hbeag阴性慢性乙型肝炎病毒感染幽门螺杆菌率及组织病理学评价

O. Özdoğan, Serkan Yaraş
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摘要

导读:幽门螺杆菌(HP)在肝脏疾病和乙型肝炎病毒(HBV)感染中的研究越来越受到关注。大多数调查HP和HBV之间关系的研究都是在肝硬化和肝细胞癌(HCC)患者中进行的,通常包括非侵入性检查。这些患者的HP频率高于健康对照组。在这些研究中没有进行组织病理学评估。我们通过侵入性胃活检和组织病理学评估,调查了hbeag阴性慢性HBV感染(以前称为“无活性携带者”)中HP的发病率。材料和方法:我们纳入90例初次治疗的非活动性乙型肝炎携带者作为患者。对照组为107名健康受试者。从胃窦和胃体进行活检,并使用胃炎的悉尼分类系统进行组织病理学评估。结果:非活动性乙肝病毒携带者HP感染率显著高于对照组(75.6% vs. 53.3%;P = 0.001)。两组间萎缩、肠化生、活动性和炎症的发生率均无差异(p > 0.05)。HBV组有11例(12.2%)出现消化性溃疡,对照组有7例(6.5%)出现消化性溃疡(p = 0.360)。HBV DNA≥2000 IU/ml的患者HP发病率高于HBV DNA < 2000 IU/ml的患者,但差异无统计学意义(分别为85% vs. 68%;P = 0.062)。结论:虽然非活动性乙型肝炎携带者的HP发生率高于对照组,但在萎缩、肠化生、活动性、炎症和消化性溃疡发生率方面,组间无差异。
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Helicobacter pylori rate and histopathological evaluation in HBeAg-negative chronic hepatitis B virus infection
Introduction: Studies of Helicobacter pylori (HP) in liver diseases and hepatitis B virus (HBV) infection have been increasingly discussed. Most studies investigating the relationship between HP and HBV have been conducted in patients with cirrhosis and hepatocellular carcinoma (HCC) and usually involving noninvasive tests. The HP frequency in these patients was higher than in healthy controls. No histopathological evaluation was performed in these studies. We investigated the incidence of HP in HBeAg-negative chronic HBV infection (previously termed “inactive carrier”) by using invasive gastric biopsies and carried out histopathological evaluation. Material and methods: We included 90 treatment-naive inactive hepatitis-B carriers as patients. The control group comprised 107 healthy subjects. Biopsies were obtained from the antrum and corpus and were evaluated histopathologically using the Sydney system of classification for gastritis. Results: The rate of HP in inactive hepatitis-B carriers was significantly higher than the control group (75.6% vs. 53.3%, respectively; p = 0.001). There was no difference in incidence of atrophy, intestinal metaplasia, activity, or inflammation (p > 0.05). Peptic ulcer was detected in 11 (12.2%) patients in the HBV group and in 7 (6.5%) patients in the control group (p = 0.360). The incidence of HP was higher in patients with HBV DNA ≥ 2000 IU/ml than in patients with HBV DNA < 2000 IU/ml, but this difference was not statistically significant (85% vs. 68%, respectively; p = 0.062). Conclusions: Although the HP rate in inactive hepatitis-B carriers was higher than the control group, there were no intergroup differences with respect to atrophy, intestinal metaplasia, activity, inflammation, and peptic ulcer frequency.
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