Literature DB >> 35101643

Clinical applicability of artificial intelligence for patients with an inherited heart disease: A scoping review.

Hidde Bleijendaal1, Philip M Croon2, Marinka D Oudkerk Pool3, Arjan Malekzadeh4, Simona Aufiero2, Ahmad S Amin5, Aeilko H Zwinderman6, Yigal M Pinto5, Arthur A M Wilde5, Michiel M Winter2.   

Abstract

The number of inherited heart disease (IHD) studies using artificial intelligence (AI) has increased rapidly over the last years. In this scoping review, we aimed to present an overview of the current literature available on the applicability of AI within the field of IHD. The literature search resulted in eighteen articles in which an AI model was trained and tested, mostly for diagnostic and predictive purposes. The areas under the receiver operating characteristic curves ranged from 0.78-0.96, but varied between IHD types, used methods and outcome measures. Only three out of eighteen did perform validation on an external dataset and most studies did not use explainable deep learning models. To be able to integrate AI as a tool to aid physicians in their diagnoses and clinical decisions within the IHD field, generalizability has to be better evaluated and explainability of DL models has to be increased.
Copyright © 2022. Published by Elsevier Inc.

Entities:  

Year:  2022        PMID: 35101643     DOI: 10.1016/j.tcm.2022.01.011

Source DB:  PubMed          Journal:  Trends Cardiovasc Med        ISSN: 1050-1738            Impact factor:   6.677


  2 in total

Review 1.  Application of non-negative matrix factorization in oncology: one approach for establishing precision medicine.

Authors:  Ryuji Hamamoto; Ken Takasawa; Hidenori Machino; Kazuma Kobayashi; Satoshi Takahashi; Amina Bolatkan; Norio Shinkai; Akira Sakai; Rina Aoyama; Masayoshi Yamada; Ken Asada; Masaaki Komatsu; Koji Okamoto; Hirokazu Kameoka; Syuzo Kaneko
Journal:  Brief Bioinform       Date:  2022-07-18       Impact factor: 13.994

2.  Homozygous Pro1066Arg MYBPC3 Pathogenic Variant in a 26Mb Region of Homozygosity Associated with Severe Hypertrophic Cardiomyopathy in a Patient of an Apparent Non-Consanguineous Family.

Authors:  Raquel Rodríguez-López; Javier García-Planells; Marina Martínez-Matilla; Cristian Pérez-García; Amor García Banacloy; Carola Guzmán Luján; Otilia Zomeño Alcalá; Joaquina Belchi Navarro; Juan Martínez-León; Rafael Salguero-Bodes
Journal:  Life (Basel)       Date:  2022-07-12
  2 in total

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