Section of Gastroenterology, Department of Medical Sciences, University of Foggia, Foggia, Italy.
J Antimicrob Chemother. 2010 Feb;65(2):327-32. doi: 10.1093/jac/dkp445. Epub 2009 Dec 11.
INTRODUCTION: Primary clarithromycin resistance is increasing worldwide, and it has been regarded as the main factor reducing the efficacy of Helicobacter pylori therapy. However, the clinical consequence of either phenotypic or genotypic resistance still remains unclear. This study aimed to evaluate: (i) the concordance between phenotypic (culture) and genotypic (real-time PCR) tests in assessing primary clarithromycin resistance; and (ii) the role of both in therapeutic outcome. METHODS: A post hoc subgroup study was selected from a double-blind, placebo-controlled trial, enrolling 146 patients with dyspepsia or peptic ulcers never previously treated. Real-time PCR and Etest on bacterial culture for assessing clarithromycin resistance were performed. [(13)C]urea breath test (UBT), histology and rapid urease tests at entry and UBT after 4-8 weeks were used to assess infection and eradication. All patients received a 10 day therapy. RESULTS: Prevalence of clarithromycin phenotypic resistance was significantly lower as compared with genotypic resistance (18.4% versus 37.6%, P < 0.001). A concordance between the two methods was present in 71.2% of cases. A significant difference in the eradication rate was seen between clarithromycin-susceptible and -resistant strains, when assessed with either Etest (92.4% versus 55.5%, P < 0.001) or a PCR-based method (94.5% versus 70.9%; P < 0.001). Of note, the eradication rate showed the lowest value (30.7%) when phenotypic bacterial resistance was genetically linked to the A2143G point mutation. CONCLUSIONS: This study showed that: (i) there is a relevant discordance between the two methods; and (ii) phenotypic clarithromycin resistance markedly reduces H. pylori eradication when it is linked to a specific point mutation.
介绍:全球范围内原发性克拉霉素耐药性日益增加,它已被认为是降低幽门螺杆菌治疗效果的主要因素。然而,表型或基因型耐药的临床后果仍不清楚。本研究旨在评估:(i)表型(培养)和基因型(实时 PCR)检测在评估原发性克拉霉素耐药性方面的一致性;(ii)两者在治疗结果中的作用。
方法:从一项双盲、安慰剂对照试验中选择了一项事后亚组研究,该研究纳入了 146 例从未接受过治疗的消化不良或消化性溃疡患者。进行了实时 PCR 和细菌培养的 Etest 以评估克拉霉素耐药性。[13C]尿素呼气试验(UBT)、组织学和快速尿素酶试验在入组时和 4-8 周后用于评估感染和根除。所有患者均接受 10 天的治疗。
结果:与基因耐药性相比,克拉霉素表型耐药的流行率显著降低(18.4%比 37.6%,P < 0.001)。两种方法之间存在 71.2%的一致性。当使用 Etest(92.4%比 55.5%,P < 0.001)或基于 PCR 的方法(94.5%比 70.9%;P < 0.001)评估时,克拉霉素敏感和耐药菌株的根除率存在显著差异。值得注意的是,当表型细菌耐药性与 A2143G 点突变存在遗传联系时,根除率最低(30.7%)。
结论:本研究表明:(i)两种方法之间存在明显差异;(ii)当表型克拉霉素耐药性与特定点突变相关时,明显降低了幽门螺杆菌的根除率。
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