Evidence map›Paper›PMID 37314195›Full record

ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2023

Leucocyte-derived micro-RNAs as candidate biomarkers in Brugada syndrome.

Christian Steinberg, Nathalie Gaudreault, Andreas I Papadakis, Cyndi Henry, Jean Champagne, François Philippon, Gilles O'Hara, Louis Blier, Benoit Plourde, Isabelle Nault and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 16% 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.

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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2023
    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

14 authors at 2 institutions in 1 country.

Christian SteinbergInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0003-4112-0028
Nathalie GaudreaultInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0002-5351-596X
Andreas I PapadakisLady Davis Institute for Medical Research, Montreal Jewish Hospital, McGill University, Montreal, Canada.ORCID 0000-0003-0026-6581
Cyndi HenryInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0003-4202-4951
Jean ChampagneInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0001-9861-9351
François PhilipponInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.
Gilles O'HaraInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0002-1115-8108
Louis BlierInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.
Benoit PlourdeInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.
Isabelle NaultInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.
Karine RoyInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0009-0004-4299-9921
Jean-François SarrazinInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0002-1114-0661
Alan SpatzLady Davis Institute for Medical Research, Montreal Jewish Hospital, McGill University, Montreal, Canada.ORCID 0000-0003-3020-1420
Yohan BosséInstitut universitaire de cardiologie et pneumologie de Québec, Université Laval, 2725, Chemin Ste-Foy, Quebec City, Canada G1V 4G5.ORCID 0000-0002-3067-3711
Institut universitaire de cardiologie et de pneumologie de Québec · CAJewish General Hospital · CA

Funding

Fonds de Recherche du Québec-SantéIUCPQ-UL
6 · The paper itself

Abstract

aimsRisk stratification for sudden cardiac death in patients with Brugada syndrome remains a major challenge. Contemporary risk prediction models have only modest predictive value. The aim of this study was to assess the role of micro-RNAs from peripheral blood as candidate biomarkers in Brugada syndrome. METHODS AND

resultsIn this prospective study, Brugada patients and unaffected control individuals were enrolled for analysis of leucocyte-derived microRNAs (miRNAs) levels. Expression levels of 798 different circulating miRNAs were analysed on the NanoString® nCounter platform. All results were cross-validated by using a quantitative polymerase chain reaction. Micro-RNA expression levels of Brugada patients were compared with clinical data. A total of 21 definite Brugada patients (38% with a history of ventricular arrhythmia or cardiac arrest) and 30 unaffected control individuals were included in the study. Micro-RNA analysis showed a distinct expression profile in Brugada patients with 42 differentially expressed markers (38 up-regulated, 4 down-regulated miRNAs). The symptom status of Brugada patients was associated with a distinct miRNA signature. Micro-RNAs 145-5p and 585-3p were significantly up-regulated in symptomatic Brugada patients (P = 0.04). Incorporating miRNAs 145-5p and 585-3p into a multivariable model demonstrated significantly increased symptom prediction (area under the curve = 0.96; 95% confidence interval: 0.88-1.00).

conclusionBrugada patients display a distinct miRNA expression profile compared with unaffected control individuals. There is also evidence that certain miRNAs (miR-145-5p and miR-585-3p) are associated with the symptom status of Brugada patients. The results suggest the principal utility of leucocyte-derived miRNAs as prognostic biomarkers for Brugada syndrome.

Indexed as

Brugada SyndromeCirculating MicroRNAMicroRNAsBiomarkersHumansProspective StudiesBiomarkersCirculating MicroRNAMicroRNAsMIRN145 microRNA, humanBiomarkerBrugada syndromeLeucocyte derivedMicroRNANanoStringRisk prediction

Identifiers

PMID37314195
PMCPMC10265963
OpenAlexW4380577581

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.