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Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study

Despite considerable success of genome wide association (GWA) studies in identifying causal variants for many human diseases, their success in unraveling the genetic basis to complex diseases has been more mitigated. Pathogen population structure may impact upon the infectious phenotype, especially...

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Autores principales: Loucoubar, Cheikh, Goncalves, Bronner, Tall, Adama, Sokhna, Cheikh, Trape, Jean-François, Diène Sarr, Fatoumata, Faye, Joseph, Badiane, Abdoulaye, Ly, Alioune Badara, Diop, Aliou, Bar-Hen, Avner, Bureau, Jean-François, Sakuntabhai, Anavaj, Paul, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207815/
https://www.ncbi.nlm.nih.gov/pubmed/22073159
http://dx.doi.org/10.1371/journal.pone.0026364
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author Loucoubar, Cheikh
Goncalves, Bronner
Tall, Adama
Sokhna, Cheikh
Trape, Jean-François
Diène Sarr, Fatoumata
Faye, Joseph
Badiane, Abdoulaye
Ly, Alioune Badara
Diop, Aliou
Bar-Hen, Avner
Bureau, Jean-François
Sakuntabhai, Anavaj
Paul, Richard
author_facet Loucoubar, Cheikh
Goncalves, Bronner
Tall, Adama
Sokhna, Cheikh
Trape, Jean-François
Diène Sarr, Fatoumata
Faye, Joseph
Badiane, Abdoulaye
Ly, Alioune Badara
Diop, Aliou
Bar-Hen, Avner
Bureau, Jean-François
Sakuntabhai, Anavaj
Paul, Richard
author_sort Loucoubar, Cheikh
collection PubMed
description Despite considerable success of genome wide association (GWA) studies in identifying causal variants for many human diseases, their success in unraveling the genetic basis to complex diseases has been more mitigated. Pathogen population structure may impact upon the infectious phenotype, especially with the intense short-term selective pressure that drug treatment exerts on pathogens. Rigorous analysis that accounts for repeated measures and disentangles the influence of genetic and environmental factors must be performed. Attempts should be made to consider whether pathogen diversity will impact upon host genetic responses to infection. We analyzed the heritability of two Plasmodium falciparum phenotypes, the number of clinical malaria episodes (PFA) and the proportion of these episodes positive for gametocytes (Pfgam), in a family-based cohort followed for 19 years, during which time there were four successive drug treatment regimes, with documented appearance of drug resistance. Repeated measures and variance components analyses were performed with fixed environmental, additive genetic, intra-individual and maternal effects for each drug period. Whilst there was a significant additive genetic effect underlying PFA during the first drug period of study, this was lost in subsequent periods. There was no additive genetic effect for Pfgam. The intra-individual effect increased significantly in the chloroquine period. The loss of an additive genetic effect following novel drug treatment may result in significant loss of power to detect genes in a GWA study. Prior genetic analysis must be a pre-requisite for more detailed GWA studies. The temporal changes in the individual genetic and the intra-individual estimates are consistent with those expected if there were specific host-parasite interactions. The complex basis to the human response to malaria parasite infection likely includes dominance/epistatic genetic effects encompassed within the intra-individual variance component. Evaluating their role in influencing the outcome of infection through host genotype by parasite genotype interactions warrants research effort.
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spelling pubmed-32078152011-11-09 Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study Loucoubar, Cheikh Goncalves, Bronner Tall, Adama Sokhna, Cheikh Trape, Jean-François Diène Sarr, Fatoumata Faye, Joseph Badiane, Abdoulaye Ly, Alioune Badara Diop, Aliou Bar-Hen, Avner Bureau, Jean-François Sakuntabhai, Anavaj Paul, Richard PLoS One Research Article Despite considerable success of genome wide association (GWA) studies in identifying causal variants for many human diseases, their success in unraveling the genetic basis to complex diseases has been more mitigated. Pathogen population structure may impact upon the infectious phenotype, especially with the intense short-term selective pressure that drug treatment exerts on pathogens. Rigorous analysis that accounts for repeated measures and disentangles the influence of genetic and environmental factors must be performed. Attempts should be made to consider whether pathogen diversity will impact upon host genetic responses to infection. We analyzed the heritability of two Plasmodium falciparum phenotypes, the number of clinical malaria episodes (PFA) and the proportion of these episodes positive for gametocytes (Pfgam), in a family-based cohort followed for 19 years, during which time there were four successive drug treatment regimes, with documented appearance of drug resistance. Repeated measures and variance components analyses were performed with fixed environmental, additive genetic, intra-individual and maternal effects for each drug period. Whilst there was a significant additive genetic effect underlying PFA during the first drug period of study, this was lost in subsequent periods. There was no additive genetic effect for Pfgam. The intra-individual effect increased significantly in the chloroquine period. The loss of an additive genetic effect following novel drug treatment may result in significant loss of power to detect genes in a GWA study. Prior genetic analysis must be a pre-requisite for more detailed GWA studies. The temporal changes in the individual genetic and the intra-individual estimates are consistent with those expected if there were specific host-parasite interactions. The complex basis to the human response to malaria parasite infection likely includes dominance/epistatic genetic effects encompassed within the intra-individual variance component. Evaluating their role in influencing the outcome of infection through host genotype by parasite genotype interactions warrants research effort. Public Library of Science 2011-11-03 /pmc/articles/PMC3207815/ /pubmed/22073159 http://dx.doi.org/10.1371/journal.pone.0026364 Text en Loucoubar 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Loucoubar, Cheikh
Goncalves, Bronner
Tall, Adama
Sokhna, Cheikh
Trape, Jean-François
Diène Sarr, Fatoumata
Faye, Joseph
Badiane, Abdoulaye
Ly, Alioune Badara
Diop, Aliou
Bar-Hen, Avner
Bureau, Jean-François
Sakuntabhai, Anavaj
Paul, Richard
Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study
title Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study
title_full Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study
title_fullStr Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study
title_full_unstemmed Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study
title_short Impact of Changing Drug Treatment and Malaria Endemicity on the Heritability of Malaria Phenotypes in a Longitudinal Family-Based Cohort Study
title_sort impact of changing drug treatment and malaria endemicity on the heritability of malaria phenotypes in a longitudinal family-based cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207815/
https://www.ncbi.nlm.nih.gov/pubmed/22073159
http://dx.doi.org/10.1371/journal.pone.0026364
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