Evidence map›Paper›PMID 33744130›Full record

ArticleJACC. Cardiovascular imaging2021

Ischemia-Mediated Dysfunction in Subpapillary Myocardium as a Marker of Functional Mitral Regurgitation.

Jonathan D Kochav, Jiwon Kim, Robert Judd, Han W Kim, Igor Klem, John Heitner, Dipan Shah, Chetan Shenoy, Afshin Farzaneh-Far, Venkateshwar Polsani and 16 more

Open access · greenAbstract read
In one paragraph

Article in JACC. Cardiovascular imaging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 9 institutions in 1 country.

Jonathan D KochavDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA; Division of Cardiology, Columbia University Irving Medical Center, New York, New York, USA.
Jiwon KimDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA.
Robert JuddDuke Cardiovascular Magnetic Resonance Center, Duke University Medical Center, Durham, North Carolina, USA.
Han W KimDuke Cardiovascular Magnetic Resonance Center, Duke University Medical Center, Durham, North Carolina, USA.
Igor KlemDuke Cardiovascular Magnetic Resonance Center, Duke University Medical Center, Durham, North Carolina, USA.
John HeitnerDivision of Cardiology, NewYork-Presbyterian Brooklyn Methodist Hospital, New York, New York, USA.
Dipan ShahDivision of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston, Texas, USA.
Chetan ShenoyDivision of Cardiology, University of Minnesota Medical Center, Minneapolis, Minnesota, USA.
Afshin Farzaneh-FarDivision of Cardiology, University of Illinois at Chicago, Chicago, Illinois, USA.
Venkateshwar PolsaniPeidmont Heart Institute, Peidmont Atlanta Hospital, Atlanta Georgia, USA.
Ramsey KalilDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA.
Pablo Villar-CalleDepartment of Cardiology, Sant Pau Hospital, Barcelona, Spain.
Lakshmi NambiarDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA.
Razia SultanaDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA.
Michele ParkerDuke Cardiovascular Magnetic Resonance Center, Duke University Medical Center, Durham, North Carolina, USA.
Preston CargileHeart Imaging Technologies, Durham, North Carolina, USA.
Omar K KhaliqueDivision of Cardiology, Columbia University Irving Medical Center, New York, New York, USA.
Martin B LeonDivision of Cardiology, Columbia University Irving Medical Center, New York, New York, USA.
Dimitrios KarmpaliotisDivision of Cardiology, Columbia University Irving Medical Center, New York, New York, USA.
Mark RatcliffeDivision of Cardiac Surgery, University of California, San Francisco, California, USA.
Robert LevineDivision of Cardiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
William A ZoghbiDivision of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston, Texas, USA.
Richard B DevereuxDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA.
Chaya S MoskowitzDepartment of Epidemiology and Biostatics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Raymond KimDuke Cardiovascular Magnetic Resonance Center, Duke University Medical Center, Durham, North Carolina, USA.
Jonathan W WeinsaftDivision of Cardiology, Weill Cornell Medicine, New York, New York, USA. Electronic address: jww2001@med.cornell.edu.
Cornell University · USDuke Medical Center · USColumbia University Irving Medical Center · USHouston Methodist · USHeart Imaging Technologies (United States) · USMassachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USUniversity of Illinois Chicago · USUniversity of Minnesota Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
POSTDOCTORAL TRAINING IN CARDIOVASCULAR DISEASET32HL007854 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Marwah Abdalla, Michael Argenziano · 1996 to 2026
$14.7M
QUANTITATIVE ANALYSIS OF LEFT VENTRICULPLASTY--CHFR01HL063348 · NHLBI · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI RATCLIFFE, MARK B · 2000 to 2017
$6.8M
Phase IA/IB Study of AAVrh.10hFXN Therapy to Treat the Cardiomyopathy of Friedreich's AtaxiaR33HL151355 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G, KAMINSKY, STEPHEN MICHAEL · 2022 to 2024
$5.9M
Improving Mitral Compensation In Ischemic RegurgitationR01HL141917 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI AIKAWA, ELENA, BISCHOFF, JOYCE E. · 2018 to 2021
$5.6M
Noninvasive measurement of oxygenation using quantitative susceptibility mapping (supplement)R01HL151686 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI SPINCEMAILLE, PASCAL, WEINSAFT, JONATHAN W. · 2021 to 2025
$4.7M
CMR Myocardial Tissue Based Prediction of Ischemic MR Revascularization ResponseR01HL128278 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI WEINSAFT, JONATHAN W. · 2015 to 2019
$3.8M
Treating Ventricle and Valve: New Synergies for Ischemic LV Remodeling with MRR01HL128099 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI AKAR, FADI GABRIEL, LEVINE, ROBERT A · 2016 to 2019
$2.8M
Cardiac Fibrosis and Risk Prediction in Cancer Treatment-Related CardiotoxicityK23HL132011 · NHLBI · UNIVERSITY OF MINNESOTA · PI SHENOY, CHETAN N · 2016 to 2020
$884k
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
Delayed Enhancement MRI for Detection of Sub-Clinical Papillary Muscle InfarctionK23HL102249 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI WEINSAFT, JONATHAN W. · 2010 to 2014
$680k
Phase IA/IB Study of AAVrh.10hFXN Therapy to Treat the Cardiomyopathy of Friedreich's AtaxiaR61HL151355 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G, KAMINSKY, STEPHEN MICHAEL · 2020 to 2020
$420k
NCI NIH HHS P30 CA008748NHLBI NIH HHS K23 HL102249NHLBI NIH HHS K23 HL132011NHLBI NIH HHS K23 HL140092NHLBI NIH HHS R01 HL063348NHLBI NIH HHS R01 HL128099NHLBI NIH HHS R01 HL128278NHLBI NIH HHS R01 HL141917NHLBI NIH HHS R01 HL151686NHLBI NIH HHS R33 HL151355NHLBI NIH HHS R61 HL151355NHLBI NIH HHS T32 HL007854
6 · The paper itself

Abstract

objectivesThe goal of this study was to test whether ischemia-mediated contractile dysfunction underlying the mitral valve affects functional mitral regurgitation (FMR) and the prognostic impact of FMR.

backgroundFMR results from left ventricular (LV) remodeling, which can stem from myocardial tissue alterations. Stress cardiac magnetic resonance can assess ischemia and infarction in the left ventricle and papillary muscles; relative impact on FMR is uncertain.

methodsVasodilator stress cardiac magnetic resonance was performed in patients with known or suspected coronary artery disease at 7 sites. Images were centrally analyzed for MR etiology/severity, mitral apparatus remodeling, and papillary ischemia.

resultsA total of 8,631 patients (mean age 60.0 ± 14.1 years; 55% male) were studied. FMR was present in 27%, among whom 16% (n = 372) had advanced (moderate or severe) FMR. Patients with ischemia localized to subpapillary regions were more likely to have advanced FMR (p = 0.003); those with ischemia localized to other areas were not (p = 0.17). Ischemic/dysfunctional subpapillary myocardium (odds ratio: 1.24/10% subpapillary myocardium; confidence interval: 1.17 to 1.31; p < 0.001) was associated with advanced FMR controlling for infarction. Among a subgroup with (n = 372) and without (n = 744) advanced FMR matched (1:2) on infarct size/distribution, patients with advanced FMR had increased adverse mitral apparatus remodeling, paralleled by greater ischemic/dysfunctional subpapillary myocardium (p < 0.001). Although posteromedial papillary ischemia was more common with advanced FMR (p = 0.006), subpapillary ischemia with dysfunction remained associated (p < 0.001), adjusting for posteromedial papillary ischemia (p = 0.074). During follow-up (median 5.1 years), 1,473 deaths occurred in the overall cohort; advanced FMR conferred increased mortality risk (hazard ratio: 1.52; 95% confidence interval: 1.25 to 1.86; p < 0.001) controlling for left ventricular ejection fraction, infarction, and ischemia.

conclusionsIschemic and dysfunctional subpapillary myocardium provides a substrate for FMR, which predicts mortality independent of key mechanistic substrates.

Indexed as

Mitral Valve InsufficiencyAgedFemaleHumansIschemiaMaleMiddle AgedPapillary MusclesPredictive Value of TestsStroke VolumeVentricular Function, Leftcardiac magnetic resonanceischemiamitral regurgitation

Identifiers

PMID33744130
PMCPMC8086776
OpenAlexW3135936753

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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.