Evaluation of agreement between tests for the diagnosis of leprosy
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442017000200100 |
Resumo: | ABSTRACT Introduction: Leprosy is a chronic infectious disease caused by the intracellular parasite Mycobacterium leprae. The diagnosis is essentially clinical, based on symptoms, skin exam, peripheral nerves and epidemiological history. Laboratory tests are carried out to complement the result of clinical diagnosis, or even serving as a confirmatory method. Objective: To investigate the positivity and agreement between skin smear, enzyme-linked immunosorbent assay (ELISA) with synthetic antigen ND-O-BSA, ML Flow test and polymerase chain reaction (PCR) for detection of Mycobacterium leprae in new cases of leprosy. Methods: We conducted a case series study assessing a convenience sample of 39 new cases of leprosy and a control group of 18 household contacts in Belém (PA) and in Igarapé-Açu (PA) from March 2014 to September 2015. Results: The agreement between ELISA, ML Flow and PCR tests combinations showed slight to absent reproducibility (Kappa ≤ 0.24). The results showed greater sensitivity in PCR assay, with higher positivity in multibacillary cases. The ELISA test showed low positivity, even in multibacillary cases, resulting in no reaction to paucibacillary cases and household contacts. Conclusion: The high sensitivity of PCR decreases the agreement with other tests. |
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Evaluation of agreement between tests for the diagnosis of leprosyleprosyenzyme-linked immunosorbent assaypolymerase chain reactionserologyABSTRACT Introduction: Leprosy is a chronic infectious disease caused by the intracellular parasite Mycobacterium leprae. The diagnosis is essentially clinical, based on symptoms, skin exam, peripheral nerves and epidemiological history. Laboratory tests are carried out to complement the result of clinical diagnosis, or even serving as a confirmatory method. Objective: To investigate the positivity and agreement between skin smear, enzyme-linked immunosorbent assay (ELISA) with synthetic antigen ND-O-BSA, ML Flow test and polymerase chain reaction (PCR) for detection of Mycobacterium leprae in new cases of leprosy. Methods: We conducted a case series study assessing a convenience sample of 39 new cases of leprosy and a control group of 18 household contacts in Belém (PA) and in Igarapé-Açu (PA) from March 2014 to September 2015. Results: The agreement between ELISA, ML Flow and PCR tests combinations showed slight to absent reproducibility (Kappa ≤ 0.24). The results showed greater sensitivity in PCR assay, with higher positivity in multibacillary cases. The ELISA test showed low positivity, even in multibacillary cases, resulting in no reaction to paucibacillary cases and household contacts. Conclusion: The high sensitivity of PCR decreases the agreement with other tests.Sociedade Brasileira de Patologia Clínica2017-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442017000200100Jornal Brasileiro de Patologia e Medicina Laboratorial v.53 n.2 2017reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)instname:Sociedade Brasileira de Patologia (SBP)instacron:SBP10.5935/1676-2444.20170014info:eu-repo/semantics/openAccessSilva,Alison R.Queiroz,Marcos Fabiano A.Ishikawa,Edna A. Y.Silvestre,Maria do Perpétuo S. A.Xavier,Marilia B.eng2017-05-16T00:00:00Zoai:scielo:S1676-24442017000200100Revistahttp://www.scielo.br/jbpmlhttps://old.scielo.br/oai/scielo-oai.php||jbpml@sbpc.org.br1678-47741676-2444opendoar:2017-05-16T00:00Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)false |
dc.title.none.fl_str_mv |
Evaluation of agreement between tests for the diagnosis of leprosy |
title |
Evaluation of agreement between tests for the diagnosis of leprosy |
spellingShingle |
Evaluation of agreement between tests for the diagnosis of leprosy Silva,Alison R. leprosy enzyme-linked immunosorbent assay polymerase chain reaction serology |
title_short |
Evaluation of agreement between tests for the diagnosis of leprosy |
title_full |
Evaluation of agreement between tests for the diagnosis of leprosy |
title_fullStr |
Evaluation of agreement between tests for the diagnosis of leprosy |
title_full_unstemmed |
Evaluation of agreement between tests for the diagnosis of leprosy |
title_sort |
Evaluation of agreement between tests for the diagnosis of leprosy |
author |
Silva,Alison R. |
author_facet |
Silva,Alison R. Queiroz,Marcos Fabiano A. Ishikawa,Edna A. Y. Silvestre,Maria do Perpétuo S. A. Xavier,Marilia B. |
author_role |
author |
author2 |
Queiroz,Marcos Fabiano A. Ishikawa,Edna A. Y. Silvestre,Maria do Perpétuo S. A. Xavier,Marilia B. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Silva,Alison R. Queiroz,Marcos Fabiano A. Ishikawa,Edna A. Y. Silvestre,Maria do Perpétuo S. A. Xavier,Marilia B. |
dc.subject.por.fl_str_mv |
leprosy enzyme-linked immunosorbent assay polymerase chain reaction serology |
topic |
leprosy enzyme-linked immunosorbent assay polymerase chain reaction serology |
description |
ABSTRACT Introduction: Leprosy is a chronic infectious disease caused by the intracellular parasite Mycobacterium leprae. The diagnosis is essentially clinical, based on symptoms, skin exam, peripheral nerves and epidemiological history. Laboratory tests are carried out to complement the result of clinical diagnosis, or even serving as a confirmatory method. Objective: To investigate the positivity and agreement between skin smear, enzyme-linked immunosorbent assay (ELISA) with synthetic antigen ND-O-BSA, ML Flow test and polymerase chain reaction (PCR) for detection of Mycobacterium leprae in new cases of leprosy. Methods: We conducted a case series study assessing a convenience sample of 39 new cases of leprosy and a control group of 18 household contacts in Belém (PA) and in Igarapé-Açu (PA) from March 2014 to September 2015. Results: The agreement between ELISA, ML Flow and PCR tests combinations showed slight to absent reproducibility (Kappa ≤ 0.24). The results showed greater sensitivity in PCR assay, with higher positivity in multibacillary cases. The ELISA test showed low positivity, even in multibacillary cases, resulting in no reaction to paucibacillary cases and household contacts. Conclusion: The high sensitivity of PCR decreases the agreement with other tests. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442017000200100 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442017000200100 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/1676-2444.20170014 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Patologia Clínica |
publisher.none.fl_str_mv |
Sociedade Brasileira de Patologia Clínica |
dc.source.none.fl_str_mv |
Jornal Brasileiro de Patologia e Medicina Laboratorial v.53 n.2 2017 reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) instname:Sociedade Brasileira de Patologia (SBP) instacron:SBP |
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Sociedade Brasileira de Patologia (SBP) |
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SBP |
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SBP |
reponame_str |
Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
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Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) |
repository.name.fl_str_mv |
Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP) |
repository.mail.fl_str_mv |
||jbpml@sbpc.org.br |
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1752122296747687936 |