Kidney Injury Molecule-1 (KIM-1): A novel biomarker for human renal proximal tubule injury
Kidney Injury Molecule-1 (KIM-1): A novel biomarker for human renal proximal tubule injury. 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...
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Veröffentlicht in: | Kidney international 2002-07, Vol.62 (1), p.237-244 |
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Zusammenfassung: | Kidney Injury Molecule-1 (KIM-1): A novel biomarker for human renal proximal tubule injury.
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.
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.
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, γ-glutamyltransferase, and alkaline phosphatase, did not correlate with clinical diagnostic groupings.
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. |
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ISSN: | 0085-2538 1523-1755 |
DOI: | 10.1046/j.1523-1755.2002.00433.x |