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A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia

BACKGROUND: Recombinant human erythropoietin (rhuEPO) has received considerable attention because of its neuroprotective properties. It has recently been reported that rhuEPO increases frataxin levels in combination with clinical improvement in rhuEPO treated patients with Friedreich ataxia (FRDA)....

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Autores principales: Santner, Wolfram, Schocke, Michael, Boesch, Sylvia, Nachbauer, Wolfgang, Egger, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184378/
https://www.ncbi.nlm.nih.gov/pubmed/25298866
http://dx.doi.org/10.1177/2047981614531573
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author Santner, Wolfram
Schocke, Michael
Boesch, Sylvia
Nachbauer, Wolfgang
Egger, Karl
author_facet Santner, Wolfram
Schocke, Michael
Boesch, Sylvia
Nachbauer, Wolfgang
Egger, Karl
author_sort Santner, Wolfram
collection PubMed
description BACKGROUND: Recombinant human erythropoietin (rhuEPO) has received considerable attention because of its neuroprotective properties. It has recently been reported that rhuEPO increases frataxin levels in combination with clinical improvement in rhuEPO treated patients with Friedreich ataxia (FRDA). PURPOSE: To determine possible therapy dependent intracranial volume changes after treatment with rhuEPO using voxel-based morphometry (VBM). MATERIAL AND METHODS: Nine FRDA patients were scanned on the same 1.5-Tesla MRI scanner before and after treatment with rhuEPO. FRDA patients received 5000 IU rhuEPO thrice weekly subcutaneously for a time period of 8 weeks followed by 2000 IU thrice weekly over 6 months. To test for re-test reliability a control group of 12 healthy volunteers were scanned twice on the same scanner without rhuEPO treatment. Neurological state was defined by the Friedreich Ataxia Rating Scale (FARS) and the Scale for the Assessment and Rating of Ataxia (SARA). Statistical parametric mapping software was used for image processing and statistical analysis. RESULTS: When comparing follow-up scans after rhuEPO treatment with baseline scans (P <0.001 uncorrected) an increase of gray matter volume was observed bilaterally in the Pulvinar and the posterior parietal cortex. Moreover, clinical improvement detected using specific Ataxia scores correlated with VBM results in the pulvinar. CONCLUSION: Given the limitation of a small sample size, our study confirms previous findings that MRI may serve as reliable biomarker in neurodegenerative diseases as well as in monitoring of microstructural changes representing disease progression and/or therapy effects.
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spelling pubmed-41843782014-10-08 A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia Santner, Wolfram Schocke, Michael Boesch, Sylvia Nachbauer, Wolfgang Egger, Karl Acta Radiol Short Rep Original Article BACKGROUND: Recombinant human erythropoietin (rhuEPO) has received considerable attention because of its neuroprotective properties. It has recently been reported that rhuEPO increases frataxin levels in combination with clinical improvement in rhuEPO treated patients with Friedreich ataxia (FRDA). PURPOSE: To determine possible therapy dependent intracranial volume changes after treatment with rhuEPO using voxel-based morphometry (VBM). MATERIAL AND METHODS: Nine FRDA patients were scanned on the same 1.5-Tesla MRI scanner before and after treatment with rhuEPO. FRDA patients received 5000 IU rhuEPO thrice weekly subcutaneously for a time period of 8 weeks followed by 2000 IU thrice weekly over 6 months. To test for re-test reliability a control group of 12 healthy volunteers were scanned twice on the same scanner without rhuEPO treatment. Neurological state was defined by the Friedreich Ataxia Rating Scale (FARS) and the Scale for the Assessment and Rating of Ataxia (SARA). Statistical parametric mapping software was used for image processing and statistical analysis. RESULTS: When comparing follow-up scans after rhuEPO treatment with baseline scans (P <0.001 uncorrected) an increase of gray matter volume was observed bilaterally in the Pulvinar and the posterior parietal cortex. Moreover, clinical improvement detected using specific Ataxia scores correlated with VBM results in the pulvinar. CONCLUSION: Given the limitation of a small sample size, our study confirms previous findings that MRI may serve as reliable biomarker in neurodegenerative diseases as well as in monitoring of microstructural changes representing disease progression and/or therapy effects. SAGE Publications 2014-05-12 /pmc/articles/PMC4184378/ /pubmed/25298866 http://dx.doi.org/10.1177/2047981614531573 Text en © The Foundation Acta Radiologica 2014 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(http://www.uk.sagepub.com/aboutus/openaccess.htm).
spellingShingle Original Article
Santner, Wolfram
Schocke, Michael
Boesch, Sylvia
Nachbauer, Wolfgang
Egger, Karl
A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
title A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
title_full A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
title_fullStr A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
title_full_unstemmed A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
title_short A longitudinal VBM study monitoring treatment with erythropoietin in patients with Friedreich ataxia
title_sort longitudinal vbm study monitoring treatment with erythropoietin in patients with friedreich ataxia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184378/
https://www.ncbi.nlm.nih.gov/pubmed/25298866
http://dx.doi.org/10.1177/2047981614531573
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