TY - JOUR
T1 - Posttransplant diabetes mellitus and acute rejection
T2 - Impact on kidney transplant outcome
AU - Matas, Arthur J.
AU - Gillingham, Kristen J.
AU - Humar, Abhinav
AU - Ibrahim, Hassan N.
AU - Payne, William D.
AU - Gruessner, Rainer W.G.
AU - Dunn, Ty B.
AU - Sutherland, David E.R.
AU - Najarian, John S.
AU - Kandaswamy, Raja
PY - 2008/2
Y1 - 2008/2
N2 - BACKGROUND. The benefits (e.g., low acute rejection [AR] rate) vs. the long-term risk of each immunosuppressive protocol may determine the protocol's value. METHODS. We studied the long-term impact of new-onset posttransplant diabetes (PTDM) and/or AR in 1,487 adult, primary transplant, nondiabetic recipients. Per Cox regression, donor source, AR, and PTDM were independent risk factors for graft loss (each, p<.0001). Recipients were subdivided by donor source and into these 4 groups: no AR, no PTDM [n=857]; no AR, PTDM [n=134]; ≥1 AR, no PTDM [n=403]; ≥1 AR, PTDM [n=93]. RESULTS. There was a significant difference between groups in 15-yr actuarial graft survival (GS) and death-censored (DC) GS (p<.0001). Importantly, ≥1 AR had more impact on 15-yr GS and DC GS than did PTDM; the worst outcome was for those having both AR and PTDM. In separate analyses, we censored those with >1 AR; and then only compared those developing AR or PTDM in the first year. The results were similar-the AR (no PTDM) group did worse than the PTDM (no AR) group (p<.001). CONCLUSIONS. Determining long-term risks associated with immunosuppressive protocols is important for treating future patients. Our data suggests that 15-year actuarial outcome (GS and DC GS) is worse for those developing AR than for those developing PTDM.
AB - BACKGROUND. The benefits (e.g., low acute rejection [AR] rate) vs. the long-term risk of each immunosuppressive protocol may determine the protocol's value. METHODS. We studied the long-term impact of new-onset posttransplant diabetes (PTDM) and/or AR in 1,487 adult, primary transplant, nondiabetic recipients. Per Cox regression, donor source, AR, and PTDM were independent risk factors for graft loss (each, p<.0001). Recipients were subdivided by donor source and into these 4 groups: no AR, no PTDM [n=857]; no AR, PTDM [n=134]; ≥1 AR, no PTDM [n=403]; ≥1 AR, PTDM [n=93]. RESULTS. There was a significant difference between groups in 15-yr actuarial graft survival (GS) and death-censored (DC) GS (p<.0001). Importantly, ≥1 AR had more impact on 15-yr GS and DC GS than did PTDM; the worst outcome was for those having both AR and PTDM. In separate analyses, we censored those with >1 AR; and then only compared those developing AR or PTDM in the first year. The results were similar-the AR (no PTDM) group did worse than the PTDM (no AR) group (p<.001). CONCLUSIONS. Determining long-term risks associated with immunosuppressive protocols is important for treating future patients. Our data suggests that 15-year actuarial outcome (GS and DC GS) is worse for those developing AR than for those developing PTDM.
KW - Acute rejection
KW - Diabetes mellitus
KW - Kidney transplant
UR - http://www.scopus.com/inward/record.url?scp=40049083710&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=40049083710&partnerID=8YFLogxK
U2 - 10.1097/TP.0b013e318160ee42
DO - 10.1097/TP.0b013e318160ee42
M3 - Article
C2 - 18301329
SN - 0041-1337
VL - 85
SP - 338
EP - 343
JO - Transplantation
JF - Transplantation
IS - 3
ER -