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评价 Allplex™ H pylori 和 ClariR PCR 检测试剂盒在胃活检标本中幽门螺杆菌检测的性能。

Evaluation of the Allplex™ H pylori and ClariR PCR Assay for Helicobacter pylori detection on gastric biopsies.

机构信息

Hôpital Pellegrin, French National Reference Centre for Campylobacters & Helicobacters, Bordeaux, France.

University of Bordeaux, INSERM, UMR1053, Bordeaux BaRITOn, Bordeaux, France.

出版信息

Helicobacter. 2020 Aug;25(4):e12702. doi: 10.1111/hel.12702. Epub 2020 May 19.

Abstract

BACKGROUND

The diagnosis of Helicobacter pylori infection can be made by PCR on gastric biopsies. The objective of this study was to evaluate retrospectively the performance of the Allplex™ H pylori and ClariR PCR Assay (Seegene).

MATERIAL AND METHODS

A collection of 180 DNA samples extracted from gastric biopsies was used in this study: 90 DNAs from H pylori-negative patients and 90 from H pylori-positive patients. The Allplex™ H pylori and ClariR Assay was performed on a CFX96™ real-time PCR System and analyzed using the Seegene Viewer software. The real-time PCR used as the reference was our in-house H pylori PCR, and discrepant results were tested by the Amplidiag® H pylori + ClariR PCR (Mobidiag).

RESULTS

The performance of the Allplex™ H pylori and ClariR Assay showed 100% sensitivity, 97.6% specificity, 98% PPV, and 100% NPV. Regarding the detection of H pylori in the 90 expected negative samples, eight late amplifications were obtained (Ct > 39). Six of these eight samples were also positive using the Amplidiag® H pylori + ClariR kit and were therefore considered as true positives. For the two remaining cases, non-pathological evidence of H pylori infection was found. H pylori was detected in all 90 positive samples. Compared with our in-house H pylori PCR, all H pylori WT cases or mutated cases were correctly detected.

CONCLUSIONS

The Allplex™ H pylori and ClariR Assay showed an excellent performance and can be integrated into the armamentarium of diagnostic tests for H pylori infection. This kit has the advantage of differentiating the main mutations associated with macrolide resistance.

摘要

背景

幽门螺杆菌感染的诊断可通过胃活检的 PCR 进行。本研究的目的是回顾性评估 Allplex™ H pylori 和 ClariR PCR 检测试剂盒(Seegene)的性能。

材料与方法

本研究使用了 180 个从胃活检中提取的 DNA 样本:90 个来自 H pylori 阴性患者,90 个来自 H pylori 阳性患者。Allplex™ H pylori 和 ClariR 检测试剂盒在 CFX96™实时 PCR 系统上进行,并使用 Seegene Viewer 软件进行分析。作为参考的实时 PCR 是我们的内部 H pylori PCR,如果结果不一致,则使用 Amplidiag® H pylori + ClariR PCR(Mobidiag)进行测试。

结果

Allplex™ H pylori 和 ClariR 检测试剂盒的性能显示 100%的灵敏度、97.6%的特异性、98%的 PPV 和 100%的 NPV。对于 90 个预期的阴性样本中 H pylori 的检测,获得了 8 个晚期扩增(Ct > 39)。这 8 个样本中的 6 个使用 Amplidiag® H pylori + ClariR 试剂盒也呈阳性,因此被认为是真正的阳性。对于另外 2 个病例,发现了非病理性 H pylori 感染的证据。在所有 90 个阳性样本中均检测到 H pylori。与我们的内部 H pylori PCR 相比,所有 H pylori WT 病例或突变病例均被正确检测。

结论

Allplex™ H pylori 和 ClariR 检测试剂盒表现出优异的性能,可整合到 H pylori 感染的诊断测试中。该试剂盒具有区分与大环内酯类耐药相关的主要突变的优势。

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