Evidence map›Paper›PMID 39314937›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Reconciling heterogeneous dengue virus infection risk estimates from different study designs.

Angkana T Huang, Darunee Buddhari, Surachai Kaewhiran, Sopon Iamsirithaworn, Direk Khampaen, Aaron Farmer, Stefan Fernandez, Stephen J Thomas, Isabel Rodriguez Barraquer, Taweewun Hunsawong and 9 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Angkana T HuangUniversity of Cambridge, Cambridge, UK.ORCID 0000-0002-9857-3506
Darunee BuddhariArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Surachai KaewhiranMinistry of Public Health, Nonthaburi, Thailand.
Sopon IamsirithawornMinistry of Public Health, Nonthaburi, Thailand.
Direk KhampaenMinistry of Public Health, Nonthaburi, Thailand.
Aaron FarmerArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Stefan FernandezArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Stephen J ThomasState University of New York Upstate Medical University, USA.
Isabel Rodriguez BarraquerUniversity of California, San Francisco, USA.
Taweewun HunsawongArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Anon SrikiatkhachornArmed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Gabriel Ribeiro Dos SantosUniversity of Cambridge, Cambridge, UK.
Megan O'DriscollUniversity of Cambridge, Cambridge, UK.
Marco Hamins-PuertolasUniversity of California, San Francisco, USA.
Timothy EndyCoalition for Epidemic Preparedness Innovations, USA.
Alan L RothmanUniversity of Rhode Island, USA.
Derek A T CummingsUniversity of Florida, Florida, USA.
Kathryn AndersonState University of New York Upstate Medical University, USA.
Henrik SaljeUniversity of Cambridge, Cambridge, UK.

Funding

VIRAL DETERMINANTS OF SEVERE DENGUE DISEASEP01AI034533 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ROTHMAN, ALAN L · 1994 to 2022
$42.0M
Defining correlates of protection from dengue illness in a long-term cohort study of multigenerational house-holds in ThailandR01AI175941 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI Kathryn B Anderson · 2023 to 2026
$2.7M
NIAID NIH HHS P01 AI034533NIAID NIH HHS R01 AI175941
6 · The paper itself

Abstract

Uncovering rates at which susceptible individuals become infected with a pathogen, i.e. the force of infection (FOI), is essential for assessing transmission risk and reconstructing distribution of immunity in a population. For dengue, reconstructing exposure and susceptibility statuses from the measured FOI is of particular significance as prior exposure is a strong risk factor for severe disease. FOI can be measured via many study designs. Longitudinal serology are considered gold standard measurements, as they directly track the transition of seronegative individuals to seropositive due to incident infections (seroincidence). Cross-sectional serology can provide estimates of FOI by contrasting seroprevalence across ages. Age of reported cases can also be used to infer FOI. Agreement of these measurements, however, have not been assessed. Using 26 years of data from cohort studies and hospital-attended cases from Kamphaeng Phet province, Thailand, we found FOI estimates from the three sources to be highly inconsistent. Annual FOI estimates from seroincidence was 2.46 to 4.33-times higher than case-derived FOI. Correlation between seroprevalence-derived and case-derived FOI was moderate (correlation coefficient=0.46) and no systematic bias. Through extensive simulations and theoretical analysis, we show that incongruences between methods can result from failing to account for dengue antibody kinetics, assay noise, and heterogeneity in FOI across ages. Extending standard inference models to include these processes reconciled the FOI and susceptibility estimates. Our results highlight the importance of comparing inferences across multiple data types to uncover additional insights not attainable through a single data type/analysis.

Indexed as

catalytic modeldengue force of infectionseroincidenceseroprevalence

Identifiers

PMID39314937
PMCPMC11419196

What OpenQuestion holds

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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.