Risk factors associated with the onset and progression of posttransplantation diabetes in renal allograft recipients

被引:80
作者
Hur, Kyu Yeon
Kim, Myoung Soo
Kim, Yu Seun
Kang, Eun Seok
Nam, Jae Hyun
Kim, So Hun
Nam, Chung Mo
Ahn, Chul Woo
Cha, Bong Soo
Kim, Soon Il
Lee, Hyun Chul
机构
[1] Yonsei Univ, Coll Med, Dept Internal Med, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Dept Surg, Seoul 120749, South Korea
[3] Yonsei Univ, Coll Med, Inst Endocrine Res, Seoul 120749, South Korea
[4] Yonsei Univ, Coll Med, Dept Prevent Med, Seoul 120749, South Korea
关键词
D O I
10.2337/dc06-1277
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - The aim of this study was to assess the incidence of posttransplantation diabetes mellitus (PTDM) in renal allograft recipients and to investigate factors contributing to the onset and progression of PTDM and its underlying pathogenic mechanism(s). RESEARCH DESIGN AND METHODS - A total of 77 patients with normal glucose tolerance (NGT) were enrolled in this study.-An oral glucose tolerance test was performed I week before transplantation and repeated at 1 and 7 years after transplantation. RESULTS - The overall incidence of PTDM was 39% at 1 year and 35.1% at 7 years posttransplantation. The incidence for each category of PTDM was as follows: persistent PTDM (P-PTDM) (patients who developed diabetes mellitus within 1 year of transplantation and remained diabetic during 7 years), 23.4%; transient PTDM (T-PTDM) (patients who developed diabetes mellitus during the 1st year after transplantation but eventually recovered to have NGT), 15.6% late PTDM (L-PTDM)) (patients who developed diabetes mellitus later than I year after transplantation), 11.7%; and non-PTDM during 7 years (N-PTDM7) (patients who did not develop diabetes mellitus during 7 years), 49.3%. Older age (>= 40 years) at transplantation was and impaired fasting glucose a higher risk factor for P-PTDM, whereas a high BMI (>= 25 kg/m(2) (IFG) at I year posttransplantation were higher risk factors for L-PTDM. Impaired insulin secretion rather than insulin resistance was significantly associated with the development of P- and L-PTDM. CONCLUSIONS - Impaired insulin secretion may be the main mechanism for the development of PTDM. Older age at transplantation seems to be associated with P-PTDM, whereas a high BMI and IFG at I year after transplantation were associated with L-PTDM.
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页码:609 / 615
页数:7
相关论文
共 39 条
[1]  
American Diabetes Association, 2004, Diabetes Care, V27 Suppl 1, pS5, DOI 10.2337/diacare.27.2007.S5
[2]   SOME CHARACTERISTICS OF STEROID DIABETES - A STUDY IN RENAL-TRANSPLANT RECIPIENTS RECEIVING HIGH-DOSE CORTICOSTEROID-THERAPY [J].
ARNER, P ;
GUNNARSSON, R ;
BLOMDAHL, S ;
GROTH, CG .
DIABETES CARE, 1983, 6 (01) :23-25
[3]   THE IMPACT OF CYCLOSPORINE AND COMBINATION IMMUNOSUPPRESSION ON THE INCIDENCE OF POSTTRANSPLANT DIABETES IN RENAL-ALLOGRAFT RECIPIENTS [J].
BOUDREAUX, JP ;
MCHUGH, L ;
CANAFAX, DM ;
ASCHER, N ;
SUTHERLAND, DER ;
PAYNE, W ;
SIMMONS, RL ;
NAJARIAN, JS ;
FRYD, DS .
TRANSPLANTATION, 1987, 44 (03) :376-381
[4]  
BOUDREAUX JP, 1987, TRANSPLANT P, V19, P1811
[5]   Beta cell function declines with age in glucose tolerant Caucasians [J].
Chiu, KC ;
Lee, NP ;
Cohan, P ;
Chuang, LM .
CLINICAL ENDOCRINOLOGY, 2000, 53 (05) :569-575
[6]   High incidence of tacrolimus-associated posttransplantation diabetes in the Korean renal allograft recipients according to American diabetes association criteria [J].
Cho, YM ;
Park, KS ;
Jung, HS ;
Jeon, HJ ;
Ahn, C ;
Ha, J ;
Kim, SJ ;
Rhee, BD ;
Kim, SY ;
Lee, HK .
DIABETES CARE, 2003, 26 (04) :1123-1128
[7]   HUMAN ADIPOSE-TISSUE IN CULTURE .8. STUDIES ON THE INSULIN-ANTAGONISTIC EFFECT OF GLUCOCORTICOIDS [J].
CIGOLINI, M ;
SMITH, U .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1979, 28 (05) :502-510
[8]   Patient survival after renal transplantation: IV. Impact of post-transplant diabetes [J].
Cosio, FG ;
Pesavento, TE ;
Kim, S ;
Osei, K ;
Henry, M ;
Ferguson, RM .
KIDNEY INTERNATIONAL, 2002, 62 (04) :1440-1446
[9]   Post-transplant diabetes mellitus: Increasing incidence in renal allograft recipients transplanted in recent years [J].
Cosio, FG ;
Pesavento, TE ;
Osei, K ;
Henry, ML ;
Ferguson, RM .
KIDNEY INTERNATIONAL, 2001, 59 (02) :732-737
[10]  
DAVID DS, 1980, JAMA-J AM MED ASSOC, V243, P532