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一种新开发的用于检测胃活检组织、唾液和粪便中幽门螺杆菌的聚合酶链反应检测方法。唾液中幽门螺杆菌高流行率的证据支持其经口传播。

A newly developed PCR assay of H. pylori in gastric biopsy, saliva, and feces. Evidence of high prevalence of H. pylori in saliva supports oral transmission.

作者信息

Li C, Ha T, Ferguson D A, Chi D S, Zhao R, Patel N R, Krishnaswamy G, Thomas E

机构信息

Department of Internal Medicine (Gastroenterology), James H. Quillen College of Medicine, East Tennessee State University, Johnson City, USA.

出版信息

Dig Dis Sci. 1996 Nov;41(11):2142-9. doi: 10.1007/BF02071393.

Abstract

We have recently developed a new PCR assay for the detection of H. pylori. In this study, the polymerase chain reaction (PCR) assay was used to detect H. pylori in 88 gastric biopsy, 85 saliva, and 71 fecal specimens from 88 patients. H. pylori infection was confirmed in 71 of 88 patients by culture and/or histological stain of gastric biopsies. Serum IgG antibody to H. pylori was also measured and resulted in 97% sensitivity and 94% specificity. H. pylori DNA was detected by the PCR assay in gastric biopsy specimens from all 71 patients (100% sensitivity) with proven gastric H. pylori infection but not from 17 noninfected patients (100% specificity). In saliva specimens, H. pylori DNA was identified in 57 of the 68 patients (84%) with proven gastric H. pylori infection and in three of the 17 patients without gastric H. pylori infection. However, the PCR assay was only able to detect H. pylori DNA in the feces from 15 of 61 patients (25%) with proven gastric H. pylori infection and one of the 10 patients without gastric H. pylori infection. The results show that the PCR assay is reliable for detecting the presence of H. pylori in gastric biopsy and saliva specimens. The data indicate that H. pylori exists in a higher prevalence in saliva than feces and that the fecal-oral route may be an important means of transmission of this infection in developing countries but not as significant as previously suspected in the developed countries. It is likely that the oral-oral route is more prominent.

摘要

我们最近开发了一种用于检测幽门螺杆菌的新型聚合酶链反应(PCR)检测方法。在本研究中,采用聚合酶链反应(PCR)检测方法对88例患者的88份胃活检标本、85份唾液标本和71份粪便标本中的幽门螺杆菌进行检测。通过胃活检的培养和/或组织学染色,在88例患者中的71例中确诊了幽门螺杆菌感染。还检测了血清抗幽门螺杆菌IgG抗体,其敏感性为97%,特异性为94%。在所有71例经证实有胃幽门螺杆菌感染的患者的胃活检标本中均通过PCR检测方法检测到了幽门螺杆菌DNA(敏感性100%),而在17例未感染患者中未检测到(特异性100%)。在唾液标本中,68例经证实有胃幽门螺杆菌感染的患者中有57例(84%)检测到幽门螺杆菌DNA,17例无胃幽门螺杆菌感染的患者中有3例检测到。然而,PCR检测方法仅能在61例经证实有胃幽门螺杆菌感染的患者中的15例(25%)粪便中检测到幽门螺杆菌DNA,10例无胃幽门螺杆菌感染的患者中有1例检测到。结果表明,PCR检测方法在检测胃活检和唾液标本中幽门螺杆菌的存在方面是可靠的。数据表明,幽门螺杆菌在唾液中的流行率高于粪便,粪-口途径可能是发展中国家这种感染的重要传播途径,但在发达国家并不像以前怀疑的那样重要。口腔-口腔途径可能更为突出。

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