Evidence map›Paper›PMID 35654493›Full record

Observational studyJournal of the American College of Cardiology2022

Precision Phenotyping of Dilated Cardiomyopathy Using Multidimensional Data.

Upasana Tayal, Job A J Verdonschot, Mark R Hazebroek, James Howard, John Gregson, Simon Newsome, Ankur Gulati, Chee Jian Pua, Brian P Halliday, Amrit S Lota and 20 more

Abstract readObservational Study
In one paragraph

Observational study in Journal of the American College of Cardiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

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

  1. Pooled it
  2. Article
  3. The Dutch cardiomyopathy registry (DCR); rationale and registry design.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Recent advances in biomarkers for cardiac fibrosis.Frontiers in cardiovascular medicine · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Upasana TayalNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom. Electronic address: u.tayal@rbht.nhs.uk.
Job A J VerdonschotCardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center, Maastricht, the Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.
Mark R HazebroekCardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center, Maastricht, the Netherlands.
James HowardNational Heart Lung Institute, Imperial College London, London, United Kingdom.
John GregsonDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Simon NewsomeDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Ankur GulatiRoyal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Chee Jian PuaNational Heart Centre, Singapore.
Brian P HallidayNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Amrit S LotaNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Rachel J BuchanNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Nicola WhiffinNational Heart Lung Institute, Imperial College London, London, United Kingdom; Medical Research Council London Institute of Medical Sciences, Imperial College London, London, United Kingdom.
Lina KanapeckaiteRoyal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Resham BaruahRoyal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Julian W E JarmanRoyal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Declan P O'ReganMedical Research Council London Institute of Medical Sciences, Imperial College London, London, United Kingdom.
Paul J R BartonNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom; Medical Research Council London Institute of Medical Sciences, Imperial College London, London, United Kingdom.
James S WareNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom; Medical Research Council London Institute of Medical Sciences, Imperial College London, London, United Kingdom.
Dudley J PennellNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Bouke P AdriaansCardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center, Maastricht, the Netherlands.
Sebastiaan C A M BekkersCardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center, Maastricht, the Netherlands.
Jackie DonovanRoyal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom.
Michael FrenneauxNational Heart Lung Institute, Imperial College London, London, United Kingdom.
Leslie T CooperMayo Clinic, Jacksonville, Florida, USA.
James L JanuzziCardiology Division, Massachusetts General Hospital, Baim Insitute for Clinical Research, Boston, Massachusetts, USA.
John G F ClelandNational Heart Lung Institute, Imperial College London, London, United Kingdom.
Stuart A CookNational Heart Centre, Singapore; Medical Research Council London Institute of Medical Sciences, Imperial College London, London, United Kingdom.
Rahul C DeoOne Brave Idea and Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Stephane R B HeymansCardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center, Maastricht, the Netherlands; Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, KU Leuven, Belgium.
Sanjay K PrasadNational Heart Lung Institute, Imperial College London, London, United Kingdom; Royal Brompton Hospital (Guy's and St Thomas's NHS Foundation Trust), London, United Kingdom. Electronic address: s.prasad@rbht.nhs.uk.

Funding

Resolving Incomplete Penetrance in the Cardiomyopathies and ChannelopathiesDP2HL123228 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEO, RAHUL CHANDRAKANT · 2013 to 2013
$2.4M
British Heart Foundation FS/ICRF/21/26019British Heart Foundation FS/ICRF/22/26039British Heart Foundation NH/17/1/32725British Heart Foundation RE/18/4/34215British Heart Foundation RG/19/6/34387British Heart Foundation SP/10/10/28431British Heart Foundation SP/17/11/32885Medical Research Council MC-A658-5QEB0Medical Research Council MC_U120085815Medical Research Council MC_UP_1102/20Medical Research Council MC_UP_1605/13Medical Research Council MR/M003191/1NHLBI NIH HHS DP2 HL123228Wellcome Trust 107469/Z/15/Z
6 · The paper itself

Abstract

backgroundDilated cardiomyopathy (DCM) is a final common manifestation of heterogenous etiologies. Adverse outcomes highlight the need for disease stratification beyond ejection fraction.

objectivesThe purpose of this study was to identify novel, reproducible subphenotypes of DCM using multiparametric data for improved patient stratification.

methodsLongitudinal, observational UK-derivation (n = 426; median age 54 years; 67% men) and Dutch-validation (n = 239; median age 56 years; 64% men) cohorts of DCM patients (enrolled 2009-2016) with clinical, genetic, cardiovascular magnetic resonance, and proteomic assessments. Machine learning with profile regression identified novel disease subtypes. Penalized multinomial logistic regression was used for validation. Nested Cox models compared novel groupings to conventional risk measures. Primary composite outcome was cardiovascular death, heart failure, or arrhythmia events (median follow-up 4 years).

resultsIn total, 3 novel DCM subtypes were identified: profibrotic metabolic, mild nonfibrotic, and biventricular impairment. Prognosis differed between subtypes in both the derivation (P < 0.0001) and validation cohorts. The novel profibrotic metabolic subtype had more diabetes, universal myocardial fibrosis, preserved right ventricular function, and elevated creatinine. For clinical application, 5 variables were sufficient for classification (left and right ventricular end-systolic volumes, left atrial volume, myocardial fibrosis, and creatinine). Adding the novel DCM subtype improved the C-statistic from 0.60 to 0.76. Interleukin-4 receptor-alpha was identified as a novel prognostic biomarker in derivation (HR: 3.6; 95% CI: 1.9-6.5; P = 0.00002) and validation cohorts (HR: 1.94; 95% CI: 1.3-2.8; P = 0.00005).

conclusionsThree reproducible, mechanistically distinct DCM subtypes were identified using widely available clinical and biological data, adding prognostic value to traditional risk models. They may improve patient selection for novel interventions, thereby enabling precision medicine.

Indexed as

CardiomyopathiesCardiomyopathy, DilatedCreatinineFemaleFibrosisHumansMaleMiddle AgedProteomicsStroke VolumeCreatinineheartmachine learningproteomics

Identifiers

PMID35654493
PMCPMC9168440

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.