Evidence map›Paper›PMID 26362230›Full record

ArticleMathematical biosciences2015

Comparison of mathematical frameworks for modeling erythropoiesis in the context of malaria infection.

Luis L Fonseca, Eberhard O Voit

Abstract readComparative Study
In one paragraph

Article in Mathematical biosciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Discrete Biochemical Systems Theory.Frontiers in molecular biosciences · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Replicative cellular age distributions in compartmentalized tissues.Journal of the Royal Society, Interface · 2018
    Article
  7. Metabolic modeling helps interpret transcriptomic changes during malaria.Biochimica et biophysica acta. Molecular basis of disease · 2018
    Article
  8. Examining the Reticulocyte Preference of TwoFrontiers in microbiology · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Luis L FonsecaThe Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 950 Atlantic Drive, Atlanta, GA 30332-2000, USA.
Eberhard O VoitThe Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 950 Atlantic Drive, Atlanta, GA 30332-2000, USA. Electronic address: eberhard.voit@bme.gatech.edu.

Funding

NIAID NIH HHS HHSN272201200031CPHS HHS HHSN272201200031C
6 · The paper itself

Abstract

Malaria is an infectious disease present all around the globe and responsible for half a million deaths per year. A within-host model of this infection requires a framework capable of properly approximating not only the blood stage of the infection but also the erythropoietic process that is in charge of overcoming the malaria induced anemia. Within this context, we compare ordinary differential equations (ODEs) with and without age classes, delayed differential equations (DDEs), and discrete recursive equations (DREs) with age classes. Results show that ODEs without age classes are fair approximations that do not provide a crisp temporal representation of the processes involved, and inclusion of age classes only mitigates the problem to some degree. DDEs perform well with respect to generating the essentially fixed delay between cell production and cell removal due to age, but the inclusion of any other processes, such as sudden blood loss, becomes cumbersome. The framework that was found to perform best in representing the dynamics of red blood cells during malaria infection is a DRE with age classes. In this model structure, the amount of time a cell remains alive is easily controlled, and the addition of age dependent or independent processes is straightforward. All events that populations of cells face during their lifespan, like growth or adaptation in differentiation or maturation rate, are properly represented in this framework.

Indexed as

ErythropoiesisModels, TheoreticalHumansMalariaDDEDiscrete recursive equationErythropoiesisMalariaODEWithin-host model

Identifiers

PMID26362230
PMCPMC4679698

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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.