Evidence map›Paper›PMID 31730697›Full record

ArticleGigaScience2019

Deep learning for clustering of multivariate clinical patient trajectories with missing values.

Johann de Jong, Mohammad Asif Emon, Ping Wu, Reagon Karki, Meemansa Sood, Patrice Godard, Ashar Ahmad, Henri Vrooman, Martin Hofmann-Apitius, Holger Fröhlich

Abstract read
In one paragraph

Article in GigaScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  11. An interpretable predictive deep learning platform for pediatric metabolic diseases.Journal of the American Medical Informatics Association : JAMIA · 2024
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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

10 authors.

Johann de JongUCB Biosciences GmbH, Alfred-Nobel-Strasse 10, 40789 Monheim, Germany.
Mohammad Asif EmonFraunhofer Institute for Algorithms and Scientific Computing, Schloss Birlinghoven, Konrad-Adenauer-Strasse, 53754 Sankt Augustin, Germany.
Ping WuUCB Pharma, Bath Road 216, Slough SL1 3WE, UK.
Reagon KarkiFraunhofer Institute for Algorithms and Scientific Computing, Schloss Birlinghoven, Konrad-Adenauer-Strasse, 53754 Sankt Augustin, Germany.
Meemansa SoodFraunhofer Institute for Algorithms and Scientific Computing, Schloss Birlinghoven, Konrad-Adenauer-Strasse, 53754 Sankt Augustin, Germany.
Patrice GodardUCB Pharma, Chemin du Foriest 1, 1420 Braine-l'Alleud, Belgium.
Ashar AhmadBonn-Aachen International Center for IT, University of Bonn, Konrad-Adenauer-Strasse, 53115 Bonn, Germany.
Henri VroomanErasmus MC, University Medical Center Rotterdam, Department of Radiology, Doctor Molewaterplein 40, PO Box 2040, 3000 CA Rotterdam, Netherlands.
Martin Hofmann-ApitiusFraunhofer Institute for Algorithms and Scientific Computing, Schloss Birlinghoven, Konrad-Adenauer-Strasse, 53754 Sankt Augustin, Germany.
Holger FröhlichUCB Biosciences GmbH, Alfred-Nobel-Strasse 10, 40789 Monheim, Germany.

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

backgroundPrecision medicine requires a stratification of patients by disease presentation that is sufficiently informative to allow for selecting treatments on a per-patient basis. For many diseases, such as neurological disorders, this stratification problem translates into a complex problem of clustering multivariate and relatively short time series because (i) these diseases are multifactorial and not well described by single clinical outcome variables and (ii) disease progression needs to be monitored over time. Additionally, clinical data often additionally are hindered by the presence of many missing values, further complicating any clustering attempts.

findingsThe problem of clustering multivariate short time series with many missing values is generally not well addressed in the literature. In this work, we propose a deep learning-based method to address this issue, variational deep embedding with recurrence (VaDER). VaDER relies on a Gaussian mixture variational autoencoder framework, which is further extended to (i) model multivariate time series and (ii) directly deal with missing values. We validated VaDER by accurately recovering clusters from simulated and benchmark data with known ground truth clustering, while varying the degree of missingness. We then used VaDER to successfully stratify patients with Alzheimer disease and patients with Parkinson disease into subgroups characterized by clinically divergent disease progression profiles. Additional analyses demonstrated that these clinical differences reflected known underlying aspects of Alzheimer disease and Parkinson disease.

conclusionsWe believe our results show that VaDER can be of great value for future efforts in patient stratification, and multivariate time-series clustering in general.

Indexed as

Databases, FactualDeep LearningDisease ProgressionModels, NeurologicalPrecision MedicineAlzheimer DiseaseFemaleHumansMaleParkinson Diseaseclusteringdeep learningmultivariate longitudinal datamultivariate time seriespatient stratification

Identifiers

PMID31730697
PMCPMC6857688

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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.