Skip to main content
. 2021 Sep 24;2(1):42–53. doi: 10.1159/000519834

Table 2.

Univariable and multivariable analyses of the associations with recurrent disease in patients with kidney failure secondary to IgAN

Variable Univariable (n = 282)
Multivariable (n = 267), N events = 69
N events HR (95% CI) p value aHR (95% CI) p value
Recipient age at transplant, per each year 80 0.96 (0.94–0.98) <0.001 0.96 (0.94–0.98) 0.001
Recipient, female gender 80 1.16 (0.73–1.85) 0.52
Recipient, European ancestry 79 1.39 (0.86–2.25) 0.18
Donor, European ancestry 62 1.09 (0.62–1.93) 0.77
Allograft source 80
 Deceased donor Ref
 Living-related 1.29 (0.80–2.11) 0.3
 Living-unrelated 1.16 (0.62–2.19) 0.64
Medical sites 80
 CUIMC Ref Ref
 OHSU 1.36 (0.83–2.22) 0.23 1.06 (0.56–2.02) 0.86
 HUC 0.70 (0.31–1.55) 0.37 0.59 (0.25–1.37) 0.22
Year of transplantation 80 1.05 (1.00–1.08) 0.06 1.08 (1.02–1.14) 0.006
# HLA matches (per antigen: 0–6) 80 1.15 (1.02–1.30) 0.02 1.12 (0.98–1.29) 0.11
Induction with thymoglobulin1 69 0.65 (0.40–1.06) 0.08 0.65 (0.36–1.15) 0.14
Steroid-free regimens 80 0.77 (0.48–1.24) 0.28
Acute rejection* 80 0.90 (0.55–1.46) 0.66
Recipient HLA-B35 80 1.40 (0.87–2.27) 0.17
Recipient HLA-DQ5 71 1.00 (0.61–1.64) 0.99
Recipient HLA-DR3 (DR17 or 18) 80 1.20 (0.65–2.23) 0.56
Recipient HLA-DR15 80 0.99 (0.56–1.78) 0.98
Recipient HLA-DQ6 71 1.04 (0.62–1.75) 0.89
Recipient HLA-DQ2 71 1.09 (0.66–1.80) 0.74
Donor HLA-B35 80 1.09 (0.63–1.89) 0.77
Donor HLA-DQ5 66 1.24 (0.75–2.04) 0.41
Donor HLA-DR3 (DR17 or 18) 80 1.38 (0.80–2.40) 0.25
Donor HLA-DR15 80 0.77 (0.44–1.36) 0.37
Donor HLA-DQ6 66 0.88 (0.54–1.46) 0.63
Donor HLA-DQ2 66 0.90 (0.53–1.53) 0.7
Pretransplant DSA 76 1.25 (0.46–3.43) 0.7

CUIMC, Columbia University Irving Medical center; DSA, donor-specific antibodies; OHSU, Oregon Health & Science University; HUC, Hospitais da Universidade de Coimbra; DSA, donor-specific autoantibodies; IgAN, IgA nephropathy; HLA, human leukocyte antigen.

*

Acute rejection is defined as any episode of acute rejection that occurred before recurrence of disease in recurrent IgAN or any time before the end of follow-up in nonrecurring controls.

1

Even when induction therapy with thymoglobulin was not included in the main multivariable analysis (information on induction therapy was lacking 15 patients, including 11 with recurrent IgAN), the new multivariable analysis (n = 282) revealed similarly that only younger age at transplant (0.96 [0.94–0.98], p < 0.001) and year of transplantation (1.10 [1.04–1.15], p < 0.001) remained independent predictors for IgAN but not HLA matches (1.13 [0.99–1.29], p = 0.06) or medical sites (OHSU: 1.38 [0.83–2.29], p = 0.21, HUC: 0.65 [0.29–1.45], p = 0.29).