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. 2019 Jun 18;14(7):1056–1066. doi: 10.2215/CJN.13401118

Table 1.

Characteristics of patients with living and deceased kidney transplantation stratified according to presence and strength of DSA

Variable Living Donation, n=1324 Deceased Donation, n=2808
No DSA DSA <3000 MFI DSA ≥3000 MFI Missing Data, n No DSA DSA <3000 MFI DSA ≥3000 MFI Missing Data, n
Patient age, yr 46 (33–55) 49 (34–55) 46 (37–53) 0 56 (46–65) 54 (44–65) 55 (43–65) 0
Patient sex, women 439 (36) 29 (49) 23 (49) 0 977 (38) 71 (49) 62 (54) 0
Current % PRA 0 (0–0) 0 (0–0) 0 (0–28) 4 0 (0–0) 0 (0–24) 15 (0–73) 0
Highest % PRA 0 (0–0) 2 (0–19) 33 (1–82) 4 0 (0–6) 10 (0–79) 57 (10–95) 0
DSA strength, maximum MFI n.a. 1142 (680–1683) 6198 (4400–11,485) 0 n.a. 1177 (657–2000) 7400 (4357–12,057) 0
DSA strength, cumulative MFI n.a. 1200 (680–1807) 7900 (4579–13,700) 0 n.a. 1279 (774–2049) 9400 (5783–15,700) 0
DSA class, n (%) 0 0
 Class 1 only n. a. 29 (49) 16 (34) n. a. 85 (58) 54 (47)
 Class 2 only n. a. 25 (42) 18 (38) n. a. 46 (32) 25 (22)
 Class 1 and 2 n. a. 5 (8) 13 (28) n. a. 15 (10) 35 (30)
Retransplant, n (%) 64 (5) 11 (19) 10 (21) 0 252 (10) 43 (29) 47 (41) 0
Preemptive transplantation, n (%) 388 (32) 19 (32) 9 (19) 0 n.a. n.a. n.a. n.a.
Time on dialysis, yr 0 (0–1) 0 (0–1) 1 (0–2) 0 5 (3–8) 5 (3–8) 6 (3–9) 62
Donor age, yr 53 (47–60) 52 (45–58) 53 (47–57) 0 55 (44–66) 57 (48–66) 51 (34–63) 0
Donor sex, women 738 (61) 38 (64) 20 (43) 0 1201 (47) 77 (53) 54 (47) 0
Kidney Donor Risk Index (11) n. a. n. a. n. a. n. a. 1.3 (1.0–1.9) 1.4 (1.1–1.9) 1.3 (1.0–1.8) 484
Cold ischemic period, min 151 (120–180) 150 (120–180) 133 (117–183) 32 713 (527–900) 717 (495–920) 782 (531–977) 43
No. of mismatches for HLA-A/B/DR 3 (2–4) 4 (3–5) 4 (3–5) 133 3 (2–4) 3 (2–4) 3 (3–4) 1
Induction therapy, n (%) 164 255
 None 177 (17) 7 (13) 3 (6) 308 (13) 13 (9) 5 (4)
 ATG 62 (6) 8 (14) 11 (23) 410 (18) 41 (29) 48 (42)
 IL-2 671 (63) 29 (52) 16 (34) 1538 (67) 77 (54) 41 (36)
 CD20 15 (1) 0 (0) 4 (9) 2 (0) 1 (1) 0 (0)
 CD52 0 (0) 0 (0) 0 (0) 6 (0) 2 (1) 5 (4)
 IL-2 and CD20 119 (11) 11 (19) 7 (15) 6 (0) 3 (2) 2 (2)
 Further combinationa 13 (1) 1 (2) 6 (13) 27 (1) 5 (4) 13 (11)
Initial immunosuppression, n (%) 165 512
 CsA/MMF/steroids 141 (13) 3 (5) 1 (2) 508 (22) 21 (15) 6 (5)
 Tac/MMF/steroids 751 (71) 44 (79) 40 (85) 1434 (63) 104 (73) 87 (76)
 Other 164 (16) 9 (16) 6 (13) 354 (15) 17 (12) 21 (18)
Desensitization, n (%) 2 1
 No desensitization 915 (75) 36 (61) 26 (55) 2456 (96) 137 (94) 95 (83)
 ABO-incompatible transplantation 266 (22) 13 (22) 9 (19) 1 (0)b 0 (0) 0 (0)
 Other desensitization 35 (3) 10 (17) 12 (26) 89 (3) 9 (6) 20 (17)

Data are displayed as number of patients (%) or median (interquartile range). DSA, donor-specific HLA antibodies; MFI, medium fluorescence intensity; PRA, panel-reactive antibodies; n.a., not applicable; ATG, antithymocyte globulin; CD20, CD20 receptor antagonist (rituximab); CD52, CD52 receptor antagonist; CsA, cyclosporin A; MMF, mycophenolate mofetil; Tac, tacrolimus.

a

Ten living donation patients without DSA (one with DSA <3000 MFI and six with DSA ≥3000 MFI) received a further combined induction therapy including ATG, as well as 27 deceased donation patients without DSA (five with DSA <3000 MFI and 13 with DSA ≥3000 MFI); 12 living donation patients without DSA (one with DSA <3000 MFI and six with DSA ≥3000 MFI) received a further combined induction therapy including CD20, as well as 14 deceased donation patients without DSA (two with DSA <3000 MFI and nine with DSA ≥3000 MFI).

b

ABO-incompatible transplantation because of clerical error.