Occurrence of Diabetic Nephropathy After Renal Transplantation Despite Intensive Glycemic Control: An Observational Cohort Study

被引:21
作者
Coemans, Maarten [1 ,2 ,3 ]
Van Loon, Elisabet [1 ,2 ]
Lerut, Evelyne [4 ,5 ]
Gillard, Pieter [6 ,7 ]
Sprangers, Ben [1 ,2 ]
Senev, Aleksandar [1 ,8 ]
Emonds, Marie-Paule [8 ]
Van Keer, Jan [1 ]
Callemeyn, Jasper [1 ,2 ]
Daniels, Liesbeth [6 ]
Sichien, Jeroen [3 ]
Verbeke, Geert [3 ]
Kuypers, Dirk [1 ,2 ]
Mathieu, Chantal [6 ,7 ]
Naesens, Maarten [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Dept Microbiol & Immunol, Lab Nephrol, Leuven, Belgium
[2] Univ Hosp Leuven, Dept Nephrol & Renal Transplantat, Leuven, Belgium
[3] Katholieke Univ Leuven, Dept Publ Hlth & Primary Care, Leuven Biostat & Stat Bioinformat Ctr, Leuven, Belgium
[4] Katholieke Univ Leuven, Dept Imaging & Pathol, Leuven, Belgium
[5] Univ Hosp Leuven, Dept Pathol, Leuven, Belgium
[6] Katholieke Univ Leuven, Dept Chron Dis Metab & Ageing, Clin & Expt Endocrinol, Leuven, Belgium
[7] Univ Hosp Leuven, Dept Diabet & Endocrinol, Leuven, Belgium
[8] Red Cross Flanders, Histocompatibil & Immunogenet Lab, Mechelen, Belgium
基金
比利时弗兰德研究基金会;
关键词
GLOMERULAR-FILTRATION-RATE; NORMAL KIDNEYS; END-POINTS; LONG-TERM; HYPERFILTRATION; PROGRESSION; LESIONS; PATHOGENESIS; SENESCENCE; PREVENTION;
D O I
10.2337/dc18-1936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE The kinetics and risk factors of diabetic nephropathy after kidney transplantation remain unclear. This study investigated the posttransplant occurrence of diabetic nephropathy and the contribution of posttransplant glycemic control. RESEARCH DESIGN AND METHODS We performed a single-center prospective cohort study of 953 renal allograft recipients and 3,458 protocol-specified renal allograft biopsy specimens up to 5 years after transplantation. The effects of pretransplant diabetes and glycemic control (glycated hemoglobin levels) on the posttransplant histology were studied. RESULTS Before transplantation, diabetes was present in 164 (17.2%) renal allograft recipients, primarily type 2 (n = 146 [89.0%]). Despite intensive glycemic control (glycated hemoglobin 7.00 +/- 1.34% [53 +/- 14.6 mmol/mol], 6.90 +/- 1.22% [52 +/- 13.3 mmol/mol], and 7.10 +/- 1.13% [54 +/- 12.4 mmol/mol], at 1, 2, and 5 years after transplantation), mesangial matrix expansion reached a cumulative incidence of 47.7% by 5 years in the pretransplant diabetes group versus 27.1% in patients without diabetes, corresponding to a hazard ratio of 1.55 (95% CI 1.07-2.26; P = 0.005). Mesangial matrix expansion was not specific for diabetic nephropathy and associated independently with increasing age. Pretransplant diabetes was associated with posttransplant proteinuria but not with estimated glomerular filtration rate, graft failure, or any other structural changes of the glomerular, vascular, or tubulointerstitial renal compartments. The occurrence of diabetic nephropathy was independent of posttransplant glycated hemoglobin levels. CONCLUSIONS Mesangial matrix expansion, an early indicator of diabetic nephropathy, can occur rapidly in patients with diabetes before transplantation, despite intensive glycemic control. Prevention of diabetic nephropathy requires more than pursuing low levels of glycated hemoglobin.
引用
收藏
页码:625 / 634
页数:10
相关论文
共 47 条
[1]   Diabetic nephropathy: Linking histology, cell biology, and genetics [J].
Adler, S .
KIDNEY INTERNATIONAL, 2004, 66 (05) :2095-2106
[2]   The relationship between microalbuminuria and glomerular filtration rate in young type 1 diabetic subjects: The Oxford Regional Prospective Study [J].
Amin, R ;
Turner, C ;
van Aken, S ;
Bahu, TK ;
Watts, A ;
Lindsell, DRM ;
Dalton, RN ;
Dunger, DB .
KIDNEY INTERNATIONAL, 2005, 68 (04) :1740-1749
[3]  
[Anonymous], 2000, J AM SOC NEPHROL
[4]   EFFECT OF GLYCEMIC CONTROL ON EARLY DIABETIC RENAL LESIONS - A 5-YEAR RANDOMIZED CONTROLLED CLINICAL-TRIAL OF INSULIN-DEPENDENT DIABETIC KIDNEY-TRANSPLANT RECIPIENTS [J].
BARBOSA, J ;
STEFFES, MW ;
SUTHERLAND, DER ;
CONNETT, JE ;
RAO, KV ;
MAUER, SM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 272 (08) :600-606
[6]   Recurrent and de novo diabetic nephropathy in renal allografts [J].
Bhalla, V ;
Nast, CC ;
Stollenwerk, N ;
Tran, S ;
Barba, L ;
Kamil, ES ;
Danovitch, G ;
Adler, SG .
TRANSPLANTATION, 2003, 75 (01) :66-71
[7]   Early diabetic nephropathy in type 1 diabetes: new insights [J].
Bjornstad, Petter ;
Cherney, David ;
Maahs, David M. .
CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2014, 21 (04) :279-286
[8]  
BOHMAN SO, 1987, TRANSPLANT P, V19, P2290
[9]   The pathobiology of diabetic complications - A unifying mechanism [J].
Brownlee, M .
DIABETES, 2005, 54 (06) :1615-1625
[10]  
CHRISTIANSEN JS, 1981, DIABETOLOGIA, V20, P451