Evidence map›Paper›PMID 40965243›Full record

ArticleCPT: pharmacometrics & systems pharmacology2025

A Dose-Aware Model for Revealing Dose-Risk Relationship of Drug-Drug Interaction.

Yi Shi, Anna Sun, Yuedi Yang, Hongmei Nan, Jing Xu, Mu Shan, Michael T Eadon, Jing Su, Pengyue Zhang

Abstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2025. 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. 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

9 authors.

Yi ShiDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0003-0145-2968
Anna SunDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0009-0009-0905-6469
Yuedi YangDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0009-0007-5067-4387
Hongmei NanDepartment of Epidemiology, Richard M. Fairbanks School of Public Health, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0002-9957-616X
Jing XuDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0003-3673-7592
Mu ShanEli Lilly and Company, Indianapolis, Indiana, USA.
Michael T EadonDivision of Nephrology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Jing SuDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.
Pengyue ZhangDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0002-9148-5589

Funding

Significant high order drug interactions in the emergency department setting among older patient populationR01AG071018 · NIA · OHIO STATE UNIVERSITY · PI Macarius M. Donneyong, Pengyue Zhang · 2022 to 2026
$2.5M
Revealing Health Trajectories of Chronic Kidney Disease for Precision MedicineR01LM013771 · NLM · INDIANA UNIVERSITY INDIANAPOLIS · PI SU, JING, ZHANG, PENGYUE · 2022 to 2025
$1.7M
A Statistical Network Pharmacology Approach for Early Detection of Adverse Drug EventsR01GM141279 · NIGMS · OHIO STATE UNIVERSITY · PI ZHANG, PENGYUE, ZHANG, PING · 2021 to 2023
$937k
NIA NIH HHS R01 AG071018NIGMS NIH HHS R01 GM141279NLM NIH HHS R01 LM013771
6 · The paper itself

Abstract

Drug-drug interaction (DDI) is a common cause of adverse drug events (ADEs). Despite real-world data-based studies have developed knowledge on DDI, the precise relationships between doses of two-drug combinations exposure and the risks of ADEs remain largely unknown. The estimation of the dose-risk relationship (DRR) under commonly used regression models could be subject to model misspecification or overspecification. We developed a dose-aware model (DAM) for revealing DRR. DAM could improve the DRR estimation by identifying the optimal model from a large number of meaningful models of doses of two-drug combinations exposure and risks of ADE. We compared DAM with commonly used models (e.g., exposed-versus-unexposed model, dose-response model, and saturated model), in which DAM had higher performance metrics on model fitting in real-world data analyses and DRR estimation in a simulation study. In conclusion, DAM is a powerful tool for estimating DRR for potential adverse two-drug combinations, which could be used to mitigate DDI-induced harm.

Indexed as

Drug-Related Side Effects and Adverse ReactionsComputer SimulationDose-Response Relationship, DrugDrug InteractionsHumansModels, Biologicaladverse drug eventdose‐aware modeldose‐dependent riskdrug–drug interactionreal‐world data

Identifiers

PMID40965243
PMCPMC12706421

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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.