<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chelban V</submitter><funding>MSA Coalition</funding><funding>European Research Council</funding><funding>French Clinical Research Programme</funding><funding>Medical Research Council</funding><funding>Horizon 2020 research and innovation programme</funding><funding>Alzheimer's Society</funding><funding>PSP Association</funding><funding>Wellcome Trust</funding><funding>Wellcome Trust equipment and strategic awards</funding><pagination>4398-4408</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9762941</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>145(12)</volume><pubmed_abstract>Disease-modifying treatments are currently being trialled in multiple system atrophy. Approaches based solely on clinical measures are challenged by heterogeneity of phenotype and pathogenic complexity. Neurofilament light chain protein has been explored as a reliable biomarker in several neurodegenerative disorders but data on multiple system atrophy have been limited. Therefore, neurofilament light chain is not yet routinely used as an outcome measure in multiple system atrophy. We aimed to comprehensively investigate the role and dynamics of neurofilament light chain in multiple system atrophy combined with cross-sectional and longitudinal clinical and imaging scales and for subject trial selection. In this cohort study, we recruited cross-sectional and longitudinal cases in a multicent</pubmed_abstract><journal>Brain : a journal of neurology</journal><pubmed_title>Neurofilament light levels predict clinical progression and death in multiple system atrophy.</pubmed_title><pmcid>PMC9762941</pmcid><funding_grant_id>WT104033/Z/14/Z</funding_grant_id><funding_grant_id>720931</funding_grant_id><funding_grant_id>004</funding_grant_id><funding_grant_id>681712</funding_grant_id><funding_grant_id>517</funding_grant_id><funding_grant_id>220258</funding_grant_id><funding_grant_id>WT093205MA</funding_grant_id><pubmed_authors>Jabbari E</pubmed_authors><pubmed_authors>Foubert-Samier A</pubmed_authors><pubmed_authors>Guo T</pubmed_authors><pubmed_authors>Gonzalez M</pubmed_authors><pubmed_authors>Ng BL</pubmed_authors><pubmed_authors>Zetterberg H</pubmed_authors><pubmed_authors>Chelban V</pubmed_authors><pubmed_authors>Wellington H</pubmed_authors><pubmed_authors>Bocchetta M</pubmed_authors><pubmed_authors>Synofzik M</pubmed_authors><pubmed_authors>Foltynie T</pubmed_authors><pubmed_authors>Leigh PN</pubmed_authors><pubmed_authors>Houlden H</pubmed_authors><pubmed_authors>Todd EG</pubmed_authors><pubmed_authors>Rohrer JD</pubmed_authors><pubmed_authors>Burn DJ</pubmed_authors><pubmed_authors>Segura B</pubmed_authors><pubmed_authors>Compta Y</pubmed_authors><pubmed_authors>Wilke C</pubmed_authors><pubmed_authors>Marti MJ</pubmed_authors><pubmed_authors>Church A</pubmed_authors><pubmed_authors>Schols L</pubmed_authors><pubmed_authors>Pavese N</pubmed_authors><pubmed_authors>Morris HR</pubmed_authors><pubmed_authors>Le Traon AP</pubmed_authors><pubmed_authors>Vijiaratnam N</pubmed_authors><pubmed_authors>Nikram E</pubmed_authors><pubmed_authors>Tariq A</pubmed_authors><pubmed_authors>Kobylecki C</pubmed_authors><pubmed_authors>Massey L</pubmed_authors><pubmed_authors>Hu MTM</pubmed_authors><pubmed_authors>Alikhwan S</pubmed_authors><pubmed_authors>Painous C</pubmed_authors><pubmed_authors>Senkevich K</pubmed_authors><pubmed_authors>Junque C</pubmed_authors><pubmed_authors>Peran P</pubmed_authors><pubmed_authors>Munoz E</pubmed_authors><pubmed_authors>Olufodun S</pubmed_authors><pubmed_authors>Perez-Soriano A</pubmed_authors><pubmed_authors>Meissner WG</pubmed_authors><pubmed_authors>Rowe JB</pubmed_authors><pubmed_authors>Heslegrave AJ</pubmed_authors><pubmed_authors>Rascol O</pubmed_authors><pubmed_authors>Pchelina S</pubmed_authors><pubmed_authors>Costantini AA</pubmed_authors><pubmed_authors>Jaunmuktane Z</pubmed_authors><pubmed_authors>Zhelcheska K</pubmed_authors><pubmed_authors>Laurens B</pubmed_authors><pubmed_authors>Wood N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neurofilament light levels predict clinical progression and death in multiple system atrophy.</name><description>Disease-modifying treatments are currently being trialled in multiple system atrophy. Approaches based solely on clinical measures are challenged by heterogeneity of phenotype and pathogenic complexity. Neurofilament light chain protein has been explored as a reliable biomarker in several neurodegenerative disorders but data on multiple system atrophy have been limited. Therefore, neurofilament light chain is not yet routinely used as an outcome measure in multiple system atrophy. We aimed to comprehensively investigate the role and dynamics of neurofilament light chain in multiple system atrophy combined with cross-sectional and longitudinal clinical and imaging scales and for subject trial selection. In this cohort study, we recruited cross-sectional and longitudinal cases in a multicent</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-18T15:21:16.999Z</modification><creation>2025-04-07T02:00:09.482Z</creation></dates><accession>S-EPMC9762941</accession><cross_references><pubmed>35903017</pubmed><doi>10.1093/brain/awac253</doi></cross_references></HashMap>