Utility of Plasma Neurofilament Light in the 1Florida Alzheimer’s Disease Research Center (ADRC)

Autor: Maria T. Greig, Ranjan Duara, Rosemarie Rodriguez, Carlos Quinonez, Monica Rosselli, Todd E. Golde, Tatjana Rundek, Kevin Hanson, Nilufer Ertekin-Taner, Malek Adjouadi, Cesar L Chirinos, David A. Loewenstein, Miriam J. Rodriguez, Glenn E. Smith, Rosie E. Curiel Cid, Karen N. McFarland, David E. Vaillancourt, Steven T. DeKosky, Raquel Behar, Warren W. Barker, Michael Marsiske
Rok vydání: 2021
Předmět:
Male
0301 basic medicine
Oncology
positron emission tomography
diagnosis
Disease
Hippocampus
plasma neurofilament light
Cohort Studies
hippocampal atrophy
Cognition
0302 clinical medicine
Neurofilament Proteins
magnetic resonance imaging
Medicine
Aged
80 and over

General Neuroscience
Age Factors
amyloid
Brain
Hispanic or Latino
General Medicine
Middle Aged
Cognitive test
Psychiatry and Mental health
Clinical Psychology
Cohort
Female
Alzheimer’s disease
Research Article
Lewy Body Disease
medicine.medical_specialty
White People
Alzheimer's disease research
03 medical and health sciences
Sex Factors
Neuroimaging
Alzheimer Disease
Internal medicine
Humans
Cognitive Dysfunction
Memory disorder
Aged
Amyloid beta-Peptides
business.industry
Dementia
Vascular

medicine.disease
Black or African American
Functional Status
030104 developmental biology
Positron-Emission Tomography
Etiology
Atrophy
Frontotemporal Lobar Degeneration
Geriatrics and Gerontology
business
030217 neurology & neurosurgery
Zdroj: Journal of Alzheimer's Disease
ISSN: 1875-8908
1387-2877
Popis: Background: Plasma NfL (pNfL) levels are elevated in many neurological disorders. However, the utility of pNfL in a clinical setting has not been established. Objective: In a cohort of diverse older participants, we examined: 1) the association of pNfL to age, sex, Hispanic ethnicity, diagnosis, and structural and amyloid imaging biomarkers; and 2) its association to baseline and longitudinal cognitive and functional performance. Methods: 309 subjects were classified at baseline as cognitively normal (CN) or with cognitive impairment. Most subjects had structural MRI and amyloid PET scans. The most frequent etiological diagnosis was Alzheimer’s disease (AD), but other neurological and neuropsychiatric disorders were also represented. We assessed the relationship of pNfL to cognitive and functional status, primary etiology, imaging biomarkers, and to cognitive and functional decline. Results: pNfL increased with age, degree of hippocampal atrophy, and amyloid load, and was higher in females among CN subjects, but was not associated with Hispanic ethnicity. Compared to CN subjects, pNfL was elevated among those with AD or FTLD, but not those with neuropsychiatric or other disorders. Hippocampal atrophy, amyloid positivity and higher pNfL levels each added unique variance in predicting greater functional impairment on the CDR-SB at baseline. Higher baseline pNfL levels also predicted greater cognitive and functional decline after accounting for hippocampal atrophy and memory scores at baseline. Conclusion: pNfL may have a complementary and supportive role to brain imaging and cognitive testing in a memory disorder evaluation, although its diagnostic sensitivity and specificity as a stand-alone measure is modest. In the absence of expensive neuroimaging tests, pNfL could be used for differentiating neurodegenerative disease from neuropsychiatric disorders.
Databáze: OpenAIRE