Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis

Abstract African children are at risk of malaria and malnutrition. We quantified relationships between malaria and malnutrition among young Ugandan children in a high malaria transmission region. Data were used from a randomized controlled trial where Ugandan HIV‐unexposed (n = 393) and HIV‐exposed...

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Main Authors: Ali Mohamed Ali, Erika Wallender, Emma Hughes, Grant Dorsey, Radojka M. Savic
Format: Article
Language:English
Published: Wiley 2023-05-01
Series:CPT: Pharmacometrics & Systems Pharmacology
Online Access:https://doi.org/10.1002/psp4.12892
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author Ali Mohamed Ali
Erika Wallender
Emma Hughes
Grant Dorsey
Radojka M. Savic
author_facet Ali Mohamed Ali
Erika Wallender
Emma Hughes
Grant Dorsey
Radojka M. Savic
author_sort Ali Mohamed Ali
collection DOAJ
description Abstract African children are at risk of malaria and malnutrition. We quantified relationships between malaria and malnutrition among young Ugandan children in a high malaria transmission region. Data were used from a randomized controlled trial where Ugandan HIV‐unexposed (n = 393) and HIV‐exposed (n = 186) children were randomized to receive no malaria chemoprevention, monthly sulfadoxine‐pyrimethamine, daily trimethoprim‐sulfamethoxazole, or monthly dihydroartemisinin‐piperaquine (DP) from age 6–24 months, and then were followed off chemoprevention until age 36 months. Monthly height and weight, and time of incident malaria episodes were obtained; 89 children who received DP contributed piperaquine (PQ) concentrations. Malaria hazard was modeled using parametric survival analysis adjusted for repeated events, and height and weight were modeled using a Brody growth model. Among 579 children, stunting (height‐for‐age z‐score [ZHA] < −2) was associated with a 17% increased malaria hazard (95% confidence interval [CI] 10–23%) compared with children with a ZHA of zero. DP was associated with a 35% lower malaria hazard (hazard ratio [HR] [95% CI], 0.65 [0.41–0.97]), compared to no chemoprevention. After accounting for PQ levels, stunted children who received DP had 2.1 times the hazard of malaria (HR [95% CI] 2.1 [1.6–3.0]) compared with children with a ZHA of zero who received DP. Each additional malaria episode was associated with a 0.4% reduced growth rate for height. Better dosing regimens are needed to optimize malaria prevention in malnourished populations, but, importantly, malaria chemoprevention may reduce the burden of malnutrition in early childhood.
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spelling doaj.art-cc8ed1a52cf64670ad17dc6d81efac332023-05-19T06:03:15ZengWileyCPT: Pharmacometrics & Systems Pharmacology2163-83062023-05-0112565666710.1002/psp4.12892Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysisAli Mohamed Ali0Erika Wallender1Emma Hughes2Grant Dorsey3Radojka M. Savic4Department of Bioengineering and Therapeutic Sciences University of California San Francisco San Francisco California USADepartment of Clinical Pharmacy University of California, San Francisco San Francisco California USADepartment of Bioengineering and Therapeutic Sciences University of California San Francisco San Francisco California USADepartment of Medicine University of California, San Francisco San Francisco California USADepartment of Bioengineering and Therapeutic Sciences University of California San Francisco San Francisco California USAAbstract African children are at risk of malaria and malnutrition. We quantified relationships between malaria and malnutrition among young Ugandan children in a high malaria transmission region. Data were used from a randomized controlled trial where Ugandan HIV‐unexposed (n = 393) and HIV‐exposed (n = 186) children were randomized to receive no malaria chemoprevention, monthly sulfadoxine‐pyrimethamine, daily trimethoprim‐sulfamethoxazole, or monthly dihydroartemisinin‐piperaquine (DP) from age 6–24 months, and then were followed off chemoprevention until age 36 months. Monthly height and weight, and time of incident malaria episodes were obtained; 89 children who received DP contributed piperaquine (PQ) concentrations. Malaria hazard was modeled using parametric survival analysis adjusted for repeated events, and height and weight were modeled using a Brody growth model. Among 579 children, stunting (height‐for‐age z‐score [ZHA] < −2) was associated with a 17% increased malaria hazard (95% confidence interval [CI] 10–23%) compared with children with a ZHA of zero. DP was associated with a 35% lower malaria hazard (hazard ratio [HR] [95% CI], 0.65 [0.41–0.97]), compared to no chemoprevention. After accounting for PQ levels, stunted children who received DP had 2.1 times the hazard of malaria (HR [95% CI] 2.1 [1.6–3.0]) compared with children with a ZHA of zero who received DP. Each additional malaria episode was associated with a 0.4% reduced growth rate for height. Better dosing regimens are needed to optimize malaria prevention in malnourished populations, but, importantly, malaria chemoprevention may reduce the burden of malnutrition in early childhood.https://doi.org/10.1002/psp4.12892
spellingShingle Ali Mohamed Ali
Erika Wallender
Emma Hughes
Grant Dorsey
Radojka M. Savic
Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis
CPT: Pharmacometrics & Systems Pharmacology
title Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis
title_full Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis
title_fullStr Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis
title_full_unstemmed Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis
title_short Interplay among malnutrition, chemoprevention, and the risk of malaria in young Ugandan children: Longitudinal pharmacodynamic and growth analysis
title_sort interplay among malnutrition chemoprevention and the risk of malaria in young ugandan children longitudinal pharmacodynamic and growth analysis
url https://doi.org/10.1002/psp4.12892
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