Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/50785
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degois.publication.firstPage997pt_PT
degois.publication.issue9pt_PT
degois.publication.lastPage1004pt_PT
degois.publication.titleJournal of Neurology, Neurosurgery & Psychiatrypt_PT
dc.relation.publisherversionhttps://jnnp.bmj.com/pt_PT
dc.contributor.authorMeeter, Lieke H. H.-
dc.contributor.authorSteketee, Rebecca M. E.-
dc.contributor.authorSalkovic, Dina-
dc.contributor.authorVos, Maartje E.-
dc.contributor.authorGrossman, Murray-
dc.contributor.authorMcMillan, Corey T.-
dc.contributor.authorIrwin, David J.-
dc.contributor.authorBoxer, Adam L.-
dc.contributor.authorRojas, Julio C.-
dc.contributor.authorOlney, Nicholas T.-
dc.contributor.authorKarydas, Anna-
dc.contributor.authorMiller, Bruce L.-
dc.contributor.authorPijnenburg, Yolande A. L.-
dc.contributor.authorBarkhof, Frederik-
dc.contributor.authorSánchez-Valle, Raquel-
dc.contributor.authorLladó, Albert-
dc.contributor.authorBorrego-Ecija, Sergi-
dc.contributor.authorDiehl-Schmid, Janine-
dc.contributor.authorGrimmer, Timo-
dc.contributor.authorGoldhardt, Oliver-
dc.contributor.authorSantillo, Alexander F.-
dc.contributor.authorHansson, Oskar-
dc.contributor.authorVestberg, Susanne-
dc.contributor.authorBorroni, Barbara-
dc.contributor.authorPadovani, Alessandro-
dc.contributor.authorGalimberti, Daniela-
dc.contributor.authorScarpini, Elio-
dc.contributor.authorRohrer, Jonathan D.-
dc.contributor.authorWoollacott, Ione O. C.-
dc.contributor.authorSynofzik, Matthis-
dc.contributor.authorWilke, Carlo-
dc.contributor.authorDe Mendonça, Alexandre-
dc.contributor.authorVandenberghe, Rik-
dc.contributor.authorBenussi, Luisa-
dc.contributor.authorGhidoni, Roberta-
dc.contributor.authorBinetti, Giuliano-
dc.contributor.authorNiessen, Wiro J.-
dc.contributor.authorPapma, Janne M.-
dc.contributor.authorSeelaar, Harro-
dc.contributor.authorJiskoot, Lize C.-
dc.contributor.authorde Jong, Frank Jan-
dc.contributor.authorDonker Kaat, Laura-
dc.contributor.authorDel Campo, Marta-
dc.contributor.authorTeunissen, Charlotte E.-
dc.contributor.authorBron, Esther E.-
dc.contributor.authorVan den Berg, Esther-
dc.contributor.authorVan Swieten, John C.-
dc.date.accessioned2022-01-12T14:59:21Z-
dc.date.available2022-01-12T14:59:21Z-
dc.date.issued2019-
dc.identifier.citationJ Neurol Neurosurg Psychiatry. 2019 Sep;90(9):997-1004pt_PT
dc.identifier.issn0022-3050-
dc.identifier.urihttp://hdl.handle.net/10451/50785-
dc.description© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.pt_PT
dc.description.abstractBackground: Semantic dementia (SD) is a neurodegenerative disorder characterised by progressive language problems falling within the clinicopathological spectrum of frontotemporal lobar degeneration (FTLD). The development of disease-modifying agents may be facilitated by the relative clinical and pathological homogeneity of SD, but we need robust monitoring biomarkers to measure their efficacy. In different FTLD subtypes, neurofilament light chain (NfL) is a promising marker, therefore we investigated the utility of cerebrospinal fluid (CSF) NfL in SD. Methods: This large retrospective multicentre study compared cross-sectional CSF NfL levels of 162 patients with SD with 65 controls. CSF NfL levels of patients were correlated with clinical parameters (including survival), neuropsychological test scores and regional grey matter atrophy (including longitudinal data in a subset). Results: CSF NfL levels were significantly higher in patients with SD (median: 2326 pg/mL, IQR: 1628-3593) than in controls (577 (446-766), p<0.001). Higher CSF NfL levels were moderately associated with naming impairment as measured by the Boston Naming Test (rs =-0.32, p=0.002) and with smaller grey matter volume of the parahippocampal gyri (rs =-0.31, p=0.004). However, cross-sectional CSF NfL levels were not associated with progression of grey matter atrophy and did not predict survival. Conclusion: CSF NfL is a promising biomarker in the diagnostic process of SD, although it has limited cross-sectional monitoring or prognostic abilities.pt_PT
dc.description.sponsorshipThis study was funded by a Memorabel grant from Deltaplan Dementie (The Netherlands Organisation for Health Research and Development, and Alzheimer Nederland grant number 7330598105), National Institutes of Health (Grants AG010124, AG032953, AG043503, NS088341, AG017586, AG052943, AG038490), the Wyncote Foundation, Dana Foundation, Brightfocus Foundation, Penn Institute on Aging, Pla estratègic de recerca i innovació en salut 2016-2020, Catalan Department of Health (grant number SLT002/16/00408), Italian Ministry of Health (Ricerca Corrente) and the German Federal Ministry of Education and Research (FTLDc 01GI1007A). MS was supported by the Else Kröner-Fresenius-Stiftung. CW was supported by the Vaillant Stiftungpt_PT
dc.language.isoengpt_PT
dc.publisherBMJ Publishing Group Ltd.pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleClinical value of cerebrospinal fluid neurofilament light chain in semantic dementiapt_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
degois.publication.volume90pt_PT
dc.identifier.doi10.1136/jnnp-2018-319784pt_PT
dc.identifier.eissn1468-330X-
Aparece nas colecções:IMM - Artigos em Revistas Internacionais
FM - Artigos em Revistas Internacionais

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