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Benefit of doxycycline treatment on articular disability caused by dialysis related amyloidosis.

Authors :
Montagna, Giovanni
Cazzulani, Benedetta
Obici, Laura
Uggetti, Carla
Giorgetti, Sofia
Porcari, Riccardo
Ruggiero, Rubina
Mangione, P. Patrizia
Brambilla, Moreno
Lucchetti, Jacopo
Guiso, Giovanna
Gobbi, Marco
Merlini, Giampaolo
Salmona, Mario
Stoppini, Monica
Villa, Giuseppe
Bellotti, Vittorio
Source :
Amyloid. Sep2013, Vol. 20 Issue 3, p173-178. 6p.
Publication Year :
2013

Abstract

Doxycycline inhibits amyloid formation in vitro and its therapeutic efficacy is under evaluation in clinical trials for different protein conformational diseases, including prion diseases, Alzheimer's disease and transthyretin amyloidosis. In patients on chronic hemodialysis, a persistently high concentration of β2-microglobulin causes a form of amyloidosis (dialysis-related amyloidosis, DRA) localized in bones and ligaments. Since doxycycline inhibits β2-microglobulin fibrillogenesis in vitro and accumulates in bones, DRA represents an ideal form of amyloidosis where doxycycline may reach a therapeutic concentration at the site of amyloid deposition. Three patients on long-term dialysis with severe articular impairment and uncontrollable pain due to DRA were treated with 100 mg of doxycycline daily. Pharmacokinetics and safety of treatment were conducted. Plasmatic levels of the drug reached a plateau after one week (1.1-2.3 µg/ml). Treatment was well tolerated in two patients for a year, while one was suspended after 5 months due to mild esophagitis. Treatment was associated with a significant reduction in articular pain and with a significant and measurable improvement in passive and active movements in all cases, despite the persistence of unchanged amyloid deposits measured by magnetic resonance imaging. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13506129
Volume :
20
Issue :
3
Database :
Academic Search Index
Journal :
Amyloid
Publication Type :
Academic Journal
Accession number :
89854100
Full Text :
https://doi.org/10.3109/13506129.2013.803463