Evidence map›Paper›PMID 41999216›Full record

ArticleInterdisciplinary cardiovascular and thoracic surgery2026

Targeted Sequencing of Human Aorta Tissue Reveals Undiagnosed Heritable Thoracic Aortic Disease.

Ha Lee, Yoonjung Kim, Myeong Su Kim, Kyung-A Lee, Suk-Won Song

Abstract read
In one paragraph

Article in Interdisciplinary cardiovascular and thoracic surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Ha LeeDepartment of Thoracic and Cardiovascular Surgery, Ewha Womans University Seoul Hospital, Ewha Womans University College of Medicine, Seoul, 07804, Republic of Korea.ORCID 0000-0003-3976-8554
Yoonjung KimDepartment of Laboratory Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, 06273, Republic of Korea.ORCID 0000-0002-4370-4265
Myeong Su KimDepartment of Thoracic and Cardiovascular Surgery, Ewha Womans University Seoul Hospital, Ewha Womans University College of Medicine, Seoul, 07804, Republic of Korea.ORCID 0000-0002-1435-6441
Kyung-A LeeDepartment of Laboratory Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, 06273, Republic of Korea.ORCID 0000-0001-5320-6705
Suk-Won SongDepartment of Thoracic and Cardiovascular Surgery, Ewha Womans University Seoul Hospital, Ewha Womans University College of Medicine, Seoul, 07804, Republic of Korea.ORCID 0000-0002-9850-9707

Funding

Research Grant from Gangnam Severance Hospital, Yonsei University College of Medicine
6 · The paper itself

Abstract

objectivesTo diagnose undiagnosed heritable thoracic aortic disease (HTAD) using targeted next-generation sequencing technology on human aorta tissue obtained from a single-centre biobank.

methodsFrom May 2016 to November 2021, 622 patients undergoing surgical repair for thoracic aortic aneurysm or acute aortic syndrome donated blood or tissue samples to the research biobank. A total of 134 aortic tissue samples were retrieved from patients suspected of HTAD. The inclusion criteria were (1) family history, (2) age ≤ 45, (3) annuloaortic ectasia, (4) bicuspid aortic valve, (5) patent ductus arteriosus, (6) polycystic kidney disease, or (7) patients previously classified as variant of uncertain significance by germline sequencing (n = 17). Exclusion criteria included patients previously classified as likely pathogenic or pathogenic by germline sequencing. The targeted panel included 96 genes.

resultsA total of 29 variants were identified including FBN1, MYH11, COL11A1, SMAD3, SMAD6, ACTA2, COL3A1, FLNA, PKD2, THSD4, ACVRL1, and FBN2. A total of 27 patients (20.1%) had variants with 2 patients having digenic variants. Clinical data were combined with genetic data, and finally, 17 patients (12.7%) were additionally diagnosed with HTAD.

conclusionsGenomic data analysis of human aortic tissue allowed for additional diagnoses of undiagnosed HTAD, contributing to resolving discrepancies between clinical and genomic data. Considering the surgical treatment of HTAD, human aortic tissue can be a valuable resource for genomic analysis.

Indexed as

Acute Aortic SyndromeAorta, ThoracicAortic Aneurysm, ThoracicGenetic TestingHigh-Throughput Nucleotide SequencingAdultAgedFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPhenotypeYoung AdultBiobankheritable thoracic aortic diseasenext-generation sequencingrare disease

Identifiers

PMID41999216
PMCPMC13148960

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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.