Evidence map›Paper›PMID 40740135›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2025

Tricuspid Aortic Valve Regurgitation Associates With Ascending Aortic Aneurysm Through Endothelial Activation and Lipoprotein Infiltration.

David Freiholtz, Claudia Reyes-Goya, Karin Lång, Otto Bergman, Christian Olsson, Malin Granbom Koski, Michael Dismorr, Cecilia Österholm, Kenneth Caidahl, Anders Franco-Cereceda and 3 more

Abstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2025. 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
–field-weighted citation impact
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. 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

13 authors.

David FreiholtzDivision of Cardiology, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (D.F., C.R.-G., K.L., O.B., P.E., H.M.B.).ORCID 0000-0001-9196-7409
Claudia Reyes-GoyaDivision of Cardiology, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (D.F., C.R.-G., K.L., O.B., P.E., H.M.B.).ORCID 0000-0002-1621-5335
Karin LångDivision of Cardiology, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (D.F., C.R.-G., K.L., O.B., P.E., H.M.B.).ORCID 0009-0008-5758-4701
Otto BergmanDivision of Cardiology, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (D.F., C.R.-G., K.L., O.B., P.E., H.M.B.).ORCID 0000-0003-4323-8150
Christian OlssonSection of Cardiothoracic Surgery, Department of Molecular Medicine and Surgery , Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (C.O., M.G.K., M.D., A.F.-C.).ORCID 0000-0002-5677-0747
Malin Granbom KoskiSection of Cardiothoracic Surgery, Department of Molecular Medicine and Surgery , Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (C.O., M.G.K., M.D., A.F.-C.).ORCID 0009-0000-6013-0120
Michael DismorrSection of Cardiothoracic Surgery, Department of Molecular Medicine and Surgery , Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (C.O., M.G.K., M.D., A.F.-C.).ORCID 0000-0002-5652-8774
Cecilia ÖsterholmDivision of Clinical Genetics, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden (C.Ö).ORCID 0000-0001-7506-084X
Kenneth CaidahlSection of Clinical Physiology, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Karolinska University Hospital, Sweden (K.C.).ORCID 0000-0002-5079-9696
Anders Franco-CerecedaSection of Cardiothoracic Surgery, Department of Molecular Medicine and Surgery , Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (C.O., M.G.K., M.D., A.F.-C.).ORCID 0000-0002-3427-9455
Per ErikssonDivision of Cardiology, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (D.F., C.R.-G., K.L., O.B., P.E., H.M.B.).ORCID 0000-0002-5635-2692
Anton GisteråDivision of Cardiovascular Medicine, Center for Molecular Medicine, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden (A.G.).ORCID 0000-0002-4614-8030
Hanna M BjörckDivision of Cardiology, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Karolinska University Hospital, Solna, Sweden (D.F., C.R.-G., K.L., O.B., P.E., H.M.B.).ORCID 0000-0002-9155-3609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn abnormal accumulation of immune cells and inflammation has been described in ascending aortic aneurysm, but the factor driving disease initiation remains elusive. Interestingly, ascending aortic dilatation often occurs alongside aortic regurgitation but rarely with aortic stenosis. We sought to investigate ascending aortic aneurysm initiation by assessing the relation between aortic regurgitation and vascular activation and inflammation.

methodsIn this prospective cohort study, patients with tricuspid aortic valves undergoing elective open-heart surgery were included. Aortic specimens from organ donors were obtained through the University of Miami Tissue Bank. Spatial transcriptomics measured gene expression in nondilated aortic endothelium, intima, and subintima. Immunohistochemistry determined protein expression. Aortic dimensions were recorded preoperatively and 10 years after surgery using echocardiography. Aortic gene expression affected by physiological blood flow was previously measured in Wistar rats.

resultsWe show a mesenchymal activation of endothelial cells, possibly mediated by bidirectional flow, in the nondilated ascending aorta of patients with aortic regurgitation, accompanied by intimal infiltration, retention, and oxidation of apoB-containing lipoproteins. We further observed intimal upregulation of genes coding for core proteins of lipoprotein-binding proteoglycans and the

conclusionsOur results highlight a distinct pathological role of aortic regurgitation in ascending aortic aneurysm formation by promoting mesenchymal activation of endothelial cells and lipoprotein-related immune cell infiltration and inflammation in patients with tricuspid aortic valves. We also provide novel insights into the long-term impact of surgical aortic valve replacement on ascending aortic growth and suggest a diagnostic or therapeutic target in oxidized low-density lipoprotein cholesterol.

Indexed as

AortaAortic AneurysmAortic Valve InsufficiencyEndothelial CellsEndothelium, VascularTricuspid ValveAgedAneurysm, Ascending AortaAnimalsFemaleHumansMacrophagesMaleMiddle AgedProspective Studiesaneurysm, ascending aortaaortic valve stenosisendothelial cellsgene expressionlipoproteinsregurgitation, aortic valve

Identifiers

PMID40740135
PMCPMC12379797

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.