Yamamoto I, Fukuda Y, Mizuta T, Fukada M, Nishigami T, Shimoyama T
Department of Internal Medicine, Hyogo College of Medicine, Japan.
J Clin Gastroenterol. 1995;21 Suppl 1:S164-8.
We investigated the relationship between the severity of Helicobacter pylori-associated gastritis and serum anti-H. pylori antibodies. A total of 158 consecutive patients underwent upper gastroduodenal endoscopy. At the time of endoscopy, three biopsy specimens were taken from the antrum and the body of the stomach for culture of H. pylori, CLO test, and histology. Specimens with a negative rapid urease test and no organisms found by culture were judged to be H. pylori-negative. The GAP test used for the antibody measurement is a kit designed to measure serum IgG, IgA, and IgM antibodies. The severity of gastritis was classified according to the Sydney System. The sensitivity and specificity of the IgG antibody measurement kit was 98.3 and 71.4%, respectively. The sensitivity and specificity of the IgM antibody measurement kit was 14.3 and 60.8%, respectively. The sensitivity and specificity of the IgA antibody measurement kit was 45.1 and 100%, respectively. Serum anti-H. pylori IgG antibody titers were correlated significantly with the severity of inflammation in both the antrum and body. Significant associations were found between serum anti-H. pylori IgG and IgA antibody titers and the development of atrophic gastritis. These results suggest that measurement of serum anti-H. pylori antibody titers is useful in the diagnosis of H. pylori infection and severity of gastritis.
我们研究了幽门螺杆菌相关性胃炎的严重程度与血清抗幽门螺杆菌抗体之间的关系。共有158例连续患者接受了上消化道内镜检查。在内镜检查时,从胃窦和胃体采集了三份活检标本,用于幽门螺杆菌培养、CLO试验和组织学检查。快速尿素酶试验阴性且培养未发现细菌的标本被判定为幽门螺杆菌阴性。用于抗体检测的GAP试验是一种用于测量血清IgG、IgA和IgM抗体的试剂盒。胃炎的严重程度根据悉尼系统进行分类。IgG抗体检测试剂盒的敏感性和特异性分别为98.3%和71.4%。IgM抗体检测试剂盒的敏感性和特异性分别为14.3%和60.8%。IgA抗体检测试剂盒的敏感性和特异性分别为45.1%和100%。血清抗幽门螺杆菌IgG抗体滴度与胃窦和胃体的炎症严重程度显著相关。血清抗幽门螺杆菌IgG和IgA抗体滴度与萎缩性胃炎的发生之间存在显著关联。这些结果表明,测量血清抗幽门螺杆菌抗体滴度有助于诊断幽门螺杆菌感染和胃炎的严重程度。