Evidence map›Paper›PMID 33057348›Full record

ArticlePloS one2020

Patch dynamics modeling framework from pathogens' perspective: Unified and standardized approach for complicated epidemic systems.

Shi Chen, Yakubu Owolabi, Ang Li, Eugenia Lo, Patrick Robinson, Daniel Janies, Chihoon Lee, Michael Dulin

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

Shi ChenDepartment of Public Health Sciences, University of North Carolina Charlotte, Charlotte, NC, United States of America.ORCID 0000-0002-2316-111X
Yakubu OwolabiDepartment of Public Health Sciences, University of North Carolina Charlotte, Charlotte, NC, United States of America.
Ang LiState Key Laboratory of Vegetation and Environmental Change, Chinese Academy of Sciences, Beijing, China.
Eugenia LoDepartment of Biological Sciences, University of North Carolina Charlotte, Charlotte, NC, United States of America.ORCID 0000-0002-5631-4709
Patrick RobinsonDepartment of Public Health Sciences, University of North Carolina Charlotte, Charlotte, NC, United States of America.
Daniel JaniesDepartment of Bioinformatics, University of North Carolina Charlotte, Charlotte, NC, United States of America.
Chihoon LeeSchool of Business, Stevens Institute of Technology, Hoboken, NJ, United States of America.
Michael DulinDepartment of Public Health Sciences, University of North Carolina Charlotte, Charlotte, NC, United States of America.

Funding

Comparative Genomics of Plasmodium vivax: Insights into Duffy Negative Erythrocyte InvasionR15AI138002 · NIAID · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI LO, EUGENIA · 2018 to 2018
$433k
NIAID NIH HHS R15 AI138002
6 · The paper itself

Abstract

Mathematical models are powerful tools to investigate, simulate, and evaluate potential interventions for infectious diseases dynamics. Much effort has focused on the Susceptible-Infected-Recovered (SIR)-type compartment models. These models consider host populations and measure change of each compartment. In this study, we propose an alternative patch dynamic modeling framework from pathogens' perspective. Each patch, the basic module of this modeling framework, has four standard mechanisms of pathogen population size change: birth (replication), death, inflow, and outflow. This framework naturally distinguishes between-host transmission process (inflow and outflow) and within-host infection process (replication) during the entire transmission-infection cycle. We demonstrate that the SIR-type model is actually a special cross-sectional and discretized case of our patch dynamics model in pathogens' viewpoint. In addition, this patch dynamics modeling framework is also an agent-based model from hosts' perspective by incorporating individual host's specific traits. We provide an operational standard to formulate this modular-designed patch dynamics model. Model parameterization is feasible with a wide range of sources, including genomics data, surveillance data, electronic health record, and from other emerging technologies such as multiomics. We then provide two proof-of-concept case studies to tackle some of the existing challenges of SIR-type models: sexually transmitted disease and healthcare acquired infections. This patch dynamics modeling framework not only provides theoretical explanations to known phenomena, but also generates novel insights of disease dynamics from a more holistic viewpoint. It is also able to simulate and handle more complicated scenarios across biological scales such as the current COVID-19 pandemic.

Indexed as

Models, TheoreticalBacterial InfectionsCommunicable DiseasesCoronavirus InfectionsCOVID-19Disease Transmission, InfectiousHumansPandemicsPneumonia, Viral

Identifiers

PMID33057348
PMCPMC7561140

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LicenceCC BY
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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.