系统评价和荟萃分析用于检测幽门螺杆菌抗生素耐药性的基因方法。

A systematic review and meta-analysis of genotypic methods for detecting antibiotic resistance in Helicobacter pylori.

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.

Department of Medical College, Nanchang University, Nanchang, Jiangxi Province, China.

出版信息

Helicobacter. 2018 Apr;23(2):e12467. doi: 10.1111/hel.12467. Epub 2018 Feb 6.

Abstract

BACKGROUND

Antibiotic susceptibility testing is essential for tailored treatments to cure Helicobacter pylori (H. pylori) infection. However, phenotypic methods have some limitations.

OBJECTIVES

To evaluate the feasibility of genotypic detection methods compared with phenotypic detection methods using samples taken from H. pylori-infected patients.

METHODS

Literature searches were conducted in the following databases (from January 2000 to November 2016): PubMed, Embase, the Cochrane Library, and Web of Science. A meta-analysis and systematic review was performed for studies that compared genotypic methods with phenotypic methods for the detection of H. pylori antibiotic susceptibility.

RESULTS

This meta-analysis showed that the pooled sensitivity, specificity, and diagnostic odds ratio (DOR) for the A2142G/C and/or A2143G combination for the detection of clarithromycin resistance in the strain samples were 0.97 (95% CI: 0.94-0.99), 1.00 (95% CI: 0.99-1.00), and 13 742 (95% CI: 1708-110 554), respectively. The pooled sensitivity, specificity, and DOR for the A2142G/C and/or A2143G combination for the detection of clarithromycin resistance in biopsy samples were 0.96 (95% CI: 0.90-0.99), 0.96 (95% CI: 0.91-0.99), and 722 (95% CI: 117-4443), respectively. The summarized sensitivity, specificity, and DOR value for the ability of the genotypic methods to detect quinolone resistance in biopsy specimens were 0.97 (95% CI: 0.87-0.99), 0.99 (95% CI: 0.92-1.00), and 6042 (95% CI: 486-75 143), respectively.

CONCLUSION

The genotypic detection methods were reliable for the diagnosis of clarithromycin and quinolone resistance in the strain and biopsy specimens. The A2142G/C and/or A2143G combination had the best sensitivity and specificity for the detection of clarithromycin resistance.

摘要

背景

抗生素药敏试验对于针对治疗幽门螺杆菌(H. pylori)感染至关重要。然而,表型方法存在一些局限性。

目的

评估基因型检测方法与表型检测方法在 H. pylori 感染患者样本中的可行性。

方法

对 2000 年 1 月至 2016 年 11 月期间的以下数据库进行文献检索:PubMed、Embase、Cochrane 图书馆和 Web of Science。对比较基因型方法与表型方法检测 H. pylori 抗生素敏感性的研究进行了荟萃分析和系统综述。

结果

该荟萃分析显示,对于菌株样本中克拉霉素耐药性检测,A2142G/C 和/或 A2143G 组合的汇总灵敏度、特异性和诊断比值比(DOR)分别为 0.97(95%CI:0.94-0.99)、1.00(95%CI:0.99-1.00)和 13742(95%CI:1708-110554)。对于活检样本中克拉霉素耐药性检测,A2142G/C 和/或 A2143G 组合的汇总灵敏度、特异性和 DOR 分别为 0.96(95%CI:0.90-0.99)、0.96(95%CI:0.91-0.99)和 722(95%CI:117-4443)。基因型方法检测活检标本中喹诺酮类药物耐药性的汇总灵敏度、特异性和 DOR 值分别为 0.97(95%CI:0.87-0.99)、0.99(95%CI:0.92-1.00)和 6042(95%CI:486-75143)。

结论

基因型检测方法对于菌株和活检标本中克拉霉素和喹诺酮类药物耐药性的诊断是可靠的。A2142G/C 和/或 A2143G 组合对克拉霉素耐药性的检测具有最佳的灵敏度和特异性。

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