诊断学理论与实践 ›› 2019, Vol. 18 ›› Issue (05): 570-574.doi: 10.16150/j.1671-2870.2019.05.016
周磊1, 王虹1(), 徐慧明2, 叶涛3, 高建萍1, 孙一骏1, 谢军1
收稿日期:
2019-08-20
出版日期:
2019-10-25
发布日期:
2019-10-25
通讯作者:
王虹
E-mail:13501762950@163.com
基金资助:
ZHOU Lei1, WANG Hong1(), XU Huiming2, YE Tao3, GAO Jianping1, SUN Yijun1, XIE Jun1
Received:
2019-08-20
Online:
2019-10-25
Published:
2019-10-25
Contact:
WANG Hong
E-mail:13501762950@163.com
摘要:
目的:评估胃蛋白酶原筛查试验在无症状胃癌高危人群中检出慢性萎缩性胃炎(chronic atrophic gastritis,CAG)的价值。方法:选取上海石门二路街道社区和南京西路街道社区中无症状的胃癌高危居民,测定其幽门螺杆菌抗体、血清胃蛋白酶原(pepsinogen,PG)Ⅰ和Ⅱ水平,并行内镜检查、胃黏膜活检,根据胃黏膜病理结果中CAG的累及范围分为无萎缩组、胃窦为主萎缩组、胃体为主萎缩组和胃广泛萎缩组4组。结果:本研究共入组居民178人,血清PGⅠ、PGⅡ水平在各组间差异无统计学意义,而与无萎缩组及胃窦为主萎缩组相比较,胃广泛萎缩组及胃体为主萎缩组的胃蛋白酶原比值(pepsinogen ratio,PGR)(PGⅠ/PGⅡ)显著降低(P<0.05)。当PGR临界值选择≤5.16时,检出胃广泛萎缩的灵敏度和特异度分别达到91.8%和61.9%,受试者工作特征曲线的曲线下面积为0.794;当临界值选择≤6.43时,诊断胃体为主萎缩性胃炎灵敏度和特异度分别达到78.7%和65.5%,曲线下面积达到0.750。结论:血清PGR在检出累及胃体的CAG中具有较高灵敏度和特异度,有望作为在胃癌高危人群中筛查CAG的血清学标志物。
中图分类号:
周磊, 王虹, 徐慧明, 叶涛, 高建萍, 孙一骏, 谢军. 血清胃蛋白酶原对上海中心城区胃癌高危人群筛查慢性萎缩性胃炎的潜在价值[J]. 诊断学理论与实践, 2019, 18(05): 570-574.
ZHOU Lei, WANG Hong, XU Huiming, YE Tao, GAO Jianping, SUN Yijun, XIE Jun. The potential value of serum pepsinogen in screening of chronic atrophic gastritis among population with high risk for gastric cancer of Shanghai central urban area[J]. Journal of Diagnostics Concepts & Practice, 2019, 18(05): 570-574.
表1
不同类型CAG的血清PG水平
项目 | 无萎缩组 | 胃窦为主萎缩组 | 胃体为主萎缩组 | 胃广泛萎缩组 | P值 |
---|---|---|---|---|---|
人数[n(%)] | 61(34.26%) | 67(37.64%) | 29(16.29%) | 21(11.79%) | |
性别(男/女) | 25/36 | 32/34 | 15/14 | 13/8 | 0.392 |
年龄(岁) | 63.36±6.94 | 65.14±7.48 | 67.14±6.97 | 67.05±7.37 | 0.071 |
PGⅠ(μg/L) | 116.94±64.42 | 129.89±92.42 | 108.13±99.48 | 92.50±71.55 | >0.050 |
PGⅡ(μg/L) | 12.80±9.97 | 14.19±11.19 | 16.03±11.93 | 17.82±11.43 | >0.050 |
PGR | 11.97±6.85 | 12.37±9.72 | 6.93±4.95a) | 6.04±4.53b) | <0.001 |
[1] |
Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2018, 68(6):394-424.
doi: 10.3322/caac.21492 URL |
[2] | 国家消化系统疾病临床医学研究中心, 中华医学会消化内镜学分会, 中华医学会健康管理学分会, 等. 中国早期胃癌筛查流程专家共识意见(草案)(2017年,上海)[J]. 胃肠病学, 2018, 23(2):92-97. |
[3] |
Venerito M, Nardone G, Selgrad M, et al. Gastric cancer--epidemiologic and clinical aspects[J]. Helicobacter, 2014, 19(Suppl 1):32-37.
doi: 10.1111/hel.12164 URL |
[4] |
Islami F, Sheikhattari P, Ren JS, et al. Gastric atrophy and risk of oesophageal cancer and gastric cardia adenocarcinoma--a systematic review and meta-analysis[J]. Ann Oncol, 2011, 22(4):754-760.
doi: S0923-7534(19)38545-X pmid: 20860989 |
[5] |
Kikuchi R, Abe Y, Iijima K, et al. Low serum levels of pepsinogen and gastrin 17 are predictive of extensive gastric atrophy with high-risk of early gastric cancer[J]. Tohoku J Exp Med, 2011, 223(1):35-44.
doi: 10.1620/tjem.223.35 URL |
[6] |
Vannella L, Lahner E, Annibale B. Risk for gastric neoplasias in patients with chronic atrophic gastritis: a critical reappraisal[J]. World J Gastroenterol, 2012, 18(12):1279-1285.
doi: 10.3748/wjg.v18.i12.1279 URL |
[7] | Hosseini M, Amoueian S, Attaranzadeh A, et al. Serum gastrin 17, pepsinogen I and pepsinogen II in atrophic gastritis patients living in North-East of Iran[J]. J Res Med Sci, 2013, 18(3):225-229. |
[8] |
Lomba-Viana R, Dinis-Ribeiro M, Fonseca F, et al. Serum pepsinogen test for early detection of gastric cancer in a European country[J]. Eur J Gastroenterol Hepatol, 2012, 24(1):37-41.
doi: 10.1097/MEG.0b013e32834d0a0a URL |
[9] |
Nasrollahzadeh D, Aghcheli K, Sotoudeh M, et al. Accuracy and cut-off values of pepsinogens I, II and gastrin 17 for diagnosis of gastric fundic atrophy: influence of gastritis[J]. PLoS One, 2011, 6(10):e26957.
doi: 10.1371/journal.pone.0026957 URL |
[10] |
Graham DY, Nurgalieva ZZ, El-Zimaity HM, et al. Noninvasive versus histologic detection of gastric atrophy in a Hispanic population in North America[J]. Clin Gastroenterol Hepatol, 2006, 4(3):306-314.
doi: 10.1016/j.cgh.2005.11.003 URL |
[11] |
Samloff IM. Pepsinogens I and II: purification from gastric mucosa and radioimmunoassay in serum[J]. Gastroenterology, 1982, 82(1):26-33.
pmid: 7053333 |
[12] |
Gritti I, Banfi G, Roi GS. Pepsinogens: physiology, pharmacology pathophysiology and exercise[J]. Pharmacol Res, 2000, 41(3):265-281.
pmid: 10675278 |
[13] |
Sipponen P. Update on the pathologic approach to the diagnosis of gastritis, gastric atrophy, and Helicobacter pylori and its sequelae[J]. J Clin Gastroenterol, 2001, 32(3):196-202.
pmid: 11246343 |
[14] |
Hansen S, Vollset SE, Derakhshan MH, et al. Two distinct aetiologies of cardia cancer; evidence from premorbid serological markers of gastric atrophy and Helicobacter pylori status[J]. Gut, 2007, 56(7):918-925.
pmid: 17317788 |
[15] |
Bornschein J, Selgrad M, Wex T, et al. Serological assessment of gastric mucosal atrophy in gastric cancer[J]. BMC Gastroenterol, 2012, 12:10.
doi: 10.1186/1471-230X-12-10 pmid: 22289789 |
[16] |
Leja M, Kupcinskas L, Funka K, et al. The validity of a biomarker method for indirect detection of gastric muco-sal atrophy versus standard histopathology[J]. Dig Dis Sci, 2009, 54(11):2377-2384.
doi: 10.1007/s10620-009-0947-5 URL |
[17] |
Kikuchi S, Kato M, Katsuyama T, et al. Design and planned analyses of an ongoing randomized trial asses-sing the preventive effect of Helicobacter pylori eradication on occurrence of new gastric carcinomas after endoscopic resection[J]. Helicobacter, 2006, 11(3):147-151.
pmid: 16684261 |
[18] |
He CY, Sun LP, Gong YH, et al. Serum pepsinogen II: a neglected but useful biomarker to differentiate between diseased and normal stomachs[J]. J Gastroenterol Hepatol, 2011, 26(6):1039-1046.
doi: 10.1111/j.1440-1746.2011.06692.x URL |
[19] | Chae H, Lee JH, Lim J, et al. Clinical utility of serum pepsinogen levels as a screening test of atrophic gastritis[J]. Korean J Lab Med, 2008, 28(3):201-206. |
[20] |
Zoalfaghari A, Aletaha N, Roushan N, et al. Accuracy of pepsinogens for early diagnosis of atrophic gastritis and gastric cancer in Iranian population[J]. Med J Islam Repub Iran, 2014, 28:150.
pmid: 25695008 |
[21] | Chae H, Lee JH, Lim J, et al. Clinical utility of serum pepsinogen levels as a screening test of atrophic gastritis[J]. Korean J Lab Med, 2008, 28(3):201-206. |
[22] |
Zoalfaghari A, Aletaha N, Roushan N, et al. Accuracy of pepsinogens for early diagnosis of atrophic gastritis and gastric cancer in Iranian population[J]. Med J Islam Repub Iran, 2014, 28:150.
pmid: 25695008 |
[23] |
Pimentel-Nunes P, Libanio D, Marcos-Pinto R, et al. Management of epithelial precancerous conditions and lesions in the stomach (MAPS II): European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter and Microbiota Study Group (EHMSG), European Society of Pathology (ESP), and Sociedade Portuguesa de Endoscopia Digestiva (SPED) guideline update 2019[J]. Endoscopy, 2019, 51(4):365-388.
doi: 10.1055/a-0859-1883 pmid: 30841008 |
[24] |
Lomba-Viana R, Dinis-Ribeiro M, Fonseca F, et al. Serum pepsinogen test for early detection of gastric cancer in a European country[J]. Eur J Gastroenterol Hepatol, 2012, 24(1):37-41.
doi: 10.1097/MEG.0b013e32834d0a0a URL |
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