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作 者:刘艳红[1] 韩素桂[1] 刘洪梅[1] 高华[1] 李玉柱[1]
机构地区:[1]河北省唐山市人民医院肿瘤医院检验科,063001
出 处:《肿瘤研究与临床》2013年第11期742-744,共3页Cancer Research and Clinic
摘 要:目的 探讨酶联免疫吸附(ELISA)法检测血清巨噬细胞抑制因子Ⅰ(MIC-1)联合甲胎蛋白异质体3(AFP-L3)对原发性肝癌的诊断价值.方法 选择116例临床确诊的原发性肝癌患者,应用ELISA法检测患者血清MIC-1和AFP-L3含量,分析二者联合检测在原发性肝癌诊断中的价值.结果 原发性肝癌组AFP-L3浓度为(127.12±51.43)ng/ml,明显高于正常对照组的(27.11±7.26) ng/ml(P< 0.001),以AFP-L3> 38.0 ng/ml为临界值时,灵敏度为85.34%(99/116),特异度为88.33%(53/60),诊断准确度为86.36%(152/176);原发性肝癌组MIC-1浓度为(3140.43±1138.23)pg/ml,明显高于正常对照组的(701.88±302.34) pg/ml(P<0.001),灵敏度为91.38%(106/116),特异度为85.00%(51/60),诊断准确度为89.20%(157/176).二者联合检测灵敏度为83.62%(97/116),特异度为91.67%(55/60),诊断准确度为86.36%(152/176).结论 MIC-1联合AFP-L3检测可提高原发性肝癌诊断的特异度,具有一定的临床价值.Objective Study on the diagnosis value of expression of serum macrophage inhibitory factor 1 (MIC-1) combined with alpha-fetoprotein isoforms 3 (AFP-L3) in primary liver cancer detected by enzyme linked immunosorbent assay (ELISA).Methods MIC-1 and AFP-L3 concentrations were detected by ELISA from selected 116 patients of primary liver cancer.Results were compared both in combined and sigle detection.Results In primary liver cancer group AFP-L3 concentration [(127.12±51.43) ngmml] was significantly higher than that in normal control group [(27.11±7.26) ng/ml,P 〈 0.001].With AFP-L3 〉 38.0 ng/ml as the critical value,the sensitivity was 85.34 % (99/116),specificity was 88.33 % (53/60) and the diagnostic accuracy was 86.36 % (152/176).In primary liver cancer group MIC-1 concentration [(3140.43±1138.23) pg/ml]was significantly higher than that in normal the control group [(701.88±302.34) pg/ml,P 〈 0.001],the sensitivity was 91.38 % (106/116),specificity was 85.00 % (51/60),the diagnostic accuracy was 89.20 %(157/176).The two combined detection sensitivity was 83.62 % (97/116),specificity was 91.67 % (55/60),diagnostic accuracy was 86.36 % (152/176).Conclusion MIC-1 combined with AFP-L3 concentration detection can improve the specificity of the diagnosis of primary liver cancer,which has certain clinical value.
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