Preclinical effects of APOE [epsilon]4 on cerebrospinal fluid Aß42 concentrations
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CitationLautner R. Insel PS. Skillbäck T. Olsson B. Landén M. Frisoni GB. Herukka SK. Hampel H. Wallin A. Minthon L. Hansson O. Blennow K. Mattsson N. Zetterberg H. (2017). Preclinical effects of APOE [epsilon]4 on cerebrospinal fluid Aß42 concentrations. Alzheimer's Research & Therapy, 9 (1) , 87. 10.1186/s13195-017-0313-3.
From earlier studies it is known that the APOE ε2/ε3/ε4 polymorphism modulates the concentrations of cerebrospinal fluid (CSF) beta-amyloid1–42 (Aβ42) in patients with cognitive decline due to Alzheimer’s disease (AD), as well as in cognitively healthy controls. Here, in a large cohort consisting solely of cognitively healthy individuals, we aimed to evaluate how the effect of APOE on CSF Aβ42 varies by age, to understand the association between APOE and the onset of preclinical AD.
APOE genotype and CSF Aβ42 concentration were determined in a cohort comprising 716 cognitively healthy individuals aged 17–99 from nine different clinical research centers.
CSF concentrations of Aβ42 were lower in APOE ε4 carriers than in noncarriers in a gene dose-dependent manner. The effect of APOE ε4 on CSF Aβ42 was age dependent. The age at which CSF Aβ42 concentrations started to decrease was estimated at 50 years in APOE ε4-negative individuals and 43 years in heterozygous APOE ε4 carriers. Homozygous APOE ε4 carriers showed a steady decline in CSF Aβ42 concentrations with increasing age throughout the examined age span.
People possessing the APOE ε4 allele start to show a decrease in CSF Aβ42 concentration almost a decade before APOE ε4 noncarriers already in early middle age. Homozygous APOE ε4 carriers might deposit Aβ42 throughout the examined age span. These results suggest that there is an APOE ε4-dependent period of early alterations in amyloid homeostasis, when amyloid slowly accumulates, that several years later, together with other downstream pathological events such as tau pathology, translates into cognitive decline.
SubjectsAlzheimer’s disease APOE Cerebrospinal fluid Beta amyloid
Link to the original itemhttp://dx.doi.org/10.1186/s13195-017-0313-3
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