Miftahussurur Muhammad, Waskito Langgeng Agung, Syam Ari Fahrial, Nusi Iswan Abbas, Wibawa I Dewa Nyoman, Rezkitha Yudith Annisa Ayu, Fauzia Kartika Afrida, Siregar Gontar Alamsyah, Akil Fardah, Waleleng Bradley Jimmy, Saudale Alexander Michael Joseph, Abubakar Azzaki, Maulahela Hasan, Richardo Marselino, Rahman Abdul, Namara Yoma Sari, Sudarmo Eko, Adi Pangestu, Maimunah Ummi, Setiawan Poernomo Boedi, Doohan Dalla, Uchida Tomohisa, Dewayani Astri, Rejeki Purwo Sri, Sugihartono Titong, Yamaoka Yoshio
Division of Gastroentero-Hepatology, Department of Internal Medicine, Faculty of Medicine, Dr. Soetomo Teaching Hospital, Universitas Airlangga, Surabaya, Indonesia.
Helicobacter pylori and Microbiota Study Group, Institute of Tropical Disease, Universitas Airlangga, Surabaya, Indonesia.
J Res Med Sci. 2022 Dec 23;27:90. doi: 10.4103/jrms.jrms_983_21. eCollection 2022.
BACKGROUND: Chronic dyspepsia's symptoms are frequently seen in primary to tertiary healthcare in Indonesia. This study aimed to describe the potential usability of pepsinogen (PG) values in determining gastric mucosal conditions, including superficial gastritis and atrophic gastritis. MATERIALS AND METHODS: We recruited 646 adult dyspeptic patients and then analyzed PG values (including PGI, PGII, and PGI/II ratio) with endoscopic findings, gastric mucosal damages, and infection. The gastric mucosal damage and infection were evaluated using histological examination based on the updated Sydney system. RESULTS: Among 646 enrolled patients, 308 (47.2%), 212 (32.8%), 91 (14.1%), 34 (5.2%), and 1 (0.2%) patient were diagnosed with normal mucosa, gastritis, reflux esophagitis, peptic ulcer disease, and gastric cancer, respectively. Significant differences in PGI, PGII, and PGI/II ratio values were observed among ethnic groups (all < 0.01). The PGI and PGII levels were significantly higher and PGI/II was significantly lower in -infected patients than in uninfected ones (all < 0.001). The optimal cutoff value for PGII and PGI/II was 12.45 ng/mL with an area under the curve (AUC) value of 0.755 (0.702-0.811), sensitivity 59.3%, and specificity 77.1%; and 4.75 with AUC value of 0.821 (0.763-0.855), sensitivity 81.5%, and specificity 78.7%, respectively, to determine moderate-severe atrophy. CONCLUSION: Serum PG levels, a useful biomarker, represent the endoscopic findings, especially for reflux esophagitis. In addition, the benefits of PG values detecting atrophic gastritis were limited to moderate-severe atrophic gastritis. This usefulness requires careful attention for several ethnic groups in Indonesia.
背景:慢性消化不良症状在印度尼西亚的初级至三级医疗保健中经常出现。本研究旨在描述胃蛋白酶原(PG)值在确定胃黏膜状况(包括浅表性胃炎和萎缩性胃炎)方面的潜在可用性。 材料与方法:我们招募了646名成年消化不良患者,然后将PG值(包括PGI、PGII和PGI/II比值)与内镜检查结果、胃黏膜损伤和感染情况进行分析。胃黏膜损伤和感染情况采用基于更新后的悉尼系统的组织学检查进行评估。 结果:在646名登记患者中,分别有308名(47.2%)、212名(32.8%)、91名(14.1%)、34名(5.2%)和1名(0.2%)患者被诊断为黏膜正常、胃炎、反流性食管炎、消化性溃疡病和胃癌。在不同种族群体中观察到PGI、PGII和PGI/II比值存在显著差异(均P<0.01)。感染患者的PGI和PGII水平显著高于未感染患者,而PGI/II则显著低于未感染患者(均P<0.001)。PGII和PGI/II用于确定中重度萎缩的最佳截断值分别为12.45 ng/mL,曲线下面积(AUC)值为0.755(0.702 - 0.811),灵敏度为59.3%,特异性为77.1%;以及4.75,AUC值为0.821(0.763 - 0.855),灵敏度为81.5%,特异性为78.7%。 结论:血清PG水平是一种有用的生物标志物,能够反映内镜检查结果,尤其是对于反流性食管炎。此外,PG值检测萎缩性胃炎的作用仅限于中重度萎缩性胃炎。在印度尼西亚,对于几个种族群体而言,这种实用性需要谨慎关注。
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