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Deep learning identified pathological abnormalities predictive of graft loss in kidney transplant biopsies.
Yi, Zhengzi; Salem, Fadi; Menon, Madhav C; Keung, Karen; Xi, Caixia; Hultin, Sebastian; Haroon Al Rasheed, M Rizwan; Li, Li; Su, Fei; Sun, Zeguo; Wei, Chengguo; Huang, Weiqing; Fredericks, Samuel; Lin, Qisheng; Banu, Khadija; Wong, Germaine; Rogers, Natasha M; Farouk, Samira; Cravedi, Paolo; Shingde, Meena; Smith, R Neal; Rosales, Ivy A; O'Connell, Philip J; Colvin, Robert B; Murphy, Barbara; Zhang, Weijia.
Afiliación
  • Yi Z; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Salem F; Pathology Division, Department of Molecular and Cell Based Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Menon MC; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA; Nephrology Division, Department of Medicine, Yale School of Medicine, New Haven, Connecticut, USA.
  • Keung K; Centre for Transplant and Renal Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia; Department of Nephrology, Prince of Wales Hospital, Sydney, New South Wales, Australia.
  • Xi C; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Hultin S; Centre for Transplant and Renal Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia.
  • Haroon Al Rasheed MR; Pathology Division, Department of Molecular and Cell Based Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Li L; Pathology Division, Department of Molecular and Cell Based Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Su F; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Sun Z; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Wei C; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Huang W; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Fredericks S; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Lin Q; Nephrology Division, Department of Medicine, Yale School of Medicine, New Haven, Connecticut, USA.
  • Banu K; Nephrology Division, Department of Medicine, Yale School of Medicine, New Haven, Connecticut, USA.
  • Wong G; Centre for Transplant and Renal Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia.
  • Rogers NM; Centre for Transplant and Renal Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia.
  • Farouk S; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Cravedi P; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Shingde M; Centre for Transplant and Renal Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia.
  • Smith RN; Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Pathology, Harvard Medical School, Boston, Massachusetts, USA.
  • Rosales IA; Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Pathology, Harvard Medical School, Boston, Massachusetts, USA.
  • O'Connell PJ; Centre for Transplant and Renal Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia; Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia; Department of Nephrology, Westmead Hospital, Sydney, New South Wales,
  • Colvin RB; Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Pathology, Harvard Medical School, Boston, Massachusetts, USA.
  • Murphy B; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Zhang W; Renal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA. Electronic address: weijia.zhang@mssm.edu.
Kidney Int ; 101(2): 288-298, 2022 02.
Article en En | MEDLINE | ID: mdl-34757124
Interstitial fibrosis, tubular atrophy, and inflammation are major contributors to kidney allograft failure. Here we sought an objective, quantitative pathological assessment of these lesions to improve predictive utility and constructed a deep-learning-based pipeline recognizing normal vs. abnormal kidney tissue compartments and mononuclear leukocyte infiltrates. Periodic acid- Schiff stained slides of transplant biopsies (60 training and 33 testing) were used to quantify pathological lesions specific for interstitium, tubules and mononuclear leukocyte infiltration. The pipeline was applied to the whole slide images from 789 transplant biopsies (478 baseline [pre-implantation] and 311 post-transplant 12-month protocol biopsies) in two independent cohorts (GoCAR: 404 patients, AUSCAD: 212 patients) of transplant recipients to correlate composite lesion features with graft loss. Our model accurately recognized kidney tissue compartments and mononuclear leukocytes. The digital features significantly correlated with revised Banff 2007 scores but were more sensitive to subtle pathological changes below the thresholds in the Banff scores. The Interstitial and Tubular Abnormality Score (ITAS) in baseline samples was highly predictive of one-year graft loss, while a Composite Damage Score in 12-month post-transplant protocol biopsies predicted later graft loss. ITASs and Composite Damage Scores outperformed Banff scores or clinical predictors with superior graft loss prediction accuracy. High/intermediate risk groups stratified by ITASs or Composite Damage Scores also demonstrated significantly higher incidence of estimated glomerular filtration rate decline and subsequent graft damage. Thus, our deep-learning approach accurately detected and quantified pathological lesions from baseline or post-transplant biopsies and demonstrated superior ability for prediction of post-transplant graft loss with potential application as a prevention, risk stratification or monitoring tool.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Aprendizaje Profundo Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Kidney Int Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Aprendizaje Profundo Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Kidney Int Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos