Evidence map›Paper›PMID 33304928›Full record

ArticleFrontiers in cardiovascular medicine2020

Neural-Network-Based Diagnosis Using 3-Dimensional Myocardial Architecture and Deformation: Demonstration for the Differentiation of Hypertrophic Cardiomyopathy.

Alessandro Satriano, Yarmaghan Afzal, Muhammad Sarim Afzal, Ali Fatehi Hassanabad, Cody Wu, Steven Dykstra, Jacqueline Flewitt, Patricia Feuchter, Rosa Sandonato, Bobak Heydari and 7 more

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Fabry Disease and the Heart: A Comprehensive Review.International journal of molecular sciences · 2021
    Review
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

17 authors.

Alessandro SatrianoStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Yarmaghan AfzalStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Muhammad Sarim AfzalStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Ali Fatehi HassanabadDivision of Cardiology, School of Medicine, University of Calgary, Calgary, AB, Canada.
Cody WuStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Steven DykstraDivision of Cardiology, School of Medicine, University of Calgary, Calgary, AB, Canada.
Jacqueline FlewittStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Patricia FeuchterStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Rosa SandonatoStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Bobak HeydariStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Naeem MerchantStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Andrew G HowarthStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Carmen P LydellStephenson Cardiac Imaging Center, Calgary, AB, Canada.
Aneal KhanDepartment of Medical Genetics, University of Calgary, Calgary, AB, Canada.
Nowell M FineLibin Cardiovascular Institute of Alberta, Calgary, AB, Canada.
Russell GreinerDepartment of Computing Science, University of Alberta, Edmonton, AB, Canada.
James A WhiteStephenson Cardiac Imaging Center, Calgary, AB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diagnosis of cardiomyopathy states may benefit from machine-learning (ML) based approaches, particularly to distinguish those states with similar phenotypic characteristics. Three-dimensional myocardial deformation analysis (3D-MDA) has been validated to provide standardized descriptors of myocardial architecture and deformation, and may therefore offer appropriate features for the training of ML-based diagnostic tools. We aimed to assess the feasibility of automated disease diagnosis using a neural network trained using 3D-MDA to discriminate hypertrophic cardiomyopathy (HCM) from its mimic states: cardiac amyloidosis (CA), Anderson-Fabry disease (AFD), and hypertensive cardiomyopathy (HTNcm). 3D-MDA data from 163 patients (mean age 53.1 ± 14.8 years; 68 females) with left ventricular hypertrophy (LVH) of known etiology was provided. Source imaging data was from cardiac magnetic resonance (CMR). Clinical diagnoses were as follows: 85 HCM, 30 HTNcm, 30 AFD, and 18 CA. A fully-connected-layer feed-forward neural was trained to distinguish HCM vs. other mimic states. Diagnostic performance was compared to threshold-based assessments of volumetric and strain-based CMR markers, in addition to baseline clinical patient characteristics. Threshold-based measures provided modest performance, the greatest area under the curve (AUC) being 0.70. Global strain parameters exhibited reduced performance, with AUC under 0.64. A neural network trained exclusively from 3D-MDA data achieved an AUC of 0.94 (sensitivity 0.92, specificity 0.90) when performing the same task. This study demonstrates that ML-based diagnosis of cardiomyopathy states performed exclusively from 3D-MDA is feasible and can distinguish HCM from mimic disease states. These findings suggest strong potential for computer-assisted diagnosis in clinical practice.

Indexed as

cardiomyopathyhypertrophicmachine learningmagnetic resonanceneural networkstrain analysis

Identifiers

PMID33304928
PMCPMC7693650

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.