Changjiang Zhao1,2, Haibo Xu1, Chengxin Yu2, Lei Gao1, Junlong Pan 2, Long Chen2, Can Zhang2, Jiangjin Chen2, Li Zhu2, Xiong Xiong2, and Xiance Zhao3
1Department of Radiology, Zhongnan Hospital of Wuhan University, Wuhan, China, 2Department of Radiology, The First College of Clinical Medical Science of China Three Gorges University, Yichang, China, 3Philips Healthcare, Shanghai, China
Synopsis
Keywords: Functional Connectivity, Stroke, functional connectivity
Motivation: How stroke at different locations affects homotopic connectivity remains incompletely understood.
Goal(s): This study aimed to examine how motor deficits resulting from acute stroke in different brain regions impact homotopic connectivity.
Approach: Patients with dyskinesia were included and divided into 4 demographically matched subgroups by stroke location: frontoparietal, radiation coronal, basal ganglia, and brain stem. Additional 37 matched healthy controls were also recruited. Interhemispheric homotopic functional and structural connectivity was obtained by resting-state functional MRI and diffusion tensor imaging.
Results: Our results suggest that post-stroke motor deficits in different regions implicate different links from cortical to subcortical areas.
Impact: Alterations in lesion topography and regional functional homotopy
provide new insights into the understanding of neural basis of motor disorders
and also inform potential individualized precisive targets.
Introduction
Motor
impairment is the most common consequence after a stroke1,2.
Interhemispheric homotopic connectivity varies
regionally and hierarchically along the somatomotor-association cortex axis and
is particularly important for maintaining normal motor function3.
However, our understanding of how stroke at different locations affects
homotopic connectivity remains incomplete. This study aimed to examine how
motor deficits resulting from acute stroke in different brain regions impact
homotopic connectivity.Methods
84
acute ischemic stroke patients with dyskinesia were included and divided into 4
demographically matched subgroups by stroke location: frontoparietal (15), radiation coronal (16), basal ganglia (30), and brain
stem (23). Additional 37 matched healthy controls were also recruited.
Multimodal MRI data, and motor function assessments were collected.
Interhemispheric homotopic functional and structural connectivity was obtained
by resting-state functional MRI and diffusion tensor imaging, respectively, and
correlated with motor function scores.Results
VMHC-based
results showed that frontoparietal and basal ganglia strokes resulted in
reduced homotopic connectivity in somatosensory/motor cortex, whereas radiation
coronal and brainstem strokes were associated with altered interhemispheric
connectivity in subcortical motor circuits (Fig. 1). Diffusion tensor imaging
based structural connectivity suggested that frontal-parietal and basal ganglia
strokes primarily affected cortical association fibers, whereas radiation
coronal and brainstem strokes involved extensive cortical-cortical and
cortical-subcortical disruption of the integrity of white matter fibers (Fig.
2).Discussion
In
the present study, we examined changes in homotopic functional and structural
connectivity in patients with acute cerebral infarction at different sites
(frontal-parietal, radial-coronal, basal ganglia, and brainstem) to provide
information about interhemispheric structural and functional involvement and
the potential relationship between these changes. Our main findings are as
follows: VMHC was reduced in the somatosensory-motor cortex in the
frontal-parietal lesion group compared with healthy controls, suggesting that
functional connectivity between sensory-motor networks is reduced in patients
with acute cortical infarction. This change may be related to post-stroke motor
dysfunction, which is in line with previous studies4-6. When compared
to acute cortical infarction, patients with acute subcortical stroke showed
significantly different VMHC changes. The results showed a decrease in VMHC in
the visual cortex but a significant increase in VMHC in the frontoparietal
network. The orbital prefrontal cortex mainly processes sensory experiences
generated by convergent information related to emotions (e.g., disgust or
uneasiness)7. This pattern of increase and decrease may reflect the
reorganization of emotional control, memory, cognitive function, higher
cognitive function, and visual function after acute cerebral infarction.Conclusion
Our results suggest that post-stroke motor
deficits in different regions implicate different links from cortical to
subcortical areas. Alterations in lesion topography and regional functional
homotopy provide new insights into the understanding of neural basis of motor
disorders and also inform potential individualized precisive targets.Acknowledgements
The authors would like to thank the patients and volunteers for
participating in this study, and to the team of Dr. Yong Qin from the
Department of Rehabilitation and Dr. Jinghua Zhou from the Department of Neurology for their help at all
stages of the project.References
1. Feigin VL, Stark BA, Johnson
CO, et al. Global, regional, and national burden of stroke and its risk
factors, 1990–2019: a systematic analysis for the
Global Burden of Disease Study 2019. The Lancet Neurology 2021; 20:795-820.
2. Hankey GJ. Potential new risk
factors for ischemic stroke: what is their potential? Stroke 2006;
37:2181-2188.
3. Feigin VL, Forouzanfar MH,
Krishnamurthi R, et al. Global and regional burden of stroke during 1990–2010: findings from the Global Burden of Disease Study 2010. The
lancet 2014; 383:245-255.
4. Zhang Y, Liu N, Wang Z, et al. Impaired
inter-hemispheric functional connectivity during resting state in female
patients with migraine. Brain Sciences 2022; 12:1505.
5. Van Meer MP, Van Der Marel K,
Wang K, et al. Recovery of sensorimotor function after experimental stroke
correlates with restoration of resting-state interhemispheric functional
connectivity. J Neurosci 2010; 30:3964-3972.
6. Van Meer MP, Van der Marel K,
Otte WM, Berkelbach Van Der Sprenkel JW, Dijkhuizen RM. Correspondence between
altered functional and structural connectivity in the contralesional
sensorimotor cortex after unilateral stroke in rats: a combined resting-state
functional MRI and manganese-enhanced MRI study. Journal of Cerebral Blood Flow
& Metabolism 2010; 30:1707-1711.
7. Burgdorf J, Panksepp J. The
neurobiology of positive emotions. Neuroscience & Biobehavioral Reviews
2006; 30:173-187.