ArticleBMC medicine2015
Identifying children with excess malaria episodes after adjusting for variation in exposure: identification from a longitudinal study using statistical count models.
Article in BMC medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed.
- Does anthropometric status at 6 months predict the over-dispersion of malaria infections in children aged 6-18 months? A prospective cohort study.Malaria journal · 2019Trial
- Natural History of Malaria Infections During Early Childhood in Twins.The Journal of infectious diseases · 2023Article
- Factors influencing severity of recurrent malaria in a conflict-affected state of South Sudan: an unmatched case-control study.Conflict and health · 2022Article
- Controlled human malaria infection (CHMI) outcomes in Kenyan adults is associated with prior history of malaria exposure and anti-schizont antibody response.BMC infectious diseases · 2022Article
- Endemic chikungunya fever in Kenyan children: a prospective cohort study.BMC infectious diseases · 2021Article
- Individual-level variations in malaria susceptibility and acquisition of clinical protection.Wellcome open research · 2021Article
- Characterization of Naturally Acquired Immunity to a Panel of Antigens Expressed in MatureFrontiers in cellular and infection microbiology · 2021Article
- Mosquito Exposure and Malaria Morbidity: A Microlevel Analysis of Household Mosquito Populations and Malaria in a Population-Based Longitudinal Cohort in Western Kenya.The Journal of infectious diseases · 2020Article
- Epidemiological profiles of recurrent malaria episodes in an endemic area along the Thailand-Myanmar border: a prospective cohort study.Malaria journal · 2019Article
- Transmission and Age Impact the Risk of Developing Febrile Malaria in Children with Asymptomatic Plasmodium falciparum Parasitemia.The Journal of infectious diseases · 2019Article
- Statistical modeling of surveillance data to identify correlates of urban malaria risk: A population-based study in the Amazon Basin.PloS one · 2019Article
- Development of B Cell Memory in Malaria.Frontiers in immunology · 2019Review
- Gametocyte carriage in an era of changing malaria epidemiology: A 19-year analysis of a malaria longitudinal cohort.Wellcome open research · 2019Article
- Variation in natural exposure to anopheles mosquitoes and its effects on malaria transmission.eLife · 2018Article
- Parasitic Protozoa and Interactions with the Host Intestinal Microbiota.Infection and immunity · 2017Review
- Linking health facility data from young adults aged 18-24 years to longitudinal demographic data: Experience from The Kilifi Health and Demographic Surveillance System.Wellcome open research · 2017Article
- From hospitalization records to surveillance: The use of local patient profiles to characterize cholera in Vellore, India.PloS one · 2017Article
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12 authors.
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Abstract
backgroundThe distribution of Plasmodium falciparum clinical malaria episodes is over-dispersed among children in endemic areas, with more children experiencing multiple clinical episodes than would be expected based on a Poisson distribution. There is consistent evidence for micro-epidemiological variation in exposure to P. falciparum. The aim of the current study was to identify children with excess malaria episodes after controlling for malaria exposure.
methodsWe selected the model that best fit the data out of the models examined and included the following covariates: age, a weighted local prevalence of infection as an index of exposure, and calendar time to predict episodes of malaria on active surveillance malaria data from 2,463 children of under 15 years of age followed for between 5 and 15 years each. Using parameters from the zero-inflated negative binomial model which best fitted our data, we ran 100 simulations of the model based on our population to determine the variation that might be seen due to chance.
resultsWe identified 212 out of 2,463 children who had a number of clinical episodes above the 95(th) percentile of the simulations run from the model, hereafter referred to as "excess malaria (EM)". We then identified exposure-matched controls with "average numbers of malaria" episodes, and found that the EM group had higher parasite densities when asymptomatically infected or during clinical malaria, and were less likely to be of haemoglobin AS genotype.
conclusionsOf the models tested, the negative zero-inflated negative binomial distribution with exposure, calendar year, and age acting as independent predictors, fitted the distribution of clinical malaria the best. Despite accounting for these factors, a group of children suffer excess malaria episodes beyond those predicted by the model. An epidemiological framework for identifying these children will allow us to study factors that may explain excess malaria episodes.
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