Josefina Yoaly Sánchez-López, Luis Carlos Díaz-Herrera, Lourdes Del Carmen Rizo-de la Torre
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引用次数: 0
摘要
简介:萎缩性胃炎和肠化生是胃癌的前兆病变:萎缩性胃炎和肠化生是胃癌的前驱病变。本研究旨在确定胃蛋白酶原 I (PgI)、胃蛋白酶原 II (PgII)、胃泌素-17 和幽门螺杆菌抗体等生物标志物在识别前驱病变中的作用:我们对 129 名有胃部症状的患者进行了研究。方法:我们对 129 名有胃部症状的患者进行了研究,通过 ELISA 技术使用 GastroPanel 对生物标志物状态进行了测定:结果:14%的受试者通过生物标志物检测到胃萎缩,49.6%的受试者幽门螺杆菌抗体呈阳性。PgI/PgII比值小于3是我们人群中前驱病变的重要风险生物标志物(OR = 9.171,95% CI:1.723-48.799,p = 0.009);然而,生物标志物与组织病理学研究的准确性较低:在墨西哥西部人群中,前驱病变(AG、IM)常见于患有消化不良的成年人(45%),但在儿童中并不常见(8%)。41.3%的成人和16.0%的儿童检测出幽门螺杆菌感染。在所研究的生物标志物中,PgI/PgII 比率小于 3 是我们人群中出现 AG 或 IM 等前驱病变的重要风险因素,OR 值为 9.171(95% CI:1.723-48.799,P = 0.009)。
Pepsinogen I, pepsinogen II, gastrin-17, and Helicobacter pylori serological biomarkers in the diagnosis of precursor lesions of gastric cancer.
Introduction: Atrophic gastritis and intestinal metaplasia are precursor lesions of gastric cancer. The aim of this study was to determine the usefulness of the biomarkers pepsinogen I(PgI), pepsinogen II (PgII), gastrin-17, and H. pylori antibodies in the identification of precursor lesions.
Methods: We studied 129 patients with gastric symptoms. The biomarker status was determined using GastroPanel by means of the ELISA-technique.
Results: Biomarkers detected atrophy in 14% of the subjects, and 49.6% had positive antibodies for H. pylori. A PgI/PgII ratio < 3 was an important risk biomarker for precursor lesions in our population (OR = 9.171, 95% CI: 1.723-48.799, p = 0.009); however, biomarkers showed low accuracy with histopathological study.
Conclusions: In the Western Mexican population, precursor lesions (AG, IM) are common in adults (45%) with dyspepsia but infrequent in children (8%). H. pylori infection was detected in 41.3% of adults and 16.0% of children. Of the studied biomarkers, a PgI/PgII ratio < 3 was an important risk factor for precursor lesions such as AG or IM in our population, with an OR of 9.171 (95% CI: 1.723-48.799, p = 0.009).
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