Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.

It is well established that human brain white matter structure changes with aging, but the timescale and spatial distribution of this change remain uncertain. Cross-sectional diffusion tensor imaging (DTI) studies indicate that, after a period of relative stability during adulthood, there is an acce...

Descrición completa

Detalles Bibliográficos
Main Authors: Sexton, C, Walhovd, K, Storsve, AB, Tamnes, C, Westlye, LT, Johansen-Berg, H, Fjell, A
Formato: Journal article
Idioma:English
Publicado: 2014
_version_ 1826278233687982080
author Sexton, C
Walhovd, K
Storsve, AB
Tamnes, C
Westlye, LT
Johansen-Berg, H
Fjell, A
author_facet Sexton, C
Walhovd, K
Storsve, AB
Tamnes, C
Westlye, LT
Johansen-Berg, H
Fjell, A
author_sort Sexton, C
collection OXFORD
description It is well established that human brain white matter structure changes with aging, but the timescale and spatial distribution of this change remain uncertain. Cross-sectional diffusion tensor imaging (DTI) studies indicate that, after a period of relative stability during adulthood, there is an accelerated decline in anisotropy and increase in diffusivity values during senescence; and, spatially, results have been discussed within the context of several anatomical frameworks. However, inferring trajectories of change from cross-sectional data can be challenging; and, as yet, there have been no longitudinal reports of the timescale and spatial distribution of age-related white matter change in healthy adults across the adult lifespan. In a longitudinal DTI study of 203 adults between 20 and 84 years of age, we used tract-based spatial statistics to characterize the pattern of annual change in fractional anisotropy, axial diffusivity, radial diffusivity, and mean diffusivity and examined whether there was an acceleration of change with age. We found extensive and overlapping significant annual decreases in fractional anisotropy, and increases in axial diffusivity, radial diffusivity, and mean diffusivity. Spatially, results were consistent with inferior-to-superior gradients of lesser-to-greater vulnerability. Annual change increased with age, particularly within superior regions, with age-related decline estimated to begin in the fifth decade. Charting white matter microstructural changes in healthy aging provides essential context to clinical studies, and future studies should compare age trajectories between healthy participants and at-risk populations and also explore the relationship between DTI rates of change and cognitive decline.
first_indexed 2024-03-06T23:40:53Z
format Journal article
id oxford-uuid:6f470e67-ef57-4b0b-a0f9-d8946245c794
institution University of Oxford
language English
last_indexed 2024-03-06T23:40:53Z
publishDate 2014
record_format dspace
spelling oxford-uuid:6f470e67-ef57-4b0b-a0f9-d8946245c7942022-03-26T19:29:39ZAccelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:6f470e67-ef57-4b0b-a0f9-d8946245c794EnglishSymplectic Elements at Oxford2014Sexton, CWalhovd, KStorsve, ABTamnes, CWestlye, LTJohansen-Berg, HFjell, AIt is well established that human brain white matter structure changes with aging, but the timescale and spatial distribution of this change remain uncertain. Cross-sectional diffusion tensor imaging (DTI) studies indicate that, after a period of relative stability during adulthood, there is an accelerated decline in anisotropy and increase in diffusivity values during senescence; and, spatially, results have been discussed within the context of several anatomical frameworks. However, inferring trajectories of change from cross-sectional data can be challenging; and, as yet, there have been no longitudinal reports of the timescale and spatial distribution of age-related white matter change in healthy adults across the adult lifespan. In a longitudinal DTI study of 203 adults between 20 and 84 years of age, we used tract-based spatial statistics to characterize the pattern of annual change in fractional anisotropy, axial diffusivity, radial diffusivity, and mean diffusivity and examined whether there was an acceleration of change with age. We found extensive and overlapping significant annual decreases in fractional anisotropy, and increases in axial diffusivity, radial diffusivity, and mean diffusivity. Spatially, results were consistent with inferior-to-superior gradients of lesser-to-greater vulnerability. Annual change increased with age, particularly within superior regions, with age-related decline estimated to begin in the fifth decade. Charting white matter microstructural changes in healthy aging provides essential context to clinical studies, and future studies should compare age trajectories between healthy participants and at-risk populations and also explore the relationship between DTI rates of change and cognitive decline.
spellingShingle Sexton, C
Walhovd, K
Storsve, AB
Tamnes, C
Westlye, LT
Johansen-Berg, H
Fjell, A
Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.
title Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.
title_full Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.
title_fullStr Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.
title_full_unstemmed Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.
title_short Accelerated changes in white matter microstructure during aging: a longitudinal diffusion tensor imaging study.
title_sort accelerated changes in white matter microstructure during aging a longitudinal diffusion tensor imaging study
work_keys_str_mv AT sextonc acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy
AT walhovdk acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy
AT storsveab acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy
AT tamnesc acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy
AT westlyelt acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy
AT johansenbergh acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy
AT fjella acceleratedchangesinwhitemattermicrostructureduringagingalongitudinaldiffusiontensorimagingstudy