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Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes

BACKGROUND: Malaria in pregnancy has been associated with maternal morbidity, placental malaria, and adverse birth outcomes. However, data are limited on the relationships between longitudinal measures of malaria during pregnancy, measures of placental malaria, and birth outcomes. METHODS: This is a...

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Autores principales: Kapisi, James, Kakuru, Abel, Jagannathan, Prasanna, Muhindo, Mary K., Natureeba, Paul, Awori, Patricia, Nakalembe, Miriam, Ssekitoleko, Richard, Olwoch, Peter, Ategeka, John, Nayebare, Patience, Clark, Tamara D., Rizzuto, Gabrielle, Muehlenbachs, Atis, Havlir, Diane V., Kamya, Moses R., Dorsey, Grant, Gaw, Stephanie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629777/
https://www.ncbi.nlm.nih.gov/pubmed/28982374
http://dx.doi.org/10.1186/s12936-017-2040-4
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author Kapisi, James
Kakuru, Abel
Jagannathan, Prasanna
Muhindo, Mary K.
Natureeba, Paul
Awori, Patricia
Nakalembe, Miriam
Ssekitoleko, Richard
Olwoch, Peter
Ategeka, John
Nayebare, Patience
Clark, Tamara D.
Rizzuto, Gabrielle
Muehlenbachs, Atis
Havlir, Diane V.
Kamya, Moses R.
Dorsey, Grant
Gaw, Stephanie L.
author_facet Kapisi, James
Kakuru, Abel
Jagannathan, Prasanna
Muhindo, Mary K.
Natureeba, Paul
Awori, Patricia
Nakalembe, Miriam
Ssekitoleko, Richard
Olwoch, Peter
Ategeka, John
Nayebare, Patience
Clark, Tamara D.
Rizzuto, Gabrielle
Muehlenbachs, Atis
Havlir, Diane V.
Kamya, Moses R.
Dorsey, Grant
Gaw, Stephanie L.
author_sort Kapisi, James
collection PubMed
description BACKGROUND: Malaria in pregnancy has been associated with maternal morbidity, placental malaria, and adverse birth outcomes. However, data are limited on the relationships between longitudinal measures of malaria during pregnancy, measures of placental malaria, and birth outcomes. METHODS: This is a nested observational study of data from a randomized controlled trial of intermittent preventive therapy during pregnancy among 282 participants with assessment of placental malaria and delivery outcomes. HIV-uninfected pregnant women were enrolled at 12–20 weeks of gestation. Symptomatic malaria during pregnancy was measured using passive surveillance and monthly detection of asymptomatic parasitaemia using loop-mediated isothermal amplification (LAMP). Placental malaria was defined as either the presence of parasites in placental blood by microscopy, detection of parasites in placental blood by LAMP, or histopathologic evidence of parasites or pigment. Adverse birth outcomes assessed included low birth weight (LBW), preterm birth (PTB), and small for gestational age (SGA) infants. RESULTS: The 282 women were divided into three groups representing increasing malaria burden during pregnancy. Fifty-two (18.4%) had no episodes of symptomatic malaria or asymptomatic parasitaemia during the pregnancy, 157 (55.7%) had low malaria burden (0–1 episodes of symptomatic malaria and < 50% of samples LAMP+), and 73 (25.9%) had high malaria burden during pregnancy (≥ 2 episodes of symptomatic malaria or ≥ 50% of samples LAMP+). Women with high malaria burden had increased risks of placental malaria by blood microscopy and LAMP [aRR 14.2 (1.80–111.6) and 4.06 (1.73–9.51), respectively], compared to the other two groups combined. Compared with women with no malaria exposure during pregnancy, the risk of placental malaria by histopathology was higher among low and high burden groups [aRR = 3.27 (1.32–8.12) and aRR = 7.07 (2.84–17.6), respectively]. Detection of placental parasites by any method was significantly associated with PTB [aRR 5.64 (1.46–21.8)], and with a trend towards increased risk for LBW and SGA irrespective of the level of malaria burden during pregnancy. CONCLUSION: Higher malaria burden during pregnancy was associated with placental malaria and together with the detection of parasites in the placenta were associated with increased risk for adverse birth outcomes. Trial Registration Current Controlled Trials Identifier NCT02163447 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-2040-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-56297772017-10-13 Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes Kapisi, James Kakuru, Abel Jagannathan, Prasanna Muhindo, Mary K. Natureeba, Paul Awori, Patricia Nakalembe, Miriam Ssekitoleko, Richard Olwoch, Peter Ategeka, John Nayebare, Patience Clark, Tamara D. Rizzuto, Gabrielle Muehlenbachs, Atis Havlir, Diane V. Kamya, Moses R. Dorsey, Grant Gaw, Stephanie L. Malar J Research BACKGROUND: Malaria in pregnancy has been associated with maternal morbidity, placental malaria, and adverse birth outcomes. However, data are limited on the relationships between longitudinal measures of malaria during pregnancy, measures of placental malaria, and birth outcomes. METHODS: This is a nested observational study of data from a randomized controlled trial of intermittent preventive therapy during pregnancy among 282 participants with assessment of placental malaria and delivery outcomes. HIV-uninfected pregnant women were enrolled at 12–20 weeks of gestation. Symptomatic malaria during pregnancy was measured using passive surveillance and monthly detection of asymptomatic parasitaemia using loop-mediated isothermal amplification (LAMP). Placental malaria was defined as either the presence of parasites in placental blood by microscopy, detection of parasites in placental blood by LAMP, or histopathologic evidence of parasites or pigment. Adverse birth outcomes assessed included low birth weight (LBW), preterm birth (PTB), and small for gestational age (SGA) infants. RESULTS: The 282 women were divided into three groups representing increasing malaria burden during pregnancy. Fifty-two (18.4%) had no episodes of symptomatic malaria or asymptomatic parasitaemia during the pregnancy, 157 (55.7%) had low malaria burden (0–1 episodes of symptomatic malaria and < 50% of samples LAMP+), and 73 (25.9%) had high malaria burden during pregnancy (≥ 2 episodes of symptomatic malaria or ≥ 50% of samples LAMP+). Women with high malaria burden had increased risks of placental malaria by blood microscopy and LAMP [aRR 14.2 (1.80–111.6) and 4.06 (1.73–9.51), respectively], compared to the other two groups combined. Compared with women with no malaria exposure during pregnancy, the risk of placental malaria by histopathology was higher among low and high burden groups [aRR = 3.27 (1.32–8.12) and aRR = 7.07 (2.84–17.6), respectively]. Detection of placental parasites by any method was significantly associated with PTB [aRR 5.64 (1.46–21.8)], and with a trend towards increased risk for LBW and SGA irrespective of the level of malaria burden during pregnancy. CONCLUSION: Higher malaria burden during pregnancy was associated with placental malaria and together with the detection of parasites in the placenta were associated with increased risk for adverse birth outcomes. Trial Registration Current Controlled Trials Identifier NCT02163447 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-2040-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-05 /pmc/articles/PMC5629777/ /pubmed/28982374 http://dx.doi.org/10.1186/s12936-017-2040-4 Text en © The Author(s) 2017 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
Kapisi, James
Kakuru, Abel
Jagannathan, Prasanna
Muhindo, Mary K.
Natureeba, Paul
Awori, Patricia
Nakalembe, Miriam
Ssekitoleko, Richard
Olwoch, Peter
Ategeka, John
Nayebare, Patience
Clark, Tamara D.
Rizzuto, Gabrielle
Muehlenbachs, Atis
Havlir, Diane V.
Kamya, Moses R.
Dorsey, Grant
Gaw, Stephanie L.
Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
title Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
title_full Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
title_fullStr Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
title_full_unstemmed Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
title_short Relationships between infection with Plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
title_sort relationships between infection with plasmodium falciparum during pregnancy, measures of placental malaria, and adverse birth outcomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629777/
https://www.ncbi.nlm.nih.gov/pubmed/28982374
http://dx.doi.org/10.1186/s12936-017-2040-4
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