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dc.contributor.authorDomínguez Vivero, Clara 
dc.contributor.authorLeira, Y.
dc.contributor.authorPineiro, M. S.
dc.contributor.authorRodríguez Osorio, Xiana 
dc.contributor.authorRamos-Cabrer, P.
dc.contributor.authorVillalba Martín, Carmen 
dc.contributor.authorSobrino Moreiras, Tomas 
dc.contributor.authorCampos Pérez, Francisco 
dc.contributor.authorCastillo Sánchez, José 
dc.contributor.authorLeira Muiño, Rogelio Manuel 
dc.date.accessioned2022-05-19T08:32:00Z
dc.date.available2022-05-19T08:32:00Z
dc.date.issued2020
dc.identifier.issn2072-6651
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32731573es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16722
dc.description.abstractPrevious studies have reported increased brain deposits of iron in patients with chronic migraine (CM). This study aims to determine the relation between iron deposits and outcome after treatment with OnabotulinumtoxinA (OnabotA). Demographic and clinical data were collected for this study through a prospective cohort study including 62 CM patients treated with OnabotA in the Hospital Clinico Universitario de Santiago de Compostela (Spain). Demographic and clinical variables were registered. Selected biomarkers in plasma during interictal periods (calcitonin gene-related peptide (CGRP) and pentraxin-3 (PTX3)) and neuroimaging changes (iron deposits in the red nucleus (RN), substantia nigra (SN), globus pallidus (GP), and periaqueductal gray matter (PAG), and white matter lesions (WML)) were determined. Subjects were classified in responders (>/=50% reduction in headache days) or non-responders (<50%). Responders to treatment were younger (mean age difference = 12.2; 95% confidence interval (CI): 5.4-18.9, p = 0.001), showed higher serum levels of CGRP (>/=50 ng/mL) and PTX3 (>/=1000 pg/mL) and smaller iron deposits in the GP and PAG (mean difference = 805.0; 95% CI: 37.9-1572.1 muL, p = 0.040 and mean difference = 69.8; 95% CI: 31.0-108.6 muL, p = 0.008; respectively). Differences in PAG iron deposits remained significant after adjusting for age (mean difference = 65.7; 95% CI: 22.8-108.6 muL, p = 0.003) and were associated with poor response to OnabotA after adjustment for clinical and biochemical variables (odds ratio (OR) = 0.963; 95% CI: 0.927-0.997, p = 0.041). We conclude that larger PAG iron deposits are associated with poor response to OnabotA in CM.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshBotulinum Toxins*
dc.subject.meshAdult*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshTreatment Outcome*
dc.subject.meshMagnetic Resonance Imaging*
dc.subject.meshNeuromuscular Agents*
dc.subject.meshIron*
dc.subject.meshMigraine Disorders*
dc.subject.meshPeriaqueductal Gray*
dc.subject.meshChronic Disease*
dc.titleIron Deposits in Periaqueductal Gray Matter Are Associated with Poor Response to OnabotulinumtoxinA in Chronic Migraineen
dc.typeJournal Articlees
dc.authorsophosVivero, C. D.;Leira, Y.;Pineiro, M. S.;Rodriguez-Osorio, X.;Ramos-Cabrer, P.;Martin, C. V.;Sobrino, T.;Campos, F.;Castillo, J.;Leira, R.
dc.identifier.doi10.3390/toxins12080479
dc.identifier.pmid32731573
dc.identifier.sophos40032
dc.issue.number8es
dc.journal.titleToxins (Basel)es
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Neuroloxíaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Radiodiagnósticoes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.rights.accessRightsopenAccess
dc.subject.decsresultado del tratamiento*
dc.subject.decstrastornos migrañosos*
dc.subject.decssustancia gris periacueductal*
dc.subject.decsenfermedad crónica*
dc.subject.decsmediana edad*
dc.subject.decsimagen por resonancia magnética*
dc.subject.decshumanos*
dc.subject.decshierro*
dc.subject.decsadulto*
dc.subject.decstoxinas botulínicas*
dc.subject.decsfármacos neuromusculares*
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number12es


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