β-amyloid deposition is associated with gait variability in usual aging

Qu Tian, Woei Nan Bair, Susan M. Resnick, Murat Bilgel, Dean Foster Wong, Stephanie A. Studenski

Research output: Contribution to journalArticle

Abstract

Background: Higher amyloid burden predicts gait slowing in aging. Whether and which gait characteristics are associated with amyloid burden is less clear. Gait variability may be more sensitive to amyloid burden than mean gait characteristics. Methods: In the Baltimore Longitudinal Study of Aging, 99 older participants without neurological disease had concurrent amyloid imaging and assessment of gait characteristics. β-amyloid burden was measured using 11C-Pittsburgh compound B (PiB) positron emission tomography. PiB+/− status was based on a mean cortical distribution volume ratio (DVR) cut point. Gait characteristics were quantified by 3D motion analysis. Cross-sectional associations of PiB+/− status and DVR in motor-related regions (primary motor cortex, putamen, caudate) with gait characteristics were examined using linear regression, adjusted for age, sex, height, body mass index, gait speed and covariates (memory, executive function, visuoperceptual speed, depressive symptoms, cardiovascular risk, ApoE ε4, cerebrovascular burden, neurodegeneration, peripheral arterial disease, knee pain). Results: Being PiB+ and higher DVR in motor-related regions were associated with greater gait speed variability, cadence variability, and gait cycle time variability but not with mean gait characteristics. Associations remained similar after adjustment for gait speed and covariates, except for memory, which attenuated associations of PiB+/− with cadence variability and gait cycle time variability. Associations were prominent in men but were not found in women. Conclusions: In usual aging, integrated temporal gait variability measures, but not mean performance, appear related to amyloid burden from cortical and motor-related cortical and subcortical regions, especially in men. Increased gait variability may be a subclinical indicator of increased amyloid burden in men.

Original languageEnglish (US)
Pages (from-to)346-352
Number of pages7
JournalGait and Posture
Volume61
DOIs
StatePublished - Mar 1 2018

Fingerprint

Gait
Amyloid
Baltimore
Peripheral Arterial Disease
Putamen
Executive Function
Motor Cortex
Apolipoproteins E
Positron-Emission Tomography
Longitudinal Studies
Linear Models
Knee
Body Mass Index
2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole
Depression
Pain

Keywords

  • Beta-amyloid
  • Gait characteristics
  • Gait variability
  • Usual aging

ASJC Scopus subject areas

  • Biophysics
  • Orthopedics and Sports Medicine
  • Rehabilitation

Cite this

β-amyloid deposition is associated with gait variability in usual aging. / Tian, Qu; Bair, Woei Nan; Resnick, Susan M.; Bilgel, Murat; Wong, Dean Foster; Studenski, Stephanie A.

In: Gait and Posture, Vol. 61, 01.03.2018, p. 346-352.

Research output: Contribution to journalArticle

Tian, Qu ; Bair, Woei Nan ; Resnick, Susan M. ; Bilgel, Murat ; Wong, Dean Foster ; Studenski, Stephanie A. / β-amyloid deposition is associated with gait variability in usual aging. In: Gait and Posture. 2018 ; Vol. 61. pp. 346-352.
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N2 - Background: Higher amyloid burden predicts gait slowing in aging. Whether and which gait characteristics are associated with amyloid burden is less clear. Gait variability may be more sensitive to amyloid burden than mean gait characteristics. Methods: In the Baltimore Longitudinal Study of Aging, 99 older participants without neurological disease had concurrent amyloid imaging and assessment of gait characteristics. β-amyloid burden was measured using 11C-Pittsburgh compound B (PiB) positron emission tomography. PiB+/− status was based on a mean cortical distribution volume ratio (DVR) cut point. Gait characteristics were quantified by 3D motion analysis. Cross-sectional associations of PiB+/− status and DVR in motor-related regions (primary motor cortex, putamen, caudate) with gait characteristics were examined using linear regression, adjusted for age, sex, height, body mass index, gait speed and covariates (memory, executive function, visuoperceptual speed, depressive symptoms, cardiovascular risk, ApoE ε4, cerebrovascular burden, neurodegeneration, peripheral arterial disease, knee pain). Results: Being PiB+ and higher DVR in motor-related regions were associated with greater gait speed variability, cadence variability, and gait cycle time variability but not with mean gait characteristics. Associations remained similar after adjustment for gait speed and covariates, except for memory, which attenuated associations of PiB+/− with cadence variability and gait cycle time variability. Associations were prominent in men but were not found in women. Conclusions: In usual aging, integrated temporal gait variability measures, but not mean performance, appear related to amyloid burden from cortical and motor-related cortical and subcortical regions, especially in men. Increased gait variability may be a subclinical indicator of increased amyloid burden in men.

AB - Background: Higher amyloid burden predicts gait slowing in aging. Whether and which gait characteristics are associated with amyloid burden is less clear. Gait variability may be more sensitive to amyloid burden than mean gait characteristics. Methods: In the Baltimore Longitudinal Study of Aging, 99 older participants without neurological disease had concurrent amyloid imaging and assessment of gait characteristics. β-amyloid burden was measured using 11C-Pittsburgh compound B (PiB) positron emission tomography. PiB+/− status was based on a mean cortical distribution volume ratio (DVR) cut point. Gait characteristics were quantified by 3D motion analysis. Cross-sectional associations of PiB+/− status and DVR in motor-related regions (primary motor cortex, putamen, caudate) with gait characteristics were examined using linear regression, adjusted for age, sex, height, body mass index, gait speed and covariates (memory, executive function, visuoperceptual speed, depressive symptoms, cardiovascular risk, ApoE ε4, cerebrovascular burden, neurodegeneration, peripheral arterial disease, knee pain). Results: Being PiB+ and higher DVR in motor-related regions were associated with greater gait speed variability, cadence variability, and gait cycle time variability but not with mean gait characteristics. Associations remained similar after adjustment for gait speed and covariates, except for memory, which attenuated associations of PiB+/− with cadence variability and gait cycle time variability. Associations were prominent in men but were not found in women. Conclusions: In usual aging, integrated temporal gait variability measures, but not mean performance, appear related to amyloid burden from cortical and motor-related cortical and subcortical regions, especially in men. Increased gait variability may be a subclinical indicator of increased amyloid burden in men.

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