Chronic Kidney Disease After Nonrenal Solid Organ Transplantation: A Histological Assessment and Utility of Chronic Allograft Damage Index Scoring

被引:27
作者
Kubal, Chandrashekhar [1 ,2 ]
Cockwell, Paul [2 ,3 ]
Gunson, Bridget [4 ]
Jesky, Mark [2 ,3 ]
Hanvesakul, Rajesh [2 ,3 ]
Dronavalli, Vamsidhar [5 ]
Bonser, Robert S. [5 ]
Neil, Desley [6 ]
机构
[1] Indiana Univ Sch Med, Dept Surg, Div Transplantat, Indianapolis, IN 46202 USA
[2] Univ Hosp Birmingham, Dept Nephrol & Renal Transplantat, Renal Inst Birmingham, Birmingham, W Midlands, England
[3] Univ Birmingham, Dept Immun & Infect, Birmingham, W Midlands, England
[4] Univ Hosp Birmingham, Dept Liver Transplantat, Birmingham, W Midlands, England
[5] Univ Hosp Birmingham, Dept Cardiac Surg & Heart Lung Transplantat, Birmingham, W Midlands, England
[6] Univ Hosp Birmingham, Dept Pathol, Birmingham, W Midlands, England
关键词
Liver transplantation; Chronic kidney disease; Renal biopsy; Calcineurin inhibitor nephrotoxicity; Hypertension; CHRONIC-RENAL-FAILURE; LIVER-TRANSPLANTATION; MYCOPHENOLATE-MOFETIL; CALCINEURIN INHIBITOR; HEART-TRANSPLANTATION; RECIPIENTS; NEPHROPATHY; BIOPSY; TRIAL;
D O I
10.1097/TP.0b013e318240e984
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. It is proposed that chronic calcineurin inhibitor (CNI) nephrotoxicity has a central role in chronic kidney disease after nonrenal solid organ transplantation (NRSOT), although there are little data on renal histology in this setting. The aim of this study was to assess the histological features and renal outcomes of a cohort of patients with chronic kidney disease after NRSOT. Methods. Renal biopsies of 62 NRSOT recipients were evaluated for histological diagnoses. Biopsies were graded for chronic allograft damage index parameters and for arteriolar hyalinosis. The sum of all chronic allograft damage index parameters and arteriolar hyalinosis scores was called chronic damage index. Results. The biopsies were performed at a median of 4 (range: 0.3-15.9) years after NRSOT and at serum creatinine of 318 +/- 17.7 mu mol/L (mean +/- standard deviation). Twenty-two (35.5%) biopsies showed predominant features of chronic CNI nephrotoxicity, 27 (43.5%) predominant features of hypertensive nephropathy, and 12 (19.3%) an alternative primary renal pathology. Twenty-four (38.7%) patients had progression to end-stage renal disease, at a median of 1.5 (0-10.1) years after biopsy and 6.9 (0.3-19.2) years after NRSOT. The risk of renal progression was associated with in situ damage measured by chronic damage index. Conclusions. Although CNI nephrotoxicity is an important cause of renal failure after NRSOT, many patients do not have overt histological evidence of CNI toxicity. Quantitative parameters of chronic damage can stratify renal prognosis.
引用
收藏
页码:406 / 411
页数:6
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