Evidence map›Paper›PMID 33862229›Full record

ArticleJournal of biomedical informatics2021

Simulation-derived best practices for clustering clinical data.

Caitlin E Coombes, Xin Liu, Zachary B Abrams, Kevin R Coombes, Guy Brock

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  7. Artificial intelligence in pediatric allergy research.European journal of pediatrics · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. SillyPutty: Improved clustering by optimizing the silhouette width.bioRxiv : the preprint server for biology · 2023
    Article
  12. Article
  13. Article
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  15. Article
  16. 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

5 authors.

Caitlin E CoombesThe Ohio State University College of Medicine, 370 W 9th Ave, Columbus, OH 43210, USA. Electronic address: Caitlin.Coombes@osumc.edu.
Xin LiuDepartment of Biomedical Informatics, The Ohio State University, 1800 Cannon Dr, Columbus, OH 43210, USA. Electronic address: liu.7302@buckeyemail.osu.edu.
Zachary B AbramsInstitute for Informatics, Washington University in St. Louis, 444 Forest Park Ave., St. Louis, MO 63108, USA. Electronic address: Zachary.Abrams@osumc.edu.
Kevin R CoombesDepartment of Biomedical Informatics, The Ohio State University, 1800 Cannon Dr, Columbus, OH 43210, USA. Electronic address: Kevin.Coombes@osumc.edu.
Guy BrockDepartment of Biomedical Informatics, The Ohio State University, 1800 Cannon Dr, Columbus, OH 43210, USA. Electronic address: Guy.Brock@osumc.edu.

Funding

The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
NCATS NIH HHS UL1 TR002733
6 · The paper itself

Abstract

introductionClustering analyses in clinical contexts hold promise to improve the understanding of patient phenotype and disease course in chronic and acute clinical medicine. However, work remains to ensure that solutions are rigorous, valid, and reproducible. In this paper, we evaluate best practices for dissimilarity matrix calculation and clustering on mixed-type, clinical data.

methodsWe simulate clinical data to represent problems in clinical trials, cohort studies, and EHR data, including single-type datasets (binary, continuous, categorical) and 4 data mixtures. We test 5 single distance metrics (Jaccard, Hamming, Gower, Manhattan, Euclidean) and 3 mixed distance metrics (DAISY, Supersom, and Mercator) with 3 clustering algorithms (hierarchical (HC), k-medoids, self-organizing maps (SOM)). We quantitatively and visually validate by Adjusted Rand Index (ARI) and silhouette width (SW). We applied our best methods to two real-world data sets: (1) 21 features collected on 247 patients with chronic lymphocytic leukemia, and (2) 40 features collected on 6000 patients admitted to an intensive care unit.

resultsHC outperformed k-medoids and SOM by ARI across data types. DAISY produced the highest mean ARI for mixed data types for all mixtures except unbalanced mixtures dominated by continuous data. Compared to other methods, DAISY with HC uncovered superior, separable clusters in both real-world data sets. DISCUSSION: Selecting an appropriate mixed-type metric allows the investigator to obtain optimal separation of patient clusters and get maximum use of their data. Superior metrics for mixed-type data handle multiple data types using multiple, type-focused distances. Better subclassification of disease opens avenues for targeted treatments, precision medicine, clinical decision support, and improved patient outcomes.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellAlgorithmsCluster AnalysisComputer SimulationHumansClinical informaticsClinical trialClusteringElectronic health recordUnsupervised machine learning

Identifiers

PMID33862229
PMCPMC9017600

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Registered trials

None linked

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.