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Volume 52, Issue 3, Pages 595-605 (September 2008)


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Neutrophil Gelatinase–Associated Lipocalin (NGAL) as a Marker of Kidney Damage

Davide Bolignano, MD, Valentina Donato, MD, Giuseppe Coppolino, MD, Susanna Campo, MD, Antoine Buemi, MD, Antonio Lacquaniti, MD, Michele Buemi, MDCorresponding Author Informationemail address

Received 20 November 2007; accepted 31 January 2008. published online 03 April 2008.

Refers to article:
NGAL in Acute Kidney Injury: From Serendipity to Utility
Prasad Devarajan
American Journal of Kidney Diseases
September 2008 (Vol. 52, Issue 3, Pages 395-399)
Full Text | Full-Text PDF (79 KB)

Neutrophil gelatinase–associated lipocalin (NGAL) is a protein belonging to the lipocalin superfamily initially found in activated neutrophils, in accordance with its role as an innate antibacterial factor. However, it subsequently was shown that many other types of cells, including in the kidney tubule, may produce NGAL in response to various injuries. The increase in NGAL production and release from tubular cells after harmful stimuli of various kinds may have self-defensive intent based on the activation of specific iron-dependent pathways, which in all probability also represent the mechanism through which NGAL promotes kidney growth and differentiation. NGAL levels predict the future appearance of acute kidney injury after treatments potentially detrimental to the kidney and even the acute worsening of unstable nephropathies. Furthermore, recent evidence also suggests that NGAL somehow may be involved in the pathophysiological process of chronic renal diseases, such as polycystic kidney disease and glomerulonephritis. NGAL levels clearly correlate with severity of renal impairment, probably expressing the degree of active damage underlying the chronic condition. For all these reasons, NGAL may become one of the most promising next-generation biomarkers in clinical nephrology and beyond.

Department of Internal Medicine, University of Messina, Messina, Italy

Corresponding Author InformationAddress correspondence to Michele Buemi, MD, Via Salita Villa Contino, 30, 98100 Messina, Italy

 Originally published online as doi:10.1053/j.ajkd.2008.01.020 on April 3, 2008.

PII: S0272-6386(08)00163-7

doi:10.1053/j.ajkd.2008.01.020


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