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dc.contributor.authorFaber, Jennifer
dc.contributor.authorSchaprian, Tamara
dc.contributor.authorBerkan, Koyak
dc.contributor.authorReetz, Kathrin
dc.contributor.authorFrança, Marcondes Cavalcante
dc.contributor.authorRezende, Thiago Junqueira Ribeiro de
dc.contributor.authorJiang Hong
dc.contributor.authorWeihua Liao
dc.contributor.authorWarrenburg, Bart van de
dc.contributor.authorGaalen, Judith van
dc.contributor.authorDurr, Alexandra
dc.contributor.authorMochel, Fanny
dc.contributor.authorGiunti, Paola
dc.contributor.authorGarcia-Moreno, Hector
dc.contributor.authorSchoels, Ludger
dc.contributor.authorHengel, Holger
dc.contributor.authorSynofzik, Matthis
dc.contributor.authorBender, Benjamin
dc.contributor.authorOz, Gulin
dc.contributor.authorInfante Ceberio, Jon 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-02-23T15:54:22Z
dc.date.available2022-02-23T15:54:22Z
dc.date.issued2021-10
dc.identifier.issn0885-3185
dc.identifier.issn1531-8257
dc.identifier.urihttp://hdl.handle.net/10902/24040
dc.description.abstractBackground: Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there is a need for markers that reflect disease-related alterations, in particular, in the preataxic stage, in which clinical scales are lacking sensitivity. Objective: The objective of this study was to quantify regional brain volumes and upper cervical spinal cord areas in spinocerebellar ataxia type 3 in vivo across the entire time course of the disease. Methods: We applied a brain segmentation approach that included a lobular subsegmentation of the cerebellum to magnetic resonance images of 210 ataxic and 48 preataxic spinocerebellar ataxia type 3 mutation carriers and 63 healthy controls. In addition, cervical cord cross-sectional areas were determined at 2 levels. Results: The metrics of cervical spinal cord segments C3 and C2, medulla oblongata, pons, and pallidum, and the cerebellar anterior lobe were reduced in preataxic mutation carriers compared with controls. Those of cervical spinal cord segments C2 and C3, medulla oblongata, pons, midbrain, cerebellar lobules crus II and X, cerebellar white matter, and pallidum were reduced in ataxic compared with nonataxic carriers. Of all metrics studied, pontine volume showed the steepest decline across the disease course. It covaried with ataxia severity, CAG repeat length, and age. The multivariate model derived from this analysis explained 46.33% of the variance of pontine volume. Conclusion: Regional brain and spinal cord tissue loss in spinocerebellar ataxia type 3 starts before ataxia onset. Pontine volume appears to be the most promising imaging biomarker candidate for interventional trials that aim at slowing the progression of spinocerebellar ataxia type 3.es_ES
dc.description.sponsorshipFunding agencies: This publication is an outcome of ESMI, an EU Joint Programme - Neurodegenerative Disease Research (JPND) Project (see www.jpnd.eu). The project is supported under the aegis of JPND through the following funding organizations: Germany, Federal Ministry of Education and Research (BMBF; funding codes 01ED1602A/B); Netherlands, The Netherlands Organisation for Health Research and Development; Portugal, Foundation for Science and Technology and Regional Fund for Science and Technology of the Azores; United Kingdom, Medical Research Council. This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement 643417. At the US sites this work was in part supported y the National Ataxia Foundation and the National Institute of Neurological Disorders and Stroke (NINDS) grant R01 NS080816. The Center for Magnetic Resonance Research is supported by the National Institute of Biomedical Imaging and Bioengineering (NIBIB) grant P41 EB027061, and the Institutional Center Cores for Advanced Neuroimaging award P30 NS076408 and S10 OD017974 grant.es_ES
dc.format.extent11 p.es_ES
dc.language.isoenges_ES
dc.publisherJohn Wiley and Sons Inc.es_ES
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposeses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceMovement Disorders, 2021, 36(10), 2021es_ES
dc.subject.otherSpinocerebellar ataxiaes_ES
dc.subject.otherMRIes_ES
dc.subject.otherVolumetryes_ES
dc.subject.otherBiomarkeres_ES
dc.titleRegional brain and spinal cord volume Loss in spinocerebellar ataxia type 3es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1002/mds.28610es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1002/mds.28610
dc.type.versionpublishedVersiones_ES


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This is an open access article under the terms of the Creative
Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposesExcepto si se señala otra cosa, la licencia del ítem se describe como This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes