Evidence map›Paper›PMID 38202009›Full record

ArticleJournal of clinical medicine2023

Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening.

Rebeca Lorca, Isaac Pascual, Maria Fernandez, Rut Alvarez-Velasco, Santiago Colunga, Maria Muñiz, Marta Izquierdo, Yolanda Fernandez, Emilio Esteban, Juan Gomez and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

12 authors at 3 institutions in 1 country.

Rebeca LorcaÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-7803-4011
Isaac PascualÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0001-5433-1364
Maria FernandezÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0001-5311-822X
Rut Alvarez-VelascoÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-2837-7374
Santiago ColungaÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Maria MuñizOncología Médica, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Marta IzquierdoOncología Médica, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Yolanda FernandezOncología Médica, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Emilio EstebanDepartamento de Medicina, Universidad de Oviedo, 33003 Oviedo, Spain.
Juan GomezInstituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain.ORCID 0000-0002-3318-4649
Pablo AvanzasÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-4958-6108
Teresa Lopez-FernandezCardiología, Hospital Universitario la Paz, IdiPAZ Research Institute, 28046 Madrid, Spain.ORCID 0000-0002-3414-7022
Hospital Universitario Central de Asturias · ESUniversidad de Oviedo · ESHospital Universitario La Paz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBasal cardiovascular risk assessment in cardio-oncology is essential. Integrating clinical information, ECG and transthoracic echocardiogram can identify concealed inherited cardiomyopathies (ICMPs) with potential added risk of cardiotoxicity. We aimed to evaluate the impact of our Cardio-Oncology Unit design in detecting concealed ICMPs.

methodsWe carried out a retrospective study of all consecutive breast cancer patients referred to the Cardio-Oncology Unit for cardiac evaluation (2020-2022). ICMPs diagnosis was provided according to ESC guidelines and underwent genetic testing. ICMPs prevalence in this cohort was compared to the highest and lowest frequency reported in the general population.

resultsAmong 591 breast cancer patients, we identified eight patients with ICMPs: one arrhythmogenic cardiomyopathy (ACM), three familial non-ischemic dilated cardiomyopathy (DCM), three hypertrophic cardiomyopathy (HCM) and one left ventricular non-compaction cardiomyopathy (LVNC), which has now been reclassified as non-dilated left ventricular cardiomyopathy. The number of ICMPs identified was within the expected range (neither overdiagnosed nor overlooked): ACM 0.0017 vs. 0.0002-0.001 (

conclusionOpportunistic screening of ICMPs during basal cardiovascular risk assessment can identify high-risk cancer patients who benefit from personalized medicine and enables extension of prevention strategies to all available relatives at concealed high cardiovascular risk.

Indexed as

cardiomyopathycardio-oncologygenetics

Identifiers

PMID38202009
PMCPMC10780282
OpenAlexW4389937991

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.