Re‐evaluation of glomerulitis using occlusion criteria based on the Banff 2013 revision: a retrospective study

Summary The presence of occlusion/near‐occlusion of glomerular capillaries was recently added to the existing definition of glomerulitis (g). We retrospectively re‐evaluated 135 renal allograft biopsies regarding g to ensure no antibody‐damaged grafts were missed. Previous and revised g scores (pg a...

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Veröffentlicht in:Transplant international 2017-06, Vol.30 (6), p.579-588
Hauptverfasser: Ozluk, Yasemin, Caliskan, Yasar, Sevinc, Mustafa, Bayram, Aysel, Arikan, Evsen A., Turkmen, Aydin, Akgul, Sebahat, Savran, Fatma O., Sever, Mehmet S., Kilicaslan, Isin
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Sprache:eng
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Zusammenfassung:Summary The presence of occlusion/near‐occlusion of glomerular capillaries was recently added to the existing definition of glomerulitis (g). We retrospectively re‐evaluated 135 renal allograft biopsies regarding g to ensure no antibody‐damaged grafts were missed. Previous and revised g scores (pg and rg, respectively) were compared for clinicopathologic correlations. The g score did not change in 100 (74.1%) biopsies. Thirty‐five (25.9%) biopsies were changed to a lower score. Sensitivity and specificity of pg and rg for the presence of donor‐specific antibodies (DSA) were 76% vs. 58% and 70% vs. 79%, respectively. Pg score indicated graft loss with 65% sensitivity and 63% specificity, whereas rg showed 46% sensitivity and 71% specificity. Area under the curve (AUC) values in ROC analysis for DSA and graft loss were as follows: pg, 0.773; rg, 0.693; and pg, 0.635; rg, 0.577, respectively. A comparison of the two AUC values revealed a significant difference between pg and rg only for DSA (P = 0.0076). Pg and post‐transplant time of biopsy independently predicted graft loss, whereas rg did not. In conclusion, revised g scores showed lesser sensitivity but higher specificity for DSA and graft loss. Recent definition of g missed antibody‐mediated rejection in few cases, and it was not an independent predictor for graft loss.
ISSN:0934-0874
1432-2277
DOI:10.1111/tri.12943