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Diagnostic values of serum levels of pepsinogens and gastrin-17 for screening gastritis and gastric cancer in a high risk area in Northern Iran

机译:血清胃蛋白酶原和胃泌素17的水平对伊朗北部高危地区筛查胃炎和胃癌的诊断价值

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摘要

Background: Gastric cancer (GC) is the second cause of cancer related death in the world. It may develop by progression from its precancerous condition, called gastric atrophy (GA) due to gastritis. The aim of this study was to evaluate the accuracy of serum levels of pepsinogens (Pg) and gastrin-17 (G17) as non-invasive methods to discriminate GA or GC (GA/GC) patients. Materials and Methods: Subjects referred to gastrointestinal clinics of Golestan province of Iran during 2010 and 2011 were invited to participate. Serum levels of PgI, PgII and G17 were measured using a GastroPanel kit. Based on the pathological examination of endoscopic biopsy samples, subjects were classified into four groups: normal, non-atrophic gastritis, GA, and GC. Receiver operating curve (ROC) analysis was used to determine cut-off values. Indices of validity were calculated for serum markers. Results: Study groups were normal individuals (n=74), non-atrophic gastritis (n=90), GA (n=31) and GC patients (n=30). The best cut-off points for PgI, PgI/II ratio, G17 and HP were 80 μg/L, 10, 6 pmol/L, and 20 EIU, respectively. PgI could differentiate GA/GC with high accuracy (AUC=0.83; 95%CI: 0.76-0.89). The accuracy of a combination of PgI and PgI/II ratio for detecting GA/GC was also relatively high (AUC=0.78; 95%CI: 0.70-0.86). Conclusions: Our findings suggested PgI alone as well as a combination of PgI and PgI/II ratio are valid markers to differentiate GA/GC. Therefore, Pgs may be considered in conducting GC screening programs in high-risk areas.
机译:背景:胃癌(GC)是世界上与癌症相关的死亡的第二大原因。它可能从其癌前状态(由于胃炎引起的胃萎缩症(GA))的进展发展而来。这项研究的目的是评估胃蛋白酶原(Pg)和胃泌素17(G17)的血清水平作为区分GA或GC(GA / GC)患者的非侵入性方法的准确性。材料和方法:2010年至2011年间,在伊朗Golestan省的胃肠病诊所就诊的受试者被邀请参加。使用GastroPanel试剂盒测量血清PgI,PgII和G17的水平。根据内窥镜活检样本的病理检查,将受试者分为四类:正常,非萎缩性胃炎,GA和GC。接收器工作曲线(ROC)分析用于确定临界值。计算血清标志物的有效性指标。结果:研究组为正常个体(n = 74),非萎缩性胃炎(n = 90),GA(n = 31)和GC患者(n = 30)。 PgI,PgI / II比,G17和HP的最佳临界点分别为80μg/ L,10、6 pmol / L和20 EIU。 PgI可以高精度地区分GA / GC(AUC = 0.83; 95%CI:0.76-0.89)。 PgI和PgI / II比值组合检测GA / GC的准确性也较高(AUC = 0.78; 95%CI:0.70-0.86)。结论:我们的研究结果表明,单独的PgI以及PgI和PgI / II比值的组合是区分GA / GC的有效标记。因此,在高风险地区进行GC筛查计划时,可以考虑使用Pg。

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