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. 2024 Sep 16;40(2):491–503. doi: 10.1007/s00467-024-06487-2

Table 6.

Risk factor analysis for graft dysfunction (defined as graft loss, an eGFR < 30 mL/min·1.73 m2 or an eGFR decline ≥ 50% of baseline)

Risk factors for graft dysfunction Unadjusted HR (95% CI) p value Adjusted HR (95% CI) p value
Age at KTx, years 0.97 (0.93–1.02) 0.266
Male sex 1.14 (0.66–1.96) 0.640
 > 1 KTx 1.81 (0.91–3.58) 0.092
Living donation 1.44 (0.84–2.48) 0.189
Donor age, years2 1.02 (1.01–1.04) 0.005 1.02 (1.00–1.04) 0.007
Cold ischemia time 0.98 (0.94–1.02) 0.289
HLA-DR mismatch (0 versus 1 or 2) 1.09 (0.73–1.62) 0.685
Delayed graft function 1.19 (0.48–2.99) 0.710
Time from dialysis to KTx (> 21 months) 1.23 (0.72–2.09) 0.447
IL-2R antibody induction 0.67 (0.38–1.17) 0.161
Potential recurrent disease1 1.14 (0.51–2.51) 0.752
BKPyV nephropathy2,3 5.45 (2.46–12.1)  < 0.001 7.20 (3.15–16.5)  < 0.001
ABMR2,3 4.06 (2.13–7.73)  < 0.001 3.30 (1.72–6.33)  < 0.001
TCMR and treated borderline rejection2,3 2.59 (1.52–4.42) 0.001 2.48 (1.44–4.30) 0.001

ABMR antibody-mediated rejection, BKPyV BK polyomavirus, CI confidence interval, HLA human leukocyte antigen, HR hazard ratio, IL-2R interleukin 2 receptor, KTx kidney transplantation, TCMR T cell-mediated rejection

1Potentional recurrent disease included: atypical hemolytic uremic syndrome, non-genetic focal segmental glomerulosclerosis, type I and type II membranoproliferative glomerulonephritis, IgA nephropathy, membranous glomerulonephritis, primary hyperoxaluria, and ANCA-associated vasculitis

2Multivariable Cox regression model with time-variable covariables adjusted for center effect

3Histopathologic diagnoses were treated as time-dependent variables