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Sex-based differences in clearance of chronic Plasmodium falciparum infection

Multiple studies have reported a male bias in incidence and/or prevalence of malaria infection in males compared to females. To test the hypothesis that sex-based differences in host-parasite interactions affect the epidemiology of malaria, we intensively followed Plasmodium falciparum infections in...

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Autores principales: Briggs, Jessica, Teyssier, Noam, Nankabirwa, Joaniter I, Rek, John, Jagannathan, Prasanna, Arinaitwe, Emmanuel, Bousema, Teun, Drakeley, Chris, Murray, Margaret, Crawford, Emily, Hathaway, Nicholas, Staedke, Sarah G, Smith, David, Rosenthal, Phillip J, Kamya, Moses, Dorsey, Grant, Rodriguez-Barraquer, Isabel, Greenhouse, Bryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591246/
https://www.ncbi.nlm.nih.gov/pubmed/33107430
http://dx.doi.org/10.7554/eLife.59872
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author Briggs, Jessica
Teyssier, Noam
Nankabirwa, Joaniter I
Rek, John
Jagannathan, Prasanna
Arinaitwe, Emmanuel
Bousema, Teun
Drakeley, Chris
Murray, Margaret
Crawford, Emily
Hathaway, Nicholas
Staedke, Sarah G
Smith, David
Rosenthal, Phillip J
Kamya, Moses
Dorsey, Grant
Rodriguez-Barraquer, Isabel
Greenhouse, Bryan
author_facet Briggs, Jessica
Teyssier, Noam
Nankabirwa, Joaniter I
Rek, John
Jagannathan, Prasanna
Arinaitwe, Emmanuel
Bousema, Teun
Drakeley, Chris
Murray, Margaret
Crawford, Emily
Hathaway, Nicholas
Staedke, Sarah G
Smith, David
Rosenthal, Phillip J
Kamya, Moses
Dorsey, Grant
Rodriguez-Barraquer, Isabel
Greenhouse, Bryan
author_sort Briggs, Jessica
collection PubMed
description Multiple studies have reported a male bias in incidence and/or prevalence of malaria infection in males compared to females. To test the hypothesis that sex-based differences in host-parasite interactions affect the epidemiology of malaria, we intensively followed Plasmodium falciparum infections in a cohort in a malaria endemic area of eastern Uganda and estimated both force of infection (FOI) and rate of clearance using amplicon deep-sequencing. We found no evidence of differences in behavioral risk factors, incidence of malaria, or FOI by sex. In contrast, females cleared asymptomatic infections at a faster rate than males (hazard ratio [HR]=1.82, 95% CI 1.20 to 2.75 by clone and HR = 2.07, 95% CI 1.24 to 3.47 by infection event) in multivariate models adjusted for age, timing of infection onset, and parasite density. These findings implicate biological sex-based differences as an important factor in the host response to this globally important pathogen.
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spelling pubmed-75912462020-10-28 Sex-based differences in clearance of chronic Plasmodium falciparum infection Briggs, Jessica Teyssier, Noam Nankabirwa, Joaniter I Rek, John Jagannathan, Prasanna Arinaitwe, Emmanuel Bousema, Teun Drakeley, Chris Murray, Margaret Crawford, Emily Hathaway, Nicholas Staedke, Sarah G Smith, David Rosenthal, Phillip J Kamya, Moses Dorsey, Grant Rodriguez-Barraquer, Isabel Greenhouse, Bryan eLife Epidemiology and Global Health Multiple studies have reported a male bias in incidence and/or prevalence of malaria infection in males compared to females. To test the hypothesis that sex-based differences in host-parasite interactions affect the epidemiology of malaria, we intensively followed Plasmodium falciparum infections in a cohort in a malaria endemic area of eastern Uganda and estimated both force of infection (FOI) and rate of clearance using amplicon deep-sequencing. We found no evidence of differences in behavioral risk factors, incidence of malaria, or FOI by sex. In contrast, females cleared asymptomatic infections at a faster rate than males (hazard ratio [HR]=1.82, 95% CI 1.20 to 2.75 by clone and HR = 2.07, 95% CI 1.24 to 3.47 by infection event) in multivariate models adjusted for age, timing of infection onset, and parasite density. These findings implicate biological sex-based differences as an important factor in the host response to this globally important pathogen. eLife Sciences Publications, Ltd 2020-10-27 /pmc/articles/PMC7591246/ /pubmed/33107430 http://dx.doi.org/10.7554/eLife.59872 Text en © 2020, Briggs et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Epidemiology and Global Health
Briggs, Jessica
Teyssier, Noam
Nankabirwa, Joaniter I
Rek, John
Jagannathan, Prasanna
Arinaitwe, Emmanuel
Bousema, Teun
Drakeley, Chris
Murray, Margaret
Crawford, Emily
Hathaway, Nicholas
Staedke, Sarah G
Smith, David
Rosenthal, Phillip J
Kamya, Moses
Dorsey, Grant
Rodriguez-Barraquer, Isabel
Greenhouse, Bryan
Sex-based differences in clearance of chronic Plasmodium falciparum infection
title Sex-based differences in clearance of chronic Plasmodium falciparum infection
title_full Sex-based differences in clearance of chronic Plasmodium falciparum infection
title_fullStr Sex-based differences in clearance of chronic Plasmodium falciparum infection
title_full_unstemmed Sex-based differences in clearance of chronic Plasmodium falciparum infection
title_short Sex-based differences in clearance of chronic Plasmodium falciparum infection
title_sort sex-based differences in clearance of chronic plasmodium falciparum infection
topic Epidemiology and Global Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591246/
https://www.ncbi.nlm.nih.gov/pubmed/33107430
http://dx.doi.org/10.7554/eLife.59872
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