Deep learning-based segmentation of kidneys and renal cysts on T2-weighted MRI from patients with autosomal dominant polycystic kidney disease.


Journal

European radiology experimental
ISSN: 2509-9280
Titre abrégé: Eur Radiol Exp
Pays: England
ID NLM: 101721752

Informations de publication

Date de publication:
30 Oct 2024
Historique:
received: 24 05 2024
accepted: 19 09 2024
medline: 31 10 2024
pubmed: 31 10 2024
entrez: 31 10 2024
Statut: epublish

Résumé

Our aim was to train and test a deep learning-based algorithm for automatically segmenting kidneys and renal cysts in patients with autosomal dominant polycystic kidney disease (ADPKD). We retrospectively selected all ADPKD patients who underwent renal MRI with coronal T2-weighted imaging at our institution from 2008 to 2022. The 20 most recent examinations constituted the test dataset, to mimic pseudoprospective enrolment. The remaining ones constituted the training dataset to which eight normal renal MRIs were added. Kidneys and cysts ground truth segmentations were performed on coronal T2-weighted images by a junior radiologist supervised by an experienced radiologist. Kidneys and cysts of the 20 test MRIs were segmented by the algorithm and three independent human raters. Segmentations were compared using overlap metrics. The total kidney volume (TKV), total cystic volume (TCV), and cystic index (TCV divided by TKV) were compared using Bland-Altman analysis. We included 164 ADPKD patients. Dice similarity coefficients ranged from 85.9% to 87.4% between the algorithms and the raters' segmentations and from 84.2% to 86.2% across raters' segmentations. For TCV assessment, the biases ± standard deviations (SD) were 3-19 ± 137-151 mL between the algorithm and the raters, and 22-45 ± 49-57 mL across raters. The algorithm underestimated TKV and TCV in two outliers with TCV > 2800 mL. For cystic index assessment, the biases ± SD were 2.5-6.9% ± 6.7-8.3% between the algorithm and the raters, and 2.1-9.4 ± 7.4-11.6% across raters. The algorithm's performance fell within the range of inter-rater variability, but large TKV and TCV were underestimated. Accurate automated segmentation of the renal cysts will enable the large-scale evaluation of the prognostic value of TCV and cystic index in ADPKD patients. If these biomarkers are prognostic, then automated segmentation will facilitate their use in daily routine. Cystic volume is an emerging biomarker in ADPKD. The algorithm's performance in segmenting kidneys and cysts fell within interrater variability. The segmentation of very large cysts, under-represented in the training dataset, needs improvement.

Sections du résumé

BACKGROUND BACKGROUND
Our aim was to train and test a deep learning-based algorithm for automatically segmenting kidneys and renal cysts in patients with autosomal dominant polycystic kidney disease (ADPKD).
METHODS METHODS
We retrospectively selected all ADPKD patients who underwent renal MRI with coronal T2-weighted imaging at our institution from 2008 to 2022. The 20 most recent examinations constituted the test dataset, to mimic pseudoprospective enrolment. The remaining ones constituted the training dataset to which eight normal renal MRIs were added. Kidneys and cysts ground truth segmentations were performed on coronal T2-weighted images by a junior radiologist supervised by an experienced radiologist. Kidneys and cysts of the 20 test MRIs were segmented by the algorithm and three independent human raters. Segmentations were compared using overlap metrics. The total kidney volume (TKV), total cystic volume (TCV), and cystic index (TCV divided by TKV) were compared using Bland-Altman analysis.
RESULTS RESULTS
We included 164 ADPKD patients. Dice similarity coefficients ranged from 85.9% to 87.4% between the algorithms and the raters' segmentations and from 84.2% to 86.2% across raters' segmentations. For TCV assessment, the biases ± standard deviations (SD) were 3-19 ± 137-151 mL between the algorithm and the raters, and 22-45 ± 49-57 mL across raters. The algorithm underestimated TKV and TCV in two outliers with TCV > 2800 mL. For cystic index assessment, the biases ± SD were 2.5-6.9% ± 6.7-8.3% between the algorithm and the raters, and 2.1-9.4 ± 7.4-11.6% across raters.
CONCLUSION CONCLUSIONS
The algorithm's performance fell within the range of inter-rater variability, but large TKV and TCV were underestimated.
RELEVANCE STATEMENT CONCLUSIONS
Accurate automated segmentation of the renal cysts will enable the large-scale evaluation of the prognostic value of TCV and cystic index in ADPKD patients. If these biomarkers are prognostic, then automated segmentation will facilitate their use in daily routine.
KEY POINTS CONCLUSIONS
Cystic volume is an emerging biomarker in ADPKD. The algorithm's performance in segmenting kidneys and cysts fell within interrater variability. The segmentation of very large cysts, under-represented in the training dataset, needs improvement.

Identifiants

pubmed: 39477840
doi: 10.1186/s41747-024-00520-7
pii: 10.1186/s41747-024-00520-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Rémi Sore (R)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Pascal Cathier (P)

Medisys, Philips Research Paris, Paris, France.

Anna Sesilia Vlachomitrou (AS)

Philips France, Suresnes, France.

Jérôme Bailleux (J)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Karine Arnaud (K)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Laurent Juillard (L)

Service de Néphrologie, Dialyse et Exploration Fonctionnelle Rénale, Centre Référence Maladie Rénale Rare MAREGE, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Faculté de Médecine Lyon Est, Université Lyon 1, Université de Lyon, Lyon, France.

Sandrine Lemoine (S)

Service de Néphrologie, Dialyse et Exploration Fonctionnelle Rénale, Centre Référence Maladie Rénale Rare MAREGE, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Faculté de Médecine Lyon Est, Université Lyon 1, Université de Lyon, Lyon, France.

Olivier Rouvière (O)

Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France. olivier.rouviere@netcourrier.com.
Faculté de Médecine Lyon Est, Université Lyon 1, Université de Lyon, Lyon, France. olivier.rouviere@netcourrier.com.
LabTau, INSERM Unit, Lyon, France. olivier.rouviere@netcourrier.com.

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