With improvements in the practice of transplantation and the introduction o
f new immunosuppressive medications, there has been a substantial increase
in 1-year allograft survival rates. Consequently, the pool of potential can
didates for organ transplants continues to grow and a greater preponderance
of older patients with more comorbidities are undergoing transplantation.
As a result, there is interest in such medical complications as posttranspl
antation diabetes mellitus (PTDM) that develop after the transplantation of
a successful allograft. PTDM is an undesirable consequence of transplantat
ion because of its associated morbidity and impairment of both patient and
graft survival. Although some controversy exists, it is likely that glucose
intolerance after transplantation results in both macrovascular and microv
ascular disease, and there is an increasing risk for infectious and cardiov
ascular diseases, to which transplant recipients are already at increased s
usceptibility. Both experimental and clinical observations have shown that
immunosuppressive agents currently used in transplantation account for a la
rge degree of the increased risk for PTDM. Consequently, improved understan
ding of the effects of currently used immunosuppressive medicines on glycem
ic tolerance is of interest in clinical transplantation. (C) 1999 by the Na
tional Kidney Foundation, Inc.