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Helicobacter pylori gastritis and serum pepsinogen levels in a healthy population: development of a biomarker strategy for gastric atrophy in high-risk groups

机译:健康人群中的幽门螺杆菌胃炎和血清胃蛋白酶原水平:高风险人群胃萎缩症生物标志物策略的发展

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This study aimed to estimate the prevalence and type of chronic gastritis in an asymptomatic working population and to determine whether a combination of serum pepsinogen levels and Helicobacter pylori serology could be used to identify a subgroup with atrophic gastritis at elevated risk of gastric carcinoma. A 10% subsample of 544 male volunteer factory workers aged 18-63 years and participating in a larger study underwent endoscopy and biopsy. Of these men, 29 were seropositive for Helicobacter pylori; all but three (89.7%) had chronic gastritis. Serum pepsinogen A levels increased with progression from a corpus predominant pattern of gastritis through pangastritis to an antral predominant pattern. Nine subjects had corpus atrophy, which was in most cases accompanied by fasting hypochlorhydria and hypergastrinaemia. A combination of pepsinogen A below 80 ng ml-1 and Helicobaceter pylori seropositivity detected corpus atrophy with sensitivity 88.9% and specificity 92.3%. A second screening stage, using a pepsinogen A/C ratio of below 2.5 as a cut-off, resulted in a reduction in numbers requiring further investigation but with some loss of sensitivity (77.8%). Application of this two-stage screening programme to the original sample of 544 workers would have resulted in 11 (2.2%) men being selected for follow-up, excluding 25 (5.1%) false negatives. Our results suggest that a combination of serum pepsinogen levels and Helicobacter pylori serology could be useful as a biomarker strategy for detection of individuals at increased risk of gastric carcinoma and for non-invasive investigation of the natural history of Helicobacter pylori gastritis.
机译:这项研究的目的是评估无症状工作人群中慢性胃炎的患病率和类型,并确定血清胃蛋白酶原水平和幽门螺杆菌血清学的组合是否可用于鉴定胃癌风险升高的萎缩性胃炎亚组。 544位年龄在18-63岁之间的男性志愿者工厂工人中有10%的子样本参加了较大的研究,并接受了内窥镜检查和活检。在这些人中,有29人对幽门螺杆菌呈血清反应阳性。除三人(89.7%)外,其余所有人均患有慢性胃炎。血清胃蛋白酶原A水平随胃炎的全胃部胃炎,胃炎和胃窦部疾病而增加。九名受试者患有体萎缩,多数情况下伴有禁食性胃酸过多和胃泌素过多血症。低于80 ng ml-1的胃蛋白酶原A和幽门螺杆菌血清阳性的组合检测到体萎缩,敏感性为88.9%,特异性为92.3%。在第二个筛查阶段,以低于2.5的胃蛋白酶原A / C比作为临界值,导致需要进一步研究的数量有所减少,但灵敏度有所下降(77.8%)。如果将这两个阶段的筛选程序应用于544名工人的原始样本,则将选择11名(2.2%)男性作为随访对象,不包括25名(5.1%)假阴性。我们的结果表明,血清胃蛋白酶原水平和幽门螺杆菌血清学的结合可能作为一种生物标志物策略,可用于检测患胃癌风险增高的个体以及用于幽门螺杆菌胃炎自然史的非侵入性研究。

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