Skip to main content
. 2023 Mar 3;58(6):639–646. doi: 10.1038/s41409-023-01944-2

Table 2.

Characteristics and outcomes according to recipient quantitative anti-CMV IgG value.

CMV seropositive recipients Group A: anti-CMV IgG ≥250 AU/ml Group B: anti-CMV IgG 6–249 AU/ml Group C: anti-CMV IgG 0–5 AU/ml p value Post-hoc p value A/B Post-hoc p value A/C Post-hoc p value B/C
n (%) 58 (13.18) 208 (47.27) 174 (39.55)
Age in years ± SD 53.8 ± 12.8 50.5 ± 14.2 46.7 ± 13.5 0.001 0.122 0.001 0.007
Female, n (%) 27 (46.55) 93 (44.71) 65 (37.36) 0.264
Donor CMV seropositive, n (%) 36 (62.07) 136 (65.38) 41 (23.56) <0.001 0.755 <0.001 <0.001
Conditioning, n (%) 0.993
 MAC 11 (18.97) 41 (19.71) 34 (19.54)
 NMA 3 (5.17) 8 (3.85) 8 (4.60)
 RIC 44 (75.86) 159 (76.44) 132 (75.86)
Disease risk, n (%)
 Low 11 (19.30) 31 (15.12) 20 (11.49)
 Intermediate 22 (38.60) 105 (51.22) 84 (48.28) 0.149
 High 21 (36.84) 48 (23.41) 57 (32.76)
 Very high 3 (5.26) 21 (10.24) 13 (7.47)
Optimal match vs. mismatch, n (%) 41 (70.69) 156 (75.00) 135 (77.59) 0.560
CMV infection event, n (%) <0.001  0.036  <0.001  <0.001
 No infection 5 (8.62) 47 (22.60) 160 (91.95)
 subCMVi 14 (24.14) 54 (25.96) 6 (3.45)
 csCMVi 39 (67.24) 107 (51.44) 8 (4.60)
CMV peak viral load in IU/ml (IQR) 3840.0 (1370.0–10900.0) 3440.0 (1190.0–9870.0) 1795.0 (364.8–7390.0) 0.551
Days of CMV reactivation (IQR) 78.5 (33.2–147.0) 88.0 (38.0–161.0) 12.5 (7.0–119.8) 0.018 0.400 0.042 0.017
Days between TX and CMV reactivation (IQR) 39.0 (25.0–52.5) 30.5 (24.0–42.0) 47.0 (37.0–116.0) 0.031 0.150 0.195 0.072
Death, n (%) 43 (74.14) 98 (47.34) 93 (53.76) 0.001 0.002 0.015 0.253

MAC myeloablative conditioning, NMA non-myeloablative, RIC reduced intensityconditioning, subCMVi subclinical infection, csCMVi clinically significantinfection, IQR interquartile range.