Fairness in Cardiac Magnetic Resonance Imaging: Assessing Sex and Racial Bias in Deep Learning-Based Segmentation.

cardiac magnetic resonance deep learning fair AI inequality fairness in deep learning-based CMR segmentation segmentation

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 21 01 2022
accepted: 02 03 2022
entrez: 25 4 2022
pubmed: 26 4 2022
medline: 26 4 2022
Statut: epublish

Résumé

Artificial intelligence (AI) techniques have been proposed for automation of cine CMR segmentation for functional quantification. However, in other applications AI models have been shown to have potential for sex and/or racial bias. The objective of this paper is to perform the first analysis of sex/racial bias in AI-based cine CMR segmentation using a large-scale database. A state-of-the-art deep learning (DL) model was used for automatic segmentation of both ventricles and the myocardium from cine short-axis CMR. The dataset consisted of end-diastole and end-systole short-axis cine CMR images of 5,903 subjects from the UK Biobank database (61.5 ± 7.1 years, 52% male, 81% white). To assess sex and racial bias, we compared Dice scores and errors in measurements of biventricular volumes and function between patients grouped by race and sex. To investigate whether segmentation bias could be explained by potential confounders, a multivariate linear regression and ANCOVA were performed. Results on the overall population showed an excellent agreement between the manual and automatic segmentations. We found statistically significant differences in Dice scores between races (white ∼94% vs. minority ethnic groups 86-89%) as well as in absolute/relative errors in volumetric and functional measures, showing that the AI model was biased against minority racial groups, even after correction for possible confounders. The results of a multivariate linear regression analysis showed that no covariate could explain the Dice score bias between racial groups. However, for the Mixed and Black race groups, sex showed a weak positive association with the Dice score. The results of an ANCOVA analysis showed that race was the main factor that can explain the overall difference in Dice scores between racial groups. We have shown that racial bias can exist in DL-based cine CMR segmentation models when training with a database that is sex-balanced but not race-balanced such as the UK Biobank.

Sections du résumé

Background UNASSIGNED
Artificial intelligence (AI) techniques have been proposed for automation of cine CMR segmentation for functional quantification. However, in other applications AI models have been shown to have potential for sex and/or racial bias. The objective of this paper is to perform the first analysis of sex/racial bias in AI-based cine CMR segmentation using a large-scale database.
Methods UNASSIGNED
A state-of-the-art deep learning (DL) model was used for automatic segmentation of both ventricles and the myocardium from cine short-axis CMR. The dataset consisted of end-diastole and end-systole short-axis cine CMR images of 5,903 subjects from the UK Biobank database (61.5 ± 7.1 years, 52% male, 81% white). To assess sex and racial bias, we compared Dice scores and errors in measurements of biventricular volumes and function between patients grouped by race and sex. To investigate whether segmentation bias could be explained by potential confounders, a multivariate linear regression and ANCOVA were performed.
Results UNASSIGNED
Results on the overall population showed an excellent agreement between the manual and automatic segmentations. We found statistically significant differences in Dice scores between races (white ∼94% vs. minority ethnic groups 86-89%) as well as in absolute/relative errors in volumetric and functional measures, showing that the AI model was biased against minority racial groups, even after correction for possible confounders. The results of a multivariate linear regression analysis showed that no covariate could explain the Dice score bias between racial groups. However, for the Mixed and Black race groups, sex showed a weak positive association with the Dice score. The results of an ANCOVA analysis showed that race was the main factor that can explain the overall difference in Dice scores between racial groups.
Conclusion UNASSIGNED
We have shown that racial bias can exist in DL-based cine CMR segmentation models when training with a database that is sex-balanced but not race-balanced such as the UK Biobank.

Identifiants

pubmed: 35463778
doi: 10.3389/fcvm.2022.859310
pmc: PMC9021445
doi:

Types de publication

Journal Article

Langues

eng

Pagination

859310

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_17228
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_QA137853
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M016560/1
Pays : United Kingdom

Informations de copyright

Copyright © 2022 Puyol-Antón, Ruijsink, Mariscal Harana, Piechnik, Neubauer, Petersen, Razavi, Chowienczyk and King.

Déclaration de conflit d'intérêts

SEP provided consultancy to and is shareholder of Circle Cardiovascular Imaging, Inc., Calgary, Alberta, Canada. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Esther Puyol-Antón (E)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.

Bram Ruijsink (B)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Department of Adult and Paediatric Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Division of Heart and Lungs, Department of Cardiology, University Medical Centre Utrecht, Utrecht, Netherlands.

Jorge Mariscal Harana (J)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.

Stefan K Piechnik (SK)

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.

Stefan Neubauer (S)

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.

Steffen E Petersen (SE)

National Institute for Health Research (NIHR) Barts Biomedical Research Centre, William Harvey Research Institute, Queen Mary University London, London, United Kingdom.
Barts Heart Centre, St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.
Health Data Research UK, London, United Kingdom.
Alan Turing Institute, London, United Kingdom.

Reza Razavi (R)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Department of Adult and Paediatric Cardiology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

Phil Chowienczyk (P)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
British Heart Foundation Centre, King's College London, London, United Kingdom.

Andrew P King (AP)

School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.

Classifications MeSH