Evidence map›Paper›PMID 31398112›Full record

ArticleIEEE transactions on medical imaging2020

Estimating Aggregate Cardiomyocyte Strain Using In Vivo Diffusion and Displacement Encoded MRI.

Ilya A Verzhbinsky, Luigi E Perotti, Kevin Moulin, Tyler E Cork, Michael Loecher, Daniel B Ennis

Abstract read
In one paragraph

Article in IEEE transactions on medical imaging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. In-silico heart model phantom to validate cardiac strain imaging.bioRxiv : the preprint server for biology · 2024
    Article
  6. Myocardial mesostructure and mesofunction.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Myofiber strain in healthy humans using DENSE and cDTI.Magnetic resonance in medicine · 2021
    Article
  13. Arbitrary Point Tracking with Machine Learning to Measure Cardiac Strains in Tagged MRI.Functional imaging and modeling of the heart : ... International Workshop, FIMH ..., proceedings. FIMH (Conference) · 2021
    Article
  14. Fully-automated global and segmental strain analysis of DENSE cardiovascular magnetic resonance using deep learning for segmentation and phase unwrapping.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2021
    Article
  15. 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

6 authors.

Ilya A Verzhbinsky
Luigi E Perotti
Kevin Moulin
Tyler E Cork
Michael Loecher
Daniel B Ennis

Funding

Validating Cardiac MRI Biomarkers and Genotype-Phenotype Correlations for DMDR01HL131975 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ENNIS, DANIEL B · 2016 to 2019
$2.5M
A New Framework for Understanding the Mechanisms of Diastolic DysfunctionR01HL131823 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ENNIS, DANIEL B · 2017 to 2020
$2.3M
Predoctoral Training in Biomedical Imaging at Stanford UniversityT32EB009653 · NIBIB · STANFORD UNIVERSITY · PI BUTTS-PAULY, KIM · 2010 to 2019
$2.1M
Defining and Measuring Diastolic Myocardial Kinematics and StiffnessK25HL135408 · NHLBI · UNIVERSITY OF CENTRAL FLORIDA · PI PEROTTI, LUIGI EMANUELE · 2017 to 2019
$494k
NHLBI NIH HHS K25 HL135408NHLBI NIH HHS R01 HL131823NHLBI NIH HHS R01 HL131975NIBIB NIH HHS T32 EB009653
6 · The paper itself

Abstract

Changes in left ventricular (LV) aggregate cardiomyocyte orientation and deformation underlie cardiac function and dysfunction. As such, in vivo aggregate cardiomyocyte "myofiber" strain ( [Formula: see text]) has mechanistic significance, but currently there exists no established technique to measure in vivo [Formula: see text]. The objective of this work is to describe and validate a pipeline to compute in vivo [Formula: see text] from magnetic resonance imaging (MRI) data. Our pipeline integrates LV motion from multi-slice Displacement ENcoding with Stimulated Echoes (DENSE) MRI with in vivo LV microstructure from cardiac Diffusion Tensor Imaging (cDTI) data. The proposed pipeline is validated using an analytical deforming heart-like phantom. The phantom is used to evaluate 3D cardiac strains computed from a widely available, open-source DENSE Image Analysis Tool. Phantom evaluation showed that a DENSE MRI signal-to-noise ratio (SNR) ≥20 is required to compute [Formula: see text] with near-zero median strain bias and within a strain tolerance of 0.06. Circumferential and longitudinal strains are also accurately measured under the same SNR requirements, however, radial strain exhibits a median epicardial bias of -0.10 even in noise-free DENSE data. The validated framework is applied to experimental DENSE MRI and cDTI data acquired in eight ( N=8 ) healthy swine. The experimental study demonstrated that [Formula: see text] has decreased transmural variability compared to radial and circumferential strains. The spatial uniformity and mechanistic significance of in vivo [Formula: see text] make it a compelling candidate for characterization and early detection of cardiac dysfunction.

Indexed as

Myocytes, CardiacAnimalsCardiovascular DiseasesHeartHeart VentriclesImage Interpretation, Computer-AssistedImage Processing, Computer-AssistedMagnetic Resonance Imaging, CinePhantoms, ImagingSwine

Identifiers

PMID31398112
PMCPMC7325525

What OpenQuestion holds

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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.