朱瑞伍, 郭晓杰, 张庆. 血清微小RNA-20a-5p、微小RNA-128-3p与缺氧缺血性脑病患儿脑神经发育的关系[J]. 实用临床医药杂志, 2023, 27(22): 50-54. DOI: 10.7619/jcmp.20232224
引用本文: 朱瑞伍, 郭晓杰, 张庆. 血清微小RNA-20a-5p、微小RNA-128-3p与缺氧缺血性脑病患儿脑神经发育的关系[J]. 实用临床医药杂志, 2023, 27(22): 50-54. DOI: 10.7619/jcmp.20232224
ZHU Ruiwu, GUO Xiaojie, ZHANG Qing. Relationships of serum microRNA-20a-5p and microRNA-128-3p with cranial nerve development in children with hypoxic-ischemic encephalopathy[J]. Journal of Clinical Medicine in Practice, 2023, 27(22): 50-54. DOI: 10.7619/jcmp.20232224
Citation: ZHU Ruiwu, GUO Xiaojie, ZHANG Qing. Relationships of serum microRNA-20a-5p and microRNA-128-3p with cranial nerve development in children with hypoxic-ischemic encephalopathy[J]. Journal of Clinical Medicine in Practice, 2023, 27(22): 50-54. DOI: 10.7619/jcmp.20232224

血清微小RNA-20a-5p、微小RNA-128-3p与缺氧缺血性脑病患儿脑神经发育的关系

Relationships of serum microRNA-20a-5p and microRNA-128-3p with cranial nerve development in children with hypoxic-ischemic encephalopathy

  • 摘要:
    目的 分析微小RNA(miR)-20a-5p、miR-128-3p在缺氧缺血性脑病(HIE)早产儿血清中的表达与脑神经发育的关系。
    方法 选取95例HIE早产儿为HIE组,根据HIE早产儿病情严重程度,将其分为轻度组(n=27)、中度组(n=46)、重度组(n=22);另选取同期95例无HIE早产儿为对照组。评估2组早产儿Apgar评分和新生儿神经行为测定评分法(NBNA)评分;采用实时荧光定量聚合酶链式反应(qRT-PCR)检测血清中miR-20a-5p和miR-128-3p表达水平;Spearman法分析血清miR-20a-5p、miR-128-3p水平与Apgar评分、NBNA评分的相关性;受试者工作特征(ROC)曲线分析血清miR-20a-5p、miR-128-3p水平对早产儿发生HIE的诊断价值。
    结果 与对照组相比,HIE组血清miR-20a-5p、miR-128-3p水平升高,Apgar评分、NBNA评分降低,差异有统计学意义(P < 0.05)。轻度组、中度组、重度组血清miR-20a-5p、miR-128-3p水平依次升高,Apgar评分、NBNA评分依次降低,差异均有统计学意义(P < 0.05)。Spearman法分析结果显示,血清miR-20a-5p水平与Apgar评分、NBNA评分呈负相关(r=-0.659、-0.548,P均 < 0.001),血清miR-128-3p水平与Apgar评分、NBNA评分呈负相关(r=-0.582、-0.499,P均 < 0.001)。血清miR-20a-5p、miR-128-3p联合预测早产儿发生HIE的曲线下面积(AUC)为0.920,敏感度为78.95%,特异度为97.89%。二者联合对早产儿发生HIE的预测效能优于miR-20a-5p、miR-128-3p单独预测,差异有统计学意义(P < 0.05)。
    结论 HIE早产儿血清miR-20a-5p、miR-128-3p水平升高,且与病情严重程度和脑神经发育密切相关。miR-20a-5p、miR-128-3p联合检测对早产儿HIE发生有较好的预测价值。

     

    Abstract:
    Objective To analyze the relationships of expressions of serum microRNA (miR)-20a-5p and miR-128-3p with cranial nerve development in the premature infants with hypoxic-ischemic encephalopathy (HIE).
    Methods A total of 95 HIE premature infants were selected as HIE group, and according to the severity of HIE, they were divided into mild group (n=27), moderate group (n=46) and severe group (n=22); another 95 premature infants without HIE in the same period were selected as control group. Apgar score and the Neonatal Behavioral Neurological Assessment (NBNA) score were performed in both groups; the expression levels of miR-20a-5p and miR-128-3p in serum were detected by real-time fluorescence quantitative polymerase chain reaction (qRT-PCR); Spearman method was used to analyze the correlations of serum miR-20a-5p and miR-128-3p levels with Apgar score and NBNA score; the values of serum miR-20a-5p and miR-128-3p levels in diagnosing HIE in premature infants were analyzed by receiver operating characteristic (ROC) curve.
    Results Compared with the control group, the levels of serum miR-20a-5p and miR-128-3p in the HIE group increased significantly, while the Apgar score and NBNA score decreased significantly (P < 0.05). In the mild, moderate, and severe groups, the levels of serum miR-20a-5p and miR-128-3p increased gradually, while the Apgar score and NBNA score decreased gradually, with the significant between-group differences (P < 0.05). Spearman analysis results showed that the level of serum miR-20a-5p was negatively correlated with the Apgar score and NBNA score (r=-0.659, -0.548, P < 0.001), and the level of serum miR-128-3p was negatively correlated with the Apgar score and NBNA score (r=-0.582, -0.499, P < 0.001). The combined prediction of serum miR-20a-5p and miR-128-3p for HIE in premature infants had an area under the curve (AUC) of 0.920, with a sensitivity of 78.95% and a specificity of 97.89%. The predictive efficacy of the combined model was superior to that of miR-20a-5p and miR-128-3p alone (P < 0.05).
    Conclusion The serum levels of miR-20a-5p and miR-128-3p increase in the premature infants with HIE, and are closely related to the severity of the disease and the development of brain nerves. The combined detection of miR-20a-5p and miR-128-3p has good predictive value for the occurrence of HIE in premature infants.

     

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