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用于检测人体弓蛔虫病抗体的快速诊断检测的现场评估。

Field evaluation of a rapid diagnostic test to detect antibodies in human toxocariasis.

作者信息

Lim P K C, Yamasaki H, Mak J W, Wong S F, Chong C W, Yap I K S, Ambu S, Kumarasamy V

机构信息

School of Medical Sciences, International Medical University, 126 Jalan Jalil Perkasa 19, Bukit Jalil, 57000 Kuala Lumpur, Malaysia.

Department of Parasitology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.

出版信息

Acta Trop. 2015 Aug;148:32-7. doi: 10.1016/j.actatropica.2015.04.011. Epub 2015 Apr 22.

Abstract

Human toxocariasis which is caused mainly by the larvae of Toxocara canis and Toxocara cati, is a worldwide zoonotic disease that can be a potentially serious human infection. The enzyme-linked immunosorbent assay (ELISA) using T. canis excretory-secretory (TES) antigens harvested from T. canis larvae is currently the serological test for confirming toxocariasis. An alternative to producing large amounts of Toxocara TES and improved diagnosis for toxocariasis is through the development of highly specific recombinant antigens such as the T. canis second stage larva excretory-secretory 30 kDa protein (recTES-30). The aim of this study was to evaluate the sensitivity and specificity of a rapid diagnostic kit (RDT, named as iToxocara kit) in comparison to recTES-30 ELISA in Serendah Orang Asli village in Selangor, Malaysia. A total of 133 subjects were included in the study. The overall prevalence rates by ELISA and RDT were 29.3% and 33.1%, respectively, with more positive cases detected in males than females. However, no association was found between toxocariasis and gender or age. The percentage sensitivity, specificity, positive predictive value and negative predictive value of RDT were 85.7%, 90.1%, 80% and 93.2%, respectively. The prevalence for toxocariasis in this population using both ELISA and RDT was 27.1% (36/133) and the K-concordance test suggested good agreement of the two tests with a Cohen's kappa of 0.722, P<0.01. In addition, the followed-up Spearman rank correlation showed a moderately high correlation at R=0.704 and P<0.01. In conclusion, the RDT kit was faster and easier to use than an ELISA and is useful for the laboratory diagnosis of hospitalized cases of toxocariasis.

摘要

人体弓首蛔虫病主要由犬弓首蛔虫和猫弓首蛔虫的幼虫引起,是一种全球性的人畜共患病,可能导致严重的人体感染。使用从犬弓首蛔虫幼虫中收获的犬弓首蛔虫排泄分泌(TES)抗原的酶联免疫吸附测定(ELISA)是目前确诊弓首蛔虫病的血清学检测方法。生产大量犬弓首蛔虫TES并改善弓首蛔虫病诊断的一种替代方法是开发高度特异性的重组抗原,如犬弓首蛔虫第二期幼虫排泄分泌30 kDa蛋白(recTES-30)。本研究的目的是在马来西亚雪兰莪州的塞伦达原住民村,将一种快速诊断试剂盒(RDT,名为iToxocara试剂盒)与recTES-30 ELISA相比较,评估其敏感性和特异性。共有133名受试者纳入本研究。ELISA和RDT的总体患病率分别为29.3%和33.1%,男性检测出的阳性病例多于女性。然而,未发现弓首蛔虫病与性别或年龄之间存在关联。RDT的敏感性、特异性、阳性预测值和阴性预测值分别为85.7%、90.1%、80%和93.2%。使用ELISA和RDT检测该人群中弓首蛔虫病的患病率为27.1%(36/133),K一致性检验表明两种检测方法一致性良好,Cohen's kappa为0.722,P<0.01。此外,后续的Spearman等级相关性显示相关性中等偏高,R=0.704,P<0.01。总之,RDT试剂盒比ELISA使用起来更快、更简便,可用于弓首蛔虫病住院病例的实验室诊断。

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