Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6370
Title: Amyloidosis, Inflammation, and Oxidative Stress in the Heart of an Alkaptonuric Patient.
Authors: Millucci, Lia 
Ghezzi, Lorenzo
Paccagnini, Eugenio
Giorgetti, Giovanna
Viti, Cecilia
Braconi, Daniela 
Laschi, Marcella
Geminiani, Michela 
Soldani, Patrizia 
Lupetti, Pietro
Orlandini, Maurizio 
Benvenuti, C
Perfetto, F
Spreafico, Adriano
Bernardini, Giulia 
Santucci, Annalisa 
Issue Date: 2014
Project: None 
Journal: MEDIATORS OF INFLAMMATION
Abstract: 
Background. Alkaptonuria, a rare autosomal recessive metabolic disorder caused by deficiency in homogentisate 1,2-dioxygenase activity, leads to accumulation of oxidised homogentisic acid in cartilage and collagenous structures present in all organs and tissues, especially joints and heart, causing a pigmentation called ochronosis. A secondary amyloidosis is associated with AKU. Here we report a study of an aortic valve from an AKU patient. Results. Congo Red birefringence, Th-T fluorescence, and biochemical assays demonstrated the presence of SAA-amyloid deposits in AKU stenotic aortic valve. Light and electron microscopy assessed the colocalization of ochronotic pigment and SAA-amyloid, the presence of calcified areas in the valve. Immunofluorescence detected lipid peroxidation of the tissue and lymphocyte/macrophage infiltration causing inflammation. High SAA plasma levels and proinflammatory cytokines levels comparable to those from rheumatoid arthritis patients were found in AKU patient. Conclusions. SAA-amyloidosis was present in the aortic valve from an AKU patient and colocalized with ochronotic pigment as well as with tissue calcification, lipid oxidation, macrophages infiltration, cell death, and tissue degeneration. A local HGD expression in human cardiac tissue has also been ascertained suggesting a consequent local production of ochronotic pigment in AKU heart.
Description: 
14675
URI: http://hdl.handle.net/20.500.12779/6370
ISSN: 1466-1861
DOI: 10.1155/2014/258471
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