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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004464naa a2200697 4500
001oai:gup.ub.gu.se/296716
003SwePub
008240528s2020 | |||||||||||000 ||eng|
024a https://gup.ub.gu.se/publication/2967162 URI
024a https://doi.org/10.1002/mds.282062 DOI
040 a (SwePub)gu
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Mollenhauer, B.4 aut
2451 0a Validation of Serum Neurofilament Light Chain as a Biomarker of Parkinson's Disease Progression
264 c 2020-08-15
264 1b Wiley,c 2020
520 a Background The objective of this study was to assess neurofilament light chain as a Parkinson's disease biomarker. Methods We quantified neurofilament light chain in 2 independent cohorts: (1) longitudinal cerebrospinal fluid samples from the longitudinal de novo Parkinson's disease cohort and (2) a large longitudinal cohort with serum samples from Parkinson's disease, other cognate/neurodegenerative disorders, healthy controls, prodromal conditions, and mutation carriers. Results In the Parkinson's Progression Marker Initiative cohort, mean baseline serum neurofilament light chain was higher in Parkinson's disease patients (13 +/- 7.2 pg/mL) than in controls (12 +/- 6.7 pg/mL),P= 0.0336. Serum neurofilament light chain increased longitudinally in Parkinson's disease patients versus controls (P< 0.01). Motor scores were positively associated with neurofilament light chain, whereas some cognitive scores showed a negative association. Conclusions Neurofilament light chain in serum samples is increased in Parkinson's disease patients versus healthy controls, increases over time and with age, and correlates with clinical measures of Parkinson's disease severity. Although the specificity of neurofilament light chain for Parkinson's disease is low, it is the first blood-based biomarker candidate that could support disease stratification of Parkinson's disease versus other cognate/neurodegenerative disorders, track clinical progression, and possibly assess responsiveness to neuroprotective treatments. However, use of neurofilament light chain as a biomarker of response to neuroprotective interventions remains to be assessed. (c) 2020 The Authors.Movement Disorderspublished by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Neurovetenskaper0 (SwePub)301052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Neurosciences0 (SwePub)301052 hsv//eng
653 a Parkinson's disease
653 a parkinsonism
653 a cohort studies
653 a outcome research
653 a cerebrospinal-fluid
653 a diagnosis
653 a pathology
653 a accuracy
653 a Neurosciences & Neurology
700a Dakna, M.4 aut
700a Kruse, N.4 aut
700a Galasko, D.4 aut
700a Foroud, T.4 aut
700a Zetterberg, Henrik,d 1973u Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry4 aut0 (Swepub:gu)xzethe
700a Schade, S.4 aut
700a Gera, R. G.4 aut
700a Wang, W. T.4 aut
700a Gao, F.4 aut
700a Frasier, M.4 aut
700a Chahine, L. M.4 aut
700a Coffey, C. S.4 aut
700a Singleton, A. B.4 aut
700a Simuni, T.4 aut
700a Weintraub, D.4 aut
700a Seibyl, J.4 aut
700a Toga, A. W.4 aut
700a Tanner, C. M.4 aut
700a Kieburtz, K.4 aut
700a Marek, K.4 aut
700a Siderowf, A.4 aut
700a Cedarbaum, J. M.4 aut
700a Hutten, S. J.4 aut
700a Trenkwalder, C.4 aut
700a Graham, D.4 aut
710a Göteborgs universitetb Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi4 org
773t Movement Disordersd : Wileyg 35:11, s. 1999-2008q 35:11<1999-2008x 0885-3185x 1531-8257
856u https://movementdisorders.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28206
8564 8u https://gup.ub.gu.se/publication/296716
8564 8u https://doi.org/10.1002/mds.28206

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