Evidence map›Paper›PMID 40460089›Full record

ArticlePloS one2025

Assessing generalizability of a dengue classifier across multiple datasets.

Bingqian Lu, Yanni Li, Ciaran Evans

Abstract read
In one paragraph

Article in PloS one, 2025. 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

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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

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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. Article
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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

3 authors.

Bingqian LuData Science Institute, Columbia University, New York, New York, United States.
Yanni LiDepartment of Statistical Sciences, Wake Forest University, Winston-Salem, North Carolina, United States.
Ciaran EvansDepartment of Statistical Sciences, Wake Forest University, Winston-Salem, North Carolina, United States.ORCID https://orcid.org/0000-0003-3256-011X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early diagnosis of dengue fever is important for individual treatment and monitoring disease prevalence in the population. To assist diagnosis, previous studies have proposed classification models to detect dengue from symptoms and clinical measurements. However, there has been little exploration of whether existing models can be used to make predictions for new populations. In this study, we assess the generalizability of dengue classification models to new datasets. We trained logistic regression models on five publicly available dengue datasets from previous studies, using three explanatory variables identified as important in prior work: age, white blood cell count, and platelet count. These five datasets were collected at different times in different locations, with a variety of disease rates and patient ages. A model was trained on each dataset, and predictive performance and model calibration was evaluated on both the original (training) dataset, and the other (test) datasets from different studies. By comparing the model's performance when applied to data from a new location, we are able to assess the model's generalizability to new populations. We further compared performance with larger models and other classification methods. In-sample area under the receiver operating characteristic curve (AUC) values for the logistic regression models ranged from 0.74 to 0.89, while out-of-sample AUCs ranged from 0.55 to 0.89. Matching age ranges in training/test datasets increased AUC values and balanced the sensitivity and specificity. Adjusting the predicted probabilities to account for differences in dengue prevalence improved calibration in 20/28 training-test pairs. Results were similar when other explanatory variables were included and when other classification methods (decision trees and support vector machines) were used. The in-sample performance of the logistic regression model was consistent with previous dengue classifiers, suggesting the chosen model is a good choice in a variety of settings and has decent overall performance. However, adjustments are required to make predictions on new datasets. Practitioners can use existing dengue classifiers in new settings but should be careful with different patient ages and disease rates.

Indexed as

DengueAdolescentAdultArea Under CurveFemaleHumansLogistic ModelsMaleMiddle AgedROC Curve

Identifiers

PMID40460089
PMCPMC12132959

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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.