Efficacy of LAMP assay for Mycobacterial spp. detection to prevent treatment delays and onset of drug resistance: a systematic review and meta-analysis.

IF 2 Q3 PHARMACOLOGY & PHARMACY Drug Target Insights Pub Date : 2023-01-01 DOI:10.33393/dti.2023.2596
Gurvinder Singh Bumbrah, Sarika Jain, Zeeshan Fatima, Saif Hameed
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Abstract

Background: Tuberculosis (TB) remains a deadly disease affecting one-third population globally. Long turnaround time and poor sensitivity of the conventional diagnostics are the major impediments for faster diagnosis of Mycobacterial spp to prevent drug resistance. To overcome these issues, molecular diagnostics have been developed. They offer enhanced sensitivity but require sophisticated infrastructure, skilled manpower and remain expensive.

Methods: In that context, loop-mediated isothermal amplification (LAMP) assay, recommended by the WHO in 2016 for TB diagnosis, sounds as a promising alternative that facilitates visual read outs. Therefore, the aim of the present study is to conduct a meta-analysis to assess the diagnostic efficiency of LAMP for the detection of a panel of Mycobacterium spp. following PRISMA guidelines using scientific databases. From 1600 studies reported on the diagnosis of Mycobacterium spp., a selection of 30 articles were identified as eligible to meet the criteria of LAMP based diagnosis.

Results: It was found that most of the studies were conducted in high disease burden nations such as India, Thailand, and Japan with sputum as the most common specimen to be used for LAMP assay. Furthermore, IS6110 gene and fluorescence-based detections ranked as the most used target and method respectively. The accuracy and precision rates mostly varied between 79.2% to 99.3% and 73.9% to 100%, respectively. Lastly, a quality assessment based on QUADAS-2 of bias and applicability was conducted.

Conclusion: LAMP technology could be considered as a feasible alternative to current diagnostics considering high burden for rapid testing in low resource regions.

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LAMP法检测分枝杆菌预防治疗延误和耐药的疗效:一项系统综述和荟萃分析。
背景:结核病(TB)仍然是影响全球三分之一人口的致命疾病。常规诊断方法的周转时间长、敏感性差是阻碍分枝杆菌快速诊断以预防耐药的主要因素。为了克服这些问题,分子诊断学得到了发展。它们提供了更高的灵敏度,但需要复杂的基础设施和熟练的人力,而且仍然昂贵。方法:在这种情况下,2016年世卫组织推荐用于结核病诊断的环介导等温扩增(LAMP)检测听起来是一种很有前途的替代方法,可以促进视觉读数。因此,本研究的目的是进行一项荟萃分析,以评估LAMP在遵循PRISMA指南使用科学数据库检测一组分枝杆菌的诊断效率。从1600篇关于分枝杆菌诊断的研究报告中,筛选出30篇符合LAMP诊断标准的文章。结果:发现大多数研究是在疾病负担高的国家进行的,如印度、泰国和日本,痰是用于LAMP测定的最常见标本。此外,IS6110基因检测和荧光检测分别是最常用的靶点和方法。准确度和精密度分别在79.2% ~ 99.3%和73.9% ~ 100%之间。最后,基于QUADAS-2进行偏倚和适用性的质量评价。结论:考虑到低资源地区快速检测的高负担,LAMP技术可被认为是现有诊断方法的可行替代方法。
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来源期刊
Drug Target Insights
Drug Target Insights PHARMACOLOGY & PHARMACY-
CiteScore
2.70
自引率
0.00%
发文量
5
审稿时长
8 weeks
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