Assessment of kidney organ quality and prediction of outcome at time of transplantation

被引:38
作者
Mueller, Thomas F. [1 ]
Solez, Kim [2 ]
Mas, Valeria [3 ,4 ]
机构
[1] Univ Alberta, Dept Med, Div Nephrol & Immunol, Edmonton, AB, Canada
[2] Univ Alberta, Dept Lab Med & Pathol, Edmonton, AB, Canada
[3] Virginia Commonwealth Univ, Dept Surg, Div Transplant, Mol Transplant Res Lab, Richmond, VA USA
[4] Virginia Commonwealth Univ, Dept Pathol, Div Transplant, Mol Transplant Res Lab, Richmond, VA USA
关键词
Kidney transplantation; Zero-hour biopsy; Ischemia-reperfusion injury; Graft outcome; Gene expression; Inflammation; DELAYED GRAFT FUNCTION; GENE-EXPRESSION PATTERNS; ACUTE TUBULAR-NECROSIS; CADAVERIC RENAL-TRANSPLANTATION; GLOMERULAR-FILTRATION-RATE; DECEASED DONOR KIDNEYS; GELATINASE-ASSOCIATED LIPOCALIN; ISCHEMIA-REPERFUSION INJURY; IDEAL SERUM CREATININE; SCORING SYSTEM;
D O I
10.1007/s00281-011-0248-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The critical importance of donor organ quality, i.e., number of surviving nephrons, ability to withstand injury, and capacity for repair in determining short- and long-term outcomes is becoming increasingly clear. This review provides an overview of studies to assess donor kidney quality and subsequent transplant outcomes based on clinical pathology and transcriptome-based variables available at time of transplantation. Prediction scores using clinical variables function when applied to large data sets but perform poorly for the individual patient. Histopathology findings in pre-implantation or post-reperfusion biopsies help to assess structural integrity of the donor kidney, provide information on pre-existing donor disease, and can serve as a baseline for tracking changes over time. However, more validated approaches of analysis and prospective studies are needed to reduce the number of discarded organs, improve allocation, and allow prediction of outcomes. Molecular profiling detects changes not seen by morphology or captured by clinical markers. In particular, molecular profiles provide a quantitative measurement of inflammatory burden or immune activation and reflect coordinated changes in pathways associated with injury and repair. However, description of transcriptome patterns is not an end in itself. The identification of predictive gene sets and the application to an individualized patient management needs the integration of clinical and pathology-based variables, as well asmore objective reference markers of transplant function, post-transplant events, and long-term outcomes.
引用
收藏
页码:185 / 199
页数:15
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