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Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon

The need to monitor changes in parasite clearance following treatment with artemisinin-based combination therapies (ACTs) is important in the containment of drug resistance. This study aimed to model Plasmodium falciparum response to ACTs among children in two different transmission settings (Muteng...

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Autores principales: Nji, Akindeh M., Ali, Innocent M., Niba, Peter Thelma Ngwa, Marie-Solange, Evehe, Heumann, Christian, Froeschl, Guenter, Mbacham, Wilfred F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465257/
https://www.ncbi.nlm.nih.gov/pubmed/34578139
http://dx.doi.org/10.3390/pathogens10091106
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author Nji, Akindeh M.
Ali, Innocent M.
Niba, Peter Thelma Ngwa
Marie-Solange, Evehe
Heumann, Christian
Froeschl, Guenter
Mbacham, Wilfred F.
author_facet Nji, Akindeh M.
Ali, Innocent M.
Niba, Peter Thelma Ngwa
Marie-Solange, Evehe
Heumann, Christian
Froeschl, Guenter
Mbacham, Wilfred F.
author_sort Nji, Akindeh M.
collection PubMed
description The need to monitor changes in parasite clearance following treatment with artemisinin-based combination therapies (ACTs) is important in the containment of drug resistance. This study aimed to model Plasmodium falciparum response to ACTs among children in two different transmission settings (Mutengene and Garoua) in Cameroon. Using the step function, a discrete-time survival model was fitted with all the covariates included that might play a role in parasite clearance. The probability of clearing parasites within 24 h following treatment was 21.6% and 70.3% for younger children aged 6 to 59 months and 29.3% and 59.8% for older children aged 60 to 120 months in Mutengene and Garoua, respectively. After two days of treatment, the conditional probability of clearing parasites given that they were not cleared on day 1 was 76.7% and 96.6% for children aged 6–59 months and 83.1% and 93.5% for children aged 60–120 months in Mutengene and Garoua, respectively. The model demonstrated that the ecological setting, age group and pretreatment serum levels of creatinine and alanine aminotransferase were the main factors that significantly influenced parasite clearance in vivo after administration of ACTs (p < 0.05). The findings highlight the need for further investigations on host differential response to ACTs in current practice.
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spelling pubmed-84652572021-09-27 Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon Nji, Akindeh M. Ali, Innocent M. Niba, Peter Thelma Ngwa Marie-Solange, Evehe Heumann, Christian Froeschl, Guenter Mbacham, Wilfred F. Pathogens Article The need to monitor changes in parasite clearance following treatment with artemisinin-based combination therapies (ACTs) is important in the containment of drug resistance. This study aimed to model Plasmodium falciparum response to ACTs among children in two different transmission settings (Mutengene and Garoua) in Cameroon. Using the step function, a discrete-time survival model was fitted with all the covariates included that might play a role in parasite clearance. The probability of clearing parasites within 24 h following treatment was 21.6% and 70.3% for younger children aged 6 to 59 months and 29.3% and 59.8% for older children aged 60 to 120 months in Mutengene and Garoua, respectively. After two days of treatment, the conditional probability of clearing parasites given that they were not cleared on day 1 was 76.7% and 96.6% for children aged 6–59 months and 83.1% and 93.5% for children aged 60–120 months in Mutengene and Garoua, respectively. The model demonstrated that the ecological setting, age group and pretreatment serum levels of creatinine and alanine aminotransferase were the main factors that significantly influenced parasite clearance in vivo after administration of ACTs (p < 0.05). The findings highlight the need for further investigations on host differential response to ACTs in current practice. MDPI 2021-08-30 /pmc/articles/PMC8465257/ /pubmed/34578139 http://dx.doi.org/10.3390/pathogens10091106 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nji, Akindeh M.
Ali, Innocent M.
Niba, Peter Thelma Ngwa
Marie-Solange, Evehe
Heumann, Christian
Froeschl, Guenter
Mbacham, Wilfred F.
Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon
title Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon
title_full Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon
title_fullStr Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon
title_full_unstemmed Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon
title_short Discrete Survival Model Analysis of Plasmodium falciparum Response to Artemisinin-Based Combination Therapies among Children in Regions of Varying Malaria Transmission in Cameroon
title_sort discrete survival model analysis of plasmodium falciparum response to artemisinin-based combination therapies among children in regions of varying malaria transmission in cameroon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465257/
https://www.ncbi.nlm.nih.gov/pubmed/34578139
http://dx.doi.org/10.3390/pathogens10091106
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