Evidence map›Paper›PMID 41603487›Full record

ArticleCPT: pharmacometrics & systems pharmacology2026

Conditional Versus Unconditional Covariate Effects in Pharmacometric Models: Implications for Interpretation, Communication, and Reporting.

E Niclas Jonsson, Siv Jönsson, Emma Hansson, Joakim Nyberg

Abstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

4 authors.

E Niclas JonssonPharmetheus AB, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-2615-0280
Siv JönssonPharmetheus AB, Uppsala, Sweden.ORCID https://orcid.org/0000-0001-8240-0865
Emma HanssonPharmetheus AB, Uppsala, Sweden.ORCID https://orcid.org/0009-0004-3053-588X
Joakim NybergPharmetheus AB, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-2839-4940

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work investigates how correlations between covariates influence the estimation of their effects in pharmacometric models. The focus is on quantifying the impact on conditional and unconditional covariate effect estimates and assessing the consequences for model interpretation, communication, and dosing recommendations. A theoretical framework was used to describe the mathematical relationship between conditional and unconditional coefficients. This was verified by simulations across a wide range of covariate correlation strengths and relative covariate effect sizes. The practical consequences of misinterpreting conditional effects were evaluated in the context of dose selection and a priori dose individualization. As predicted by theory, covariate correlation had a substantial effect on the conditional covariate coefficient estimates, while unconditional estimates remained stable. Interpreting conditional covariate effects in isolation led to incorrect conclusions about dosing needs and introduced bias and imprecision in individual dose predictions. In contrast, both the complete conditional model and the unconditional model gave accurate predictions when applied appropriately. Unconditional covariate effects offer greater interpretability, making them more suitable for communicating individual covariate impacts in drug labels, publications, and forest plots. We demonstrate that conditional effects are highly sensitive to model context and covariate correlation, making them poor proxies for the unconditional effect, which is often the quantity of interest for dosing and communication. To minimize misinterpretation, unconditional effects should be reported when describing the influence of individual covariates, while the complete conditional model should be used for simulations and exposure predictions. This dual approach can improve clarity and reduce the risk of misunderstanding in model-informed decision-making.

Indexed as

Models, BiologicalComputer SimulationDose-Response Relationship, DrugHumanscovariate effectsdosing recommendationsinferencepharmacometric modelsstatistics

Identifiers

PMID41603487
PMCPMC12849216

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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.