Austin Health

Title
Smaller spared subcortical nuclei are associated with worse post-stroke sensorimotor outcomes in 28 cohorts worldwide.
Publication Date
2021-10-27
Author(s)
Liew, Sook-Lei
Zavaliangos-Petropulu, Artemis
Schweighofer, Nicolas
Jahanshad, Neda
Lang, Catherine E
Lohse, Keith R
Banaj, Nerisa
Barisano, Giuseppe
Baugh, Lee A
Bhattacharya, Anup K
Bigjahan, Bavrina
Borich, Michael R
Boyd, Lara A
Brodtmann, Amy
Buetefisch, Cathrin M
Byblow, Winston D
Cassidy, Jessica M
Charalambous, Charalambos C
Ciullo, Valentina
Conforto, Adriana B
Craddock, Richard C
Dula, Adrienne N
Egorova, Natalia
Feng, Wuwei
Fercho, Kelene A
Gregory, Chris M
Hanlon, Colleen A
Hayward, Kathryn S
Holguin, Jess A
Hordacre, Brenton
Hwang, Darryl H
Kautz, Steven A
Khlif, Mohamed Salah
Kim, Bokkyu
Kim, Hosung
Kuceyeski, Amy
Lo, Bethany
Liu, Jingchun
Lin, David
Lotze, Martin
MacIntosh, Bradley J
Margetis, John L
Mohamed, Feroze B
Nordvik, Jan Egil
Petoe, Matthew A
Piras, Fabrizio
Raju, Sharmila
Ramos-Murguialday, Ander
Revill, Kate P
Roberts, Pamela
Robertson, Andrew D
Schambra, Heidi M
Seo, Na Jin
Shiroishi, Mark S
Soekadar, Surjo R
Spalletta, Gianfranco
Stinear, Cathy M
Suri, Anisha
Tang, Wai Kwong
Thielman, Gregory T
Thijs, Vincent N
Vecchio, Daniela
Ward, Nick S
Westlye, Lars T
Winstein, Carolee J
Wittenberg, George F
Wong, Kristin A
Yu, Chunshui
Wolf, Steven L
Cramer, Steven C
Thompson, Paul M
Subject
MRI
rehabilitation
sensorimotor behaviour
stroke
subcortical volumes
Type of document
Journal Article
OrcId
0000-0001-5935-4215
0000-0001-5598-1369
0000-0001-8145-8176
0000-0002-2828-4549
0000-0003-3469-0399
0000-0002-1547-1839
0000-0002-9244-2900
0000-0001-5240-3264
0000-0002-7129-6684
0000-0002-1111-9176
0000-0002-6575-9849
0000-0003-4519-4956
0000-0003-0981-648X
0000-0001-5456-5056
0000-0002-9095-9877
0000-0001-6446-5905
0000-0002-9404-1959
0000-0001-8644-956X
DOI
10.1093/braincomms/fcab254
Abstract
Up to two-thirds of stroke survivors experience persistent sensorimotor impairments. Recovery relies on the integrity of spared brain areas to compensate for damaged tissue. Deep grey matter structures play a critical role in the control and regulation of sensorimotor circuits. The goal of this work is to identify associations between volumes of spared subcortical nuclei and sensorimotor behaviour at different timepoints after stroke. We pooled high-resolution T1-weighted MRI brain scans and behavioural data in 828 individuals with unilateral stroke from 28 cohorts worldwide. Cross-sectional analyses using linear mixed-effects models related post-stroke sensorimotor behaviour to non-lesioned subcortical volumes (Bonferroni-corrected, P < 0.004). We tested subacute (≤90 days) and chronic (≥180 days) stroke subgroups separately, with exploratory analyses in early stroke (≤21 days) and across all time. Sub-analyses in chronic stroke were also performed based on class of sensorimotor deficits (impairment, activity limitations) and side of lesioned hemisphere. Worse sensorimotor behaviour was associated with a smaller ipsilesional thalamic volume in both early (n = 179; d = 0.68) and subacute (n = 274, d = 0.46) stroke. In chronic stroke (n = 404), worse sensorimotor behaviour was associated with smaller ipsilesional putamen (d = 0.52) and nucleus accumbens (d = 0.39) volumes, and a larger ipsilesional lateral ventricle (d = -0.42). Worse chronic sensorimotor impairment specifically (measured by the Fugl-Meyer Assessment; n = 256) was associated with smaller ipsilesional putamen (d = 0.72) and larger lateral ventricle (d = -0.41) volumes, while several measures of activity limitations (n = 116) showed no significant relationships. In the full cohort across all time (n = 828), sensorimotor behaviour was associated with the volumes of the ipsilesional nucleus accumbens (d = 0.23), putamen (d = 0.33), thalamus (d = 0.33) and lateral ventricle (d = -0.23). We demonstrate significant relationships between post-stroke sensorimotor behaviour and reduced volumes of deep grey matter structures that were spared by stroke, which differ by time and class of sensorimotor measure. These findings provide additional insight into how different cortico-thalamo-striatal circuits support post-stroke sensorimotor outcomes.
Link
Citation
Brain Communications 2021; 3(4): fcab254
Jornal Title
Brain Communications

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