Evidence map›Paper›PMID 31957077›Full record

ArticleBiometrical journal. Biometrische Zeitschrift2020

Developing risk models for multicenter data using standard logistic regression produced suboptimal predictions: A simulation study.

Nora Falconieri, Ben Van Calster, Dirk Timmerman, Laure Wynants

Abstract read
In one paragraph

Article in Biometrical journal. Biometrische Zeitschrift, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Nora FalconieriDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0002-9533-0859
Ben Van CalsterDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0003-1613-7450
Dirk TimmermanDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0002-3707-6645
Laure WynantsDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID 0000-0002-3037-122X

Funding

Fonds Wetenschappelijk Onderzoek G0B4716NKU Leuven C24/15/037
6 · The paper itself

Abstract

Although multicenter data are common, many prediction model studies ignore this during model development. The objective of this study is to evaluate the predictive performance of regression methods for developing clinical risk prediction models using multicenter data, and provide guidelines for practice. We compared the predictive performance of standard logistic regression, generalized estimating equations, random intercept logistic regression, and fixed effects logistic regression. First, we presented a case study on the diagnosis of ovarian cancer. Subsequently, a simulation study investigated the performance of the different models as a function of the amount of clustering, development sample size, distribution of center-specific intercepts, the presence of a center-predictor interaction, and the presence of a dependency between center effects and predictors. The results showed that when sample sizes were sufficiently large, conditional models yielded calibrated predictions, whereas marginal models yielded miscalibrated predictions. Small sample sizes led to overfitting and unreliable predictions. This miscalibration was worse with more heavily clustered data. Calibration of random intercept logistic regression was better than that of standard logistic regression even when center-specific intercepts were not normally distributed, a center-predictor interaction was present, center effects and predictors were dependent, or when the model was applied in a new center. Therefore, to make reliable predictions in a specific center, we recommend random intercept logistic regression.

Indexed as

Models, StatisticalBiometryFemaleHumansLogistic ModelsOvarian NeoplasmsRisk Assessmentcalibrationdiscriminationmulticenterrandom effectsrisk prediction model

Identifiers

PMID31957077
PMCPMC7383814

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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.