Evidence map›Paper›PMID 28130096›Full record

ArticleJournal of theoretical biology2017

Model distinguishability and inference robustness in mechanisms of cholera transmission and loss of immunity.

Elizabeth C Lee, Michael R Kelly, Brad M Ochocki, Segun M Akinwumi, Karen E S Hamre, Joseph H Tien, Marisa C Eisenberg

Abstract read
In one paragraph

Article in Journal of theoretical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  4. Benchmarking tools for a priori identifiability analysis.Bioinformatics (Oxford, England) · 2023
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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

7 authors.

Elizabeth C LeeDepartment of Biology, Georgetown University, 37th and O Streets, NW, Washington, DC 20057, United States. Electronic address: ecl48@georgetown.edu.
Michael R KellyDivision of Natural Sciences and Mathematics, Transylvania University, 300 North Broadway, Lexington, KY 40508, United States; Department of Mathematics, The Ohio State University, 231 West 18th Ave, Columbus, OH 43210, United States. Electronic address: mikelly@transy.edu.
Brad M OchockiDepartment of BioSciences, Program in Ecology and Evolutionary Biology, Rice University, 6100 Main Street, MS-170, Houston, TX 77005-1892, United States. Electronic address: brad.ochocki@rice.edu.
Segun M AkinwumiDepartment of Mathematical and Statistical Sciences, University of Alberta, Edmonton, AB, Canada T6G 2G1. Electronic address: segunmic@ualberta.ca.
Karen E S HamreDivision of Global Pediatrics and Division of Epidemiology and Community Health, University of Minnesota, 717 Delaware Street SE, 3rd Floor, Minneapolis, MN 55414, United States. Electronic address: hamr0091@umn.edu.
Joseph H TienDepartment of Mathematics, The Ohio State University, 231 West 18th Ave, Columbus, OH 43210, United States. Electronic address: jtien@math.ohio-state.edu.
Marisa C EisenbergDepartments of Epidemiology and Mathematics, University of Michigan, Ann Arbor, 1415 Washington Heights, Ann Arbor 48109, United States. Electronic address: marisae@umich.edu.

Funding

Modeling the Effects of the Environment on Enteric Pathogen DynamicsU01GM110712 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EISENBERG, JOSEPH N. S. · 2014 to 2018
$3.0M
NIGMS NIH HHS U01 GM110712
6 · The paper itself

Abstract

Mathematical models of cholera and waterborne disease vary widely in their structures, in terms of transmission pathways, loss of immunity, and a range of other features. These differences can affect model dynamics, with different models potentially yielding different predictions and parameter estimates from the same data. Given the increasing use of mathematical models to inform public health decision-making, it is important to assess model distinguishability (whether models can be distinguished based on fit to data) and inference robustness (whether inferences from the model are robust to realistic variations in model structure). In this paper, we examined the effects of uncertainty in model structure in the context of epidemic cholera, testing a range of models with differences in transmission and loss of immunity structure, based on known features of cholera epidemiology. We fit these models to simulated epidemic and long-term data, as well as data from the 2006 Angola epidemic. We evaluated model distinguishability based on fit to data, and whether the parameter values, model behavior, and forecasting ability can accurately be inferred from incidence data. In general, all models were able to successfully fit to all data sets, both real and simulated, regardless of whether the model generating the simulated data matched the fitted model. However, in the long-term data, the best model fits were achieved when the loss of immunity structures matched those of the model that simulated the data. Two parameters, one representing person-to-person transmission and the other representing the reporting rate, were accurately estimated across all models, while the remaining parameters showed broad variation across the different models and data sets. The basic reproduction number (R

Indexed as

Models, TheoreticalUncertaintyAngolaBasic Reproduction NumberCholeraComputer SimulationEpidemicsHumansComparative modelingModel misspecificationModel structureParameter estimation

Identifiers

PMID28130096
PMCPMC5412123

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Registered trials

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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.