Evidence map›Paper›PMID 26287609›Full record

ArticlePloS one2015

Outcome Prediction in Mathematical Models of Immune Response to Infection.

Manuel Mai, Kun Wang, Greg Huber, Michael Kirby, Mark D Shattuck, Corey S O'Hern

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. The dynamics ofmSphere · 2025
    Article
  2. Article
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

6 authors.

Manuel MaiDepartment of Physics, Yale University, New Haven, Connecticut, United States of America.
Kun WangDepartment of Mathematics, Colorado State University, Fort Collins, Colorado, United States of America; Department of Mechanical Engineering and Material Science, Yale University, New Haven, Connecticut, United States of America.
Greg HuberKavli Institute for Theoretical Physics, Kohn Hall, University of California Santa Barbara, Santa Barbara, California, United States of America.
Michael KirbyDepartment of Mathematics, Colorado State University, Fort Collins, Colorado, United States of America; Department of Computer Science, Colorado State University, Fort Collins, Colorado, United States of America.
Mark D ShattuckDepartment of Mechanical Engineering and Material Science, Yale University, New Haven, Connecticut, United States of America; Benjamin Levich Institute and Physics Department, The City College of New York, New York, New York, United States of America.
Corey S O'HernDepartment of Physics, Yale University, New Haven, Connecticut, United States of America; Department of Mechanical Engineering and Material Science, Yale University, New Haven, Connecticut, United States of America; Department of Applied Physics, Yale University, New Haven, Connecticut, United States of America; Graduate Program in Computational Biology and Bioinformatics, Yale University, New Haven, Connecticut, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinicians need to predict patient outcomes with high accuracy as early as possible after disease inception. In this manuscript, we show that patient-to-patient variability sets a fundamental limit on outcome prediction accuracy for a general class of mathematical models for the immune response to infection. However, accuracy can be increased at the expense of delayed prognosis. We investigate several systems of ordinary differential equations (ODEs) that model the host immune response to a pathogen load. Advantages of systems of ODEs for investigating the immune response to infection include the ability to collect data on large numbers of 'virtual patients', each with a given set of model parameters, and obtain many time points during the course of the infection. We implement patient-to-patient variability v in the ODE models by randomly selecting the model parameters from distributions with coefficients of variation v that are centered on physiological values. We use logistic regression with one-versus-all classification to predict the discrete steady-state outcomes of the system. We find that the prediction algorithm achieves near 100% accuracy for v = 0, and the accuracy decreases with increasing v for all ODE models studied. The fact that multiple steady-state outcomes can be obtained for a given initial condition, i.e. the basins of attraction overlap in the space of initial conditions, limits the prediction accuracy for v > 0. Increasing the elapsed time of the variables used to train and test the classifier, increases the prediction accuracy, while adding explicit external noise to the ODE models decreases the prediction accuracy. Our results quantify the competition between early prognosis and high prediction accuracy that is frequently encountered by clinicians.

Indexed as

Models, TheoreticalAlgorithmsBacterial InfectionsHumansModels, BiologicalNonlinear DynamicsOutcome Assessment, Health CarePrognosisSystems BiologyVirus Diseases

Identifiers

PMID26287609
PMCPMC4545748

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.