Age and amyloid effects on human central nervous system amyloid-beta kinetics

作者：Patterson Bruce W; Elbert Donald L; Mawuenyega Kwasi G; Kasten Tom; Ovod Vitaliy; Ma Shengmei; Xiong Chengjie; Chott Robert; Yarasheski Kevin; Sigurdson Wendy; Zhang Lily; Goate Alison; Benzinger Tammie; Morris John C; Holtzman David; Bateman Randall J^*

来源：Annals of Neurology, 2015, 78(3): 439-453.

DOI：10.1002/ana.24454

ObjectiveAge is the single greatest risk factor for Alzheimer's disease (AD), with the incidence doubling every 5 years after age 65. However, our understanding of the mechanistic relationship between increasing age and the risk for AD is currently limited. We therefore sought to determine the relationship between age, amyloidosis, and amyloid-beta (A) kinetics in the central nervous system (CNS) of humans.
MethodsA kinetics were analyzed in 112 participants and compared to the ages of participants and the amount of amyloid deposition.
ResultsWe found a highly significant correlation between increasing age and slowed A turnover rates (2.5-fold longer half-life over five decades of age). In addition, we found independent effects on A42 kinetics specifically in participants with amyloid deposition. Amyloidosis was associated with a higher (>50%) irreversible loss of soluble A42 and a 10-fold higher A42 reversible exchange rate.
InterpretationThese findings reveal a mechanistic link between human aging and the risk of amyloidosis, which may be owing to a dramatic slowing of A turnover, increasing the likelihood of protein misfolding that leads to deposition. Alterations in A kinetics associated with aging and amyloidosis suggest opportunities for diagnostic and therapeutic strategies. More generally, this study provides an example of how changes in protein turnover kinetics can be used to detect physiological and pathophysiological changes and may be applicable to other proteinopathies. Ann Neurol 2015;78:439-453

• 出版日期2015-9