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Dynamic prediction of renal survival among deeply phenotyped kidney transplant recipients using artificial intelligence: an observational, international, multicohort study

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  • معلومة اضافية
    • Contributors:
      Paris-Centre de Recherche Cardiovasculaire (PARCC (UMR_S 970/ U970)); Hôpital Européen Georges Pompidou APHP (HEGP); Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité); Hôpital Necker - Enfants Malades AP-HP; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP); University of Pennsylvania; Centre Hospitalier Universitaire de Toulouse (CHU Toulouse); Université Toulouse III - Paul Sabatier (UT3); Université de Toulouse (UT); Hôpital Bretonneau; Centre Hospitalier Régional Universitaire de Tours (CHRU Tours); Service de Néphrologie CHRU Nancy; Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy); Université de Lorraine (UL); Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier); Cellules Souches, Plasticité Cellulaire, Médecine Régénératrice et Immunothérapies (IRMB); Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM); Hôpital Foch Suresnes; University of Zagreb; University Hospital Centre Zagreb; Partenaires INRAE; IMIM-Hospital del Mar; Generalitat de Catalunya; Universidade Federal de São Paulo; Universidade de São Paulo = University of São Paulo (USP); Albert Einstein College of Medicine New York; Cedars-Sinai Medical Center; Mayo Clinic Rochester; New York University Langone Medical Center (NYU Langone Medical Center); NYU System (NYU); Medizinische Universität Wien = Medical University of Vienna; Johns Hopkins University School of Medicine Baltimore; Northwestern University Feinberg School of Medicine; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO); Hopital Saint-Louis AP-HP (AP-HP)
    • بيانات النشر:
      HAL CCSD
      Elsevier
    • الموضوع:
      2021
    • Collection:
      Archive ouverte HAL (Hyper Article en Ligne, CCSD - Centre pour la Communication Scientifique Directe)
    • نبذة مختصرة :
      International audience ; Background: Kidney allograft failure is a common cause of end-stage renal disease. We aimed to develop a dynamic artificial intelligence approach to enhance risk stratification for kidney transplant recipients by generating continuously refined predictions of survival using updates of clinical data.Methods: In this observational study, we used data from adult recipients of kidney transplants from 18 academic transplant centres in Europe, the USA, and South America, and a cohort of patients from six randomised controlled trials. The development cohort comprised patients from four centres in France, with all other patients included in external validation cohorts. To build deeply phenotyped cohorts of transplant recipients, the following data were collected in the development cohort: clinical, histological, immunological variables, and repeated measurements of estimated glomerular filtration rate (eGFR) and proteinuria (measured using the proteinuria to creatininuria ratio). To develop a dynamic prediction system based on these clinical assessments and repeated measurements, we used a Bayesian joint models-an artificial intelligence approach. The prediction performances of the model were assessed via discrimination, through calculation of the area under the receiver operator curve (AUC), and calibration. This study is registered with ClinicalTrials.gov, NCT04258891.Findings: 13 608 patients were included (3774 in the development cohort and 9834 in the external validation cohorts) and contributed 89 328 patient-years of data, and 416 510 eGFR and proteinuria measurements. Bayesian joint models showed that recipient immunological profile, allograft interstitial fibrosis and tubular atrophy, allograft inflammation, and repeated measurements of eGFR and proteinuria were independent risk factors for allograft survival. The final model showed accurate calibration and very high discrimination in the development cohort (overall dynamic AUC 0·857 [95% CI 0·847-0·866]) with a persistent improvement ...
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/34756569; hal-03645221; https://hal.umontpellier.fr/hal-03645221; https://hal.umontpellier.fr/hal-03645221/document; https://hal.umontpellier.fr/hal-03645221/file/1-s2.0-S2589750021002090-main.pdf; PUBMED: 34756569
    • الرقم المعرف:
      10.1016/S2589-7500(21)00209-0
    • Rights:
      http://creativecommons.org/licenses/by-nc-nd/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.A74772EF