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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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7591246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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