TY - JOUR
T1 - The Associations Between Grey Matter Volume Covariance Patterns and Gait Variability—The Tasmanian Study of Cognition and Gait
AU - Jayakody, Oshadi
AU - Breslin, Monique
AU - Beare, Richard
AU - Srikanth, Velandai K.
AU - Blumen, Helena M.
AU - Callisaya, Michele L.
N1 - Funding Information:
National Health and Medical Research Council (Grant Nos. 403000BH and 491109). Physiotherapy Research Foundation (Grant No. BH036/05). Perpetual Trustees. Brain Foundation. Royal Hobart Hospital Research Foundation (Grant No. 341 M). ANZ Charitable Trust. Masonic Centenary Medical Research Foundation. VS is funded by NHMRC Practitioner Fellowship (APP1137837). MC is funded by NHMRC Boosting Dementia Research Leadership Fellowship (1135761).
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2021/7
Y1 - 2021/7
N2 - Greater gait variability predicts dementia. However, little is known about the neural correlates of gait variability. The aims of this study were to determine (1) grey matter volume covariance patterns associated with gait variability and (2) whether these patterns were associated with specific cognitive domains. Participants (n = 351; mean age 71.9 ± 7.1) were randomly selected from the Southern Tasmanian electoral roll. Step time, step length, step width and double support time were measured using an electronic walkway. Gait variability was calculated as the standard deviation of all steps for each gait measure. Voxel-based morphometry and multivariate covariance-based analyses were used to identify grey matter patterns associated with each gait variability measure. The individual expressions of grey matter patterns were correlated with processing speed, memory, executive and visuospatial functions. The grey matter covariance pattern of double support time variability included frontal, medial temporal, anterior cingulate, insula, cerebellar and striatal regions. Greater expression of this pattern was correlated with poorer performance in all cognitive functions (p < 0.001). The covariance pattern of step length variability included frontal, temporal, insula, occipital and cerebellar regions and was correlated with all cognitive functions (p < 0.05), except memory (p = 0.76). The covariance pattern of step width variability was limited to the cerebellum and correlated only with memory (p = 0.047). No significant pattern was identified for step time variability. In conclusion, different grey matter covariance patterns were associated with individual gait variability measures. These patterns were also correlated with specific cognitive functions, suggesting common neural networks may underlie both gait and cognition.
AB - Greater gait variability predicts dementia. However, little is known about the neural correlates of gait variability. The aims of this study were to determine (1) grey matter volume covariance patterns associated with gait variability and (2) whether these patterns were associated with specific cognitive domains. Participants (n = 351; mean age 71.9 ± 7.1) were randomly selected from the Southern Tasmanian electoral roll. Step time, step length, step width and double support time were measured using an electronic walkway. Gait variability was calculated as the standard deviation of all steps for each gait measure. Voxel-based morphometry and multivariate covariance-based analyses were used to identify grey matter patterns associated with each gait variability measure. The individual expressions of grey matter patterns were correlated with processing speed, memory, executive and visuospatial functions. The grey matter covariance pattern of double support time variability included frontal, medial temporal, anterior cingulate, insula, cerebellar and striatal regions. Greater expression of this pattern was correlated with poorer performance in all cognitive functions (p < 0.001). The covariance pattern of step length variability included frontal, temporal, insula, occipital and cerebellar regions and was correlated with all cognitive functions (p < 0.05), except memory (p = 0.76). The covariance pattern of step width variability was limited to the cerebellum and correlated only with memory (p = 0.047). No significant pattern was identified for step time variability. In conclusion, different grey matter covariance patterns were associated with individual gait variability measures. These patterns were also correlated with specific cognitive functions, suggesting common neural networks may underlie both gait and cognition.
KW - Covariance patterns
KW - Grey matter volume
KW - Intra-individual gait variability
KW - Population-based
KW - Specific cognitive functions
UR - http://www.scopus.com/inward/record.url?scp=85105539627&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85105539627&partnerID=8YFLogxK
U2 - 10.1007/s10548-021-00841-5
DO - 10.1007/s10548-021-00841-5
M3 - Article
C2 - 33914190
AN - SCOPUS:85105539627
SN - 0896-0267
VL - 34
SP - 478
EP - 488
JO - Brain Topography
JF - Brain Topography
IS - 4
ER -