Evidence map›Paper›PMID 39511342›Full record

ArticleScientific reports2024

Genetic insights from a Brazilian cohort of aortopathies through targeted next-generation sequencing and FBN1 direct sequencing.

Juliana Rocha Ferreira, Julia Passarelli Pereira, Anna Paula Arpini Botelho, Daniele do Nascimento Aprijo, Marcelo Machado Melo, Helena Cramer Veiga Rey, Glauber Monteiro Dias

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In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Juliana Rocha FerreiraNational Institute of Cardiology, Rio de Janeiro, RJ, 22240-002, Brazil.
Julia Passarelli PereiraNational Institute of Cardiology, Rio de Janeiro, RJ, 22240-002, Brazil.
Anna Paula Arpini BotelhoNational Institute of Cardiology, Rio de Janeiro, RJ, 22240-002, Brazil.
Daniele do Nascimento AprijoNational Institute of Cardiology, Rio de Janeiro, RJ, 22240-002, Brazil.
Marcelo Machado MeloNational Institute of Cardiology, Rio de Janeiro, RJ, 22240-002, Brazil.
Helena Cramer Veiga ReyNational Institute of Cardiology, Rio de Janeiro, RJ, 22240-002, Brazil.
Glauber Monteiro DiasCellular and Tissue Biology Laboratory, State University of Norte Fluminense Darcy Ribeiro, Campos dos Goytacazes, RJ, 28013-602, Brazil. glauber@uenf.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thoracic aortic diseases (or aortopathies) result from complex interactions between genetic and hemodynamic factors. Often clinically silent, these diseases can lead to lethal complications such as aortic dissection or rupture. This study focused on a Brazilian cohort of 79 individuals with thoracic aortic diseases and explored genetic factors through targeted next-generation sequencing (tNGS) of 15 priority genes and FBN1 direct sequencing. The majority of individuals had nonsyndromic aortopathy, with eight diagnosed with Marfan syndrome (MFS). Pathogenic or likely pathogenic variants (PV/LPV) were found in five genes, namely, FBN1, ACTA2, TGFBR2, MYLK, and SMAD3. Notably, novel variants in FBN1 were identified that contributed to Marfan-like phenotypes. The diagnostic yield for isolated aortopathies was 7.1%, which increased to 55.5% for syndromic cases. Variants of uncertain significance (VUS) were identified, emphasizing the need for further research and familial investigations to refine variant classifications. This study provides valuable insights into the genetic landscape of aortopathies in Brazil, aiding early diagnosis and personalized management.

Indexed as

Fibrillin-1High-Throughput Nucleotide SequencingActinsAdipokinesAdolescentAdultAgedAortic DiseasesBrazilChildCohort StudiesFemaleGenetic Predisposition to DiseaseHumansMaleMarfan SyndromeACTA2 protein, humanActinsAdipokinesFBN1 protein, humanFibrillin-1Receptor, Transforming Growth Factor-beta Type IISmad3 ProteinSMAD3 protein, humanTGFBR2 protein, humanAortic aneurysm and dissectionGenetic variant pathogenicityMarfan syndromeNext-generation sequencingThoracic aortic disease

Identifiers

PMID39511342
PMCPMC11543835

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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.