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通过快速检测和酶联免疫吸附试验检测非结构蛋白-1抗原及其与聚合酶链反应在登革热早期诊断中的相关性比较

Comparison of nonstructural protein-1 antigen detection by rapid and enzyme-linked immunosorbent assay test and its correlation with polymerase chain reaction for early diagnosis of dengue.

作者信息

Gaikwad Seema, Sawant Sandhya S, Shastri Jayanthi S

机构信息

Department of Microbiology, B.Y.L. Nair Charitable Hospital, Mumbai, Maharashtra, India.

出版信息

J Lab Physicians. 2017 Jul-Sep;9(3):177-181. doi: 10.4103/0974-2727.208265.

DOI:10.4103/0974-2727.208265
PMID:28706387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5496295/
Abstract

INTRODUCTION

Early diagnosis of dengue is important for appropriate clinical management and vector control. Different serological tests based on the principle of immunochromatography and enzyme-linked immunosorbent assay (ELISA) are commonly used for detection of antigen and antibodies of dengue virus. The performance of these tests depends on the sensitivity and specificity. Hence, the study was undertaken to compare nonstructural protein-1 (NS1) antigen detection by rapid and ELISA with real-time polymerase chain reaction (RT-PCR) for diagnosis of dengue.

MATERIALS AND METHODS

Prospective laboratory study was carried out on sera samples ( = 200) from clinically suspected cases of dengue. The sera samples were subjected for NS1 antigen detection test by rapid test, NS1 ELISA, and RT-PCR. The results of rapid and ELISA tests were compared with real Time PCR.

RESULTS

The sensitivity, specificity, positive, and negative predictive value of rapid dengue NS1 antigen test were 81.5%, 66.7%, 78.2%, and 71.1%, respectively whereas that of NS1 ELISA were 89.9%, 100%, 100%, and 94%, respectively. Concordance of Rapid NS1 and NS1 ELISA with PCR was 75.5% and 94%.

DISCUSSION AND CONCLUSION

NS1 antigen ELISA can be implemented in diagnostic laboratories for diagnosis of dengue in the acute phase of illness. The test also has great potential value for use in epidemic situations, as it could facilitate the early screening of patients and limit disease expansion.

摘要

引言

登革热的早期诊断对于适当的临床管理和病媒控制至关重要。基于免疫层析原理和酶联免疫吸附测定(ELISA)的不同血清学检测常用于检测登革热病毒的抗原和抗体。这些检测的性能取决于敏感性和特异性。因此,开展本研究以比较采用快速检测法和ELISA检测非结构蛋白1(NS1)抗原与实时聚合酶链反应(RT-PCR)用于诊断登革热的效果。

材料与方法

对临床疑似登革热病例的血清样本(n = 200)进行前瞻性实验室研究。血清样本接受快速检测法、NS1 ELISA和RT-PCR的NS1抗原检测试验。将快速检测法和ELISA检测的结果与实时PCR结果进行比较。

结果

快速登革热NS1抗原检测的敏感性、特异性、阳性预测值和阴性预测值分别为81.5%、66.7%、78.2%和71.1%,而NS1 ELISA的相应值分别为89.9%、100%、100%和94%。快速NS1检测和NS1 ELISA与PCR的一致性分别为75.5%和94%。

讨论与结论

NS1抗原ELISA可在诊断实验室用于疾病急性期登革热的诊断。该检测在疫情情况下也具有很大的潜在价值,因为它有助于对患者进行早期筛查并限制疾病传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0a/5496295/8a14a1774a27/JLP-9-177-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0a/5496295/7156a0927a2a/JLP-9-177-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0a/5496295/8a14a1774a27/JLP-9-177-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0a/5496295/7156a0927a2a/JLP-9-177-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0a/5496295/8a14a1774a27/JLP-9-177-g003.jpg

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