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. 2021 Jan 13;6(3):813–816. doi: 10.1016/j.ekir.2020.12.028

Table 2.

Clinical and pathologic characteristics of the study population

Clinical and Pathologic Characteristics De novo GN (n = 46) Recurrent GN (n = 77) P value
Induction agenta
 Antithymocyte globulin 24/44 (54.6) 46/68 (67.7) 0.2
 Alemtuzumab 5/44 (11.4) 11/68 (16.2) 0.6
 Interleukin 2 receptor antagonists 15/44 (34.1) 10/68 (14.7) 0.02
Total HLA mismatch (0–6)b,c 4 (2, 5) 3 (2, 5) 0.2
DSAd
 Pre-KT DSAs 5/36 (13.9) 8/64 (12.5) >0.9
 DSAs at time of GN discovery 15/41 (36.6) 10/59 (17.0) 0.03
Glomerulonephritis at index biopsy
 Anti-GBM GN 0/46 (0) 1/77 (1) >0.9
 C3 glomerulopathy 0/46 (0) 9/77 (12) 0.03
 IgA nephropathy 11/46 (24) 46/77 (60) 0.0002
 Membranous nephropathy 8/46 (17) 14/77 (18) >0.9
 HCV-related GN 4/46 (9) 0/77 (0) 0.02
 Infection related GN 2/46 (4) 0/77 (0) 0.1
 ICGN-NOS 21/46 (46) 7/77 (9) <0.0001
 Graft outcomes
 Graft failure 11/46 (23.9) 21/77 (27.3) 0.8
 Time from KT to graft failure, yrc 7.9 (4.5, 12.7) 6.8 (4.9, 12.2) 0.9
 Time from GN discovery to graft failure, yrc 1.4 (0.2, 3.5) 1.2 (0.7, 2.6) 0.7
 Last creatinine if graft has not failedc 1.8 (1.3, 2.5) 1.7 (1.4 2.6) 0.8

Anti-GBM, anti–glomerular basement membrane; DSA, donor-specific antibody; GN, glomerulonephritis; HCV, hepatitis C virus; HLA, human leukocyte antigen; IGCN-NOS, immune complex–mediated glomerulonephritis not otherwise specified; KT, kidney transplant.

Unless otherwise noted, values are n (%).

HLA mismatch is calculated based on A, B, and DR antigens.

a

Induction agent is unknown in 2 subjects in the de novo group and in 9 subjects in the recurrent group. One patient in the recurrent group did not receive any induction therapy as the transplant was from a twin sibling.

b

HLA typing is missing in 2 patients in the de novo group and in 7 patients in the recurrent group.

c

Values are median (25th, 75th percentile).

d

DSAs at the time of transplant is missing in 10 patients in the de novo group and in 13 patients in the recurrent group. DSAs at the time of index biopsy is missing in 5 patients in the de novo group and in 18 patients in the recurrent group.