Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32802
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dc.contributor.authorKang, Matthew Jy-
dc.contributor.authorEratne, Dhamidhu-
dc.contributor.authorDobson, Hannah-
dc.contributor.authorMalpas, Charles B-
dc.contributor.authorKeem, Michael-
dc.contributor.authorLewis, Courtney-
dc.contributor.authorGrewal, Jasleen-
dc.contributor.authorTsoukra, Vivian-
dc.contributor.authorDang, Christa-
dc.contributor.authorMocellin, Ramon-
dc.contributor.authorKalincik, Tomas-
dc.contributor.authorSantillo, Alexander F-
dc.contributor.authorZetterberg, Henrik-
dc.contributor.authorBlennow, Kaj-
dc.contributor.authorStehmann, Christiane-
dc.contributor.authorVarghese, Shiji-
dc.contributor.authorLi, Qiao-Xin-
dc.contributor.authorMasters, Colin L-
dc.contributor.authorCollins, Steven-
dc.contributor.authorBerkovic, Samuel F-
dc.contributor.authorEvans, Andrew-
dc.contributor.authorKelso, Wendy-
dc.contributor.authorFarrand, Sarah-
dc.contributor.authorLoi, Samantha M-
dc.contributor.authorWalterfang, Mark-
dc.contributor.authorVelakoulis, Dennis-
dc.date2023-
dc.date.accessioned2023-05-10T23:23:30Z-
dc.date.available2023-05-10T23:23:30Z-
dc.date.issued2024-02-
dc.identifier.citationActa Neuropsychiatrica 2024-02; 36(1)en_US
dc.identifier.issn1601-5215-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32802-
dc.description.abstractPeople with neuropsychiatric symptoms often experience delay in accurate diagnosis. Although cerebrospinal fluid neurofilament light (CSF NfL) shows promise in distinguishing neurodegenerative disorders (ND) from psychiatric disorders (PSY), its accuracy in a diagnostically challenging cohort longitudinally is unknown. We collected longitudinal diagnostic information (mean=36 months) from patients assessed at a neuropsychiatry service, categorising diagnoses as ND/mild cognitive impairment/other neurological disorders (ND/MCI/other), and PSY. We pre-specified NfL>582pg/mL as indicative of ND/MCI/other. Diagnostic category changed from initial to final diagnosis for 23% (49/212) of patients. NfL predicted the final diagnostic category for 92% (22/24) of these and predicted final diagnostic category overall (ND/MCI/other vs. PSY) in 88% (187/212), compared to 77% (163/212) with clinical assessment alone. CSF NfL improved diagnostic accuracy, with potential to have led to earlier, accurate diagnosis in a real-world setting using a pre-specified cut-off, adding weight to translation of NfL into clinical practice.en_US
dc.language.isoeng-
dc.subjectbiomarkeren_US
dc.subjectdementiaen_US
dc.subjectdiagnosisen_US
dc.subjectdiagnostic delayen_US
dc.subjectneurofilamenten_US
dc.subjectneuropsychiatryen_US
dc.subjectpsychiatric disordersen_US
dc.titleCerebrospinal fluid neurofilament light predicts longitudinal diagnostic change in patients with psychiatric and neurodegenerative disorders.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleActa Neuropsychiatricaen_US
dc.identifier.affiliationNeuropsychiatry, Royal Melbourne Hospital, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationMelbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationAlfred Mental and Addiction Health, Alfred Health, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, Royal Melbourne Hospital, Parkville, Victoria, Australia.;en_US
dc.identifier.affiliationMelbourne School of Psychological Sciences, University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationNeuropsychiatry, Royal Melbourne Hospital, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Neurology, Evangelismos Hospital, Athens, Greece.en_US
dc.identifier.affiliationNational Ageing Research Institute; University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationDelmont Private Hospital, Glen Iris, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, Royal Melbourne Hospital, Parkville, Victoria, Australia.;Department of Neurology, Royal Melbourne Hospital, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Clinical Sciences Malmö, Clinical Memory Research Unit, Lund University, Lund, Sweden.;Memory Clinic, Skåne University Hospital, Malmo, Sweden.en_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationNational Dementia Diagnostic Laboratory, The Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationEpilepsy Research Centreen_US
dc.identifier.affiliationDepartment of Medicine, Royal Melbourne Hospital, Parkville, Victoria, Australia.;National Dementia Diagnostic Laboratory, The Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationDepartment of Neurology, Evangelismos Hospital, Athens, Greece.en_US
dc.identifier.doi10.1017/neu.2023.25en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-9375-3762en_US
dc.identifier.orcid0000-0002-4953-4500en_US
dc.identifier.orcid0000-0002-1389-3691en_US
dc.identifier.pubmedid37114460-
dc.description.startpage1-
dc.description.endpage36-
local.name.researcherBerkovic, Samuel F-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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