山东大学学报(医学版) ›› 2015, Vol. 53 ›› Issue (11): 59-63.doi: 10.6040/j.issn.1671-7554.0.2015.837
丁娟, 郑桂喜, 杜鲁涛, 尹作花, 张建, 王传新
DING Juan, ZHENG Guixi, DU Lutao, YIN Zuohua, ZHANG Jian, WANG Chuanxin
摘要: 目的 检测血浆可溶性HLA-G(sHLA-G)及胃蛋白酶原PGI、PGII胃泌素-17(G-17)在胃癌及相关胃病患者外周血中的表达水平,评估sHLA-G与PGR(PGI/PGII)、GPR(G-17/PGI)联合检测在胃癌诊断中的效能.方法 采用化学发光微粒子免疫分析技术检测50例健康对照组、46例萎缩性胃炎组、50例胃上皮内瘤变组、36例早期胃癌组及74例进展期胃癌组PGI、PGII的表达,同时采用酶联免疫吸附试验(ELISA)法检测G-17、sHLA-G的表达水平,通过Logistic回归将各标志物引入方程,构建胃癌诊断模型,利用ROC曲线评估其在胃癌诊断中的效能.结果 与健康对照组、萎缩性胃炎组和胃上皮内瘤变组比较,早期胃癌和进展期胃癌组的PGR较低(P<0.05),而GPR与sHLA-G较高(P<0.05);sHLA-G与PGR诊断胃癌的ROC曲线下面积(AUC)分别为0.846(95%CI,0.760~0.910)和0.835(95%CI,0.748~0.902),均高于GPR的AUC 0.716(95%CI,0.617~0.802, P<0.05);构建联合检测胃癌诊断模型的方程为logit(Y)=0.41+0.03×sHLA-G-5.90×PGR,得到新变量Y诊断胃癌的AUC为0.924(95%CI,0.873~0.967),高于sHLA-G和PGR(P<0.05).结论 sHLA-G和PGR联合检测对胃癌具有较高的诊断价值,可作为传统肿瘤标志物的有益补充.
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