Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers : a multimodal imaging investigation. / Hodgetts, Carl J; Shine, Jonathan P; Williams, Huw; Postans, Mark; Sims, Rebecca; Williams, Julie; Lawrence, Andrew D; Graham, Kim S.

In: Neurobiology of aging, Vol. 73, 01.2019, p. 82-91.

Research output: Contribution to journalArticle

Published
  • Carl J Hodgetts
  • Jonathan P Shine
  • Huw Williams
  • Mark Postans
  • Rebecca Sims
  • Julie Williams
  • Andrew D Lawrence
  • Kim S Graham

Abstract

Young adult APOE-ε4 carriers show increased activity in posterior regions of the default mode network (pDMN), but how this is related to structural connectivity is unknown. Thirty young adults (one half of whom were APOE-ε4 carriers; mean age 20 years) were scanned using both diffusion and functional magnetic resonance imaging. The parahippocampal cingulum bundle (PHCB)-which links the pDMN and the medial temporal lobe-was manually delineated in individual participants using deterministic tractography. Measures of tract microstructure (mean diffusivity and fractional anisotropy) were then extracted from these tract delineations. APOE-ε4 carriers had lower mean diffusivity and higher fractional anisotropy relative to noncarriers in PHCB, but not in a control tract (the inferior longitudinal fasciculus). Furthermore, PHCB microstructure was selectively associated with pDMN (and medial temporal lobe) activity during a scene discrimination task known to be sensitive to Alzheimer's disease. These findings are consistent with a lifespan view of Alzheimer's disease risk, where early-life, connectivity-related changes in specific, vulnerable "hubs" (e.g., pDMN) lead to increased neural activity. Critically, such changes may reflect reduced network efficiency/flexibility in APOE-ε4 carriers, which in itself may portend a faster decline in connectivity over the lifespan and ultimately trigger early amyloid-β deposition in later life.

Original languageEnglish
Pages (from-to)82-91
Number of pages10
JournalNeurobiology of aging
Volume73
Early online date22 Sep 2018
DOIs
Publication statusPublished - Jan 2019
This open access research output is licenced under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.

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