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. 2017 Aug 18;13:1043–1051. doi: 10.2147/TCRM.S142348

Table 3.

Demographic data of recipients using different immunosuppressant regimens

Demographic data TAC+MMF
(N=1,380)
CsA+MMF
(N=163)
CsA+TAC+MMF
(N=81)
p-value
Age 49.83 (±12.07) 27.04 (±24.01) 42.56 (±18.45) <0.0001*
Sex <0.0001*
 Female 375 (27.17%) 72 (44.17%) 25 (30.86%)
 Male 1,005 (72.83%) 91 (55.83%) 56 (69.14%)
Pre-transplant diseases
 Alcoholic hepatitis 280 (20.29%) 14 (8.59%) 11 (13.58%) 0.0007*
 Hepatitis B 762 (55.22%) 42 (25.77%) 29 (35.80%) <0.0001*
 Hepatitis C 286 (20.72%) 22 (13.5%) 23 (28.4%) 0.0177*
 Esophageal varices 735 (53.26%) 75 (46.01%) 36 (44.44%) 0.0793
 Ascites 699 (50.65%) 86 (52.76%) 40 (49.38%) 0.8488
 Liver cancer 690 (50.00%) 30 (18.40%) 31 (38.27%) <0.0001*
 Non-liver malignancy 33 (2.39%) 5 (3.07%) 2 (2.47%) 0.8705
 Hypertension 237 (17.17%) 12 (7.36%) 12 (14.81%) 0.0052*
 Coronary artery disease 88 (6.38%) 1 (0.61%) 3 (3.70%) 0.0079*
 Chronic renal failure 44 (3.19%) 4 (2.45%) 1 (1.24%) 0.5503
End point
 New-onset diabetes 127 (9.2%) 6 (3.68%) 23 (28.4%) <0.0001*

Notes: Considering pre-transplant comorbidities, liver transplant recipients of regimen TAC+MMF were of significantly older age, male sex, alcoholic hepatitis, hepatitis B, hepatitis C, liver cancer, hypertension, and coronary artery disease compared to regimen CsA+MMF. Regarding NODALT incidence, CsA+TAC+MMF regimen had the highest correlation while CsA+MMF regimen had the lowest risk. The values given for “Age” represent mean age (years) ± standard deviation;

*

p<0.05.

Abbreviations: NODALT, new-onset diabetes after liver transplantation; TAC, tacrolimus; MMF, mycophenolate mofetil; CsA, cyclosporine; DM, diabetes mellitus.