Converging patterns of aging-associated brain volume loss and tissue microstructure differences

Neurobiol Aging. 2020 Apr:88:108-118. doi: 10.1016/j.neurobiolaging.2020.01.006. Epub 2020 Jan 15.

Abstract

Given the worldwide increasing socioeconomic burden of aging-associated brain diseases, there is pressing need to gain in-depth knowledge about the neurobiology of brain anatomy changes across the life span. Advances in quantitative magnetic resonance imaging sensitive to brain's myelin, iron, and free water content allow for a detailed in vivo investigation of aging-related changes while reducing spurious morphometry differences. Main aim of our study is to link previous morphometry findings in aging to microstructural tissue properties in a large-scale cohort (n = 966, age range 46-86 y). Addressing previous controversies in the field, we present results obtained with different approaches to adjust local findings for global effects. Beyond the confirmation of age-related atrophy, myelin, and free water decreases, we report proportionally steeper volume, iron, and myelin decline in sensorimotor and subcortical areas paralleled by free water increase. We demonstrate aging-related white matter volume, myelin, and iron loss in frontostriatal projections. Our findings provide robust evidence for spatial overlap between volume and tissue property differences in aging that affect predominantly motor and executive networks.

Keywords: Brain; Healthy cognitive ageing; Iron; Magnetic resonance imaging; Myelin; Voxel-based quantification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Aging / metabolism*
  • Aging / pathology*
  • Animals
  • Atrophy
  • Body Water / metabolism
  • Cohort Studies
  • Female
  • Humans
  • Iron / metabolism
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Myelin Sheath / metabolism
  • Organ Size*
  • White Matter / diagnostic imaging
  • White Matter / metabolism
  • White Matter / pathology*

Substances

  • Iron