| Literature DB >> 31376729 |
Luiza Kvitko Axelrud1, João Ricardo Sato2, Marcos Leite Santoro3, Fernanda Talarico3, Daniel Samuel Pine4, Luis Augusto Rohde1, Andre Zugman5, Edson Amaro Junior6, Rodrigo Affonseca Bressan5, Rodrigo Grassi-Oliveira7, Pedro Mario Pan5, Maurício Scopel Hoffmann1, Andre Rafael Simioni1, Salvador Martin Guinjoan8, Hakon Hakonarson9, Elisa Brietzke10, Ary Gadelha5, Renata Pellegrino da Silva9, Marcelo Queiroz Hoexter11, Euripedes Constantino Miguel12, Sintia Iole Belangero3, Giovanni Abrahão Salum13.
Abstract
Research suggested accumulation of tau proteins might lead to the degeneration of functional networks. Studies investigating the impact of genetic risk for Alzheimer's disease (AD) on early brain connections might shed light on mechanisms leading to AD development later in life. Here, we aim to investigate whether the polygenic risk score for Alzheimer's disease (AD-PRS) influences the connectivity among regions susceptible to tau pathology during childhood and adolescence. Participants were youth, aged 6-14 years, and recruited in Porto Alegre (discovery sample, n = 332) and São Paulo (replication sample, n = 304), Brazil. Subjects underwent genotyping and 6-min resting state funcional magnetic resonance imaging. Connections between the local maxima of tau pathology networks were used as dependent variables. The AD-PRS was associated with the connectivity between the right precuneus and the right superior temporal gyrus (discovery sample: β = 0.180, padjusted = 0.036; replication sample: β = 0.202, p = 0.031). This connectivity was also associated with inhibitory control (β = 0.157, padjusted = 0.035) and moderated the association between the AD-PRS and both immediate and delayed recall. These findings suggest the AD-PRS may affect brain connectivity in youth, which might impact memory performance and inhibitory control in early life.Entities:
Keywords: Alzheimer's disease; Functional connectivity; Polygenic risk score; Tau protein
Mesh:
Year: 2019 PMID: 31376729 PMCID: PMC7658444 DOI: 10.1016/j.neurobiolaging.2019.06.011
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673