NMR-SPECTROSCOPY AS A NOVEL-APPROACH TO THE MONITORING OF RENAL-TRANSPLANT FUNCTION

被引:106
作者
FOXALL, PJD
MELLOTTE, GJ
BENDING, MR
LINDON, JC
NICHOLSON, JK
机构
[1] UNIV LONDON,BIRKBECK COLL,DEPT CHEM,GORDON HOUSE,29 GORDON SQ,LONDON WC1H 0PP,ENGLAND
[2] ST HELIER HOSP,SW THAMES REG RENAL UNIT,CARSHALTON SM5 1AA,SURREY,ENGLAND
[3] WELLCOME RES LABS,DEPT PHYS SCI,BECKENHAM BR3 3BS,KENT,ENGLAND
关键词
D O I
10.1038/ki.1993.37
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
High field H-1 NMR spectroscopy was used for the rapid multicomponent analysis of low molecular wt compounds in urine in order to investigate the patterns of metabolic changes associated with early renal allograft dysfunction. Urine samples were collected daily for 14 days from 33 patients who underwent primary renal allograft transplantation, and analyzed by 500 and/or 600 MHz H-1 NMR spectroscopy. All patients received 20 mg prednisolone and 5 mg/kg b.d. oral cyclosporin A (CsA) solution. In this study no patient showed clinical or histopathological evidence of CsA nephrotoxicity. For each patient the NMR-generated metabolite data were correlated with the clinical observations, graft biopsy pathology, and data from conventional laboratory techniques for assessing renal function. The NMR spectra of urine from patients with immediate functioning grafts were similar with respect to their patterns of amino acids, organic acids and organic amines, whereas the patients with delayed or non-functioning grafts showed significantly different metabolite excretion patterns. In longitudinal studies on individual patients there were increased urinary levels of trimethylamine-N-oxide (TMAO), dimethylamine (DMA), lactate, acetate, succinate, glycine and alanine during episodes of graft dysfunction. However, only the urinary concentration of TMAO was statistically significantly higher (P < 0.025) in the urine collected from patients during episodes of graft dysfunction (410 +/- 102 muM TMAO/mM creatinine) than in patients with good graft function (91 +/- 18 muM TMAO/mM creatinine) or healthy control subjects (100 +/- 50 muM TMAO/mM creatinine). These findings suggest that graft dysfunction is associated with damage to the renal medulla which causes the release of TMAO into the urine from the damaged renal medullary cells. This provides a possible novel urinary marker for post-transplant graft dysfunction. This study shows that NMR spectroscopy of biofluids, when used in combination with conventional laboratory techniques, is a valuable aid to renal transplant monitoring.
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收藏
页码:234 / 245
页数:12
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