Kidney Injury Molecule-1 (KIM-1): A novel biomarker for human renal proximal tubule injury

被引:1406
作者
Han, WK
Bailly, V
Abichandani, R
Thadhani, R
Bonventre, JV
机构
[1] Harvard Univ, Sch Med, Harvard MIT Div Hlth Sci & Technol, Massachusetts Gen Hosp,Med Serv,Dept Med, Charlestown, MA USA
[2] Biogen Corp, Cambridge, MA USA
关键词
acute renal failure; acute tubular necrosis; contrast nephropathy; urinary biomarker; ischemia; dialysis; nephrotoxicity;
D O I
10.1046/j.1523-1755.2002.00433.x
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
Background. Traditional blood and urine markers for the diagnosis of various renal diseases are insensitive and nonspecific. Kidney Injury Molecule-1 (KIM-1) is a type 1 transmembrane protein, with an immunoglobulin and mucin domain, whose expression is markedly up-regulated in the proximal tubule in the post-ischemic rat kidney. The ectodomain of KIM-1 is shed from cells. The current studies were carried out to evaluate whether KIM-1 is present in human acute renal failure and might serve as a urinary marker of acute renal tubular injury. Methods. Kidney tissue samples from six patients with biopsy-proven acute tubular necrosis (ATN) were evaluated by immunohistochemistry for expression of KIM-1. Urine samples were collected from an additional thirty-two patients with various acute and chronic renal diseases, as well as from eight normal controls. Urinary KIM-1 protein was detected by immunoassay and was quantified by ELISA. Results. There was extensive expression of KIM-1 in proximal tubule cells in biopsies from 6 of 6 patients with confirmed ATN. The normalized urinary KIM-1 levels were significantly higher in patients with ischemic ATN (2.92 +/- 0.61 N = 7) compared to levels in patients with other forms of acute renal failure (0.63 +/- 0.17, P < 0.01; N = 16) or chronic renal disease (0.72 +/- 0.37, P < 0.01: N = 9). Adjusted for age, gender, length of time delay between the initial insult and sampling of the urine, a one-unit increase in normalized KIM-1 was associated with a greater than 12-fold (OR 12.4, 95% CI 1.2 to 119) risk for the presence of ATN. Concentrations of other urinary biomarkers, including total protein. gamma-glutamyltransferase, and alkaline phosphatase, did not correlate with clinical diagnostic groupings. Conclusions. A soluble form of human KIM-1 can be detected in the urine of patients with ATN and may serve as a useful biomarker for renal proximal tubule injury facilitating the early diagnosis of the disease and serving as a diagnostic discriminator.
引用
收藏
页码:237 / 244
页数:8
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