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Deep learning-based automated kidney and cyst segmentation of autosomal dominant polycystic kidney disease using single vs. multi-institutional data.
Schmidt, Emma K; Krishnan, Chetana; Onuoha, Ezinwanne; Gregory, Adriana V; Kline, Timothy L; Mrug, Michal; Cardenas, Carlos; Kim, Harrison.
Affiliation
  • Schmidt EK; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Krishnan C; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Onuoha E; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Gregory AV; Department of Radiology, Mayo Clinic, Rochester, MN 55902, USA.
  • Kline TL; Department of Radiology, Mayo Clinic, Rochester, MN 55902, USA.
  • Mrug M; Department of Veterans Affairs Medical Center, Birmingham, AL 35233, USA; Department of Nephrology, The University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Cardenas C; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL 35294, USA; Department of Radiation Oncology, The University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: cecarden@uab.edu.
  • Kim H; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL 35294, USA; Department of Radiology, The University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: Hyunkikim@uabmc.edu.
Clin Imaging ; 106: 110068, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38101228
ABSTRACT

PURPOSE:

This study aimed to investigate if a deep learning model trained with a single institution's data has comparable accuracy to that trained with multi-institutional data for segmenting kidney and cyst regions in magnetic resonance (MR) images of patients affected by autosomal dominant polycystic kidney disease (ADPKD).

METHODS:

We used TensorFlow with a Keras custom UNet on 2D slices of 756 MRI images of kidneys with ADPKD obtained from four institutions in the Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease (CRISP) study. The ground truth was determined via a manual plus global thresholding method. Five models were trained with 80 % of all institutional data (n = 604) and each institutional data (n = 232, 172, 148, or 52), respectively, and validated with 10 % and tested on an unseen 10 % of the data. The model's performance was evaluated using the Dice Similarity Coefficient (DSC).

RESULTS:

The DSCs by the model trained with all institutional data ranged from 0.92 to 0.95 for kidney image segmentation, only 1-2 % higher than those by the models trained with single institutional data (0.90-0.93).In cyst segmentation, however, the DSCs by the model trained with all institutional data ranged from 0.83 to 0.89, which were 2-20 % higher than those by the models trained with single institutional data (0.66-0.86).

CONCLUSION:

The UNet performance, when trained with a single institutional dataset, exhibited similar accuracy to the model trained on a multi-institutional dataset. Segmentation accuracy increases with models trained on larger sample sizes, especially in more complex cyst segmentation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycystic Kidney, Autosomal Dominant / Cysts / Deep Learning Limits: Humans Language: En Journal: Clin Imaging Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycystic Kidney, Autosomal Dominant / Cysts / Deep Learning Limits: Humans Language: En Journal: Clin Imaging Year: 2024 Document type: Article