Increased alloreactivity and adverse outcomes in obese kidney transplant recipients are limited to those with diabetes mellitus

被引:10
作者
Schachtner, Thomas [1 ,2 ,3 ]
Stein, Maik [2 ]
Reinke, Petra [1 ,2 ]
机构
[1] Charite, Dept Nephrol & Internal Intens Care, Campus Virchow Clin,Augustenburger Pl 1, D-13353 Berlin, Germany
[2] Berlin Brandenburg Ctr Regenerat Therapies BCRT, Berlin, Germany
[3] Berlin Inst Hlth, Charite & Max Delbruck Ctr, Berlin, Germany
关键词
Obesity; Diabetes mellitus; Renal transplantation; Alloreactivity; BODY-MASS-INDEX; RENAL-TRANSPLANTATION; HEMODIALYSIS-PATIENTS; PROSPECTIVE COHORT; MORBID-OBESITY; UNITED-STATES; RISK-FACTOR; MORTALITY; SURVIVAL; DISEASE;
D O I
10.1016/j.trim.2016.11.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies on patient and allograft outcomes of obese kidney transplant recipients (KTRs) remain controversial. To what extent obesity-related comorbidities contribute to adverse outcomes, however, hasn't been addressed. We studied all KTRs from 2005 to 2012.29 (4%), 317 (48%), 217 (33%), 76 (12%), and 21 KTRs (4%) were identified as underweight, normal-weight, overweight, obese, and morbid obese, respectively. 33 of 97 obese KTRs (34%) had pre-existent diabetes. Samples were collected before transplantation and at +1, +2, +3 months post transplantation. Donor-reactive T-cells were measured using an interferon-gamma Elispot assay. Obese KTRs showed an increased incidence pre-existent diabetes (p <0.001), but no differences for hypertension and coronary artery disease (p> 0.05). Among obese KTRs, those with pre-existent diabetes showed inferior patient and allograft survival, worse allograft function, delayed graft function, and prolonged hospitalization (p < 0.05). Interestingly, no differences were observed between obese non-diabetic, normal-weight diabetic, and normal-weight non-diabetic KTRs (p> 0.05). Obese diabetic KTRs showed higher frequencies of donor-reactive T-cells pretransplantation (p < 0.05). Our results suggest that the increased risk of mortality, allograft loss, delayed graft function, and prolonged hospitalization in obese ICTRs is limited to those with diabetes. A state of obesity-related inflammation plus hyperglycemia may trigger increased alloreactivity and should call for adequate immunosuppression. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 16
页数:9
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