Potential and Uncertainties of RejectClass in Acute Kidney Graft Dysfunction: An Independent Validation Study

Author:

von Samson-Himmelstjerna Friedrich A.1,Kakavand Nassim1,Gleske Charlotte2,Schraml Florian2,Basta Agathe A.2,Braunisch Matthias C.2,Bräsen Jan H.3,Schmitz Jessica3,Kraus Daniel4,Weinmann-Menke Julia4,Zacharias Helena U.5,Vaulet Thibaut6,Naesens Maarten6,Krautter Markus7,Schwenger Vedat7,Esser Grit1,Kolbrink Benedikt1,Amann Kerstin8,Holzmann-Littig Christopher2,Echterdiek Fabian2,Kunzendorf Ulrich1,Renders Lutz2,Schulte Kevin1,Heemann Uwe2,

Affiliation:

1. Department of Nephrology and Hypertension, University Hospital Schleswig-Holstein—Campus Kiel, Kiel, Germany.

2. Department of Nephrology, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.

3. Nephropathology Unit, Department of Pathology, Hannover Medical School, Hannover, Germany.

4. Department of Nephrology, Department of Internal Medicine 1, University Medical Center Mainz, Mainz, Germany.

5. Peter L. Reichertz Institute for Medical Informatics of TU Braunschweig and Hannover Medical School, Hannover, Germany.

6. Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Leuven, Belgium.

7. Department of Nephrology, Transplant Center, Klinikum Stuttgart, Stuttgart, Germany.

8. Department of Nephropathology, University Hospital Erlangen, University of Erlangen-Nürnberg, Erlangen, Germany.

Abstract

Background. Kidney graft rejections are classified based on the Banff classification. The RejectClass algorithm, initially derived from a cohort comprising mostly protocol biopsies, identifies data-driven phenotypes of acute rejection and chronic pathology using Banff lesion scores. It also provides composite scores for inflammation activity and chronicity. This study independently evaluates the performance of RejectClass in a cohort consisting entirely of indication biopsies. Methods. We retrospectively applied RejectClass to 441 patients from the German TRABIO (TRAnsplant BIOpsies) cohort who had received indication biopsies. The primary endpoint was death-censored graft failure during 2 y of follow-up. Results. The application of RejectClass to our cohort demonstrated moderately comparable phenotypic features with the derivation cohort, and most clusters indicated an elevated risk of graft loss. However, the reproduction of all phenotypes and the associated risks of graft failure, as depicted in the original studies, was not fully accomplished. In contrast, adjusted Cox proportional hazards analyses substantiated that both the inflammation score and the chronicity score are independently associated with graft loss, exhibiting hazard ratios of 1.7 (95% confidence interval, 1.2-2.3; P = 0.002) and 2.2 (95% confidence interval, 1.8-2.6; P < 0.001), respectively, per 0.25-point increment (scale: 0.0–1.0). Conclusions. The composite inflammation and chronicity scores may already have direct utility in quantitatively assessing the disease stage. Further refinement and validation of RejectClass clusters are necessary to achieve more reliable and accurate phenotyping of rejection.

Funder

Chiesi GmbH

Stiftung Lebendspende

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation

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