Evidence map›Paper›PMID 26872470›Full record

ReviewInternational journal of legal medicine2016

Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?

Georgia Sarquella-Brugada, Oscar Campuzano, Sergi Cesar, Anna Iglesias, Anna Fernandez, Josep Brugada, Ramon Brugada

Abstract readReview
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In one paragraph

Review in International journal of legal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Georgia Sarquella-BrugadaArrhythmias Unit, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Oscar CampuzanoCardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain.
Sergi CesarArrhythmias Unit, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Anna IglesiasCardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain.
Anna FernandezCardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain.
Josep BrugadaArrhythmias Unit, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Ramon BrugadaCardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain. ramon@brugada.org.
Institut d'Investigació Biomèdica de Girona · ESUniversitat de Barcelona · ESUniversity of Girona · ESHospital Sant Joan de Déu Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudden infant death syndrome is the unexpected demise of a child younger than 1 year of age which remains unexplained after a complete autopsy investigation. Usually, it occurs during sleep, in males, and during the first 12 weeks of life. The pathophysiological mechanism underlying the death is unknown, and the lethal episode is considered multifactorial. However, in cases without a conclusive post-mortem diagnosis, suspicious of cardiac arrhythmias may also be considered as a cause of death, especially in families suffering from any cardiac disease associated with sudden cardiac death. Here, we review current understanding of sudden infant death, focusing on genetic causes leading to lethal cardiac arrhythmias, considering both genes encoding ion channels as well as structural proteins due to recent association of channelopathies and desmosomal genes. We support a comprehensive analysis of all genes associated with sudden cardiac death in families suffering of infant death. It allows the identification of the most plausible cause of death but also of family members at risk, providing cardiologists with essential data to adopt therapeutic preventive measures in families affected with this lethal entity.

Indexed as

Arrhythmias, CardiacChannelopathiesGenetic VariationHumansInfantMutationSudden Infant DeathArrhythmiasCardiomyopathiesChannelopathiesGeneticsMolecular autopsySIDS

Identifiers

PMID26872470
OpenAlexW2337156907

What OpenQuestion holds

Textmetadata
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.