Departments of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea.
Departments of Pathology, Konkuk University School of Medicine, Seoul, Korea.
Helicobacter. 2018 Jun;23(3):e12480. doi: 10.1111/hel.12480. Epub 2018 Mar 8.
Helicobacter pylori is unevenly distributed in hypochlorhydric environments. The study aim was to elucidate the risk factors for a negative Giemsa staining finding in seropositive subjects by measuring the secretory ability of the stomach.
Subjects aged over 18 years were included consecutively after endoscopic biopsy at gastric lesions with color or structural changes. Blood was sampled for the serum pepsinogen (PG) assay and H. pylori serology test. After excluding the subjects with past H. pylori eradication, the risk factors for a negative Giemsa staining finding in seropositive subjects were analyzed.
Among 872 included subjects, a discrepancy between the serum anti-H. pylori IgG and Giemsa staining findings was found in 158 (18.1%) subjects, including 145 Giemsa-negative, seropositive subjects. Gastric adenocarcinoma/adenoma (OR = 11.090, 95% CI = 3.490-35.236) and low serum PG II level (OR = 0.931, 95% CI = 0.899-0.963) were the independent risk factors for a negative Giemsa staining finding in seropositive subjects. The cutoff value of serum PG II level was 7.45 ng/mL (area under curve [AUC] = 0.904, 95% CI = 0.881-0.927). Follow-up studies of Giemsa staining at different sites of the stomach revealed that 75% of the Giemsa-negative seropositive subjects with adenocarcinoma are positive, whereas none of those with low serum PG II level of <7.45 ng/mL revealed positive findings.
The risk of a negative Giemsa staining finding in seropositive subjects is increased in gastric adenocarcinoma/adenoma specimens and in subjects with a diminished gastric secretory ability with low serum PG II level of <7.45 ng/mL. A false-negative Giemsa staining finding is common in subjects with adenocarcinoma, and therefore, additional biopsies at different sites should be performed in these subjects.
幽门螺杆菌在低胃酸环境中分布不均。本研究旨在通过测量胃的分泌能力来阐明血清学阳性者中胃黏膜染色呈阴性的危险因素。
经内镜活检发现胃病变存在颜色或结构改变后,连续纳入年龄大于 18 岁的受试者。采集血样进行血清胃蛋白酶原(PG)检测和 H. pylori 血清学检测。排除既往 H. pylori 根除的受试者后,分析血清学阳性者胃黏膜染色呈阴性的危险因素。
在 872 例纳入的受试者中,158 例(18.1%)受试者的血清抗 H. pylori IgG 与胃黏膜染色结果不一致,包括 145 例胃黏膜染色阴性、血清学阳性者。胃腺癌/腺瘤(OR=11.090,95%CI=3.490-35.236)和低血清 PG II 水平(OR=0.931,95%CI=0.899-0.963)是血清学阳性者胃黏膜染色呈阴性的独立危险因素。血清 PG II 水平的截断值为 7.45ng/mL(曲线下面积[AUC]为 0.904,95%CI=0.881-0.927)。对胃不同部位胃黏膜染色的随访研究显示,75%的胃黏膜染色阴性、血清学阳性的腺癌患者呈阳性,而无一例血清 PG II 水平<7.45ng/mL 的患者呈阳性。
胃腺癌/腺瘤标本和血清 PG II 水平降低(<7.45ng/mL)的胃分泌能力降低的血清学阳性者中,胃黏膜染色呈阴性的风险增加。胃黏膜染色呈假阴性在腺癌患者中较为常见,因此,应在这些患者的不同部位进行额外的活检。