首页|血清LncRNA-ZFAS1、miR-15a-5p相对表达量对癫痫持续状态患者预后不良的预测效能

血清LncRNA-ZFAS1、miR-15a-5p相对表达量对癫痫持续状态患者预后不良的预测效能

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目的 观察癫痫持续状态(SE)患者血清LncRNA-ZFAS1、miR-15a-5p表达变化,分析血清LncRNA-ZFAS1、miR-15a-5p相对表达量对SE患者预后不良的预测效能。方法 SE患者100例(SE组)、同期体检健康者68例(对照组),采用实时荧光定量聚合酶链式反应检测受检者血清LncRNA-ZFAS1、miR-15a-5p,通过starBase数据库预测LncRNA-ZFAS1与miR-15a-5p的结合位点。收集SE患者性别、年龄、病程、发作类型、基础疾病、院内并发症、脑组织异常、脑脊液异常、脑电图异常、伴发热、既往癫痫发作史≥2次、癫痫持续时间、机械通气、癫痫持续状态严重程度评分(STESS)、重症监护室时间、住院时间和治疗药物种类等一般资料,并根据格拉斯哥预后量表将SE患者分为不良预后组31例和良好预后组69例,比较不良预后组、良好预后组患者的一般资料及血清LncRNA-ZFAS1、miR-15a-5p相对表达量。以SE患者预后不良为因变量,以单因素分析中有统计学差异的变量为自变量,采用多因素Logistic回归分析法分析SE患者预后不良的危险因素。采用受试者工作特征曲线(ROC)分析血清LncRNA-ZFAS1、miR-15a-5p相对表达量及二者联合对SE患者预后不良的预测效能。结果 SE组受检者血清LncRNA-ZFAS1相对表达量高于对照组,miR-15a-5p相对表达量低于对照组(P均<0。05)。SE患者血清LncRNA-ZFAS1、miR-15a-5p相对表达量呈负相关关系(r=-0。742,P<0。001)。LncRNA-ZFAS1与miR-15a-5p的3'非翻译端存在互补序列。不良预后组惊厥性、癫痫持续时间≥1 h、机械通气比例、STESS评分、血清LncRNA-ZFAS1相对表达量高于良好预后组,血清miR-15a-5p相对表达量低于良好预后组(P均<0。05)。惊厥性SE、癫痫持续时间≥1 h、机械通气、STESS评分增加和血清LncRNA-ZFAS1相对表达量升高为SE患者不良预后的独立危险因素,血清miR-15a-5p相对表达量升高为独立保护因素(P均<0。05)。血清LncRNA-ZFAS1预测SE患者不良预后的AUC为 0。786,敏感度为 67。74%、特异度为75。36%;血清miR-15a-5p预测SE患者不良预后的AUC为 0。781,敏感度为 90。32%、特异度为 53。62%;血清LncRNA-ZFAS1联合miR-15a-5p预测SE患者不良预后的AUC为0。879,敏感度为87。10%、特异度为73。91%。结论 SE患者血清LncRNA-ZFAS1高表达、miR-15a-5p低表达,呈负相关关系。血清LncRNA-ZFAS1相对表达量升高为SE患者不良预后的独立危险因素,血清miR-15a-5p相对表达量升高为独立保护因素。检测血清LncRNA-ZFAS1、miR-15a-5p可用于SE患者预后不良的预测,且二者联合预测效能更高。
Predictive efficacy of relative expression of serum LncRNA-ZFAS1 and miR-15a-5p for poor prognosis in patients with status epilepticus
Objective To observe the changes in the expression levels of serum LncRNA-ZFAS1 and miR-15a-5p in patients with status epilepticus(SE),and to analyze the predictive efficacy of the relative expression of serum LncRNA-ZFAS1 and miR-15a-5p for the poor prognosis of SE patients.Methods Totally 100 cases of SE patients(SE group)and 68 cases of healthy people with physical examination in the same period(control group)were selected,and real-time fluo-rescence quantitative polymerase chain reaction was used to detect serum LncRNA-ZFAS1 and miR-15a-5p levels in the subjects,and the binding sites of LncRNA-ZFAS1 and miR-15a-5p were predicted by starBase database.General data such as gender,age,disease duration,seizure type,underlying disease,in-hospital complications,brain tissue abnormal-ities,cerebrospinal fluid abnormalities,electroencephalogram abnormalities,concomitant fever,history of≥2 previous seizures,duration of epilepsy,mechanical ventilation,status epilepticus severity score(STESS),time in the intensive care unit,length of hospital stay,and types of therapeutic medications were collected from the patients with SE.According to the Glasgow Prognostic Score,the SE patients were divided into the poor prognosis group of 31 cases and the good prog-nosis group of 69 cases.We compared the general data and the relative expression levels of serum LncRNA-ZFAS1 and miR-15a-5p of the patients in the poor prognosis group and the good prognosis group.Risk factors for poor prognosis in SE patients were analyzed by multifactorial Logistic regression analysis.Using poor prognosis in SE patients as the dependent variable,and variables that were statistically different in univariate analyses as independent variables.The risk factors for poor prognosis in SE patients were analyzed using multivariate Logistic regression analysis.The predictive efficacy of the combination of relative expression of serum LncRNA-ZFAS1 and miR-15a-5p on poor prognosis in SE patients was ana-lyzed using receiver operating characteristic(ROC)curve.Results The relative expression of serum LncRNA-ZFAS1 in the SE group was higher than that of the control group,and the relative expression of miR-15a-5p was lower than that of the control group(both P<0.05).There was a negative correlation between the relative expression of serum LncRNA-ZFAS1 and miR-15a-5p in the SE patients(r=-0.742,P<0.05).LncRNA-ZFAS1 had a complementary sequence to the 3'un-translated end of miR-15a-5p.The convulsive SE,seizure duration≥1 h,the proportion of mechanical ventilation,STESS score,and serum LncRNA-ZFAS1 were higher in the poor prognosis group than in the good prognosis group,and the rela-tive expression of serum miR-15a-5p was lower than that of the good prognosis group(all P<0.05).The AUC of serum Ln-cRNA-ZFAS1 in predicting poor prognosis of SE patients was 0.786,with a sensitivity of 67.74%and a specificity of 75.36%;the AUC of serum miR-15a-5p in predicting poor prognosis of SE patients was 0.781,with a sensitivity of 90.32%and a specificity of 53.62%;and the AUC of serum LncRNA-ZFAS1 combined with miR-15a-5p in predicting poor prognosis of SE patients was 0.879,with the sensitivity of 87.10%and specificity of 73.91%.Conclusions Se-rum LncRNA-ZFAS1 is highly expressed and miR-15a-5p is low expressed in SE patients,which shows a negative correla-tion.Elevated relative expression of serum LncRNA-ZFAS1 is an independent risk factor for poor prognosis of SE patients,and elevated relative expression of serum miR-15a-5p is an independent protective factor.Detection of serum LncRNA-ZFAS1 and miR-15a-5p can be used for the prediction of poor prognosis in SE patients,and the predictive value of the two combined is higher.

epilepsystatus epilepticuslong non-coding RNA zinc finger NFX1-type containing 1 antisense RNA 1microRNA-15a-5pprognostic prediction

陈倩、韩忠海、宋志刚、黄陈、王华、王海滨

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资阳市中心医院神经内科,四川资阳 641300

资阳市中心医院实验医学科

癫痫 癫痫持续状态 长链非编码核糖核酸锌指NFX1型核转录因子反义链1 微小核糖核酸-15a-5p 预后预测

四川省卫生健康科研课题项目

20PJ308

2024

山东医药
山东卫生报刊社

山东医药

CSTPCD
影响因子:1.225
ISSN:1002-266X
年,卷(期):2024.64(21)