TY - JOUR
T1 - Neurofilament Light Predicts Decline in Attention but Not Episodic Memory in Preclinical Alzheimer's Disease
AU - Aschenbrenner, Andrew J.
AU - Gordon, Brian A.
AU - Fagan, Anne M.
AU - Schindler, Suzanne E.
AU - Balota, David A.
AU - Morris, John C.
AU - Hassenstab, Jason J.
AU - Tales, Andrea
N1 - Funding Information:
We would like to express our gratitude to the research volunteers who participated in the studies from which these data were obtained and their supportive families. We thank the Clinical, Biomarker and Imaging Cores at the Knight Alzheimer Disease Research Center for sample and data collection. We acknowledge Ms. Rachel Henson for performing the assays for CSF NfL. We acknowledge Drs. Carlos Cruchaga, Tammie L.S. Benzinger, and Laura Piccio for providing partial funding of the NfL assays.∥This study was supported by National Institute on Aging grants R03AG050921 and K23AG053426 (SE Schindler), RF1AG058501 (C Cruchaga and L Piccio), R01AG054567 (TLS Benzinger and Y Wang), the Foundation for Barnes-Jewish Hospital (JC Morris), P50AG005681 (JC Morris), P01AG003991 (JC Morris), and P01AG026276 (JC Morris).
Publisher Copyright:
© 2020 - IOS Press and the authors. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Background: Cerebrospinal fluid tau and neurofilament light (NfL) are two biomarkers of neurodegeneration in Alzheimer's disease. Previous reports have shown that the influence of tau on cognitive decline depends on levels of amyloid burden whereas NfL predicts decline independently of amyloid. Most studies use a global cognitive composite as the primary outcome, and it is unknown if critical cognitive domain scores are similarly sensitive to rates of decline due to neurodegeneration. Objective: To examine the unique contribution of amyloid, tau, and NfL to rates of cognitive decline in multiple cognitive composites in a cognitively healthy, middle-aged to older adult cohort. Methods: A total of 255 participants (55% female; mean age=66.2 years, range=42.5-86.7 years) completed CSF studies and serial cognitive assessments to measure global cognition, episodic memory, and attentional control. Linear mixed effects models were used to examine rates of change on each composite score as a function of baseline biomarker levels. Results: Total tau predicted decline in attention regardless of amyloid status, but the relationship to global cognition and episodic memory was dependent on amyloid, replicating prior literature. NfL predicted decline in attention and global cognition, but not memory, and this effect was independent of amyloid status. Conclusions: These findings suggest that NfL can be used to monitor cognitive decline in aging and Alzheimer's disease and that an attentional control composite may be a better outcome for tracking general neurodegenerative effects on cognition.
AB - Background: Cerebrospinal fluid tau and neurofilament light (NfL) are two biomarkers of neurodegeneration in Alzheimer's disease. Previous reports have shown that the influence of tau on cognitive decline depends on levels of amyloid burden whereas NfL predicts decline independently of amyloid. Most studies use a global cognitive composite as the primary outcome, and it is unknown if critical cognitive domain scores are similarly sensitive to rates of decline due to neurodegeneration. Objective: To examine the unique contribution of amyloid, tau, and NfL to rates of cognitive decline in multiple cognitive composites in a cognitively healthy, middle-aged to older adult cohort. Methods: A total of 255 participants (55% female; mean age=66.2 years, range=42.5-86.7 years) completed CSF studies and serial cognitive assessments to measure global cognition, episodic memory, and attentional control. Linear mixed effects models were used to examine rates of change on each composite score as a function of baseline biomarker levels. Results: Total tau predicted decline in attention regardless of amyloid status, but the relationship to global cognition and episodic memory was dependent on amyloid, replicating prior literature. NfL predicted decline in attention and global cognition, but not memory, and this effect was independent of amyloid status. Conclusions: These findings suggest that NfL can be used to monitor cognitive decline in aging and Alzheimer's disease and that an attentional control composite may be a better outcome for tracking general neurodegenerative effects on cognition.
KW - Alzheimer's disease
KW - attention
KW - cerebrospinal fluid
KW - memory
KW - neurofilament light
UR - http://www.scopus.com/inward/record.url?scp=85083883234&partnerID=8YFLogxK
U2 - 10.3233/JAD-200018
DO - 10.3233/JAD-200018
M3 - Article
C2 - 32144992
AN - SCOPUS:85083883234
SN - 1387-2877
VL - 74
SP - 1119
EP - 1129
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 4
ER -