Evidence map›Paper›PMID 39255368›Full record

ArticleBiostatistics (Oxford, England)2025

Dynamic and concordance-assisted learning for risk stratification with application to Alzheimer's disease.

Wen Li, Ruosha Li, Ziding Feng, Jing Ning, Alzheimer’s Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2025. 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

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.

Wen LiDivision of Clinical and Translational Sciences, Department of Internal Medicine, The University of Texas McGovern Medical School, Houston, TX 77030, United States.ORCID 0000-0002-7538-5422
Ruosha LiDepartment of Biostatistics and Data Science, The University of Texas School of Public Health, Houston, TX 77030, United States.ORCID 0000-0003-3595-4392
Ziding FengDepartment of Biostatistics, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States.ORCID 0000-0003-3051-8882
Jing NingDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.ORCID 0000-0002-5289-331X
Alzheimer’s Disease Neuroimaging Initiative

Funding

The Early Detection Research Network: Data Management and Coordinating CenterU24CA086368 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RUTH D ETZIONI, Ziding Feng · 2010 to 2026
$75.7M
Convalescent Plasma to Limit Coronavirus Associated ComplicationsUL1TR003167 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARP, DANIEL D, MCPHERSON, DAVID D · 2019 to 2023
$45.3M
Consortium on Translational Research in Early Detection of Liver Cancer:Data Management and Coordinating Center (DMCC)U24CA230144 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Ziding Feng · 2018 to 2026
$5.8M
Statistical Methods for Integration of Multiple Data Sources toward Precision Cancer MedicineR01CA269696 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI JING NING, YU SHEN · 2022 to 2026
$1.7M
NCATS NIH HHS UL1 TR003167NCI NIH HHS R01 CA269696NCI NIH HHS U24 CA086368NCI NIH HHS U24 CA230144NIH HHS R01CA269696
6 · The paper itself

Abstract

Dynamic prediction models capable of retaining accuracy by evolving over time could play a significant role for monitoring disease progression in clinical practice. In biomedical studies with long-term follow up, participants are often monitored through periodic clinical visits with repeat measurements until an occurrence of the event of interest (e.g. disease onset) or the study end. Acknowledging the dynamic nature of disease risk and clinical information contained in the longitudinal markers, we propose an innovative concordance-assisted learning algorithm to derive a real-time risk stratification score. The proposed approach bypasses the need to fit regression models, such as joint models of the longitudinal markers and time-to-event outcome, and hence enjoys the desirable property of model robustness. Simulation studies confirmed that the proposed method has satisfactory performance in dynamically monitoring the risk of developing disease and differentiating high-risk and low-risk population over time. We apply the proposed method to the Alzheimer's Disease Neuroimaging Initiative data and develop a dynamic risk score of Alzheimer's Disease for patients with mild cognitive impairment using multiple longitudinal markers and baseline prognostic factors.

Indexed as

Alzheimer DiseaseMachine LearningModels, StatisticalAlgorithmsCognitive DysfunctionDisease ProgressionHumansLongitudinal StudiesNeuroimagingRisk AssessmentAlzheimer’s diseaseconcordance-assisted learningdynamic predictionlongitudinal markersrisk stratification

Identifiers

PMID39255368
PMCPMC11823260

What OpenQuestion holds

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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.