高敏感α-胎蛋白变异比在肝癌诊断和治疗中的临床应用

Xuan Yang, Guirong Sun, Qiang Xi, Chong Peng, Lin Wang, Mingjun Liu, Z. Tian
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引用次数: 0

摘要

目的探讨血清高敏α-胎蛋白变异比(hs-AFP-L3%)在肝癌诊断和治疗中的临床应用价值。方法选取2016年10月至2018年3月青岛大学附属医院160例肝癌患者、32例肝内胆管癌(ICC)患者、52例乙肝后肝硬化患者、53例慢性乙肝患者和50例健康对照。测定血清hs-AFP-L3%和α-胎蛋白水平。采用Mann-Whitney U检验、Spearman相关分析、Wilcoxon符号秩检验和卡方检验进行统计学分析。结果肝癌组血清hs-AFP-L3%和α-胎蛋白水平分别为24.90%(4.68% ~ 61.85%)和113.45 μg/L (11.18 ~ 1 803.48 μg/L),高于肝癌组(0.50%、0.50% ~ 0.50%;2.79 μg/L、1.72 μg/L ~ 4.04 μg/L),肝硬化组(0.50%、0.50% ~ 5.25%;18.35 μg/L、3.95 μg/L ~ 31.93 μg/L),慢性肝炎组(0.50%、0.50% ~ 4.25%;2.70 μg/L、1.80 μg/L ~ 17.00 μg/L),健康对照组(0.50%、0.50% ~ 0.50%;1.94 μg/L、1.46 μg/L ~ 2.63 μg/L),差异有统计学意义(U=461.00、1 485.50、1 141.00、625.00;401.50, 2 207.00, 1 254.00, 266.00;P < 0.05)。联合检测的敏感性为82.5%,高于单独检测,差异有统计学意义(χ2=24.04、18.05,P均为0.05)。hs-AFP-L3%对α-胎蛋白阴性患者的诊断敏感性(α-胎蛋白0.05)。结论hs-AFP-L3%对肝癌的诊断敏感性与α-胎蛋白相近,但特异性高于α-胎蛋白。两种标志物联合检测可提高肝癌的诊断率。hs-AFP-L3%对α-胎蛋白阴性肝细胞癌具有较高的诊断价值。关键词:甲胎蛋白;癌,肝细胞;荧光抗体技术;变体
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical application of highly sensitive α-fetoprotein variant ratio in the diagnosis and treatment of hepatocellular carcinoma
Objective To evaluate the clinical application value of serum high sensitive α-fetoprotein variant ratio (hs-AFP-L3%) in the diagnosis and treatment of hepatocellular carcinoma. Methods From October 2016 to March 2018, at Affiliated Hospital of Qingdao University, 160 patients diagnosed with hepatocellular carcinoma, 32 patients with intrahepatic cholangiocarcinoma (ICC), 52 patients with post-hepatitis B liver cirrhosis, 53 patients with chronic hepatitis B and 50 healthy controls were enrolled. The serum levels of hs-AFP-L3% and α-fetoprotein were measured. Mann-Whitney U test, Spearman correlation analysis, Wilcoxon signed rank test and chi-square test were performed for statistical analysis. Results The serum levels of hs-AFP-L3% and α-fetoprotein in hepatocellular carcinoma group were 24.90% (4.68% to 61.85%) and 113.45 μg/L (11.18 μg/L to 1 803.48 μg/L), respectively, which were higher than those in ICC group (0.50%, 0.50% to 0.50%; and 2.79 μg/L, 1.72 μg/L to 4.04 μg/L), cirrhosis group (0.50%, 0.50% to 5.25%; and 18.35 μg/L, 3.95 μg/L to 31.93 μg/L), chronic hepatitis group (0.50%, 0.50% to 4.25%; and 2.70 μg/L, 1.80 μg/L to 17.00 μg/L), and healthy control group (0.50%, 0.50% to 0.50%; and 1.94 μg/L, 1.46 μg/L to 2.63 μg/L), and the differences were statistically significant (U=461.00, 1 485.50, 1 141.00, 625.00; 401.50, 2 207.00, 1 254.00, 266.00; all P 0.05). The sensitivity of the combined detection was 82.5%, which was higher than that of the separate detection, and the differences were statistically significant (χ2=24.04 and 18.05, both P 0.05). The sensitivity of hs-AFP-L3% in the diagnosis of patients with α-fetoprotein-negative (α-fetoprotein 0.05). Conclusions The sensitivity of hs-AFP-L3% is similar to that of α-fetoprotein in the diagnosis of hepatocellular carcinoma, while the specificity of hs-AFP-L3% is higher than that of α-fetoprotein. The combined detection of the two markers can improve the diagnostic rate of hepatocellular carcinoma. The hs-AFP-L3% has a high diagnostic value in α-fetoprotein-negative hepatocellular carcinoma. Key words: Alpha-fetoprotein; Carcinoma, hepatocellular; Fluorescent antibody technique; Variant
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