粪便miR-296-3p联合癌胚抗原在结直肠癌筛查中的应用价值[]
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承德医学院附属医院

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河北省省级科技计划资助项目(No:203777106D);河北省高层次人才资助项目(No:A201902016)


Application value of fecal miR-296-3p combined with Carcinoembryonic Antigen in Colorectal Cancer screening*
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    摘要:

    目的 探讨粪便miR-296-3p联合癌胚抗原(carcinoembryonic antigen,CEA)在结直肠癌(colorectal cancer,CRC)筛查中的临床价值。方法 收集2021年6月至2023年2月由我院收治并经病理检查确诊的104例CRC患者作为CRC组,选取同期在承德医学院附属医院进行体检的61例健康人群作为健康对照组(healthy control,HC),比较两组临床资料。用实时荧光定量PCR法(real-time fluorescence quantitative polymerase chain reaction ,RT-qPCR)检测两组粪便中miR-296-3p的表达情况;logistic回归分析CRC发生的独立危险因素;受试者工作曲线(ROC)评估miR-296-3p、CEA及两者联合预测模型对CRC的预测价值。结果 RT-qPCR结果显示,与HC组相比,CRC组粪便中miR-296-3p的表达下调(P<0.05)。单因素分析结果提示,CRC组与HC组患者在miR-296-3p的表达水平(x1)(P<0.05)、CEA的表达水平(x2)(P<0.05)比较差异有统计学意义。多因素分析结果提示miR-296-3p的表达(OR=0.7,95%Cl:0.5-0.9,P<0.05)与CEA表达水平(OR=1.8,95%Cl:1.3-2.4,P<0.05)为影响CRC发生的独立危险因素。个体预测概率方程为P=1/e-(-0.399-0.351x1+0.577x2)。miR-296-3p预测模型诊断CRC的敏感度和特异度分别是79.8%、42.6%(AUC=0.687,95%Cl:0.6-0.8),CEA预测模型诊断CRC的敏感度和特异度分别是81.4% 、59.6%,(AUC=0.800,95%Cl:0.7-0.9),miR-296-3p联合CEA预测模型诊断CRC的灵敏度和特异度为86.3%、63.5%,(AUC=0.847,95%Cl:0.8-0.9)。结论 miR-296-3p在CRC组中的表达水平低于HC组,miR-296-3p联合CEA的预测模型对CRC有较好的预测价值。

    Abstract:

    Objective To explore the clinical value of fecal miR-296-3p combined with carcinoembryonic antigen (CEA) in colorectal cancer (CRC) screening. Methods 104 CRC patients admitted to our hospital and confirmed by pathological examination from June 2021 to February 2023 were selected as CRC group, and 61 healthy people who underwent physical examination in the Affiliated Hospital of Chengde Medical College during the same period were selected as healthy control group (HC), and the clinical data of the two groups were compared. real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) was used to detect the expression of miR-296-3p in the feces of both groups. The independent risk factors of colorectal cancer were analyzed by logistic regression. The receiver operating curve (ROC) evaluated the predictive value of miR-296-3p, CEA, and their combined predictive models for CRC. Results RT-qPCR results showed that compared with HC group, the expression of miR-296-3p in feces of CRC group was down-regulated (P < 0.05). The results of univariate analysis indicated that there were statistically significant differences in the expression level of miR-296-3p (x1) and CEA (x2) between CRC group and HC group (P < 0.05). The results of multivariate analysis suggested that the expression of miR-296-3p (OR=0.7, 95%Cl: 0.5-0.9, P < 0.05) and CEA (OR=1.8, 95%Cl: 1.3-2.4, P < 0.05) were independent risk factors for CRC. The individual prediction probability equation is P=1/e- (-0.399-0.351x1+0.577x2). The sensitivity and specificity of miR-296-3p predictive model in the diagnosis of colorectal cancer were 79.8% and 42.6%, respectively (AUC=0.687, 95%Cl: 0.6-0.8), the sensitivity and specificity of CEA prediction model in the diagnosis of colorectal cancer were 81.4% and 59.6%, respectively (AUC=0.800, 95%Cl: 0.7-0.9), the sensitivity and specificity of miR-296-3p combined with CEA were 86.3% and 63.5% (AUC=0.847, 95%Cl: 0.8-0.9). Conclusion The expression level of miR-296-3p in CRC group is lower than that in healthy group, and the predictive model of miR-296-3p combined with CEA has good predictive value for CRC.

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  • 收稿日期:2023-06-01
  • 最后修改日期:2023-08-08
  • 录用日期:2023-09-13
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