Evidence map›Paper›PMID 38717617›Full record

ArticleLifetime data analysis2024

A constrained maximum likelihood approach to developing well-calibrated models for predicting binary outcomes.

Yaqi Cao, Weidong Ma, Ge Zhao, Anne Marie McCarthy, Jinbo Chen

Abstract read
In one paragraph

Article in Lifetime data analysis, 2024. 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
–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

1 citing paper in PubMed.

  1. Improved risk prediction via cross-domain calibration in a retrospective case-control study.The Canadian journal of statistics = Revue canadienne de statistique · 2026
    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

5 authors.

Yaqi CaoDepartment of Statistics, School of Science, Minzu University of China, Beijing, China.
Weidong MaDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Ge ZhaoDepartment of Mathematics and Statistics, Portland State University, Portland, PA, 97201, USA.
Anne Marie McCarthyDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Jinbo ChenDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA. jinboche@pennmedicine.upenn.edu.

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
Data and Information Integration for Risk Prediction in the Era of Big DataR01CA236468 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CHEN, JINBO · 2019 to 2024
$2.2M
Statistical Methods for Analyzing Electronic Health Record DataR01HL138306 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CHEN, JINBO · 2018 to 2020
$1.2M
Division of Cancer Epidemiology and Genetics, National Cancer Institute R01-CA236468NCATS NIH HHS UL1 TR001878NCI NIH HHS R01 CA236468NHLBI Division of Intramural Research R01-HL138306NHLBI NIH HHS R01 HL138306
6 · The paper itself

Abstract

The added value of candidate predictors for risk modeling is routinely evaluated by comparing the performance of models with or without including candidate predictors. Such comparison is most meaningful when the estimated risk by the two models are both unbiased in the target population. Very often data for candidate predictors are sourced from nonrepresentative convenience samples. Updating the base model using the study data without acknowledging the discrepancy between the underlying distribution of the study data and that in the target population can lead to biased risk estimates and therefore an unfair evaluation of candidate predictors. To address this issue assuming access to a well-calibrated base model, we propose a semiparametric method for model fitting that enforces good calibration. The central idea is to calibrate the fitted model against the base model by enforcing suitable constraints in maximizing the likelihood function. This approach enables unbiased assessment of model improvement offered by candidate predictors without requiring a representative sample from the target population, thus overcoming a significant practical challenge. We study theoretical properties for model parameter estimates, and demonstrate improvement in model calibration via extensive simulation studies. Finally, we apply the proposed method to data extracted from Penn Medicine Biobank to inform the added value of breast density for breast cancer risk assessment in the Caucasian woman population.

Indexed as

Breast NeoplasmsModels, StatisticalCalibrationComputer SimulationFemaleHumansLikelihood FunctionsRisk AssessmentCalibrationConstrained maximum likelihood estimationLogistic regressionRisk prediction

Identifiers

PMID38717617
PMCPMC11634939

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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.