White matter hyperintensities and cognitive reserve during a working memory task: a functional magnetic resonance imaging study in cognitively normal older adults

Neurobiol Aging. 2016 Dec;48:23-33. doi: 10.1016/j.neurobiolaging.2016.08.008. Epub 2016 Aug 20.

Abstract

Cognitive reserve (CR) models posit that lifestyle factors such as education modulate the relationship between brain damage and cognition. However, the functional correlates of CR in healthy aging are still under investigation. White matter hyperintensities (WMHs) are a common age-associated finding that impacts cognition. In this study, we used functional magnetic resonance imaging to characterize the patterns of brain activation during a working memory task in older participants with high and low levels of education (as a proxy of CR) and high and low WMH volumes. Ninety older volunteers (aged 63-76 years) and 16 young adults (aged 21-27) completed the study. We found that older adults with higher education had better working memory performance than their less educated peers. Among the highly educated participants, those with WMH over-recruited areas engaged by young volunteers and showed activation in additional cortical and subcortical structures. However, those with low WMH differed little with respect to their younger counterparts. Our findings demonstrate that the functional mechanisms subtending the effects of education, as a proxy of CR, are modulated according to the WMH burden.

Trial registration: ClinicalTrials.gov NCT01634841.

Keywords: Aging; Cognitive reserve; Compensation; Education; Neural efficiency; White matter hyperintensities; Working memory; fMRI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aging / pathology*
  • Aging / psychology*
  • Cognition / physiology*
  • Cognitive Reserve / physiology*
  • Educational Status
  • Female
  • Humans
  • Magnetic Resonance Imaging*
  • Male
  • Memory / physiology*
  • Middle Aged
  • White Matter / diagnostic imaging*
  • White Matter / pathology*
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT01634841