Evidence map›Paper›PMID 35862421›Full record

ArticlePloS one2022

Analysis of epidemiological association patterns of serum thyrotropin by combining random forests and Bayesian networks.

Ann-Kristin Becker, Till Ittermann, Markus Dörr, Stephan B Felix, Matthias Nauck, Alexander Teumer, Uwe Völker, Henry Völzke, Lars Kaderali, Neetika Nath

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Ann-Kristin BeckerInstitute of Bioinformatics, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0003-1906-0583
Till IttermannInstitute for Community Medicine, SHIP/Clinical-Epidemiological Research, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0002-0154-7353
Markus DörrDZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, Greifswald, Germany.ORCID 0000-0001-7471-475X
Stephan B FelixDZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, Greifswald, Germany.
Matthias NauckDZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, Greifswald, Germany.ORCID 0000-0002-6678-7964
Alexander TeumerInstitute for Community Medicine, SHIP/Clinical-Epidemiological Research, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0002-8309-094X
Uwe VölkerDZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, Greifswald, Germany.ORCID 0000-0002-5689-3448
Henry VölzkeDZHK (German Centre for Cardiovascular Research), Partner Site Greifswald, Greifswald, Germany.
Lars KaderaliInstitute of Bioinformatics, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0002-2359-2294
Neetika NathInstitute of Bioinformatics, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0002-2156-9576

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproaching epidemiological data with flexible machine learning algorithms is of great value for understanding disease-specific association patterns. However, it can be difficult to correctly extract and understand those patterns due to the lack of model interpretability.

methodWe here propose a machine learning workflow that combines random forests with Bayesian network surrogate models to allow for a deeper level of interpretation of complex association patterns. We first evaluate the proposed workflow on synthetic data. We then apply it to data from the large population-based Study of Health in Pomerania (SHIP). Based on this combination, we discover and interpret broad patterns of individual serum TSH concentrations, an important marker of thyroid functionality.

resultsEvaluations using simulated data show that feature associations can be correctly recovered by combining random forests and Bayesian networks. The presented model achieves predictive accuracy that is similar to state-of-the-art models (root mean square error of 0.66, mean absolute error of 0.55, coefficient of determination of R2 = 0.15). We identify 62 relevant features from the final random forest model, ranging from general health variables over dietary and genetic factors to physiological, hematological and hemostasis parameters. The Bayesian network model is used to put these features into context and make the black-box random forest model more understandable.

conclusionWe demonstrate that the combination of random forest and Bayesian network analysis is helpful to reveal and interpret broad association patterns of individual TSH concentrations. The discovered patterns are in line with state-of-the-art literature. They may be useful for future thyroid research and improved dosing of therapeutics.

Indexed as

AlgorithmsMachine LearningBayes TheoremThyrotropinWorkflowThyrotropin

Identifiers

PMID35862421
PMCPMC9302835

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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.