Few-shot biomedical image segmentation using diffusion models: Beyond image generation.

Diffusion models Generative AI Orthopedics surgery Pelvis radiographs Semantic segmentation Synthetic data

Journal

Computer methods and programs in biomedicine
ISSN: 1872-7565
Titre abrégé: Comput Methods Programs Biomed
Pays: Ireland
ID NLM: 8506513

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 03 05 2023
revised: 12 09 2023
accepted: 25 09 2023
medline: 14 11 2023
pubmed: 2 10 2023
entrez: 1 10 2023
Statut: ppublish

Résumé

Medical image analysis pipelines often involve segmentation, which requires a large amount of annotated training data, which is time-consuming and costly. To address this issue, we proposed leveraging generative models to achieve few-shot image segmentation. We trained a denoising diffusion probabilistic model (DDPM) on 480,407 pelvis radiographs to generate 256 ✕ 256 px synthetic images. The DDPM was conditioned on demographic and radiologic characteristics and was rigorously validated by domain experts and objective image quality metrics (Frechet inception distance [FID] and inception score [IS]). For the next step, three landmarks (greater trochanter [GT], lesser trochanter [LT], and obturator foramen [OF]) were annotated on 45 real-patient radiographs; 25 for training and 20 for testing. To extract features, each image was passed through the pre-trained DDPM at three timesteps and for each pass, features from specific blocks were extracted. The features were concatenated with the real image to form an image with 4225 channels. The feature-set was broken into random patches, which were fed to a U-Net. Dice Similarity Coefficient (DSC) was used to compare the performance with a vanilla U-Net trained on radiographs. Expert accuracy was 57.5 % in determining real versus generated images, while the model reached an FID = 7.2 and IS = 210. The segmentation UNet trained on the 20 feature-sets achieved a DSC of 0.90, 0.84, and 0.61 for OF, GT, and LT segmentation, respectively, which was at least 0.30 points higher than the naively trained model. We demonstrated the applicability of DDPMs as feature extractors, facilitating medical image segmentation with few annotated samples.

Sections du résumé

BACKGROUND BACKGROUND
Medical image analysis pipelines often involve segmentation, which requires a large amount of annotated training data, which is time-consuming and costly. To address this issue, we proposed leveraging generative models to achieve few-shot image segmentation.
METHODS METHODS
We trained a denoising diffusion probabilistic model (DDPM) on 480,407 pelvis radiographs to generate 256 ✕ 256 px synthetic images. The DDPM was conditioned on demographic and radiologic characteristics and was rigorously validated by domain experts and objective image quality metrics (Frechet inception distance [FID] and inception score [IS]). For the next step, three landmarks (greater trochanter [GT], lesser trochanter [LT], and obturator foramen [OF]) were annotated on 45 real-patient radiographs; 25 for training and 20 for testing. To extract features, each image was passed through the pre-trained DDPM at three timesteps and for each pass, features from specific blocks were extracted. The features were concatenated with the real image to form an image with 4225 channels. The feature-set was broken into random patches, which were fed to a U-Net. Dice Similarity Coefficient (DSC) was used to compare the performance with a vanilla U-Net trained on radiographs.
RESULTS RESULTS
Expert accuracy was 57.5 % in determining real versus generated images, while the model reached an FID = 7.2 and IS = 210. The segmentation UNet trained on the 20 feature-sets achieved a DSC of 0.90, 0.84, and 0.61 for OF, GT, and LT segmentation, respectively, which was at least 0.30 points higher than the naively trained model.
CONCLUSION CONCLUSIONS
We demonstrated the applicability of DDPMs as feature extractors, facilitating medical image segmentation with few annotated samples.

Identifiants

pubmed: 37778140
pii: S0169-2607(23)00498-4
doi: 10.1016/j.cmpb.2023.107832
pii:
doi:

Substances chimiques

dihydroxydiphenyl-pyridyl methane R09078E41Y
Bisacodyl 10X0709Y6I

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107832

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no actual or potential conflict of interest.

Auteurs

Bardia Khosravi (B)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA; Department of Radiology, Mayo Clinic, Rochester, MN, USA.

Pouria Rouzrokh (P)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA; Department of Radiology, Mayo Clinic, Rochester, MN, USA.

John P Mickley (JP)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

Shahriar Faghani (S)

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

Kellen Mulford (K)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

Linjun Yang (L)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

A Noelle Larson (AN)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

Benjamin M Howe (BM)

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

Bradley J Erickson (BJ)

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

Michael J Taunton (MJ)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

Cody C Wyles (CC)

Department of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA; Department of Clinical Anatomy, Mayo Clinic, Rochester, MN, USA. Electronic address: Wyles.Cody@mayo.edu.

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