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Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection
BACKGROUND: We compared the diagnostic accuracy and reproducibility of commercially available NS1-based dengue tests and explored factors influencing their sensitivities. METHODS: Paired analysis of 310 samples previously characterized as positive (n = 218) and negative (n = 92) for viral isolation...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3016282/ https://www.ncbi.nlm.nih.gov/pubmed/21134275 http://dx.doi.org/10.1186/1743-422X-7-361 |
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author | Osorio, Lyda Ramirez, Meleny Bonelo, Anilza Villar, Luis A Parra, Beatriz |
author_facet | Osorio, Lyda Ramirez, Meleny Bonelo, Anilza Villar, Luis A Parra, Beatriz |
author_sort | Osorio, Lyda |
collection | PubMed |
description | BACKGROUND: We compared the diagnostic accuracy and reproducibility of commercially available NS1-based dengue tests and explored factors influencing their sensitivities. METHODS: Paired analysis of 310 samples previously characterized as positive (n = 218) and negative (n = 92) for viral isolation and/or RT-PCR and/or IgM seroconversion. Masked samples were tested by two observers with Platelia™ Dengue NS1 Ag, second generation Pan-E™ Dengue Early ELISA, SD Dengue NS1 Ag ELISA, Dengue NS1 Ag STRIP™, and SD BIOLINE™ Dengue Duo (NS1/IgM/IgG). RESULTS: SD BIOLINE™ NS1/IgM/IgG had the highest sensitivity (80.7% 95%CI 75-85.7) with likelihood ratios of 7.4 (95%CI 4.1-13.8) and 0.21 (95%CI 0.16-0.28). The ELISA-format tests showed comparable sensitivities; all below 75%. STRIP™ and SD NS1 had even lower sensitivities (<65%). The sensitivities significantly decreased in samples taken after 3 days of fever onset, in secondary infections, viral serotypes 2 and 4, and severe dengue. Adding IgM or IgG to SD NS1 increased its sensitivity in all these situations. CONCLUSIONS: The simultaneous detection of NS1/IgM/IgG would be potentially useful for dengue diagnosis in both endemic and non endemic areas. A negative result does not rule out dengue. Further studies are required to assess the performance and impact of early laboratory diagnosis of dengue in the routine clinical setting. |
format | Text |
id | pubmed-3016282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30162822011-01-06 Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection Osorio, Lyda Ramirez, Meleny Bonelo, Anilza Villar, Luis A Parra, Beatriz Virol J Research BACKGROUND: We compared the diagnostic accuracy and reproducibility of commercially available NS1-based dengue tests and explored factors influencing their sensitivities. METHODS: Paired analysis of 310 samples previously characterized as positive (n = 218) and negative (n = 92) for viral isolation and/or RT-PCR and/or IgM seroconversion. Masked samples were tested by two observers with Platelia™ Dengue NS1 Ag, second generation Pan-E™ Dengue Early ELISA, SD Dengue NS1 Ag ELISA, Dengue NS1 Ag STRIP™, and SD BIOLINE™ Dengue Duo (NS1/IgM/IgG). RESULTS: SD BIOLINE™ NS1/IgM/IgG had the highest sensitivity (80.7% 95%CI 75-85.7) with likelihood ratios of 7.4 (95%CI 4.1-13.8) and 0.21 (95%CI 0.16-0.28). The ELISA-format tests showed comparable sensitivities; all below 75%. STRIP™ and SD NS1 had even lower sensitivities (<65%). The sensitivities significantly decreased in samples taken after 3 days of fever onset, in secondary infections, viral serotypes 2 and 4, and severe dengue. Adding IgM or IgG to SD NS1 increased its sensitivity in all these situations. CONCLUSIONS: The simultaneous detection of NS1/IgM/IgG would be potentially useful for dengue diagnosis in both endemic and non endemic areas. A negative result does not rule out dengue. Further studies are required to assess the performance and impact of early laboratory diagnosis of dengue in the routine clinical setting. BioMed Central 2010-12-06 /pmc/articles/PMC3016282/ /pubmed/21134275 http://dx.doi.org/10.1186/1743-422X-7-361 Text en Copyright ©2010 Osorio et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Osorio, Lyda Ramirez, Meleny Bonelo, Anilza Villar, Luis A Parra, Beatriz Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection |
title | Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection |
title_full | Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection |
title_fullStr | Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection |
title_full_unstemmed | Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection |
title_short | Comparison of the diagnostic accuracy of commercial NS1-based diagnostic tests for early dengue infection |
title_sort | comparison of the diagnostic accuracy of commercial ns1-based diagnostic tests for early dengue infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3016282/ https://www.ncbi.nlm.nih.gov/pubmed/21134275 http://dx.doi.org/10.1186/1743-422X-7-361 |
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