Evaluation of the Modified Oxford Score in Recurrent IgA Nephropathy in North American Kidney Transplant Recipients: The Banff Recurrent Glomerulonephritis Working Group Report

Author:

Alachkar Nada1,Delsante Marco2,Greenberg Ross S.1,Koirala Abbal3,Alhamad Tarek4,Abdalla Basmah5,Anand Manish6,Boonpheng Ben3,Blosser Christopher3,Maggiore Umberto2,Bagnasco Serena M.7

Affiliation:

1. Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD.

2. Department of Medicine and Surgery, University of Parma, Parma, Italy.

3. Department of Medicine, University of Washington, Seattle, WA.

4. Department of Medicine, Washington University, St Louis, MO.

5. Department of Medicine, University of California, Los Angeles, Los Angeles, CA.

6. Department of Medicine, Division of Nephrology, University of Cincinnati, Cincinnati, OH.

7. Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD.

Abstract

Background. The modified Oxford classification mesangial and endocapillary hypercellularity, segmental sclerosis, interstitial fibrosis/tubular atrophy, and the presence of crescents (MEST-C) of immunoglobulin A nephropathy (IgAN) was recently shown to be a predictor of graft failure in Asians with recurrent IgAN. We aimed to validate these findings in a cohort from North American centers participating in the Banff Recurrent Glomerulopathies Working Group. Methods. We examined 171 transplant recipients with end-stage kidney disease because of IgAN; 100 of them with biopsy-proven recurrent IgAN (57 of them had complete MEST-C scores) and 71 with no recurrence. Results. IgAN recurrence, which was associated with younger age at transplantation (P = 0.012), strongly increased the risk of death-censored graft failure (adjusted hazard ratio, 5.10 [95% confidence interval (CI), 2.26-11.51]; P < 0.001). Higher MEST-C score sum was associated with death-censored graft failure (adjusted hazard ratio, 8.57 [95% CI, 1.23-59.85; P = 0.03] and 61.32 [95% CI, 4.82-779.89; P = 0.002] for score sums 2–3 and 4–5 versus 0, respectively), and so were the single components endocapillary hypercellularity, interstitial fibrosis/tubular atrophy, and crescents (P < 0.05 each). Overall, most of the pooled adjusted hazard ratio estimates associated with each MEST-C component were consistent with those from the Asian cohort (heterogeneity I 2 close to 0%, and P > 0.05). Conclusions. Our findings may validate the prognostic usefulness of the Oxford classification for recurrent IgAN and support the inclusion of the MEST-C score in allograft biopsies diagnostic reports.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation

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