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Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso

Asymptomatic malaria infections may affect red blood cell (RBC) homeostasis. Reports indicate a role for chronic hemolysis and splenomegaly, however, the underlying processes are incompletely understood. New hematology analysers provide parameters for a more comprehensive analysis of RBC hemostasis....

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Autores principales: Kaboré, Berenger, Post, Annelies, Berendsen, Mike L. T., Diallo, Salou, Lompo, Palpouguini, Derra, Karim, Rouamba, Eli, Jacobs, Jan, Tinto, Halidou, de Mast, Quirijn, van der Ven, Andre J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703889/
https://www.ncbi.nlm.nih.gov/pubmed/33253198
http://dx.doi.org/10.1371/journal.pone.0242507
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author Kaboré, Berenger
Post, Annelies
Berendsen, Mike L. T.
Diallo, Salou
Lompo, Palpouguini
Derra, Karim
Rouamba, Eli
Jacobs, Jan
Tinto, Halidou
de Mast, Quirijn
van der Ven, Andre J.
author_facet Kaboré, Berenger
Post, Annelies
Berendsen, Mike L. T.
Diallo, Salou
Lompo, Palpouguini
Derra, Karim
Rouamba, Eli
Jacobs, Jan
Tinto, Halidou
de Mast, Quirijn
van der Ven, Andre J.
author_sort Kaboré, Berenger
collection PubMed
description Asymptomatic malaria infections may affect red blood cell (RBC) homeostasis. Reports indicate a role for chronic hemolysis and splenomegaly, however, the underlying processes are incompletely understood. New hematology analysers provide parameters for a more comprehensive analysis of RBC hemostasis. Complete blood counts were analysed in subjects from all age groups (n = 1118) living in a malaria hyperendemic area and cytokines and iron biomarkers were also measured. Subjects were divided into age groups (<2 years, 2–4, 5–14 and ≥15 years old) and clinical categories (smear-negative healthy subjects, asymptomatic malaria and clinical malaria). We found that hemoglobin levels were similar in smear-negative healthy children and asymptomatic malaria children but significantly lower in clinical malaria with a maximum difference of 2.2 g/dl in children <2 years decreasing to 0.1 g/dl in those aged ≥15 years. Delta-He, presenting different hemoglobinization of reticulocytes and RBC, levels were lower in asymptomatic and clinial malaria, indicating a recent effect of malaria on erythropoiesis. Reticulocyte counts and reticulocyte production index (RPI), indicating the erythropoietic capacity of the bone marrow, were higher in young children with malaria compared to smear-negative subjects. A negative correlation between reticulocyte counts and Hb levels was found in asymptomatic malaria (ρ = -0.32, p<0.001) unlike in clinical malaria (ρ = -0.008, p = 0.92). Free-Hb levels, indicating hemolysis, were only higher in clinical malaria. Phagocytozing monocytes, indicating erythophagocytosis, were highest in clinical malaria, followed by asymptomatic malaria and smear-negative subjects. Circulating cytokines and iron biomarkers (hepcidin, ferritin) showed similar patterns. Pro/anti-inflammatory (IL-6/IL-10) ratio was higher in clinical than asymptomatic malaria. Cytokine production capacity of ex-vivo whole blood stimulation with LPS was lower in children with asymptomatic malaria compared to smear-negative healthy children. Bone marrow response can compensate the increased red blood cell loss in asymptomatic malaria, unlike in clinical malaria, possibly because of limited level and length of inflammation. Trial registration: Prospective diagnostic study: ClinicalTrials.gov identifier: NCT02669823. Explorative cross-sectional field study: ClinicalTrials.gov identifier: NCT03176719.
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spelling pubmed-77038892020-12-03 Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso Kaboré, Berenger Post, Annelies Berendsen, Mike L. T. Diallo, Salou Lompo, Palpouguini Derra, Karim Rouamba, Eli Jacobs, Jan Tinto, Halidou de Mast, Quirijn van der Ven, Andre J. PLoS One Research Article Asymptomatic malaria infections may affect red blood cell (RBC) homeostasis. Reports indicate a role for chronic hemolysis and splenomegaly, however, the underlying processes are incompletely understood. New hematology analysers provide parameters for a more comprehensive analysis of RBC hemostasis. Complete blood counts were analysed in subjects from all age groups (n = 1118) living in a malaria hyperendemic area and cytokines and iron biomarkers were also measured. Subjects were divided into age groups (<2 years, 2–4, 5–14 and ≥15 years old) and clinical categories (smear-negative healthy subjects, asymptomatic malaria and clinical malaria). We found that hemoglobin levels were similar in smear-negative healthy children and asymptomatic malaria children but significantly lower in clinical malaria with a maximum difference of 2.2 g/dl in children <2 years decreasing to 0.1 g/dl in those aged ≥15 years. Delta-He, presenting different hemoglobinization of reticulocytes and RBC, levels were lower in asymptomatic and clinial malaria, indicating a recent effect of malaria on erythropoiesis. Reticulocyte counts and reticulocyte production index (RPI), indicating the erythropoietic capacity of the bone marrow, were higher in young children with malaria compared to smear-negative subjects. A negative correlation between reticulocyte counts and Hb levels was found in asymptomatic malaria (ρ = -0.32, p<0.001) unlike in clinical malaria (ρ = -0.008, p = 0.92). Free-Hb levels, indicating hemolysis, were only higher in clinical malaria. Phagocytozing monocytes, indicating erythophagocytosis, were highest in clinical malaria, followed by asymptomatic malaria and smear-negative subjects. Circulating cytokines and iron biomarkers (hepcidin, ferritin) showed similar patterns. Pro/anti-inflammatory (IL-6/IL-10) ratio was higher in clinical than asymptomatic malaria. Cytokine production capacity of ex-vivo whole blood stimulation with LPS was lower in children with asymptomatic malaria compared to smear-negative healthy children. Bone marrow response can compensate the increased red blood cell loss in asymptomatic malaria, unlike in clinical malaria, possibly because of limited level and length of inflammation. Trial registration: Prospective diagnostic study: ClinicalTrials.gov identifier: NCT02669823. Explorative cross-sectional field study: ClinicalTrials.gov identifier: NCT03176719. Public Library of Science 2020-11-30 /pmc/articles/PMC7703889/ /pubmed/33253198 http://dx.doi.org/10.1371/journal.pone.0242507 Text en © 2020 Kaboré et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kaboré, Berenger
Post, Annelies
Berendsen, Mike L. T.
Diallo, Salou
Lompo, Palpouguini
Derra, Karim
Rouamba, Eli
Jacobs, Jan
Tinto, Halidou
de Mast, Quirijn
van der Ven, Andre J.
Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso
title Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso
title_full Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso
title_fullStr Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso
title_full_unstemmed Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso
title_short Red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in Burkina Faso
title_sort red blood cell homeostasis in children and adults with and without asymptomatic malaria infection in burkina faso
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703889/
https://www.ncbi.nlm.nih.gov/pubmed/33253198
http://dx.doi.org/10.1371/journal.pone.0242507
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