Cargando…

Clinical consequences of submicroscopic malaria parasitaemia in Uganda

BACKGROUND: Submicroscopic malaria parasitaemia is common in both high- and low-endemicity settings, but its clinical consequences are unclear. METHODS: A cohort of 364 children (0.5–10 years of age) and 106 adults was followed from 2011 to 2016 in Tororo District, Uganda using passive surveillance...

Descripción completa

Detalles Bibliográficos
Autores principales: Katrak, Shereen, Nayebare, Patience, Rek, John, Arinaitwe, Emmanuel, Nankabirwa, Joaniter I., Kamya, Moses, Dorsey, Grant, Rosenthal, Philip J., Greenhouse, Bryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800031/
https://www.ncbi.nlm.nih.gov/pubmed/29402282
http://dx.doi.org/10.1186/s12936-018-2221-9
_version_ 1783298123848744960
author Katrak, Shereen
Nayebare, Patience
Rek, John
Arinaitwe, Emmanuel
Nankabirwa, Joaniter I.
Kamya, Moses
Dorsey, Grant
Rosenthal, Philip J.
Greenhouse, Bryan
author_facet Katrak, Shereen
Nayebare, Patience
Rek, John
Arinaitwe, Emmanuel
Nankabirwa, Joaniter I.
Kamya, Moses
Dorsey, Grant
Rosenthal, Philip J.
Greenhouse, Bryan
author_sort Katrak, Shereen
collection PubMed
description BACKGROUND: Submicroscopic malaria parasitaemia is common in both high- and low-endemicity settings, but its clinical consequences are unclear. METHODS: A cohort of 364 children (0.5–10 years of age) and 106 adults was followed from 2011 to 2016 in Tororo District, Uganda using passive surveillance for malaria episodes and active surveillance for parasitaemia. Participants presented every 90 days for routine visits (n = 9075); a subset was followed every 30 days. Participants who presented with fever and a positive blood smear were treated for malaria. At all routine visits microscopy was performed and samples from subjects with a negative blood smear underwent loop-mediated isothermal amplification for detection of plasmodial DNA. RESULTS: Submicroscopic parasitaemia was common; the proportion of visits with submicroscopic parasitemia was 25.8% in children and 39.2% in adults. For children 0.5–10 years of age, but not adults, having microscopic and submicroscopic parasitaemia at routine visits was significantly associated with both fever (adjusted risk ratios [95% CI], 2.64 [2.16–3.22], 1.67 [1.37–2.03]) and non-febrile illness (aRR [CI], 1.52 [1.30–1.78], 1.26 [1.09–1.47]), compared to not having parasitaemia. After stratifying by age, significant associations were seen between submicroscopic parasitaemia and fever in children aged 2–< 5 and 5–10 years (aRR [CI], 1.42 [1.03–1.98], 2.01 [1.49–2.71]), and submicroscopic parasitaemia and non-febrile illness in children aged 5–10 years (aRR [CI], 1.44 [1.17–1.78]). These associations were maintained after excluding individuals with a malaria episode within the preceding 14 or following 7 days, and after adjusting for household wealth. CONCLUSIONS: Submicroscopic malaria infections were associated with fever and non-febrile illness in Ugandan children. These findings support malaria control strategies that target low-density infections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2221-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5800031
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-58000312018-02-13 Clinical consequences of submicroscopic malaria parasitaemia in Uganda Katrak, Shereen Nayebare, Patience Rek, John Arinaitwe, Emmanuel Nankabirwa, Joaniter I. Kamya, Moses Dorsey, Grant Rosenthal, Philip J. Greenhouse, Bryan Malar J Research BACKGROUND: Submicroscopic malaria parasitaemia is common in both high- and low-endemicity settings, but its clinical consequences are unclear. METHODS: A cohort of 364 children (0.5–10 years of age) and 106 adults was followed from 2011 to 2016 in Tororo District, Uganda using passive surveillance for malaria episodes and active surveillance for parasitaemia. Participants presented every 90 days for routine visits (n = 9075); a subset was followed every 30 days. Participants who presented with fever and a positive blood smear were treated for malaria. At all routine visits microscopy was performed and samples from subjects with a negative blood smear underwent loop-mediated isothermal amplification for detection of plasmodial DNA. RESULTS: Submicroscopic parasitaemia was common; the proportion of visits with submicroscopic parasitemia was 25.8% in children and 39.2% in adults. For children 0.5–10 years of age, but not adults, having microscopic and submicroscopic parasitaemia at routine visits was significantly associated with both fever (adjusted risk ratios [95% CI], 2.64 [2.16–3.22], 1.67 [1.37–2.03]) and non-febrile illness (aRR [CI], 1.52 [1.30–1.78], 1.26 [1.09–1.47]), compared to not having parasitaemia. After stratifying by age, significant associations were seen between submicroscopic parasitaemia and fever in children aged 2–< 5 and 5–10 years (aRR [CI], 1.42 [1.03–1.98], 2.01 [1.49–2.71]), and submicroscopic parasitaemia and non-febrile illness in children aged 5–10 years (aRR [CI], 1.44 [1.17–1.78]). These associations were maintained after excluding individuals with a malaria episode within the preceding 14 or following 7 days, and after adjusting for household wealth. CONCLUSIONS: Submicroscopic malaria infections were associated with fever and non-febrile illness in Ugandan children. These findings support malaria control strategies that target low-density infections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2221-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-05 /pmc/articles/PMC5800031/ /pubmed/29402282 http://dx.doi.org/10.1186/s12936-018-2221-9 Text en © The Author(s) 2018 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
Katrak, Shereen
Nayebare, Patience
Rek, John
Arinaitwe, Emmanuel
Nankabirwa, Joaniter I.
Kamya, Moses
Dorsey, Grant
Rosenthal, Philip J.
Greenhouse, Bryan
Clinical consequences of submicroscopic malaria parasitaemia in Uganda
title Clinical consequences of submicroscopic malaria parasitaemia in Uganda
title_full Clinical consequences of submicroscopic malaria parasitaemia in Uganda
title_fullStr Clinical consequences of submicroscopic malaria parasitaemia in Uganda
title_full_unstemmed Clinical consequences of submicroscopic malaria parasitaemia in Uganda
title_short Clinical consequences of submicroscopic malaria parasitaemia in Uganda
title_sort clinical consequences of submicroscopic malaria parasitaemia in uganda
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800031/
https://www.ncbi.nlm.nih.gov/pubmed/29402282
http://dx.doi.org/10.1186/s12936-018-2221-9
work_keys_str_mv AT katrakshereen clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT nayebarepatience clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT rekjohn clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT arinaitweemmanuel clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT nankabirwajoaniteri clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT kamyamoses clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT dorseygrant clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT rosenthalphilipj clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda
AT greenhousebryan clinicalconsequencesofsubmicroscopicmalariaparasitaemiainuganda