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评价 Loopamp 克鲁兹锥虫检测试剂盒在非流行地区用于诊断恰加斯病的性能,西班牙。

Evaluation of the Performance of the Loopamp Trypanosoma cruzi Detection Kit for the Diagnosis of Chagas Disease in an Area Where It Is Not Endemic, Spain.

机构信息

National Centre for Microbiology, Instituto de Salud Carlos III, Madrid, Spain

Fundación Mundo Sano-España, Madrid, Spain.

出版信息

J Clin Microbiol. 2021 Apr 20;59(5). doi: 10.1128/JCM.01860-20.

Abstract

In Spain, PCR is the tool of choice for the diagnosis of congenital Chagas disease (CD) and serology for diagnosing chronic CD. A loop-mediated isothermal amplification test for DNA detection showed good analytical performance and ease of use. We aimed to evaluate the performance of the Loopamp detection kit (Eiken Chemical Co. Ltd., Japan) (-LAMP) for congenital and chronic CD diagnosis using well-characterized samples. We included samples from 39 congenital and 174 chronic CD cases and from 48 uninfected children born to infected mothers and 34 nonchagasic individuals. The sensitivity, specificity, and accuracy of -LAMP were estimated using standard case definitions for congenital CD (positive result by parasitological or PCR tests or serology after 9 months of age) and chronic CD (positive serology by at least two tests). The -LAMP results were read by visual examination and a real-time fluorimeter. For congenital CD, -LAMP sensitivity was 97% for both types of reading; specificity was 92% by visual examination and 94% by fluorimeter. For chronic CD, sensitivity was 47% and specificity 100%. The accuracy in congenital CD was >94% versus 56% in chronic CD. The agreement of -LAMP with PCR tests was better in congenital CD (kappa, 0.86 to 0.91) than in chronic CD (kappa, 0.67 to 0.83). The Loopamp detection kit showed good performance for the diagnosis of congenital CD. -LAMP, like PCR, can be useful for the screening and early diagnosis of congenital infection.

摘要

在西班牙,PCR 是诊断先天性克氏锥虫病 (CD) 的首选工具,而血清学检查则用于诊断慢性 CD。一种用于 DNA 检测的环介导等温扩增试验显示出良好的分析性能和易用性。我们旨在使用经过充分验证的样本评估 Loopamp 检测试剂盒 (Eiken Chemical Co. Ltd.,日本) (-LAMP) 对先天性和慢性 CD 诊断的性能。我们纳入了 39 例先天性 CD 和 174 例慢性 CD 病例,以及 48 例来自感染母亲的未感染儿童和 34 例非恰加斯病个体的样本。使用先天性 CD 的标准病例定义 (寄生虫学或 PCR 检测阳性或 9 个月后血清学阳性) 和慢性 CD (至少两次血清学检测阳性) 来估计 -LAMP 的灵敏度、特异性和准确性。-LAMP 的结果通过目视检查和实时荧光计读取。对于先天性 CD,两种读取方式的灵敏度均为 97%;目视检查的特异性为 92%,荧光计的特异性为 94%。对于慢性 CD,灵敏度为 47%,特异性为 100%。先天性 CD 的准确性>94%,而慢性 CD 的准确性为 56%。-LAMP 与 PCR 检测的一致性在先天性 CD 中更好(kappa 值为 0.86 至 0.91),而在慢性 CD 中则较差(kappa 值为 0.67 至 0.83)。Loopamp 检测试剂盒在诊断先天性 CD 方面表现良好。-LAMP 与 PCR 一样,可用于先天性感染的筛查和早期诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f24/8091841/2aba8cf31181/JCM.01860-20-f0001.jpg

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