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dc.contributor.authorPavy-Le Traon, A.es
dc.contributor.authorPiedvache, A.es
dc.contributor.authorPérez Lloret, Santiagoes
dc.contributor.authorCalandra-Buonaura, G.es
dc.contributor.authorCochen De Cock, Valériees
dc.contributor.authorColosimo, C.es
dc.contributor.authorCortelli, P.es
dc.contributor.authorDebs, R.es
dc.contributor.authorDuerr, S.es
dc.contributor.authorFanciulli, A.es
dc.contributor.authorFoubert Samier, Alexandraes
dc.contributor.authorGerdelat, A.es
dc.contributor.authorGurevich, T.es
dc.contributor.authorKrismer, F.es
dc.contributor.authorPoewe, W.es
dc.contributor.authorTison, F.es
dc.contributor.authorTranchant, C.es
dc.contributor.authorWenning, G.es
dc.contributor.authorRascol, O.es
dc.contributor.authorMeissner, W. G.es
dc.date.accessioned2022-06-27T13:22:18Z-
dc.date.available2022-06-27T13:22:18Z-
dc.date.issued2016-
dc.identifier.citationPavy-Le Traon, A., et al. New insights into orthostatic hypotension in multiple system atrophy : a European multicentre cohort study [en líena]. Journal of Neurology, Neurosurgery and Psychiatry. 2016, 87(5) doi:10.1136/jnnp-2014-309999 Disponible en: https://repositorio.uca.edu.ar/handle/123456789/14266es
dc.identifier.issn0022-3050-
dc.identifier.issn1468-330X (online)-
dc.identifier.urihttps://repositorio.uca.edu.ar/handle/123456789/14266-
dc.description.abstractAbstract: Objectives Orthostatic hypotension (OH) is a key feature of multiple system atrophy (MSA), a fatal progressive neurodegenerative disorder associated with autonomic failure, parkinsonism and ataxia. This study aims (1) to determine the clinical spectrum of OH in a large European cohort of patients with MSA and (2) to investigate whether a prolonged postural challenge increases the sensitivity to detect OH in MSA. Methods: Assessment of OH during a 10 min orthostatic test in 349 patients with MSA from seven centres of the European MSA-Study Group (age: 63.6±8.8 years; disease duration: 4.2±2.6 years). Assessment of a possible relationship between OH and MSA subtype (P with predominant parkinsonism or C with predominant cerebellar ataxia), Unified MSA Rating Scale (UMSARS) scores and drug intake. Results: 187 patients (54%) had moderate (>20 mm Hg (systolic blood pressure (SBP)) and/or >10 mm Hg (diastolic blood pressure (DBP)) or severe OH (>30 mm Hg (SBP) and/or >15 mm Hg (DBP)) within 3 min and 250 patients (72%) within 10 min. OH magnitude was significantly associated with disease severity (UMSARS I, II and IV), orthostatic symptoms (UMSARS I) and supine hypertension. OH severity was not associated with MSA subtype. Drug intake did not differ according to OH magnitude except for antihypertensive drugs being less frequently, and antihypotensive drugs more frequently, prescribed in severe OH. Conclusions: This is the largest study of OH in patients with MSA. Our data suggest that the sensitivity to pick up OH increases substantially by a prolonged 10 min orthostatic challenge. These results will help to improve OH management and the design of future clinical trials.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherBMJ Publishing Groupes
dc.rightsinfo:eu-repo/semantics/closedAccess*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceJournal of Neurology, Neurosurgery and Psychiatry. 2016, 87(5)es
dc.subjectCOMORBILIDADes
dc.subjectTRASTORNOS DEL MOVIMIENTOes
dc.subjectATROFIA MULTISISTÉMICAes
dc.subjectHIPOTENSION ORTOSTATICAes
dc.titleNew insights into orthostatic hypotension in multiple system atrophy : a European multicentre cohort studyes
dc.typeArtículoes
dc.identifier.doi10.1136/jnnp-2014-309999-
dc.identifier.pmid25977316-
uca.disciplinaMEDICINAes
uca.issnrd1es
uca.affiliationFil: Pavy-Le Traon, A. University Hospital of Toulouse. French Reference Center for MSA. Neurology Department; Franciaes
uca.affiliationFil: Pavy-Le Traon, A. Unité Institut national de la santé et de la recherche médicale U; Franciaes
uca.affiliationFil: Piedvache, A. Paul Sabatier University. Faculty of Mathematics; Franciaes
uca.affiliationFil: Pérez Lloret, Santiago. University of Toulouse. University Hospital of Toulouse. Clinical Investigation Center CIC. Department of Clinical Pharmacology; Franciaes
uca.affiliationFil: Pérez Lloret, Santiago. Institut national de la santé et de la recherche médicale; Franciaes
uca.affiliationFil: Pérez Lloret, Santiago. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Biomédicas; Argentinaes
uca.affiliationFil: Pérez Lloret, Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes
uca.affiliationFil: Calandra-Buonaura, G. Università di Bologna; Italiaes
uca.affiliationFil: Calandra-Buonaura, G. Istituto delle Scienze Neurologiche di Bologna; Italiaes
uca.affiliationFil: Cochen De Cock, Valérie. University Hospital of Toulouse. French Reference Center for MSA. Neurology Department; Franciaes
uca.affiliationFil: Cochen De Cock, Valérie. University of Montpellier; Franciaes
uca.affiliationFil: Colosimo, C. Sapienza Università di Roma. Dipartimento di Neurologia e Psichiatria; Italiaes
uca.affiliationFil: Cortelli, P. Università di Bologna; Italiaes
uca.affiliationFil: Cortelli, P. Istituto delle Scienze Neurologiche di Bologna; Italiaes
uca.affiliationFil: Debs, R. University Hospital of Toulouse. French Reference Center for MSA. Neurology Department; Franciaes
uca.affiliationFil: Debs, R. Medical University. Department of Neurology; Austriaes
uca.affiliationFil: Fanciulli, A. Medical University. Department of Neurology; Austriaes
uca.affiliationFil: Foubert-Samier, A. CHU de Bordeaux. Centre de référence atrophie multisystématisée; Franciaes
uca.affiliationFil: Foubert-Samier, A. CHU de Bordeaux. Service de Neurologie; Franciaes
uca.affiliationFil: Foubert-Samier, A. Université de Bordeaux. Institut des Maladies Neurodégénératives; Franciaes
uca.affiliationFil: Gerdelat, A. University Hospital of Toulouse. French Reference Center for MSA. Neurology Department; Franciaes
uca.affiliationFil: Gurevich, T. Tel-Aviv University. Sourasky Medical Center. Department of Neurology. Movement Disorders Unit; Israeles
uca.affiliationFil: Krismer, F. Medical University. Department of Neurology; Austriaes
uca.affiliationFil: Poewe, W. Medical University. Division of Neurobiology; Austriaes
uca.affiliationFil: Tison, F. CHU de Bordeaux. Centre de référence atrophie multisystématisée; Franciaes
uca.affiliationFil: Tison, F. CHU de Bordeaux. Service de Neurologie; Franciaes
uca.affiliationFil: Tison, F. Université de Bordeaux. Institut des Maladies Neurodégénératives; Franciaes
uca.affiliationFil: Tranchant, C. University Hospital Hautepierre. Neurology Department; Franciaes
uca.affiliationFil: Wenning, G. Medical University. Department of Neurology; Austriaes
uca.affiliationFil: Wenning, G. Medical University. Division of Neurobiology; Austriaes
uca.affiliationFil: Rascol, O. University Hospital of Toulouse. French Reference Center for MSA. Neurology Department; Franciaes
uca.affiliationFil: Rascol, O. University of Toulouse. University Hospital of Toulouse. Clinical Investigation Center CIC. Department of Clinical Pharmacology; Franciaes
uca.affiliationFil: Rascol, O. Institut national de la santé et de la recherche médicale; Franciaes
uca.affiliationFil: Meissner, W. G. CHU de Bordeaux. Centre de référence atrophie multisystématisée; Franciaes
uca.affiliationFil: Meissner, W. G. CHU de Bordeaux. Service de Neurologie; Franciaes
uca.affiliationFil: Meissner, W. G. Université de Bordeaux. Institut des Maladies Neurodégénératives; Franciaes
uca.versionpublishedVersiones
item.languageiso639-1en-
item.grantfulltextembargo_21000101-
item.fulltextWith Fulltext-
crisitem.author.deptLaboratorio de Neurobiología Molecular-
crisitem.author.deptConsejo Nacional de Investigaciones Científicas y Técnicas-
crisitem.author.orcid0000-0001-9069-6512-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
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