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Machine Learning-Based Prediction of Drug-Induced QTc Changes in a Large Finnish Biobank Cohort.

Code ↔ Paper

6 matches between paragraphs of the paper and lines of its authors' code, computed by the harvester (lexical-v1). Click a colored paragraph or line to see its counterpart.

The 6 matches
  1. [1] § Methods › Statistical Methods ↔ R/xgb_optmizer.R, lines 61–99 · score 0.75 · child weight, mlrMBO, depth, hyperparameters, subsample, optimization
  2. [2] § Methods › Statistical Methods ↔ R/nested_xgboost_cox_cv_inner_loop.R, lines 1–12 · score 0.74 · nested cross validated, tune model, loops, split, inner, xgboost
  3. [3] § Methods › Statistical Methods ↔ vignettes/linear_plot.Rmd, lines 44–60 · score 0.67 · chronic kidney disease, heart failure, coronary, diabetes, PGS, risk
  4. [4] § Methods › Statistical Methods ↔ vignettes/linear.Rmd, lines 52–75 · score 0.66 · chronic kidney disease, heart failure, coronary, diabetes, risk, sex
  5. [5] § Methods › Variable Definitions ↔ vignettes/linear.Rmd, lines 52–75 · score 0.60 · Chronic kidney disease, Heart failure, Coronary, Diabetes
  6. [6] § Methods › Variable Definitions ↔ vignettes/linear_plot.Rmd, lines 44–60 · score 0.60 · Chronic kidney disease, Heart failure, Coronary, Diabetes

Paper

Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC

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The authors' code

R Markdown · 171 lines · 6.6 KB · no license · 2 matches

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It can be read at the source: vignettes/linear_plot.Rmd.

Overview

  1. Division of Medicine, Turku University Hospital and University of Turku, Turku, Finland
  2. Department of Geriatric Medicine, Turku University Hospital and University of Turku, Turku, Finland
  3. Department of Mathematics and Statistics, University of Turku, Turku, Finland
  4. FinnGen Consortium, Helsinki, Finland
  5. Department of Internal Medicine, University of Turku, Turku, Finland
  6. Cardiac Unit, Department of Internal Medicine, Satasairaala, Pori, Finland
  7. Central Finland Biobank, Wellbeing Services County of Central Finland, Jyväskylä, Finland
  8. Department of Medicine, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland
  9. Biobank of Eastern Finland, University of Eastern Finland, Kuopio, Finland
  10. Kuopio University Hospital, Kuopio, Finland
Journal: Clinical and translational science, volume 19, issue 5, article e70577
Dates: received 21 December 2025; accepted 20 April 2026; published online 4 May 2026; in print May 2026
Type: Research article · Language: English
License: CC BY-NC
Identifiers: DOI 10.1111/cts.70577 · PMID 42083122 · PMCID PMC13139045 · OpenAlex W7160303939
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: genetics / omics (modality), other (modality), human (organism), clinical / translational (subfield)
Methods: Statistics, Smoothing, state filtering, decompositions, Machine learning
Keywords: biobank research, drug safety, machine learning, polygenic risk score, QT interval
MeSH: Long QT Syndrome*, Machine Learning*, Aged, Biological Specimen Banks, Cohort Studies, Electrocardiography, Female, Finland, Genetic Risk Score, Humans, Male, Middle Aged, Prediction Algorithms, Predictive Learning Models, Risk Assessment (* major topic)
Topic: Cardiac electrophysiology and arrhythmias (Cardiology and Cardiovascular Medicine, Medicine), according to OpenAlex
Funding: State Research Funding of the Wellbeing Services County of Southwest Finland; Paavo Nurmi Foundation; Alkoholitutkimussäätiö; Business Finland (UH 4386/31/2016, HUS 4685/31/2016); Paavo Nurmen Säätiö; The Finnish Foundation for Alcohol studies; The Finnish Foundation for Cardiovascular Research; The Finnish Medical Foundation
Citations: not cited yet (Europe PMC); 24 references in the paper

Abstract

Prolongation of the QT interval is a known precursor to serious arrhythmias and sudden cardiac death, often triggered by medication use. Current medication risk evaluation platforms rely on literature‐based synthesis and may lag behind real‐world developments. We aimed to evaluate whether a machine learning (ML) model trained on real‐world genomic and medication data can identify associations between drug use and QTc duration, potentially enabling automated risk detection in clinical workflows. We included 10,208 individuals from the FinnGen biobank Expansion Area 3 substudy, integrating prescription records, clinical variables, and genetic information. We applied a nested‐cross‐validation approach to develop an ML framework to predict QTc duration using clinical characteristics, recent medication purchases, and polygenic score for QTc duration. We performed conventional linear regression analyses to estimate the robustness of the findings. Only a minority of ML‐detected drug–QTc associations aligned with known effects listed in expert‐curated reference. Several apparent false positives were observed, and effect sizes for true positives, such as amiodarone, were small and likely interpreted as clinically not meaningful (+1 ms in ML vs. +49 ms in linear regression). These findings highlight challenges in using ML to detect meaningful drug effects on ECG. ML models did not reliably identify medications associated with QT‐interval prolongation. Consequently, risk quantification using QTc as an intermediate marker of electrophysiological vulnerability was limited in this framework. While new approaches continue to develop in medication safety assessment, a systematic evidence review conducted by clinical pharmacology experts is unlikely to be supplanted in the foreseeable future.

Reproduced under the paper's license (CC BY-NC), from the paper cited above.

Repositories

Its files are read in the Code ↔ Paper reader above, with 6 matches between paragraphs and lines of code.

Zenodo 15223007

License: CC-BY-4.0
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Size: 1 file
Software Heritage: not checked
Found in: “Data Availability Statement”
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Tools: tidyverse (34 files), XGBoost (15 files), ggplot2 (5 files), data.table (4 files), patchwork (3 files), caret (2 files), broom (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers (HTTP 200)
  • 27 September 2026: the link answers (HTTP 200)
42 files

jjmpal/ecg_qtc

License: none: the authors keep all their rights
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: abca3806d39a31fbf5d61b2d664e2aef5ad9b713, 20 April 2025
Languages: R (41)
Size: 52 files, 41 scripts
Software Heritage: not archived
Found in: the Zenodo archive record
Holds: README, environment (DESCRIPTION), documentation, 7 notebooks
Not found: license file, CITATION.cff, tests, continuous integration
Tools: tidyverse (34 files), XGBoost (15 files), ggplot2 (5 files), data.table (4 files), patchwork (3 files), caret (2 files), broom (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
42 files, not copied: shown from their source

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Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 2 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 82 scripts, each with its path and the digest of its content;
  • 6 matches between paragraphs of the paper and lines of the code (method lexical-v1);
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

No dataset and no data link were found in the paper.

Data Availability Statement

The analysis codes for this study have been deposited in the Zenodo repository with the following DOI 10.5281/zenodo.15223007 (https://doi.org/10.5281/zenodo.15223007).

Reproduced under the paper's license (CC BY-NC), from the paper cited above.

Versions

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Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 5 keywords, 15 MeSH terms, 8 funders, 22 references.

Cite

This paper

Langén, V., Winstén, A., Teppo, K., Pohjonen, T., Laukkanen, J., Mannermaa, A., Niiranen, T. J., & Palmu, J. (2026). Machine Learning-Based Prediction of Drug-Induced QTc Changes in a Large Finnish Biobank Cohort. Clinical and translational science, 19(5), e70577. https://doi.org/10.1111/cts.70577

BibTeX

@article{langen2026machine,
author = {Langén, Ville and Winstén, Aleksi and Teppo, Konsta and Pohjonen, Timo and Laukkanen, Jari and Mannermaa, Arto and Niiranen, Teemu J and Palmu, Joonatan},
title = {{Machine Learning-Based Prediction of Drug-Induced QTc Changes in a Large Finnish Biobank Cohort}},
journal = {Clinical and translational science},
year = {2026},
month = may,
volume = {19},
number = {5},
pages = {e70577},
publisher = {Wiley},
issn = {1752-8054},
doi = {10.1111/cts.70577},
url = {https://doi.org/10.1111/cts.70577},
pmid = {42083122},
pmcid = {PMC13139045}
}

RIS

TY - JOUR
AU - Langén, Ville
AU - Winstén, Aleksi
AU - Teppo, Konsta
AU - Pohjonen, Timo
AU - Laukkanen, Jari
AU - Mannermaa, Arto
AU - Niiranen, Teemu J
AU - Palmu, Joonatan
TI - Machine Learning-Based Prediction of Drug-Induced QTc Changes in a Large Finnish Biobank Cohort
T2 - Clinical and translational science
J2 - Clin Transl Sci
PY - 2026
DA - 2026/05/01
VL - 19
IS - 5
SP - e70577
SN - 1752-8054
PB - Wiley
DO - 10.1111/cts.70577
UR - https://doi.org/10.1111/cts.70577
LA - en
ER -

CSL-JSON

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