Evidence map›Paper›PMID 37208380›Full record

ArticleScientific reports2023

Correcting bias in cardiac geometries derived from multimodal images using spatiotemporal mapping.

Debbie Zhao, Charlène A Mauger, Kathleen Gilbert, Vicky Y Wang, Gina M Quill, Timothy M Sutton, Boris S Lowe, Malcolm E Legget, Peter N Ruygrok, Robert N Doughty and 4 more

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Longitudinal trajectories of left ventricular myocardial remodeling: associations with cardiovascular risk factors in the multi-ethnic study of atherosclerosis.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Debbie ZhaoAuckland Bioengineering Institute, University of Auckland, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand. debbie.zhao@auckland.ac.nz.
Charlène A MaugerAuckland Bioengineering Institute, University of Auckland, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
Kathleen GilbertAuckland Bioengineering Institute, University of Auckland, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
Vicky Y WangAuckland Bioengineering Institute, University of Auckland, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
Gina M QuillAuckland Bioengineering Institute, University of Auckland, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
Timothy M SuttonCounties Manukau Health Cardiology, Middlemore Hospital, Auckland, New Zealand.
Boris S LoweGreen Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
Malcolm E LeggetDepartment of Medicine, University of Auckland, Auckland, New Zealand.
Peter N RuygrokGreen Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
Robert N DoughtyGreen Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
João PedrosaInstitute for Systems and Computer Engineering, Technology and Science (INESC TEC), Porto, Portugal.
Jan D'hoogeDepartment of Cardiovascular Sciences, KU Leuven, Leuven, Belgium.
Alistair A YoungDepartment of Anatomy and Medical Imaging, University of Auckland, Auckland, New Zealand.
Martyn P NashAuckland Bioengineering Institute, University of Auckland, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.

Funding

The Cardiac Atlas ProjectR01HL121754 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MCCULLOCH, ANDREW D., OMENS, JEFFREY H. · 2014 to 2023
$5.0M
NHLBI NIH HHS R01 HL121754
6 · The paper itself

Abstract

Cardiovascular imaging studies provide a multitude of structural and functional data to better understand disease mechanisms. While pooling data across studies enables more powerful and broader applications, performing quantitative comparisons across datasets with varying acquisition or analysis methods is problematic due to inherent measurement biases specific to each protocol. We show how dynamic time warping and partial least squares regression can be applied to effectively map between left ventricular geometries derived from different imaging modalities and analysis protocols to account for such differences. To demonstrate this method, paired real-time 3D echocardiography (3DE) and cardiac magnetic resonance (CMR) sequences from 138 subjects were used to construct a mapping function between the two modalities to correct for biases in left ventricular clinical cardiac indices, as well as regional shape. Leave-one-out cross-validation revealed a significant reduction in mean bias, narrower limits of agreement, and higher intraclass correlation coefficients for all functional indices between CMR and 3DE geometries after spatiotemporal mapping. Meanwhile, average root mean squared errors between surface coordinates of 3DE and CMR geometries across the cardiac cycle decreased from 7 ± 1 to 4 ± 1 mm for the total study population. Our generalised method for mapping between time-varying cardiac geometries obtained using different acquisition and analysis protocols enables the pooling of data between modalities and the potential for smaller studies to leverage large population databases for quantitative comparisons.

Indexed as

Echocardiography, Three-DimensionalBiasHeart VentriclesHumansMagnetic Resonance ImagingReproducibility of ResultsStroke VolumeVentricular Function, Left

Identifiers

PMID37208380
PMCPMC10199025

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.