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Diagnosis of placental malaria in poorly fixed and processed placental tissue
BACKGROUND: Placental histopathology has been considered the gold standard for diagnosis of malaria during pregnancy. However, in under-resourced areas placental tissue is often improperly fixed and processed; the resulting formalin pigment is difficult to distinguish from malaria pigment. This stud...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863337/ https://www.ncbi.nlm.nih.gov/pubmed/27165119 http://dx.doi.org/10.1186/s12936-016-1314-6 |
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author | Liu, Yunhao Griffin, Jennifer B. Muehlenbachs, Atis Rogerson, Stephen J. Bailis, Anya J. Sharma, Rajni Sullivan, David J. Tshefu, Antoinette K. Landis, Sarah H. Kabongo, Jean-Marie M. Taylor, Steve M. Meshnick, Steven R. |
author_facet | Liu, Yunhao Griffin, Jennifer B. Muehlenbachs, Atis Rogerson, Stephen J. Bailis, Anya J. Sharma, Rajni Sullivan, David J. Tshefu, Antoinette K. Landis, Sarah H. Kabongo, Jean-Marie M. Taylor, Steve M. Meshnick, Steven R. |
author_sort | Liu, Yunhao |
collection | PubMed |
description | BACKGROUND: Placental histopathology has been considered the gold standard for diagnosis of malaria during pregnancy. However, in under-resourced areas placental tissue is often improperly fixed and processed; the resulting formalin pigment is difficult to distinguish from malaria pigment. This study examines two alternative diagnostic methods: polymerase chain reaction (PCR) and a novel immunohistochemistry (IHC)-based method using an antibody against histidine-rich protein 2 (HRP2). METHODS: Placental histopathology from 151 pregnant women in Kinshasa was assessed by two blinded microscopists and compared with peripheral blood PCR and IHC for HRP2. The Cohen’s kappa coefficients were calculated to assess the test agreement. The sensitivity and specificity of individual tests were calculated using PCR or IHC as the reference standard as well as latent class analysis (LCA). RESULTS: PCR and IHC correlated fairly well. The correlation between the two blinded microscopists was poor, as there was widespread formalin pigment. Using LCA, all of the tests had high specificities. The most sensitive test was IHC (67.7 %), with PCR as second-best (56.1 %). CONCLUSIONS: PCR and/or IHC are suitable diagnostics when the presence of formalin pigment substantially compromises placental histopathology. |
format | Online Article Text |
id | pubmed-4863337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48633372016-05-12 Diagnosis of placental malaria in poorly fixed and processed placental tissue Liu, Yunhao Griffin, Jennifer B. Muehlenbachs, Atis Rogerson, Stephen J. Bailis, Anya J. Sharma, Rajni Sullivan, David J. Tshefu, Antoinette K. Landis, Sarah H. Kabongo, Jean-Marie M. Taylor, Steve M. Meshnick, Steven R. Malar J Research BACKGROUND: Placental histopathology has been considered the gold standard for diagnosis of malaria during pregnancy. However, in under-resourced areas placental tissue is often improperly fixed and processed; the resulting formalin pigment is difficult to distinguish from malaria pigment. This study examines two alternative diagnostic methods: polymerase chain reaction (PCR) and a novel immunohistochemistry (IHC)-based method using an antibody against histidine-rich protein 2 (HRP2). METHODS: Placental histopathology from 151 pregnant women in Kinshasa was assessed by two blinded microscopists and compared with peripheral blood PCR and IHC for HRP2. The Cohen’s kappa coefficients were calculated to assess the test agreement. The sensitivity and specificity of individual tests were calculated using PCR or IHC as the reference standard as well as latent class analysis (LCA). RESULTS: PCR and IHC correlated fairly well. The correlation between the two blinded microscopists was poor, as there was widespread formalin pigment. Using LCA, all of the tests had high specificities. The most sensitive test was IHC (67.7 %), with PCR as second-best (56.1 %). CONCLUSIONS: PCR and/or IHC are suitable diagnostics when the presence of formalin pigment substantially compromises placental histopathology. BioMed Central 2016-05-10 /pmc/articles/PMC4863337/ /pubmed/27165119 http://dx.doi.org/10.1186/s12936-016-1314-6 Text en © Liu et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Liu, Yunhao Griffin, Jennifer B. Muehlenbachs, Atis Rogerson, Stephen J. Bailis, Anya J. Sharma, Rajni Sullivan, David J. Tshefu, Antoinette K. Landis, Sarah H. Kabongo, Jean-Marie M. Taylor, Steve M. Meshnick, Steven R. Diagnosis of placental malaria in poorly fixed and processed placental tissue |
title | Diagnosis of placental malaria in poorly fixed and processed placental tissue |
title_full | Diagnosis of placental malaria in poorly fixed and processed placental tissue |
title_fullStr | Diagnosis of placental malaria in poorly fixed and processed placental tissue |
title_full_unstemmed | Diagnosis of placental malaria in poorly fixed and processed placental tissue |
title_short | Diagnosis of placental malaria in poorly fixed and processed placental tissue |
title_sort | diagnosis of placental malaria in poorly fixed and processed placental tissue |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863337/ https://www.ncbi.nlm.nih.gov/pubmed/27165119 http://dx.doi.org/10.1186/s12936-016-1314-6 |
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