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Eradication of Helicobacter pylori according to 23S ribosomal RNA point mutations associated with clarithromycin resistance.根据与克拉霉素耐药相关的 23S 核糖体 RNA 点突变根除幽门螺杆菌。
J Infect Dis. 2013 Oct 1;208(7):1123-30. doi: 10.1093/infdis/jit287. Epub 2013 Jun 24.
2
Validation of a fluorescence in situ hybridization method using peptide nucleic acid probes for detection of Helicobacter pylori clarithromycin resistance in gastric biopsy specimens.使用肽核酸探针的荧光原位杂交法检测胃活检标本中幽门螺杆菌克拉霉素耐药性的验证。
J Clin Microbiol. 2013 Jun;51(6):1887-93. doi: 10.1128/JCM.00302-13. Epub 2013 Apr 17.
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Detection of Helicobacter pylori in Gastric Aspirates Using a Monoclonal Antibody-Based Test.应用单克隆抗体试验检测胃抽吸物中的幽门螺杆菌。
Gut Liver. 2013 Jan;7(1):30-4. doi: 10.5009/gnl.2013.7.1.30. Epub 2012 Dec 5.
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PCR-Based Detection and Genotyping of Helicobacter pylori in Endoscopic Biopsy Samples from Brazilian Patients.基于 PCR 的巴西患者内镜活检样本中幽门螺杆菌的检测和基因分型。
Gastroenterol Res Pract. 2013;2013:951034. doi: 10.1155/2013/951034. Epub 2013 Jan 16.
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Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy.在萎缩性胃炎背景下,额外的胃黏膜活检可提高幽门螺杆菌感染的检出率。
BMC Gastroenterol. 2012 Dec 29;12:182. doi: 10.1186/1471-230X-12-182.
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Detection of primary clarithromycin resistance of Helicobacter pylori and association between cagA (+) status and clinical outcome.检测幽门螺杆菌对克拉霉素的原发性耐药性及 cagA(+)状态与临床转归的关系。
Folia Microbiol (Praha). 2013 Mar;58(2):141-6. doi: 10.1007/s12223-012-0192-8. Epub 2012 Sep 6.
7
Detection of clarithromycin resistance in Helicobacter pylori following noncryogenic storage of rapid urease tests for 30 days.30 天内非冷冻保存快速尿素酶试验检测幽门螺杆菌克拉霉素耐药性。
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DPO multiplex PCR as an alternative to culture and susceptibility testing to detect Helicobacter pylori and its resistance to clarithromycin.DPO 多重 PCR 替代培养和药敏试验检测幽门螺杆菌及其对克拉霉素的耐药性。
BMC Gastroenterol. 2011 Oct 17;11:112. doi: 10.1186/1471-230X-11-112.
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Real-time PCR improves Helicobacter pylori detection in patients with peptic ulcer bleeding.实时 PCR 提高消化性溃疡出血患者幽门螺杆菌的检出率。
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Helicobacter pylori treatment in the era of increasing antibiotic resistance.幽门螺杆菌在抗生素耐药时代的治疗。
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基于双引物寡核苷酸的多重聚合酶链反应在快速尿素酶试验中使用组织样本检测幽门螺杆菌感染

Dual-priming oligonucleotide-based multiplex PCR using tissue samples in rapid urease test in the detection of Helicobacter pylori infection.

作者信息

Chung Woo Chul, Jung Sung Hoon, Oh Jung Hwan, Kim Tae Ho, Cheung Dae Young, Kim Byung Wook, Kim Sung Soo, Kim Jin Il, Sin Eun Young

机构信息

Woo Chul Chung, Sung Hoon Jung, Jung Hwan Oh, Tae Ho Kim, Dae Young Cheung, Byung Wook Kim, Sung Soo Kim, Jin Il Kim, Department of Internal Medicine, the Catholic University of Korea, Seoul 130-709, South Korea.

出版信息

World J Gastroenterol. 2014 Jun 7;20(21):6547-53. doi: 10.3748/wjg.v20.i21.6547.

DOI:10.3748/wjg.v20.i21.6547
PMID:24914376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4047340/
Abstract

AIM

To investigate whether tissue samples processed by the rapid urease test (RUT) kit are suitable for dual-priming oligonucleotide-based multiplex polymerase chain reaction (DPO-PCR) to detect Helicobacter pylori (H. pylori).

METHODS

A total of 54 patients with specific gastrointestinal symptom were enrolled in this study. During endoscopy, gastric biopsy specimens were taken for histology, RUT, and DPO-PCR. DPO-PCR was performed on gastric biopsy samples and tissue samples that were analyzed by RUT at 2 separate institutes. In detecting H. pylori, the concordance rate of the DPO-PCR tests between the tissue samples that had been submitted to RUT and the gastric biopsy samples was investigated.

RESULTS

H. pylori co-occurred with 76.0% (19/25) of gastric ulcers, 64.3% (9/14) of duodenal ulcers, and 33.3% (4/12) of gastritis cases. H. pylori infection was found in 100% (3/3) of the patients with both gastric and duodenal ulcers. Overall, H. pylori was detected in 35 of 54 (64.8%) patients. The diagnostic sensitivities of histology, RUT, and DPO-PCR were 85.7% (30/35), 74.3% (26/35), and 97.1% (34/35), respectively (P = 0.02). The positive predictive value (PPV) of DPO-PCR was 94.4%, whereas the negative predictive value (NPV) was 94.7%. In the rapid urease test (CLOtest)-negative cases, the frequency of positive DPO-PCR and histologic results was 20.0% (7/35). The concordance rate of the DPO-PCR tests between the tissue samples from the RUT kit and the gastric biopsy samples was 94.4% (51/54). The rate of DPO-PCR and silver stain positivity in the RUT-negative cases was 20.0% (7/35).

CONCLUSION

In diagnosing H. pylori infection, DPO-PCR can be performed on tissue samples that have been processed by the RUT kit. Particularly, in patients with RUT-negative results, DPO-PCR on these tissue samples could be helpful in detecting of H. pylori infection.

摘要

目的

研究经快速尿素酶试验(RUT)试剂盒处理的组织样本是否适用于基于双引物寡核苷酸的多重聚合酶链反应(DPO-PCR)来检测幽门螺杆菌(H. pylori)。

方法

本研究共纳入54例有特定胃肠道症状的患者。在内镜检查期间,采集胃活检标本进行组织学检查、RUT检测和DPO-PCR检测。DPO-PCR在2个独立机构对胃活检样本和经RUT分析的组织样本进行。在检测H. pylori时,研究经RUT检测的组织样本与胃活检样本之间DPO-PCR检测的一致性率。

结果

H. pylori在76.0%(19/25)的胃溃疡、64.3%(9/14)的十二指肠溃疡和33.3%(4/12)的胃炎病例中同时存在。在患有胃溃疡和十二指肠溃疡的患者中,100%(3/3)检测到H. pylori感染。总体而言,54例患者中有35例(64.8%)检测到H. pylori。组织学检查、RUT检测和DPO-PCR检测的诊断敏感性分别为85.7%(30/35)、74.3%(26/35)和97.1%(34/35)(P = 0.02)。DPO-PCR的阳性预测值(PPV)为94.4%,而阴性预测值(NPV)为94.7%。在快速尿素酶试验(CLOtest)阴性的病例中,DPO-PCR阳性和组织学结果阳性的频率为20.0%(7/35)。RUT试剂盒的组织样本与胃活检样本之间DPO-PCR检测的一致性率为94.4%(51/54)。RUT阴性病例中DPO-PCR和银染阳性率为20.0%(7/35)。

结论

在诊断H. pylori感染时,DPO-PCR可在经RUT试剂盒处理的组织样本上进行。特别是在RUT检测结果为阴性的患者中,对这些组织样本进行DPO-PCR检测有助于检测H. pylori感染。