Evidence map›Paper›PMID 31333075›Full record

ArticleJournal of the American Heart Association2019

RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy.

Nadya Al-Wakeel-Marquard, Franziska Degener, Christopher Herbst, Jirko Kühnisch, Josephine Dartsch, Boris Schmitt, Titus Kuehne, Daniel Messroghli, Felix Berger, Sabine Klaassen

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03572569 (Risk Stratification in Children and Adolescents With Primary Cardiomyopathy), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
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.

NCT03572569 unknown statusnot on this map

Risk Stratification in Children and Adolescents With Primary Cardiomyopathy

TypeobservationalSponsorGerman Heart InstituteRan2013 to 2020Enrolled200ConditionsPrimary Cardiomyopathy, Dilated Cardiomyopathy, Hypertrophic Cardiomyopathy, Left Ventricular Noncompaction
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Genomics of pediatric cardiomyopathy.Pediatric research · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. A Systematic Review of Ebstein's Anomaly with Left Ventricular Noncompaction.Journal of cardiovascular development and disease · 2022
    Review
  11. The genetic architecture of pediatric cardiomyopathy.American journal of human genetics · 2022
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy.Journal of the American Heart Association · 2019
    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

10 authors at 5 institutions in 1 country.

Nadya Al-Wakeel-MarquardDepartment of Congenital Heart Disease-Pediatric Cardiology German Heart Center Berlin Berlin Germany.
Franziska DegenerDepartment of Congenital Heart Disease-Pediatric Cardiology German Heart Center Berlin Berlin Germany.
Christopher HerbstDepartment of Congenital Heart Disease-Pediatric Cardiology German Heart Center Berlin Berlin Germany.
Jirko KühnischDZHK (German Centre for Cardiovascular Research), partner site Berlin Berlin Germany.
Josephine DartschCharité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin Humboldt-Universität zu Berlin, and Berlin Institute of Health Experimental and Clinical Research Center, a joint cooperation between the Charité Medical Faculty and the Max-Delbrück-Center for Molecular Medicine Berlin Germany.
Boris SchmittDepartment of Congenital Heart Disease-Pediatric Cardiology German Heart Center Berlin Berlin Germany.
Titus KuehneDepartment of Congenital Heart Disease-Pediatric Cardiology German Heart Center Berlin Berlin Germany.
Daniel MessroghliDZHK (German Centre for Cardiovascular Research), partner site Berlin Berlin Germany.
Felix BergerDepartment of Congenital Heart Disease-Pediatric Cardiology German Heart Center Berlin Berlin Germany.
Sabine KlaassenDZHK (German Centre for Cardiovascular Research), partner site Berlin Berlin Germany.
Freie Universität Berlin · DECharité - Universitätsmedizin Berlin · DEDeutsches Herzzentrum München · DEHumboldt-Universität zu Berlin · DEGerman Centre for Cardiovascular Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Cardiomyopathies are heterogeneous diseases with clinical presentations varying from asymptomatic to life-threatening events, including severe heart failure and sudden cardiac death. The role of underlying genetic and disease-modulating factors in children and adolescents is relatively unknown. In this prospective study, in-depth phenotypic and genetic characterization of pediatric patients with primary cardiomyopathy and their first-degree family members (FMs) was performed. Outcome was assessed to identify clinical risk factors. Methods and Results Sixty index patients with primary cardiomyopathy (median age: 7.8 years) and 124 FMs were enrolled in the RIKADA (Risk Stratification in Children and Adolescents with Primary Cardiomyopathy) study. Family screening included cardiac workup and genetic testing. Using cardiologic screening, we identified 17 FMs with cardiomyopathies and 30 FMs with suspected cardiomyopathies. Adverse events appeared in 32% of index patients and were more common in those with lower body surface area (P=0.019), increased NT-proBNP (N-terminal pro-brain natriuretic peptide; P<0.001), and left ventricular dysfunction (P<0.001) and dilatation (P=0.005). The worst prognosis was observed in dilated and restrictive cardiomyopathies. Genetic variants of interest were detected in patients (79%) and FMs (67%). In all 15 families with at least 1 FM with cardiomyopathy, we found a variant of interest in the index patient. Increased number of variants of interest per patient was associated with adverse events (P=0.021). Late gadolinium enhancement was related to positive genotypes in patients (P=0.041). Conclusions Lower body surface area, increased NT-proBNP, left ventricular dysfunction or dilatation, late gadolinium enhancement, and increased number of variants of interest were associated with adverse outcome and should be considered for risk assessment in pediatric primary cardiomyopathies. Clinical Trial Registration URL: https://www.clinicaltrials.gov/. Unique identifier: NCT03572569.

Indexed as

Risk AssessmentAdolescentCardiomyopathiesChildChild, PreschoolFemaleHumansInfantMalePhenotypeProspective StudiesRisk Factorscardiomyopathyheart failurepediatricsrisk assessment

Identifiers

PMID31333075
PMCPMC6761660
OpenAlexW2964224905

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.