Evidence map›Paper›PMID 40608040›Full record

ArticleJACC. Cardiovascular imaging2025

Nonischemic Septal Fibrosis in Functional Tricuspid Regurgitation Provides Incremental Stratification of Adverse Remodeling and Prognosis.

Pablo Villar-Calle, Varun Pai, Robert S Zhang, Mahniz Reza, Lily Jin, Rachel Axman, Zachary Falk, Giorgia Falco, Arindam RoyChoudhury, Shmuel Chen and 6 more

Abstract read
In one paragraph

Article in JACC. Cardiovascular imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Clinical and imaging phenotypes.European heart journal supplements : journal of the European Society of Cardiology · 2026
    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

16 authors.

Pablo Villar-CalleDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Varun PaiDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Robert S ZhangDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Mahniz RezaDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Lily JinDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Rachel AxmanDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Zachary FalkDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Giorgia FalcoDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Arindam RoyChoudhuryDivision of Biostatistics and Epidemiology, Department of Population Health Sciences, Weill Cornell Medicine, New York, New York, USA.
Shmuel ChenDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Bobak MosadeghDalio Institute of Cardiovascular Imaging, Department of Radiology, Weill Cornell Medicine, New York, New York, USA.
Susheel K KodaliDivision of Cardiology, Columbia University Medical Center, NewYork-Presbyterian Hospital, New York, New York, USA.
Omar K KhaliqueDivision of Cardiovascular Imaging, Saint Francis Hospital and Heart Center, Roslyn, New York, USA.
Evelyn M HornDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Jonathan W WeinsaftDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.
Jiwon KimDivision of Cardiology, Weill Cornell Medicine, NewYork-Presbyterian Hospital, New York, New York, USA. Electronic address: jik9027@med.cornell.edu.

Funding

Cardiac Magnetic Resonance Tissue Characterization of Ischemic and Non-Ischemic Myocardium to Predict Left Ventricular Functional Recovery and Outcomes after Multivessel Coronary RevascularizationR01HL170566 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Mario FL Gaudino, Jonathan W. Weinsaft · 2023 to 2026
$3.0M
Advanced CMR Tissue-Based Prediction of Right Ventricular Dysfunction and Revascularization ResponseK23HL140092 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI KIM, JIWON · 2018 to 2022
$847k
NHLBI NIH HHS K23 HL140092NHLBI NIH HHS R01 HL170566
6 · The paper itself

Abstract

backgroundFunctional tricuspid regurgitation (TR) arises from impaired valve integrity resulting from contractile dysfunction, chamber dilation, or myocardial tissue alterations. Whereas right ventricular (RV) dysfunction is a recognized driver of adverse outcomes in TR, the impact of myocardial tissue injury, particularly nonischemic septal fibrosis (NIsF), remains largely unexplored.

objectivesThis study aims to evaluate the association of NIsF with adverse right-sided chamber remodeling and to assess its incremental prognostic value for mortality in patients with functional TR.

methodsPatients with advanced (≥ moderate) functional TR underwent comprehensive cardiac magnetic resonance (CMR) evaluation. Late gadolinium enhancement (LGE) was used to identify NIsF, defined as hyperenhancement in the midmyocardial or epicardial regions of the interventricular septum. Cine CMR measured functional and geometric indices of the left and right sides of the heart. Follow-up data were obtained for all-cause mortality.

resultsA total of 663 patients with advanced TR (mean age: 63.8 ± 16.0 years; 53% male) were studied, and 29.4% were found to have NIsF. NIsF was strongly associated with adverse chamber remodeling, including larger left ventricular and RV volumes, reduced systolic function, and increased TR severity (all P < 0.001). TR regurgitant fraction increased stepwise with NIsF extent (no NIsF, 34.9% ± 1.5%; 1 segment, 38.1% ± 13.0%; 2 segments, 40.8% ± 13.8%; P < 0.001). Over a mean follow-up of 4.3 ± 4.3 years, 25.3% of patients died. NIsF was independently associated with mortality (HR: 1.79 [95% CI: 1.26-2.56]; P = 0.001), even after adjusting for conventional risk markers, including age, TR severity, RV dysfunction, and dilation. Kaplan-Meier analysis demonstrated significantly higher mortality risk among patients with NIsF compared with patients without NIsF (P < 0.001).

conclusionsAmong patients with advanced TR, NIsF is an important marker of adverse right-sided chamber remodeling and provides incremental prognostic utility beyond conventional risk markers.

Indexed as

Magnetic Resonance Imaging, CineTricuspid ValveTricuspid Valve InsufficiencyVentricular Function, RightVentricular RemodelingAgedFemaleFibrosisHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesRisk AssessmentRisk Factorscardiac magnetic resonancenonischemic fibrosisprognostic markertricuspid regurgitation

Identifiers

PMID40608040
PMCPMC12362310

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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.