首页|血清微小核糖核酸-1297和微小核糖核酸-4458在骨肉瘤患者诊断及预后评估中的价值

血清微小核糖核酸-1297和微小核糖核酸-4458在骨肉瘤患者诊断及预后评估中的价值

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目的:探讨微小核糖核酸-1297(miR-1297)和微小核糖核酸-4458(miR-4458)在骨肉瘤患者血清中的表达水平,以及在诊断和预后评估中的价值。方法:收集2019年1月至2020年1月手术治疗的90例骨肉瘤患者(骨肉瘤组)作为研究对象,所有患者术后均进行3年的随访,根据生存情况将患者分为生存组(49例)和死亡组(41例);另选取同期在本院体检的90例健康者作为对照组。比较各组血清miR-1297和miR-4458水平,多因素Logistic回归分析骨肉瘤患者预后的影响因素,用受试者工作特征(ROC)曲线分析血清miR-1297和miR-4458对骨肉瘤的诊断价值以及对预后的评估价值。结果:骨肉瘤组miR-1297和miR-4458水平低于对照组,差异有统计学意义(P<0。05)。miR-1297和miR-4458联合诊断骨肉瘤的曲线下面积(AUC)为0。863,敏感性为88。89%,特异性为65。56%,二者联合优于血清 miR-1297 和 miR-4458 各自单独诊断(Z二者联合-miR-1297=3。043,Z二者联合-miR-4458=3。826;P=0。002,<0。001)。肿瘤淋巴结转移(TNM)分期为ⅡB/Ⅲ期、发生远处转移的骨肉瘤患者血清miR-1297和miR-4458 表达水平低于TNM分期为Ⅱ A期、未发生远处转移的患者,差异有统计学意义(P<0。05)。死亡组血清miR-1297和miR-4458表达水平低于生存组,差异有统计学意义(P<0。05)。血清miR-1297和miR-4458二者联合预测骨肉瘤患者预后的曲线下面积为0。951,敏感性为97。56%,特异性为83。67%,二者联合优于各自单独预测(Z二者联合-miR-1297=2。080,Z二者联合-miR-4458=2。530;P=0。038,0。011)。多因素Logistic回归分析结果显示,血清miR-1297和miR-4458表达水平高为骨肉瘤患者预后的保护因素,TNM分期晚、远处转移为危险因素(P<0。05)。结论:骨肉瘤患者血清miR-1297和miR-4458下调,二者联合对诊断骨肉瘤和预测患者预后有较好的参考价值。
The Value of Serum miR-1297 and miR-4458 in the Diagnosis and Prognosis Evaluation of Osteosarcoma Patients
Objective:To investigate the expression levels of microRNA-1297(miR-1297)and microRNA-4458(miR-4458)in the serum of patients with osteosarcoma,and their value in diagnosis and prognosis evaluation.Methods:90 patients with osteosarcoma(osteosarcoma group)who underwent surgical treatment from January 2019 to January 2020 were collected as research subjects,and all patients were followed up for 3 years after surgery.According to survival status,patients were grouped into survival group(49 cases)and death group(41 cases).Another 90 healthy individuals who underwent physi-cal examination during the same period and matched the general information of osteosarcoma patients were regarded as the control group.The levels of serum miR-1297 and miR-4458 in each group were compared,multivariate Logistic regression was applied to analyze the influencing factors of prognosis in patients with osteosarcoma.Receiver operator characteristic(ROC)curve was applied to analyze the diagnostic value of serum miR-1297 and miR-4458 for osteosarcoma and their prognostic value.Results:The levels of miR-1297 and miR-4458 in the osteosarcoma group were reduced than those in control group.The differences were statistically significant(P<0.05).The area under the curve(AUC)of the combined diagnosis of miR-1297 and miR-4458 for osteosarcoma was 0.863,with a sensitivity of 88.89%and a specificity of 65.56%,the combination of the two was superior to the individual diag-nosis of serum miR-1297 and miR-4458(Zcombination-miR-1297=3.043,Zcombination-miR-4458=3.826,P=0.002,<0.001).The expression levels of miR-1297 and miR-4458 in serum of osteosarcoma patients with TNM stage ⅡB/Ⅲ and distant metastasis were lower than those of patients with TNM stage Ⅱ A and no distant metastasis,the differences were statistically significant(P<0.05).The expression levels of serum miR-1297 and miR-4458 in the death group were lower than those in the survival group,the differences were statistically significant(P<0.05).The combined prediction of serum miR-1297 and miR-4458 for the prognosis of osteosarcoma had an AUC of 0.951,a sensitivity of 97.56%,and a specificity of 83.67%,the combi-nation of the two was superior to their individual predictions(Zcombination-miR-1297=2.080,Zcombination-miR-4458=2.530,P=0.038,0.011).The results of multivariate Logistic regression analysis showed that serum miR-1297 and miR-4458 were protec-tive factors for the prognosis of osteosarcoma patients,while TNM staging and distant metastasis were risk factors(P<0.05).Conclusion:Serum miR-1297 and miR-4458 are obviously down-regulated in patients with osteosarcoma,and the combination of the two has good reference value for diagnosing osteosarcoma and predicting prognosis.

osteosarcomamicroRNA-1297microRNA-4458diagnosisprognosis

龚高进、许泽川、黄海汛

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成都医学院第二附属医院/核工业四一六医院(成都,610051)

骨肉瘤 微小核糖核酸-1297 微小核糖核酸-4458 诊断 预后

成都市医学科研项目(2023)

202304073353

2024

中国中医骨伤科杂志
中华中医药学会,湖北省中医药研究院

中国中医骨伤科杂志

CSTPCD
影响因子:0.732
ISSN:1005-0205
年,卷(期):2024.32(4)
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