Evidence map›Paper›PMID 35896809›Full record

ArticleVirchows Archiv : an international journal of pathology2023

Familial acute aortic dissection associated with a novel ACTA2 germline variant.

Thomas Strecker, Felix Wiesmueller, Sabine Rudnik-Schöneborn, Juliane Hoyer, André Reis, Michael Weyand, Abbas Agaimy

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2023. 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
0.5field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Predictive Value of Normalized Lactate Load for Patients with Acute Type A Aortic Dissection: Based on the MIMIC-IV Database.Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia · 2025
    Article
  4. Aortic dissection: A story of rural assessment, evacuation, and survival.Canadian family physician Medecin de famille canadien · 2024
    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

7 authors at 3 institutions in 3 countries.

Thomas StreckerCenter of Cardiac Surgery, Friedrich-Alexander-University Erlangen-Nuremberg, Östliche Stadtmauerstraße 27, 91054, Erlangen, Germany. thomas.strecker@uk-erlangen.de.ORCID http://orcid.org/0000-0002-8292-7066
Felix WiesmuellerDivision of Cardiothoracic Surgery, Brigham and Woman's Hospital, Harvard Medical School, Boston, MA, USA.
Sabine Rudnik-SchönebornInstitute of Human Genetics, University of Innsbruck, Innsbruck, Austria.
Juliane HoyerInstitute of Genetics, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
André ReisInstitute of Genetics, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
Michael WeyandCenter of Cardiac Surgery, Friedrich-Alexander-University Erlangen-Nuremberg, Östliche Stadtmauerstraße 27, 91054, Erlangen, Germany.
Abbas AgaimyInstitute of Pathology, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEHarvard University · USUniversität Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aortic dissection is a life-threatening cardiovascular disease. Hereditary disorders are responsible for a small percentage of cases. Nonetheless, it is important to identify genetic causes, as they are often autosomal dominantly inherited and are of life-saving importance if we can identify persons at risk. Mutations of the ACTA2 gene are the most common cause of non-syndromic familial aortic disease. Exploration of the genetic background in suspected familial cases and determination of the exact etiology are mandatory for management and establishing appropriate follow-up strategies due to the risk of fatal recurrences. Herein, we present a 21-year-old male with a familial acute aortic dissection associated with novel ACTA2 germline variant and discuss the management and surveillance considerations.

Indexed as

Aortic Aneurysm, ThoracicAortic DissectionActinsAdultGerm CellsHumansMaleMutationYoung AdultACTA2 protein, humanActinsACTA2 mutationAortic dissectionCardiac surgeryEchocardiography, Computer tomographyHuman geneticsPathology

Identifiers

PMID35896809
PMCPMC9931827
OpenAlexW4288060261

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.