Evidence map›Paper›PMID 38724564›Full record

ArticleScientific reports2024

A novel multi-task machine learning classifier for rare disease patterning using cardiac strain imaging data.

Nanda K Siva, Yashbir Singh, Quincy A Hathaway, Partho P Sengupta, Naveena Yanamala

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Nanda K SivaSchool of Medicine, West Virginia University, Morgantown, WV, USA.
Yashbir SinghDivision of Cardiology, Heart and Vascular Institute, West Virginia University, Morgantown, WV, USA.
Quincy A HathawaySchool of Medicine, West Virginia University, Morgantown, WV, USA.
Partho P SenguptaDivision of Cardiovascular Disease and Hypertension, Rutgers Robert Wood Johnson Medical School, 125 Patterson St, New Brunswick, NJ, 08901, USA. partho.sengupta@rutgers.edu.
Naveena YanamalaDivision of Cardiovascular Disease and Hypertension, Rutgers Robert Wood Johnson Medical School, 125 Patterson St, New Brunswick, NJ, 08901, USA. ny128@rwjms.rutgers.edu.

Funding

American Heart Association-American Stroke Association 17PRE33660333/QAH/2017 (QAH)
6 · The paper itself

Abstract

To provide accurate predictions, current machine learning-based solutions require large, manually labeled training datasets. We implement persistent homology (PH), a topological tool for studying the pattern of data, to analyze echocardiography-based strain data and differentiate between rare diseases like constrictive pericarditis (CP) and restrictive cardiomyopathy (RCM). Patient population (retrospectively registered) included those presenting with heart failure due to CP (n = 51), RCM (n = 47), and patients without heart failure symptoms (n = 53). Longitudinal, radial, and circumferential strains/strain rates for left ventricular segments were processed into topological feature vectors using Machine learning PH workflow. In differentiating CP and RCM, the PH workflow model had a ROC AUC of 0.94 (Sensitivity = 92%, Specificity = 81%), compared with the GLS model AUC of 0.69 (Sensitivity = 65%, Specificity = 66%). In differentiating between all three conditions, the PH workflow model had an AUC of 0.83 (Sensitivity = 68%, Specificity = 84%), compared with the GLS model AUC of 0.68 (Sensitivity = 52% and Specificity = 76%). By employing persistent homology to differentiate the "pattern" of cardiac deformations, our machine-learning approach provides reasonable accuracy when evaluating small datasets and aids in understanding and visualizing patterns of cardiac imaging data in clinically challenging disease states.

Indexed as

EchocardiographyMachine LearningAdultAgedCardiomyopathy, RestrictiveFemaleHeart FailureHeart VentriclesHumansMaleMiddle AgedPericarditis, ConstrictiveRare DiseasesRetrospective StudiesConstrictive pericarditisEchocardiographyMachine learningRare diseaseRestrictive cardiomyopathy

Identifiers

PMID38724564
PMCPMC11082231

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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.