Evidence map›Paper›PMID 25633459›Full record

ArticleBMC medicine2015

Time-to-infection by Plasmodium falciparum is largely determined by random factors.

Mykola Pinkevych, Kiprotich Chelimo, John Vulule, James W Kazura, Ann M Moormann, Miles P Davenport

Abstract read
In one paragraph

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Mykola Pinkevych
Kiprotich Chelimo
John Vulule
James W Kazura
Ann M Moormann
Miles P DavenportCentre for Vascular Research, University of New South Wales Australia, Kensington NSW 2052, Sydney, Australia. m.davenport@unsw.edu.au.

Funding

Naturally Acquired Immunity to Malaria during the Epidemiologic Transition in KenR01AI095192 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 2011 to 2015
$3.2M
Human immunity to MSP-1 in Western KenyaR01AI043906 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 2004 to 2008
$3.0M
CWRU-Kenya Infectious Diseases Research Training ProgramD43TW006576 · FIC · CASE WESTERN RESERVE UNIVERSITY · PI KING, CHARLES HARDING · 2003 to 2008
$830k
FIC NIH HHS 1D43TW006576FIC NIH HHS D43 TW006576NIAID NIH HHS R01 AI043906NIAID NIH HHS R01 AI095192
6 · The paper itself

Abstract

backgroundThe identification of protective immune responses to P. falciparum infection is an important goal for the development of a vaccine for malaria. This requires the identification of susceptible and resistant individuals, so that their immune responses may be studied. Time-to-infection studies are one method for identifying putative susceptible individuals (infected early) versus resistant individuals (infected late). However, the timing of infection is dependent on random factors, such as whether the subject was bitten by an infected mosquito, as well as individual factors, such as their level of immunity. It is important to understand how much of the observed variation in infection is simply due to chance.

methodsWe analyse previously published data from a treatment-time-to-infection study of 201 individuals aged 0.5 to 78 years living in Western Kenya. We use a mathematical modelling approach to investigate the role of immunity versus random factors in determining time-to-infection in this cohort. We extend this analysis using a modelling approach to understand what factors might increase or decrease the utility of these studies for identifying susceptible and resistant individuals.

resultsWe find that, under most circumstances, the observed distribution of time-to-infection is consistent with this simply being a random process. We find that age, method for detection of infection (PCR versus microscopy), and underlying force of infection are all factors in determining whether time-to-infection is a useful correlate of immunity.

conclusionsMany epidemiological studies of P. falciparum infection assume that the observed variation in infection outcomes, such as time-to-infection or presence or absence of infection, is determined by host resistance or susceptibility. However, under most circumstances, this distribution appears largely due to the random timing of infection, particularly in children. More direct measurements, such as parasite growth rate, may be more useful than time-to-infection in segregating patients based on their level of immunity.

Indexed as

Models, BiologicalPlasmodium falciparumAdolescentAgedAge FactorsChildChild, PreschoolFemaleHumansInfantKenyaMalaria, FalciparumMaleMicroscopyMiddle AgedPolymerase Chain Reaction

Identifiers

PMID25633459
PMCPMC4311447

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.