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首页> 外文期刊>Journal of clinical laboratory analysis. >Clinical evaluation of serum alpha-fetoprotein-IgM immune complexes on the diagnosis of primary hepatocellular carcinoma.
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Clinical evaluation of serum alpha-fetoprotein-IgM immune complexes on the diagnosis of primary hepatocellular carcinoma.

机译:血清甲胎蛋白-IgM免疫复合物在原发性肝细胞癌诊断中的临床评估。

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We evaluated clinical significance of serum alpha-fetoprotein (AFP)-IgM immune complexes, in comparison with free AFP, on the diagnosis of primary hepatocellular carcinoma (HCC). Serum levels of AFP-IgM immune complexes and free AFP were determined by the ELISA method and electrochemiluminescence, respectively, in 103 healthy controls, 74 patients suffering from primary HCC, 27 patients suffering from liver cirrhosis, and 63 patients suffering from chronic hepatitis. The best cut-off value of AFP-IgM and free AFP for diagnosis of primary HCC were 300 AU/mL and 10 microg/L respectively, according to the area under the curve (AUC) in this study. The sensitivity of AFP-IgM and free AFP were 64.9 and 79.7%, and the specificity were 75.6 and 80.3%, respectively, when all cases of primary HCC were analyzed, and the AUC of free AFP was larger than that of AFP-IgM (0.85 vs. 0.72, Z=3.21). However, in case of primary HCC at early stages (stages I and II) were analyzed, the AUC of AFP-IgM was larger than that of free AFP (0.91 vs. 0.82, Z=1.73), which demonstrated that the sensitivity of AFP-IgM and free AFP were 94.4 and 72.2%, and the specificity were 81.9 and 79.9%, respectively. When both AFP-IgM and free AFP were positive, the specificity of diagnosis of primary HCC was 89.1%, and the efficacy was 79.0%. It is concluded that either sensitivity or specificity of serum level of AFP-IgM immune complexes was higher than that of free AFP in the diagnosis of primary HCC at early stages. As there was false positive AFP-IgM existed in the patients suffering from cirrhosis and chronic hepatitis, the combination of free AFP and AFP-IgM could significantly increase specificity and decrease false negative and/or false positive in the primary HCC at early stages.
机译:我们评估了血清α甲胎蛋白(AFP)-IgM免疫复合物与游离AFP相比在诊断原发性肝细胞癌(HCC)中的临床意义。采用ELISA法和电化学发光法分别测定103例健康对照者,74例原发性HCC患者,27例肝硬化患者和63例慢性肝炎患者血清AFP-IgM免疫复合物和游离AFP的水平。根据这项研究的曲线下面积(AUC),AFP-IgM和游离AFP诊断原发性HCC的最佳截止值分别为300 AU / mL和10 microg / L。当分析所有原发性肝癌病例时,AFP-IgM和游离AFP的敏感性分别为64.9和79.7%,特异性为75.6和80.3%,并且游离AFP的AUC大于AFP-IgM( 0.85比0.72,Z = 3.21)。但是,如果分析早期(第一阶段和第二阶段)原发性肝癌,则AFP-IgM的AUC大于游离AFP的AUC(0.91 vs. 0.82,Z = 1.73),这表明AFP的敏感性-IgM和游离AFP分别为94.4%和72.2%,特异性分别为81.9%和79.9%。当AFP-IgM和游离AFP均为阳性时,诊断原发性肝癌的特异性为89.1%,疗效为79.0%。结论是,在早期诊断原发性肝癌时,AFP-IgM免疫复合物的血清水平的敏感性或特异性均高于游离AFP。由于患有肝硬化和慢性肝炎的患者中存在假阳性AFP-IgM,因此游离AFP和AFP-IgM的组合可显着提高特异性,并在早期肝癌中减少假阴性和/或假阳性。

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