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首页> 外文期刊>Annals of laboratory medicine. >A Comparison Analysis on the Diagnosis of Helicobacter pylori Infection and the Detection of Clarithromycin Resistance according to Biopsy Sites
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A Comparison Analysis on the Diagnosis of Helicobacter pylori Infection and the Detection of Clarithromycin Resistance according to Biopsy Sites

机译:根据活检部位进行幽门螺杆菌感染诊断和克拉霉素耐药性检测的比较分析

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Background : This study was performed to determine the biopsy sites that are suitable for the diagnosis of Helicobacter pylori infection and to assess the sensitivity of culture, histology, and dual-priming oligonucleotide (DPO)-based multiplex PCR. Moreover, we evaluated the usefulness of PCR for the detection of 23S rRNA mutations, which are responsible for the clarithromycin resistance of H. pylori. Methods : From 90 patients, we obtained biopsy specimens for culture, histology, and Seeplex? ClaR-H. pylori PCR (Seegene Inc., Korea). Phenotypic susceptibility to clarithromycin was evaluated using the E-test (AB Biodisk, Sweden). Results : H. pylori was detected in 48 of 90 patients. The positive rates of infection in the antrum and body were higher than those in the biopsies obtained from the duodenal bulb. The positive rates in histology, PCR, and culture were 46.7%, 42.2%, and 34.4%, respectively. Using histology or PCR, we identified H. pylori in 46 of the 48 patients. 23S rRNA mutations were detected in 8 patients. The clarithromycin E-test showed that all the 10 wild-type patients were susceptible. However, the results of the PCR and E-test of 3 of the 8 mutation-positive patients were discrepant. Conclusions : We observed that a combination of histology and PCR affords a high detection rate of H.pylori infection and that DPO-based PCR can be practically used for the diagnosis of H. pylori infection and the determination of clarithromycin resistance. These techniques were useful for biopsy sampling simultaneously from the antrum and body for the detection of clarithromycin resistance of multiple strain infection or heteroresistance.
机译:背景:进行这项研究是为了确定适合诊断幽门螺杆菌感染的活检部位,并评估培养物,组织学和基于双引物寡核苷酸(DPO)的多重PCR的敏感性。此外,我们评估了PCR检测23S rRNA突变的有用性,这是造成幽门螺杆菌对克拉霉素耐药的原因。方法:从90例患者中,我们获得了用于文化,组织学和Seeplex的活检标本。 ClaR-H。幽门螺杆菌PCR(韩国Seegene Inc.)。使用E-test(AB Biodisk,瑞典)评估对克拉霉素的表型敏感性。结果:90例患者中有48例检出幽门螺杆菌。窦腔和体内感染的阳性率高于十二指肠鳞茎活检的阳性率。组织学,PCR和培养的阳性率分别为46.7%,42.2%和34.4%。使用组织学或PCR,我们在48例患者中的46例中鉴定了幽门螺杆菌。在8例患者中检测到23S rRNA突变。克拉霉素E检验显示所有10位野生型患者均易感。但是,这8例突变阳性患者中有3例的PCR和E-test结果不一致。结论:我们观察到组织学和PCR的结合提供了较高的H.pylori感染检测率,并且基于DPO的PCR可实际用于诊断H. pylori感染和确定克拉霉素抗性。这些技术可用于从胃窦和身体同时进行活检取样,以检测对多种菌株感染或异抗性的克拉霉素抗性。

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