Reduced incidence of new-onset posttransplantation diabetes mellitus during the last decade

被引:57
|
作者
Valderhaug, Tone Gretland
Hjelmesaeth, Joran
Rollag, Halvor
Leivestad, Torbjorn
Roislien, Jo
Jenssen, Trond
Hartmann, Anders
机构
[1] Hosp Buskerud, Dept Med, Drammen, Norway
[2] Hosp Vestfold, Morbid Obes Ctr, Tonsberg, Norway
[3] Univ Oslo, Rikshosp, Inst Microbiol, N-0027 Oslo, Norway
[4] Univ Oslo, Rikshosp, Dept Med, N-0027 Oslo, Norway
[5] Univ Oslo, Rikshosp, Inst Immunol, N-0027 Oslo, Norway
[6] Univ Oslo, Inst Basic Med Sci, Dept Biostat, Oslo, Norway
[7] Univ Tromso, Inst Clin Med, N-9001 Tromso, Norway
关键词
posttransplantation diabetes mellitus; cytomegalovirus; immunosuppression;
D O I
10.1097/01.tp.0000287191.45032.38
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. A previous study (1995-1996) of 173 nondiabetic renal transplant recipients (historical cohort; HQ revealed a 20% incidence of new-onset posttransplantation diabetes mellitus (PTDM) and 32% with impaired glucose tolerance (IGT) or impaired fasting glucose (IFG). We examined whether glucose tolerance has improved after recent changes in our immunosuppressive protocol and a switch from deferred to preemptive cytomegalovirus (CMV) therapy. Methods. A total of 321 consecutive, nondiabetic patients (new cohort; NC were examined 10 weeks after kidney transplantation with an oral glucose tolerance test (n=301) between January 2004 and December 2005. Results. Although recipients in the NC were on average 3 years older [mean (SD): 50.3 (14.6) vs. 47.4 (16.0), P=0.0381 and had a higher mean body mass index [24.5 (3.6) vs. 23.5 (3.8) kg/M-2, P=0.003], a significantly lower incidence of both PTDM (13%) and IGT/IFG (18%) was observed in the NC (P<0.001) as compared to the HC The patients in the NC received a significantly lower mean daily oral prednisolone dose [13.2 (4.7) vs. 15.3 (6.6) mg/day, P<0.001], and had lower frequencies of rejections (36% vs. 57%, P<0.001) and CMV infection (54% vs. 63%, P=0.071). Patients in the NC had significantly lower odds of developing PTDM, even after adjustment for age, prednisolone dose, HLA-B27 status and CMV infection (odds ratio: 0.42, 95% Cl: 0.23-0.77, P=0.005). Conclusions. The odds of developing PTDM are more than halved over the last decade. Possible explanations are changes in immunosuppressive therapy, fewer rejections, and lower doses of steroids.
引用
收藏
页码:1125 / 1130
页数:6
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