Plasma neurofilament light as a potential biomarker for cognitive decline in a longitudinal study of middle-aged urban adults

dc.contributor.authorBeydoun, May A.
dc.contributor.authorHooten, Nicole Noren
dc.contributor.authorBeydoun, Hind A.
dc.contributor.authorMaldonado, Ana I.
dc.contributor.authorWeiss, Jordan
dc.contributor.authorEvans, Michele K.
dc.contributor.authorZonderman, Alan B.
dc.date.accessioned2021-09-15T17:26:29Z
dc.date.available2021-09-15T17:26:29Z
dc.date.issued2021-08-21
dc.description.abstractPlasma neurofilament light (NfL) is a marker for neurodegenerative diseases. Few studies have examined the association of NfL with middle-aged changes in cognitive performance, and no studies have examined differential NfL effects by race. Using data from the Healthy Aging in Neighborhoods of Diversity across the Life Span (HANDLS) study (n = 625, Agev1: 30–66 y, 41.6% male, 56.3% African American, 27.8% below poverty), we investigated the associations of initial NfL levels and annualized change with cognitive performance over time in global mental status, verbal and visual memory, fluency, attention, and executive function. We used ordinary least squares and mixed-effects regressions stratified by race, while exploring differential associations by age group, sex, and poverty status. Over a mean follow-up of 4.3 years, we found initial NfL level was associated with a faster decline on normalized mental status scores in Whites only and in those >50 years old. Annualized increase in NfL was associated with a greater decline in verbal fluency in men. In other exploratory analyses, annualized increase in NfL was associated with a slower decline in verbal memory among individuals living above poverty; in the older group (>50 years), first-visit NfL was linked with better performance at baseline in global mental status and verbal memory. In summary, first-visit NfL was primarily associated with the global mental status decline among Whites, while exhibiting inconsistent relationships in some exploratory analyses. Plasma NfL levels can be detected and quantified in non-demented middle-aged adults and changes can be analyzed over time. More longitudinal studies are needed to address the clinical utility of this biomarker for early cognitive defects.en_US
dc.description.sponsorshipThis work was supported in part by the Intramural Research Program of the NIH, National Institute on Aging, Project number AG000513. MAB had full access to the data used in this paper and completed all the statistical analyses.en_US
dc.description.urihttps://www.nature.com/articles/s41398-021-01563-9en_US
dc.format.extent2 filesen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m2jtgj-jxrx
dc.identifier.citationBeydoun, May A. et al.; Plasma neurofilament light as a potential biomarker for cognitive decline in a longitudinal study of middle-aged urban adults; Translational Psychiatry, volume 11, Article number: 436, 21 August, 2021; https://doi.org/10.1038/s41398-021-01563-9en_US
dc.identifier.urihttps://doi.org/10.1038/s41398-021-01563-9
dc.identifier.urihttp://hdl.handle.net/11603/22988
dc.language.isoen_USen_US
dc.publisherNatureen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Psychology Department Collection
dc.relation.ispartofUMBC Student Collection
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.en_US
dc.rightsPublic Domain Mark 1.0*
dc.rightsThis work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
dc.rights.urihttp://creativecommons.org/publicdomain/mark/1.0/*
dc.titlePlasma neurofilament light as a potential biomarker for cognitive decline in a longitudinal study of middle-aged urban adultsen_US
dc.typeTexten_US
dcterms.creatorhttps://orcid.org/0000-0002-7247-3363en_US

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