4.6 Article

Deep-Learning-Driven Quantification of Interstitial Fibrosis in Digitized Kidney Biopsies

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 191, Issue 8, Pages 1442-1453

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajpath.2021.05.005

Keywords

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Categories

Funding

  1. Karen Toffler Charitable Trust
  2. National Center for Advancing Translational Sciences grant
  3. NIH, through Boston University Clinical AMP
  4. Translational Science Institute (BU-CTSI) [1UL1TR001430]
  5. American Heart Association Strategically Focused Research Network Center [20SFRN35460031]
  6. Hariri Institute for Computing and Computational Science and Engineering at Boston University
  7. NIH [R01-AG06 2109, R21-CA253 498, R21-DK11974 0, R01-HL1323 25, R21-DK11975 1, U01-DK085 660]
  8. German Research Foundation (DFG) [BO3755/13, 454024652, 322900939]
  9. German Federal Ministries of Education and Research [STOP-FSGS-01GM1901A]
  10. Economic Affairs and Energy (EMPAIA)
  11. European Research Council (ERC) AIM.imaging.CKD [101001791]
  12. National Science Foundation [1838193, 1551572]
  13. DEEP LIVER [ZMVI1-2520DAT111]
  14. [17SDG33670323]
  15. Div Of Information & Intelligent Systems
  16. Direct For Computer & Info Scie & Enginr [1551572] Funding Source: National Science Foundation
  17. Div Of Information & Intelligent Systems
  18. Direct For Computer & Info Scie & Enginr [1838193] Funding Source: National Science Foundation
  19. European Research Council (ERC) [101001791] Funding Source: European Research Council (ERC)

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Interstitial fibrosis and tubular atrophy (IFTA) on renal biopsy are strong indicators of disease chronicity and prognosis. Developing a deep-learning framework to analyze trichrome-stained whole-slide images (WSIs) can provide accurate assessment of IFTA grade, assisting in clinicopathologic diagnosis.
Interstitial fibrosis and tubular atrophy (IFTA) on a renal biopsy are strong indicators of disease chronicity and prognosis. Techniques that are typically used for IFTA grading remain manual, leading to variability among pathologists. Accurate IFTA estimation using computational techniques can reduce this variability and provide quantitative assessment. Using trichrome-stained whole-slide images (WSIs) processed from human renal biopsies, we developed a deep-learning framework that captured finer pathologic structures at high resolution and overall context at the WSI level to predict IFTA grade. WSIs (n = 67) were obtained from The Ohio State University Wexner Medical Center. Five nephropathologists independently reviewed them and provided fibrosis scores that were converted to IFTA grades: <= 10% (none or minimal), 11% to 25% (mild), 26% to 50% (moderate), and >50% (severe). The model was developed by associating the WSIs with the IFTA grade determined by majority voting (reference estimate). Model performance was evaluated on WSIs (n = 28) obtained from the Kidney Precision Medicine Project. There was good agreement on the IFTA grading between the pathologists and the reference estimate (kappa = 0.622 +/- 0.071). The accuracy of the deep-learning model was 71.8%+/- 5.3% on The Ohio State University Wexner Medical Center and 65.0%+/- 4.2% on Kidney Precision Medicine Project data sets. Our approach to analyzing microscopic- and WSI-level changes in renal biopsies attempts to mimic the pathologist and provides a regional and contextual estimation of IFTA. Such methods can assist clinicopathologic diagnosis.

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