Abstract
Alzheimer's disease is hypothesized to be caused by an imbalance between β-amyloid (Aβ) production and clearance that leads to Aβ accumulation in the central nervous system (CNS). Aβ production and clearance are key targets in the development of disease-modifying therapeutic agents for Alzheimer's disease. However, there has not been direct evidence of altered Aβ production or clearance in Alzheimer's disease. By using metabolic labeling, we measured Aβ42 and Aβ40 production and clearance rates in the CNS of participants with Alzheimer's disease and cognitively normal controls. Clearance rates for both Aβ42 and Aβ40 were impaired in Alzheimer's disease compared with controls. On average, there were no differences in Aβ40 or Aβ42 production rates. Thus, the common late-onset form of Alzheimer's disease is characterized by an overall impairment in Aβ clearance.
MeSH Terms
Aged
Aged, 80 and over
Alzheimer Disease/cerebrospinal fluid,metabolism
Amyloid beta-Peptides/cerebrospinal fluid,metabolism
Brain/metabolism
Female
Humans
Kinetics
Male
Middle Aged
Peptide Fragments/cerebrospinal fluid,metabolism
Chemicals
Amyloid beta-Peptides
Peptide Fragments
amyloid beta-protein (1-40)
amyloid beta-protein (1-42)
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Mawuenyega Kwasi G
Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Sigurdson Wendy
Ovod Vitaliy
Munsell Ling
Kasten Tom
Morris John C
Yarasheski Kevin E
Bateman Randall J
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