Evidence map›Paper›PMID 25360520›Full record

ArticlePloS one2014

Atlas-based quantification of cardiac remodeling due to myocardial infarction.

Xingyu Zhang, Brett R Cowan, David A Bluemke, J Paul Finn, Carissa G Fonseca, Alan H Kadish, Daniel C Lee, Joao A C Lima, Avan Suinesiaputra, Alistair A Young and 1 more

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
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  9. Atlas-based methods for efficient characterization of patient-specific ventricular activation patterns.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2021
    Article
  10. Article
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  14. Modeling left ventricular dynamics with characteristic deformation modes.Biomechanics and modeling in mechanobiology · 2019
    Article
  15. A Statistical Shape Model Approach for Computing Left Ventricle Volume and Ejection Fraction Using Multi-plane Ultrasound Images.VipIMAGE 2019 : proceedings of the VII ECCOMAS Thematic Conference on Computational Vision and Medical Image Processing, October 16-18, 2019, Porto, Portugal. VipIMAGE (Conference) (2019 : Porto, Portugal) · 2019
    Article
  16. Right ventricular shape and function: cardiovascular magnetic resonance reference morphology and biventricular risk factor morphometrics in UK Biobank.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2019
    Article
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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

11 authors.

Xingyu ZhangDepartment of Anatomy with Radiology, University of Auckland, Auckland, New Zealand.
Brett R CowanDepartment of Anatomy with Radiology, University of Auckland, Auckland, New Zealand.
David A BluemkeNational Institute of Biomedical Imaging and Bioengineering, Bethesda, Maryland, United States of America.
J Paul FinnDepartment of Radiology, University of California Los Angeles, Los Angeles, California, United States of America.
Carissa G FonsecaDepartment of Radiology, University of California Los Angeles, Los Angeles, California, United States of America.
Alan H KadishFeinberg Cardiovascular Research Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America.
Daniel C LeeFeinberg Cardiovascular Research Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America.
Joao A C LimaThe Donald W. Reynolds Cardiovascular Clinical Research Center, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Avan SuinesiaputraDepartment of Anatomy with Radiology, University of Auckland, Auckland, New Zealand.
Alistair A YoungDepartment of Anatomy with Radiology, University of Auckland, Auckland, New Zealand.
Pau Medrano-GraciaDepartment of Anatomy with Radiology, University of Auckland, Auckland, New Zealand.

Funding

Institute for Clinical and Translational Research (UL1)UL1RR025005 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$75.8M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024156 · NCRR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2006 to 2011
$53.0M
PRE-DETERMINE: Biologic Markers and MRI SCD Cohort StudyR01HL091069 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ALBERT, CHRISTINE M · 2008 to 2020
$12.9M
The Cardiac Atlas ProjectR01HL121754 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MCCULLOCH, ANDREW D., OMENS, JEFFREY H. · 2014 to 2023
$5.0M
Molecular Biomedical Imaging Laboratory (NIBIB)ZIAEB000072 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI BLUEMKE, DAVID · 2010 to 2017
$5.0M
The Cardiac Atlas Project: Establishment of a Cardiac MRI Database.R01HL087773 · NHLBI · UNIVERSITY OF AUCKLAND · PI YOUNG, ALISTAIR ANDREW · 2008 to 2010
$1.4M
SUBCLINICAL CARDIOVASCULAR DISEASE STUDYN01HC095166 · HC · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI TRACY, RUSSELL P · 1999 to 2001
$758k
SUBCLINICAL CARDIOVASCULAR DISEASE STUDY-FIELD CENTERN01HC095162 · HC · JOHNS HOPKINS UNIVERSITY · PI SZKLO, MOYSES A · 1999 to 2000
$694k
SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--FIELD CENTERN01HC095161 · HC · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHEA, STEVEN · 1999 to 2001
$642k
SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--FIELD CENTERN01HC095165 · HC · WAKE FOREST UNIVERSITY · PI BURKE, GREGORY L · 1999 to 2001
$616k
SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--FIELD CENTERN01HC095160 · HC · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAAD, MOHAMMED F · 1999 to 2001
$592k
SUBCLINICAL CARDIOVASCULAR DISEASE STUDY-FIELD CENTERN01HC095164 · HC · NORTHWESTERN UNIVERSITY · PI LIU, KIANG JOHN · 1999 to 2001
$511k
Intramural NIH HHSNCRR NIH HHS UL1 RR024156NCRR NIH HHS UL1-RR-024156NCRR NIH HHS UL1 RR025005NCRR NIH HHS UL1-RR-025005NHLBI NIH HHS N01 HC095159NHLBI NIH HHS N01 HC095169NHLBI NIH HHS N01-HC-95159NHLBI NIH HHS N01-HC-95160NHLBI NIH HHS N01-HC-95161NHLBI NIH HHS N01-HC-95162NHLBI NIH HHS N01-HC-95163NHLBI NIH HHS N01-HC-95164NHLBI NIH HHS N01-HC-95165NHLBI NIH HHS N01-HC-95166NHLBI NIH HHS N01-HC-95167NHLBI NIH HHS N01-HC-95168NHLBI NIH HHS N01-HC-95169NHLBI NIH HHS R01 HL087773NHLBI NIH HHS R01HL087773NHLBI NIH HHS R01 HL091069NHLBI NIH HHS R01 HL121754NHLBI NIH HHS R01HL121754NHLBI NIH HHS R01HL91069
6 · The paper itself

Abstract

Myocardial infarction leads to changes in the geometry (remodeling) of the left ventricle (LV) of the heart. The degree and type of remodeling provides important diagnostic information for the therapeutic management of ischemic heart disease. In this paper, we present a novel analysis framework for characterizing remodeling after myocardial infarction, using LV shape descriptors derived from atlas-based shape models. Cardiac magnetic resonance images from 300 patients with myocardial infarction and 1991 asymptomatic volunteers were obtained from the Cardiac Atlas Project. Finite element models were customized to the spatio-temporal shape and function of each case using guide-point modeling. Principal component analysis was applied to the shape models to derive modes of shape variation across all cases. A logistic regression analysis was performed to determine the modes of shape variation most associated with myocardial infarction. Goodness of fit results obtained from end-diastolic and end-systolic shapes were compared against the traditional clinical indices of remodeling: end-diastolic volume, end-systolic volume and LV mass. The combination of end-diastolic and end-systolic shape parameter analysis achieved the lowest deviance, Akaike information criterion and Bayesian information criterion, and the highest area under the receiver operating characteristic curve. Therefore, our framework quantitatively characterized remodeling features associated with myocardial infarction, better than current measures. These features enable quantification of the amount of remodeling, the progression of disease over time, and the effect of treatments designed to reverse remodeling effects.

Indexed as

Magnetic Resonance ImagingVentricular RemodelingAsymptomatic DiseasesFemaleFinite Element AnalysisHumansImaging, Three-DimensionalLogistic ModelsMaleMiddle AgedMovementMyocardial InfarctionMyocardiumOrgan SizePrincipal Component Analysis

Identifiers

PMID25360520
PMCPMC4215861

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