Additive effects of cerebrovascular disease functional connectome phenotype and plasma p-tau181 on longitudinal neurodegeneration and cognitive outcomes

Alzheimers Dement. 2024 Dec;20(12):8739-8757. doi: 10.1002/alz.14328. Epub 2024 Nov 13.

Abstract

Introduction: We investigated the effects of multiple cerebrovascular disease (CeVD) neuroimaging markers on brain functional connectivity (FC), and how such CeVD-related FC changes interact with plasma phosphorylated tau (p-tau)181 (an Alzheimer's disease [AD] marker) to influence downstream neurodegeneration and cognitive changes.

Methods: Multivariate associations among four CeVD markers and whole-brain FC in 529 participants across the dementia spectrum were examined using partial least squares correlation. Interactive effects of CeVD-related FC patterns and p-tau181 on longitudinal gray matter volume (GMV) and cognitive changes were investigated using linear mixed-effects models.

Results: We identified a brain FC phenotype associated with high CeVD burden across all markers. Further, expression of this general CeVD-related FC phenotype and p-tau181 contributed additively, but not synergistically, to baseline and longitudinal GMV and cognitive changes.

Discussion: Our findings suggest that CeVD exerts global effects on the brain connectome and highlight the additive nature of AD and CeVD on neurodegeneration and cognition.

Highlights: Effects of multiple cerebrovascular disease (CeVD) markers on functional connectivity were studied. A global network phenotype linked to high burden across CeVD markers was identified. CeVD phenotype and plasma phosphorylated tau 181 contributed additively to downstream outcomes.

Keywords: Alzheimer's disease; atrophy; cerebrovascular disease; cognition; functional connectivity; longitudinal; phosphorylated tau 181; plasma biomarkers.

MeSH terms

  • Aged
  • Alzheimer Disease / blood
  • Biomarkers / blood
  • Brain* / diagnostic imaging
  • Brain* / pathology
  • Cerebrovascular Disorders* / blood
  • Cerebrovascular Disorders* / diagnostic imaging
  • Cerebrovascular Disorders* / physiopathology
  • Cognition / physiology
  • Cognitive Dysfunction / blood
  • Cognitive Dysfunction / physiopathology
  • Connectome*
  • Female
  • Gray Matter / diagnostic imaging
  • Gray Matter / pathology
  • Humans
  • Longitudinal Studies
  • Magnetic Resonance Imaging*
  • Male
  • Middle Aged
  • Phenotype
  • Phosphorylation
  • tau Proteins* / blood

Substances

  • tau Proteins
  • Biomarkers