TY - JOUR
T1 - Utility of Plasma Neurofilament Light in the 1Florida Alzheimer's Disease Research Center (ADRC)
AU - Barker, Warren
AU - Quinonez, Carlos
AU - Greig, Maria T.
AU - Behar, Raquel
AU - Chirinos, Cesar
AU - Rodriguez, Rosemarie A.
AU - Rosselli, Monica
AU - Rodriguez, Miriam J.
AU - Cid, Rosie Curiel
AU - Rundek, Tatjana
AU - McFarland, Karen
AU - Hanson, Kevin
AU - Smith, Glenn
AU - Dekosky, Steven
AU - Vaillancourt, David
AU - Adjouadi, Malek
AU - Marsiske, Michael
AU - Ertekin-Taner, Nilufer
AU - Golde, Todd
AU - Loewenstein, David A.
AU - Duara, Ranjan
N1 - Funding Information:
Our findings suggest that pNfL provides a convenient marker of the severity of neurodegeneration and is associated with global cognitive and functional impairment, independent of hippocampal atrophy and abnormal amyloid load. An elevated pNfL concentration, similar to an elevated cholesterol, fasting glucose, or blood pressure measurement, could indicate the need for more detailed diagnostic evaluation and the institution of therapeutic and behavioral This research was supported by the National Institute of Aging Grant numbers 5P50AG0477266021 Florida Alzheimer’s Disease Research Center (Todd Golde, PI) and 1P30AG066506-01 Florida Alzheimer’s Disease Research Center (Todd Golde, PI).
Publisher Copyright:
© 2021-The authors. Published by IOS Press.
PY - 2021
Y1 - 2021
N2 - 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.
AB - 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.
KW - Alzheimer's disease
KW - amyloid
KW - diagnosis
KW - hippocampal atrophy
KW - magnetic resonance imaging
KW - plasma neurofilament light
KW - positron emission tomography
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U2 - 10.3233/JAD-200901
DO - 10.3233/JAD-200901
M3 - Article
C2 - 33216030
AN - SCOPUS:85099030267
SN - 1387-2877
VL - 79
SP - 59
EP - 70
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 1
ER -