慢性萎缩性胃炎患者血清胃蛋白酶原、胃泌素17水平及意义

H. Su
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The levels of serum pepsinogen Ⅰ (PG Ⅰ), pepsinogen Ⅱ (PG Ⅱ) and G-17 were measured by enzyme-linked immunosorbent assay. And pepsinogen ratio (PGR), PG Ⅰ/PG Ⅱ, was calculated. Qualitative detection of Helicobacter pylori (Hp) was performed by 13C urea breath test. The levels of PGⅠ, PGⅡ, PGR, and G-17 in each group were analyzed and compared among groups. \n \n \nResults \nThe levels of serum PG Ⅰ and G-17 in the chronic atrophic gastritis group were significantly lower than those in the non-atrophic gastritis group (P 0.05), the difference in PGR between the two groups was statistically significant (P 0.05). \n \n \nConclusions \nDecreased levels of PGⅠ, PGR and G-17 are biological markers of chronic atrophic gastritis. 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摘要

目的分析慢性萎缩性胃炎患者血清胃蛋白酶原、胃泌素17 (G-17)水平及其临床意义。方法选取2016年1月至2019年1月在临汾市中心医院行胃镜检查的胃十二指肠疾病患者196例作为研究对象。根据胃镜检查结果将患者分为慢性萎缩性胃炎组和非萎缩性胃炎组,每组98例。慢性萎缩性胃炎组根据病变部位进一步分为萎缩性胃体炎组(34例)、萎缩性胃窦炎组(42例)和全萎缩性胃多灶性胃炎组(22例)。采用酶联免疫吸附法测定血清胃蛋白酶原Ⅰ(PGⅠ)、胃蛋白酶原Ⅱ(PGⅡ)和G-17的水平。计算胃蛋白酶原比值(PGR), PGⅠ/PGⅡ。13C尿素呼气试验定性检测幽门螺杆菌(Hp)。分析各组PGⅠ、PGⅡ、PGR、G-17水平,并进行组间比较。结果慢性萎缩性胃炎组血清PGⅠ、G-17水平显著低于非萎缩性胃炎组(P < 0.05),两组间PGR差异有统计学意义(P < 0.05)。结论PGⅠ、PGR、G-17水平降低是慢性萎缩性胃炎的生物学标志物。可根据血清PGⅠ和PGR截止值进行大规模人群筛查和慢性萎缩性胃炎筛查,进一步胃镜检查可提高胃癌的早期诊断率。关键词:胃肿瘤;慢性萎缩性胃炎;胃蛋白酶原我;胃蛋白酶原Ⅱ;胃泌激素17;胃蛋白酶原比例
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Levels and significance of pepsinogen, gastrin 17 in serum in patients with chronic atrophic gastritis
Objective To analyze the levels of serum pepsinogen, gastrin 17 (G-17) in patients with chronic atrophic gastritis and their clinical significance. Methods A total of 196 patients with gastroduodenal disease who underwent gastroscopy in Linfen Central Hospital from January 2016 to January 2019 were selected as the study objects. According to the results of gastroscopy, they were divided into chronic atrophic gastritis group and non-atrophic gastritis group, with 98 cases in each group. The patients in chronic atrophic gastritis group were further divided into atrophic gastric body inflammation group (34 cases), atrophic gastric antrum inflammation group (42 cases), and the whole atrophic gastric multifocal gastritis group (22 cases) according to the lesion sites. The levels of serum pepsinogen Ⅰ (PG Ⅰ), pepsinogen Ⅱ (PG Ⅱ) and G-17 were measured by enzyme-linked immunosorbent assay. And pepsinogen ratio (PGR), PG Ⅰ/PG Ⅱ, was calculated. Qualitative detection of Helicobacter pylori (Hp) was performed by 13C urea breath test. The levels of PGⅠ, PGⅡ, PGR, and G-17 in each group were analyzed and compared among groups. Results The levels of serum PG Ⅰ and G-17 in the chronic atrophic gastritis group were significantly lower than those in the non-atrophic gastritis group (P 0.05), the difference in PGR between the two groups was statistically significant (P 0.05). Conclusions Decreased levels of PGⅠ, PGR and G-17 are biological markers of chronic atrophic gastritis. Large-scale population screening and screening for chronic atrophic gastritis can be performed based on serum PGⅠ and PGR cutoffs, and further examination with gastroscopy can improve the early diagnostic rate of gastric cancer. Key words: Stomach neoplasms; Chronic atrophic gastritis; Pepsinogen I; Pepsinogen Ⅱ; Gastrin 17; Pepsinogen ratio
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