Associations between plasma neurofilament light, in vivo brain pathology, and cognition in non-demented individuals with autosomal-dominant Alzheimer's disease

被引:17
作者
Guzman-Velez, Edmarie [1 ]
Zetterberg, Henrik [2 ,3 ,4 ,5 ]
Fox-Fuller, Joshua T. [1 ,6 ]
Vila-Castelar, Clara [1 ]
Sanchez, Justin S. [1 ]
Baena, Ana [7 ]
Garcia-Ospina, Gloria [7 ]
Aguillon, David [7 ]
Pardilla-Delgado, Enmanuelle [1 ]
Gatchel, Jennifer R. [1 ,8 ]
Sperling, Reisa A. [1 ,9 ]
Johnson, Keith [1 ,9 ]
Reiman, Eric M. [10 ,11 ,12 ,13 ]
Blennow, Kaj [2 ,3 ]
Lopera, Francisco [7 ]
Quiroz, Yakeel T. [1 ,7 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Boston, MA 02115 USA
[2] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[3] Univ Gothenburg, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Sahlgrenska Acad, Molndal Campus, Molndal, Sweden
[4] UCL, UK Dementia Res Inst, London, England
[5] UCL Inst Neurol, Dept Neurodegenerat Dis, London, England
[6] Boston Univ, Dept Psychol & Brain Sci, Boston, MA 02215 USA
[7] Univ Antioquia, Grp Neurociencias Antioquia, Medellin, Colombia
[8] McLean Hosp, Div Geriatr Psychiat & Psychiat Neurotherapeut, 115 Mill St, Belmont, MA 02178 USA
[9] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[10] Banner Alzheimers Inst, Phoenix, AZ USA
[11] Univ Arizona, Phoenix, AZ USA
[12] Arizona State Univ, Phoenix, AZ USA
[13] Translat Genom Res Inst, Phoenix, AZ USA
基金
英国医学研究理事会;
关键词
Alzheimer' s disease; biomarkers; NfL; pathology; preclinical; presenilin‐ 1; AMYLOID-BETA; CHAIN; TAU; PET; NEURODEGENERATION; SEVERITY; MARKERS;
D O I
10.1002/alz.12248
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Neurofilament light (NfL) is a promising biomarker of early neurodegeneration in Alzheimer's disease (AD). We examined whether plasma NfL was associated with in vivo amyloid beta and tau, and cognitive performance in non-demented presenilin-1 (PSEN1) E280A mutation carriers. Methods Twenty-five mutation carriers and 19 non-carriers (age range: 28 to 49 years) were included in this study. Participants underwent 11C Pittsburgh compound B (PiB)-PET (positron emission tomography), flortaucipir-PET, blood sampling, and cognitive testing. Results Mutation carriers exhibited higher plasma NfL levels than non-carriers. In carriers, higher NfL levels were related to greater regional tau burden and worse cognition, but not amyloid beta load. When we adjusted for age, a proxy of disease progression, elevated plasma NfL levels were only correlated with worse memory recall. Conclusions Findings support an association between plasma NfL, cognition, and tau pathology in non-demented individuals at genetic risk for developing AD dementia. Plasma NfL may be useful for selecting individuals at increased risk and tracking disease progression in AD.
引用
收藏
页码:813 / 821
页数:9
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