Evidence map›Paper›PMID 36812266›Full record

ArticlePLoS computational biology2023

Hidden variable models reveal the effects of infection from changes in host survival.

Jake M Ferguson, Andrea González-González, Johnathan A Kaiser, Sara M Winzer, Justin M Anast, Ben Ridenhour, Tanya A Miura, Christine E Parent

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Jake M FergusonDepartment of Biology, University of Hawai'i at Mānoa, Honolulu, Hawaii, United States of America.ORCID 0000-0002-5034-9089
Andrea González-GonzálezInstitute for Modeling Collaboration and Innovation, University of Idaho, Moscow, Idaho, United States of America.ORCID 0000-0002-3161-1555
Johnathan A KaiserDepartment of Biological Sciences, University of Idaho, Moscow, Idaho, United States of America.ORCID 0000-0001-5339-3387
Sara M WinzerDepartment of Biological Sciences, University of Idaho, Moscow, Idaho, United States of America.
Justin M AnastDepartment of Biological Sciences, University of Idaho, Moscow, Idaho, United States of America.
Ben RidenhourDepartment of Mathematics, University of Idaho, Moscow, Idaho, United States of America.ORCID 0000-0001-8271-4629
Tanya A MiuraInstitute for Modeling Collaboration and Innovation, University of Idaho, Moscow, Idaho, United States of America.ORCID 0000-0002-7289-4926
Christine E ParentInstitute for Modeling Collaboration and Innovation, University of Idaho, Moscow, Idaho, United States of America.
University of Idaho · USUniversity of Hawaiʻi at Mānoa · US

Funding

Sequence-structure-function relationships in human visual photopigmentsP20GM104420 · NIGMS · UNIVERSITY OF IDAHO · PI VAN LEUVEN, JAMES · 2015 to 2024
$22.9M
Genomics Resources Core (GRC)P30GM103324 · NIGMS · UNIVERSITY OF IDAHO · PI SETTLES, MATTHEW · 2013 to 2017
$5.0M
NIGMS NIH HHS P20 GM104420NIGMS NIH HHS P30 GM103324
6 · The paper itself

Abstract

The impacts of disease on host vital rates can be demonstrated using longitudinal studies, but these studies can be expensive and logistically challenging. We examined the utility of hidden variable models to infer the individual effects of infectious disease from population-level measurements of survival when longitudinal studies are not possible. Our approach seeks to explain temporal deviations in population-level survival after introducing a disease causative agent when disease prevalence cannot be directly measured by coupling survival and epidemiological models. We tested this approach using an experimental host system (Drosophila melanogaster) with multiple distinct pathogens to validate the ability of the hidden variable model to infer per-capita disease rates. We then applied the approach to a disease outbreak in harbor seals (Phoca vituline) that had data on observed strandings but no epidemiological data. We found that our hidden variable modeling approach could successfully detect the per-capita effects of disease from monitored survival rates in both the experimental and wild populations. Our approach may prove useful for detecting epidemics from public health data in regions where standard surveillance techniques are not available and in the study of epidemics in wildlife populations, where longitudinal studies can be especially difficult to implement.

Indexed as

Drosophila melanogasterPhocaAnimalsAnimals, WildDisease OutbreaksPrevalence

Identifiers

PMID36812266
PMCPMC9987815
OpenAlexW4321481425

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.