Earliest accumulation of β-amyloid occurs within the default-mode network and concurrently affects brain connectivity

• Published in: Nature communications Vol. 8; no. 1; pp. 1214 - 13
• Main Authors: Palmqvist, Sebastian, Schöll, Michael, Strandberg, Olof, Mattsson, Niklas, Stomrud, Erik, Zetterberg, Henrik, Blennow, Kaj, Landau, Susan, Jagust, William, Hansson, Oskar
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 31.10.2017; Nature Publishing Group; Nature Portfolio
• Subjects: 631/1647/245/2092; 631/378/1689/1283; 692/308/53/2421; Accumulation; Aged; Alzheimer Disease - cerebrospinal fluid; Alzheimer Disease - pathology; Alzheimer Disease - physiopathology; Alzheimer's disease; Amyloid beta-Peptides - cerebrospinal fluid; Amyloid beta-Peptides - metabolism; Atrophy; Basic Medicine; Brain; Brain - metabolism; Brain - pathology; Brain - physiopathology; Cerebrospinal fluid; Cohort Studies; Cortex (parietal); Female; Fibrils; Glucose - metabolism; Humanities and Social Sciences; Humans; Hypometabolism; Male; Medical and Health Sciences; Medicin och hälsovetenskap; Medicinska och farmaceutiska grundvetenskaper; multidisciplinary; Nerve Net - metabolism; Nerve Net - pathology; Nerve Net - physiopathology; Neural networks; Neurochemistry; Neurodegeneration; Neurodegenerative diseases; Neurologi; Neurology; Neurosciences; Neurovetenskaper; Organ Size; Positron emission; Positron emission tomography; Radiologi och bildbehandling; Radiology and Medical Imaging; Reproducibility of Results; Science; Science (multidisciplinary); Tomography; β-Amyloid
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-017-01150-x

It is not known exactly where amyloid-β (Aβ) fibrils begin to accumulate in individuals with Alzheimer’s disease (AD). Recently, we showed that abnormal levels of Aβ42 in cerebrospinal fluid (CSF) can be detected before abnormal amyloid can be detected using PET in individuals with preclinical AD. Using these approaches, here we identify the earliest preclinical AD stage in subjects from the ADNI and BioFINDER cohorts. We show that Aβ accumulation preferentially starts in the precuneus, medial orbitofrontal, and posterior cingulate cortices, i.e., several of the core regions of the default mode network (DMN). This early pattern of Aβ accumulation is already evident in individuals with normal Aβ42 in the CSF and normal amyloid PET who subsequently convert to having abnormal CSF Aβ42. The earliest Aβ accumulation is further associated with hypoconnectivity within the DMN and between the DMN and the frontoparietal network, but not with brain atrophy or glucose hypometabolism. Our results suggest that Aβ fibrils start to accumulate predominantly within certain parts of the DMN in preclinical AD and already then affect brain connectivity. Abnormal levels of Aβ42 in the cerebrospinal fluid occur prior to a positive amyloid PET scan in the brain of individuals with Alzheimer’s disease and here the authors use this temporal pattern to identify individuals with very early stage AD. They show that Aβ fibrils start to accumulate in some of the regions of the default mode network and affect brain connectivity before neurodegeneration occurs.