Background. Acute rejection (AR) is a strong predictor of renal allograft s
urvival. Recent advances in immunosuppression have reduced considerably the
incidence of AR. Still, approximately 25% of patients have AR early post-t
ransplant, and the factors that predispose to AR have not been fully clarif
ied.
Methods. The study includes 1641 adults, recipients of first cadaveric (CAD
, N = 1195) or living related renal grafts (LRD, N = 446), transplanted in
one institution. The variables associated with the occurrence of AR during
the first year posttransplant were identified.
Results. By univariate analyses, AR was associated with the following varia
bles: younger (P < 0.001); heavier (P = 0.003); and African American recipi
ents (P = 0.002); CAD transplants (P = 0.001); higher number of HLA mismatc
hes (P = 0.001); delayed graft function (DGF, P = 0.001); higher levels of
serum creatinine post-transplant (P = 0.003); and higher levels of systolic
and/or diastolic blood pressure (BP) post-transplant (P < 0.001). Higher B
P levels were also associated with earlier AR episodes (P < 0.0001). By mul
tivariable analysis AR was significantly associated with recipient age, num
ber of HLA mismatches, DGF, pre-PRA and systolic BP. Analysis of BP measure
d weekly post-transplant indicated that elevated BP levels, even three week
s prior to the AR episode, were significantly associated with AR. For every
level of BP, the use of BP medications was associated with a lower inciden
ce of AR (P < 0.0001). Furthermore, the use of calcium channel blockers was
also associated with lower incidence of AR (P = 0.001). Of note, 81% of re
cipients whose BP increased after the transplant had AR. In contrast, 22% o
f patients whose BP declined post-transplant had AR.
Conclusions. Elevated BP levels post-transplant identify patients at high r
isk of AR independently of graft function. Treatment of BP and reduction of
BP levels appears to be associated with a decreased risk of AR. We hypothe
size that high BP may be an indicator of a particular type of allograft dam
age, perhaps ischemic, that may predispose to AR.