-182-5p in the observation group was significantly lower, and the expression level of miR-31-5p was significantly higher than that in the control group (P < 0.05). The more severe the condition of UC patients were, the lower the expression level of serum miR-182-5p and the higher the expression level of serum miR-31-5p would be(P < 0.05). The expression level of serum miR-182-5p in patients with poor prognosis was significantly lower than that in patients with good prognosis, and the level of miR-31-5p was significantly higher than that in patients with good prognosis (P < 0.05). Elevated serum miR-31-5p expression (OR=3.153) and decreased miR-182-5p levels (OR=0.695) were risk factors for poor prognosis in UC patients (P < 0.05). The area under the curve (AUC) of serum miR-182-5p and miR-31-5p alone for predicting poor prognosis in UC patients was 0.723 and 0.811, respectively. The AUC of the combined prediction of the two indicators was 0.913, with a sensitivity of 94.12% and a specificity of 85.90%. The combined prediction of serum miR-182-5p and miR-31-5p was superior to their individual prediction (P < 0.05).
    Conclusion As the condition of UC patients worsens, the expression level of serum miR-182-5p decreases, while the expression level of miR-31-5p increases.

     

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