A novel pan-Leishmania loop-mediated isothermal amplification (Loopamp) assay for diagnosis of cutaneous and visceral leishmaniasis: a systematic review and meta-analysis.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Behailu Taye, Habtamu Gebrie, Alayu Bogale, Eyob Getu, Gemechu Churiso
{"title":"A novel pan-Leishmania loop-mediated isothermal amplification (Loopamp) assay for diagnosis of cutaneous and visceral leishmaniasis: a systematic review and meta-analysis.","authors":"Behailu Taye, Habtamu Gebrie, Alayu Bogale, Eyob Getu, Gemechu Churiso","doi":"10.1186/s12879-025-11091-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>There is an urgent need for accurate and robust point-of-care (PoC) assays for visceral and cutaneous leishmaniasis (VL and CL). The Loopamp™ Leishmania detection kit (Loopamp), a novel loop-mediated isothermal amplification (LAMP) assay, has shown promise for VL and CL diagnosis using Qiagen and simpler boil-and-spin (B&S) DNA extraction methods. But diagnostic performances were inconsistent across studies. This systematic review and meta-analysis aimed to evaluate the pooled sensitivity and specificity of Loopamp for CL and VL diagnosis.</p><p><strong>Methods: </strong>A comprehensive search of PubMed, Scopus, EMBASE, and Google Scholar was conducted to identify studies that evaluated the diagnostic performance of Loopamp for VL and CL suspects. Using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2), the methodological qualities of the included studies were evaluated. A bivariate random-effects meta-analysis was performed using R and Stata 14.2.</p><p><strong>Results: </strong>Ten studies comprising 18 datasets were included. Sensitivity among individual VL studies ranged from 92 to 100%, while specificity varied from 41 to 100%. For CL, sensitivity varied from 48 to 100% and specificity from 31 to 100%. Pooled sensitivity was 96% (95% CI, 94-98%) for VL and 93% (95% CI, 70-99%) for CL. Pooled specificity was 99% (95% CI, 94-100%) for VL and 87% (95% CI, 55-97%) for CL. Subgroup analysis revealed that whole-blood B&S-Loopamp for VL had similar sensitivity (96%, 95% CI: 93-98%) and specificity (99%, 95% CI: 89-100%) to Qiagen-Loopamp.</p><p><strong>Conclusions: </strong>Loopamp demonstrated robust diagnostic performance for VL in whole blood, meeting the 95% sensitivity and 99% specificity criteria outlined in the Target Product Profile (TPP). Similar to Loopamp-Qiagen, Loopamp-B&S performed excellently for VL diagnosis and is feasible to deploy in remote endemic areas. Loopamp showed high sensitivity and good specificity for CL diagnosis but fell short of the 95% sensitivity and 90% specificity required for CL PoC tests. Data on CL are limited, and its effectiveness in New World VL patients is unclear. Future research is needed to address this gap.</p><p><strong>Trial registration: </strong>CRD42023489463.</p>","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":"25 1","pages":"718"},"PeriodicalIF":3.4000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12087146/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12879-025-11091-2","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: There is an urgent need for accurate and robust point-of-care (PoC) assays for visceral and cutaneous leishmaniasis (VL and CL). The Loopamp™ Leishmania detection kit (Loopamp), a novel loop-mediated isothermal amplification (LAMP) assay, has shown promise for VL and CL diagnosis using Qiagen and simpler boil-and-spin (B&S) DNA extraction methods. But diagnostic performances were inconsistent across studies. This systematic review and meta-analysis aimed to evaluate the pooled sensitivity and specificity of Loopamp for CL and VL diagnosis.

Methods: A comprehensive search of PubMed, Scopus, EMBASE, and Google Scholar was conducted to identify studies that evaluated the diagnostic performance of Loopamp for VL and CL suspects. Using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2), the methodological qualities of the included studies were evaluated. A bivariate random-effects meta-analysis was performed using R and Stata 14.2.

Results: Ten studies comprising 18 datasets were included. Sensitivity among individual VL studies ranged from 92 to 100%, while specificity varied from 41 to 100%. For CL, sensitivity varied from 48 to 100% and specificity from 31 to 100%. Pooled sensitivity was 96% (95% CI, 94-98%) for VL and 93% (95% CI, 70-99%) for CL. Pooled specificity was 99% (95% CI, 94-100%) for VL and 87% (95% CI, 55-97%) for CL. Subgroup analysis revealed that whole-blood B&S-Loopamp for VL had similar sensitivity (96%, 95% CI: 93-98%) and specificity (99%, 95% CI: 89-100%) to Qiagen-Loopamp.

Conclusions: Loopamp demonstrated robust diagnostic performance for VL in whole blood, meeting the 95% sensitivity and 99% specificity criteria outlined in the Target Product Profile (TPP). Similar to Loopamp-Qiagen, Loopamp-B&S performed excellently for VL diagnosis and is feasible to deploy in remote endemic areas. Loopamp showed high sensitivity and good specificity for CL diagnosis but fell short of the 95% sensitivity and 90% specificity required for CL PoC tests. Data on CL are limited, and its effectiveness in New World VL patients is unclear. Future research is needed to address this gap.

Trial registration: CRD42023489463.

一种新的泛利什曼原虫环介导的等温扩增(Loopamp)检测诊断皮肤和内脏利什曼病:系统回顾和荟萃分析。
背景:迫切需要对内脏和皮肤利什曼病(VL和CL)进行准确和强大的即时检测(PoC)。Loopamp™利什曼原虫检测试剂盒(Loopamp)是一种新型的环介导等温扩增(LAMP)检测试剂盒,已显示出使用Qiagen和更简单的煮沸旋转(B&S) DNA提取方法诊断VL和CL的前景。但是诊断表现在不同的研究中是不一致的。本系统综述和荟萃分析旨在评估Loopamp对CL和VL诊断的敏感性和特异性。方法:对PubMed、Scopus、EMBASE和谷歌Scholar进行综合检索,以确定评估Loopamp对VL和CL疑似诊断性能的研究。使用诊断准确性研究质量评估-2 (QUADAS-2),对纳入研究的方法学质量进行评估。采用R和Stata 14.2进行双变量随机效应荟萃分析。结果:纳入了10项研究,包括18个数据集。在个别VL研究中,敏感性从92%到100%不等,而特异性从41%到100%不等。对于CL,敏感性从48%到100%不等,特异性从31%到100%不等。VL的总敏感性为96% (95% CI, 94-98%), CL的总敏感性为93% (95% CI, 70-99%)。VL的合并特异性为99% (95% CI, 94-100%), CL的合并特异性为87% (95% CI, 55-97%)。亚组分析显示,全血B&S-Loopamp对VL的敏感性(96%,95% CI: 93-98%)和特异性(99%,95% CI: 89-100%)与Qiagen-Loopamp相似。结论:Loopamp在全血VL诊断中表现出强大的性能,满足目标产品简介(TPP)中概述的95%敏感性和99%特异性标准。与Loopamp-Qiagen类似,Loopamp-B&S在VL诊断方面表现出色,可在偏远流行地区部署。Loopamp显示出CL诊断的高灵敏度和良好的特异性,但低于CL PoC测试所需的95%灵敏度和90%特异性。关于CL的数据有限,其在新世界VL患者中的有效性尚不清楚。未来的研究需要解决这一差距。试验注册:CRD42023489463。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信