Living donor kidney transplants:: a biopsy study 1 year after transplantation, compared with baseline changes and correlation to kidney function at 1 and 3 years

被引:45
作者
Sund, S [1 ]
Reisæter, AV
Fauchald, P
Bentdal, O
Hall, KS
Hovig, T
机构
[1] Univ Oslo, Natl Hosp Norway, Rikshosp, Inst Pathol, N-0027 Oslo, Norway
[2] Univ Oslo, Natl Hosp Norway, Rikshosp, Dept Med, N-0027 Oslo, Norway
[3] Univ Oslo, Natl Hosp Norway, Rikshosp, Dept Surg, N-0027 Oslo, Norway
[4] Univ Oslo, Natl Hosp Norway, Rikshosp, Dept Clin Chem, N-0027 Oslo, Norway
关键词
kidney transplant biopsy; baseline; prognosis; transplant outcome; reproducibility;
D O I
10.1093/ndt/14.10.2445
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Introduction. Chronic changes in biopsies from long-term stable kidney allografts have been reported to correlate with graft prognosis. Morphological changes in baseline ('zero-hour') biopsies have been described as well, but their importance for long-term prognosis have been less clear. The aim of the present study was to evaluate biopsy changes from baseline to 1 year after transplantation in patients receiving kidneys from living donors, and to assess the possible prognostic implications of these findings. Methods. Light microscopical changes in 18 gauge full-core biopsies were scored semi-quantitatively in 33 patients 1 year after transplantation, and compared to baseline changes previously reported [1]. All cases were also examined with transmission electron microscopy. The semi-quantitative data from baseline and at 1 year were correlated with kidney function 1 and 3 years after transplantation. The reproducibility of baseline findings regarding arteriosclerosis and arteriolar hyalinosis was tested by comparison with biopsies 1 week after transplantation (n = 43). Results. We found a significant increase in mesangial glomerular sclerosis (P < 0.001), interstitial fibrosis/ tubular atrophy (if/ta) (P = 0.002), and mononuclear cell interstitial infiltration (P = 0.003) after 1 year, compared to baseline changes. There was an increase of arteriosclerosis (P = 0.028) and arteriolar hyalinosis (P = 0.006) when compared to biopsies taken 1 week after transplantation, but not when compared to the 'zero-hour' findings. Electron microscopy revealed one case of recurrent immune-complex glomerulonephritis and another case of recurrent light chain deposition kidney disease. Comparing 1-week vascular findings with baseline gave a low level of reproducibility, probably due to sampling error. Baseline biopsy findings could not predict long-term kidney function. In the 1-year biopsy, if/ta was significantly correlated with serum creatinine (P = 0.007) and glomerular filtration rate (GFR) (P < 0.001) at 1 year, with serum creatinine at 3 years (P = 0.011), and with the first-year cumulative dose of methylprednisolone (P = 0.004). Serum creatinine at 1 year, however, was found to be the most accurate predictor of 3-year kidney function (P < 0.001). Donor age was correlated to kidney function at 3 years (P = 0.013) but not at 1 year after transplantation. Conclusion. Morphological changes in baseline biopsies of living donor kidneys tend to become more pronounced in well-functioning allografts during the first year after transplantation. In the 1 year biopsy, if/ta seems to be the most reliable variate for grading of chronic changes. However, 1-year serum creatinine predicted long-term kidney function more precisely than did the biopsy scores. Based on the results of the present study, a protocol 1-year biopsy does not seem warranted in the management of the graft recipient with a stable kidney function.
引用
收藏
页码:2445 / 2454
页数:10
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