Literature DB >> 22085605

Globotriaosylceramide is correlated with oxidative stress and inflammation in Fabry patients treated with enzyme replacement therapy.

Giovana B Biancini1, Camila S Vanzin, Daiane B Rodrigues, Marion Deon, Graziela S Ribas, Alethéa G Barschak, Vanusa Manfredini, Cristina B O Netto, Laura B Jardim, Roberto Giugliani, Carmen R Vargas.   

Abstract

Fabry disease is an X-linked inborn error of glycosphingolipid catabolism due to deficient activity of α-galactosidase A that leads to accumulation of the enzyme substrates, mainly globotriaosylceramide (Gb3), in body fluids and lysosomes of many cell types. Some pathophysiology hypotheses are intimately linked to reactive species production and inflammation, but until this moment there is no in vivo study about it. Hence, the aim of this study was to investigate oxidative stress parameters, pro-inflammatory cytokines and Gb3 levels in Fabry patients under treatment with enzyme replacement therapy (ERT) and finally to establish a possible relation between them. We analyzed urine and blood samples of patients under ERT (n=14) and healthy age-matched controls (n=14). Patients presented decreased levels of antioxidant defenses, assessed by reduced glutathione (GSH), glutathione peroxidase (GPx) activity and increased superoxide dismutase/catalase (SOD/CAT) ratio in erythrocytes. Concerning to the damage to biomolecules (lipids and proteins), we found that plasma levels of malondialdehyde (MDA) and protein carbonyl groups and di-tyrosine (di-Tyr) in urine were increased in patients. The pro-inflammatory cytokines IL-6 and TNF-α were also increased in patients. Urinary Gb3 levels were positively correlated with the plasma levels of IL-6, carbonyl groups and MDA. IL-6 levels were directly correlated with di-Tyr and inversely correlated with GPx activity. This data suggest that pro-inflammatory and pro-oxidant states occur, are correlated and seem to be induced by Gb3 in Fabry patients.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22085605     DOI: 10.1016/j.bbadis.2011.11.001

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  33 in total

1.  Unravelling the mechanism of action of enzyme replacement therapy in Fabry disease.

Authors:  Younhee Ko; CheolHo Lee; Myeong Hee Moon; Geu-Ru Hong; Chong-Kun Cheon; Jin-Sung Lee
Journal:  J Hum Genet       Date:  2015-10-22       Impact factor: 3.172

2.  Oxidative stress biomarkers in Fabry disease: is there a room for them?

Authors:  C Simoncini; S Torri; V Montano; L Chico; F Gruosso; A Tuttolomondo; A Pinto; I Simonetta; V Cianci; A Salviati; V Vicenzi; G Marchi; D Girelli; D Concolino; S Sestito; M Zedde; G Siciliano; Michelangelo Mancuso
Journal:  J Neurol       Date:  2020-07-27       Impact factor: 4.849

3.  Age at First Cardiac Symptoms in Fabry Disease: Association with a Chinese Hotspot Fabry Mutation (IVS4+919G>A), Classical Fabry Mutations, and Sex in a Taiwanese Population from the Fabry Outcome Survey (FOS).

Authors:  Hao-Chuan Liu; Amandine Perrin; Ting-Rong Hsu; Chia-Feng Yang; Hsiang-Yu Lin; Wen-Chung Yu; Dau-Ming Niu
Journal:  JIMD Rep       Date:  2015-03-12

4.  Evidence for inflammation in Fabry's disease? Headache and muscle involvement responding to corticosteroid and methotrexate treatment.

Authors:  Markus Kraemer; N Karabul; P Berlit; A Rolfs
Journal:  J Neurol       Date:  2017-01-27       Impact factor: 4.849

5.  α-galactosidase A deficiency promotes von Willebrand factor secretion in models of Fabry disease.

Authors:  Justin J Kang; Nayiri M Kaissarian; Karl C Desch; Robert J Kelly; Liming Shu; Peter F Bodary; James A Shayman
Journal:  Kidney Int       Date:  2018-11-22       Impact factor: 10.612

6.  Innate and Adaptive Immune Response in Fabry Disease.

Authors:  Wladimir Mauhin; Olivier Lidove; Elisa Masat; Federico Mingozzi; Kuberaka Mariampillai; Jean-Marc Ziza; Olivier Benveniste
Journal:  JIMD Rep       Date:  2015-02-18

7.  Imbalanced Production of Reactive Oxygen Species and Mitochondrial Antioxidant SOD2 in Fabry Disease-Specific Human Induced Pluripotent Stem Cell-Differentiated Vascular Endothelial Cells.

Authors:  Wei-Lien Tseng; Shih-Jie Chou; Huai-Chih Chiang; Mong-Lien Wang; Chian-Shiu Chien; Kuan-Hsuan Chen; Hsin-Bang Leu; Chien-Ying Wang; Yuh-Lih Chang; Yung-Yang Liu; Yuh-Jyh Jong; Shinn-Zong Lin; Shih-Hwa Chiou; Shing-Jong Lin; Wen-Chung Yu
Journal:  Cell Transplant       Date:  2016-12-06       Impact factor: 4.064

8.  First experience of simultaneous PET/MRI for the early detection of cardiac involvement in patients with Anderson-Fabry disease.

Authors:  Carmela Nappi; Michele Altiero; Massimo Imbriaco; Emanuele Nicolai; Caterina Anna Giudice; Marco Aiello; Claudio Tommaso Diomiaiuti; Antonio Pisani; Letizia Spinelli; Alberto Cuocolo
Journal:  Eur J Nucl Med Mol Imaging       Date:  2015-03-26       Impact factor: 9.236

Review 9.  Progress in the understanding and treatment of Fabry disease.

Authors:  James J Miller; Adam J Kanack; Nancy M Dahms
Journal:  Biochim Biophys Acta Gen Subj       Date:  2019-09-14       Impact factor: 3.770

10.  Increased Serum Interleukin-6 and Tumor Necrosis Factor Alpha Levels in Fabry Disease: Correlation with Disease Burden.

Authors:  Nilton Salles Rosa Neto; Judith Campos de Barros Bento; Valéria de Falco Caparbo; Rosa Maria Rodrigues Pereira
Journal:  Clinics (Sao Paulo)       Date:  2021-07-16       Impact factor: 2.365

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