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Background: Mirror therapy (MT) has been demonstrated as an effective intervention for promoting motor recovery post-stroke. Existing neuroimaging studies have demonstrated that the efficacy of MT is associated with its effect to increase the strength of brain activity and functional connectivity in the bilateral M1. However, its modulation on brain dynamics, which also hold physiological significance, remains unknown.
Aim: To investigate the potential influence of MT on brain dynamics in stroke patients.
Design: A randomized, single-blinded, controlled trial.
Setting: Inpatient.
Population: Fifty first-ever unilateral stroke patients with motor dysfunctions were recruited and randomly assigned to either an MT group (N.=25) or a conventional therapy (CT) group (N.=25) for a 4-week intervention.
Methods: Motor function assessments and resting-state fMRI scans were conducted both before and after the intervention. Images from sixteen healthy subjects were used as controls. A dynamic analysis of the fMRI data was performed using measures of the dynamic fractional amplitude of low-frequency fluctuation (dfALFF) and dynamic voxel-mirrored homotopic connectivity (dVMHC).
Results: Aberrant dynamics, characterized by increased variability (decreased stability) in spontaneous activity and interhemispheric functional connectivity in sensorimotor networks, were observed in stroke patients. MT but not CT intervention led to reduced variability of spontaneous activity in the ipsilesional primary motor cortex (M1) and interhemispheric M1 functional connectivity, which further exhibited a correlation with motor improvement. Notably, reduced variability of spontaneous activity showed significant mediation effects in the prediction of motor recovery with reduced variability of interhemispheric functional connectivity.
Conclusions: MT may reduce the excessive variability of interhemispheric M1 functional connectivity, thereby stabilizing the activity of ipsilesional M1 and then facilitating motor recovery.
Clinical Rehabilitation Impact: This study highlights the unique role of MT in addressing abnormal brain dynamics, emphasizing its addition to standard rehabilitation protocols.
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http://dx.doi.org/10.23736/S1973-9087.25.08844-6 | DOI Listing |
Proc Natl Acad Sci U S A
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Martin A. Fisher School of Physics, Brandeis University, Waltham, MA 02453.
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The Kids Research Institute Australia, The University of Western Australia, P.O. Box 855, West Perth, WA, 6872, Australia.
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School of Biological Sciences, University of the Punjab, Quaid-E-Azam Campus, P.O. 54590, Lahore, Pakistan.
Recombinant DNA technology is widely used to produce industrially and pharmaceutically important proteins. In silico analysis, performed before executing wet lab experiments has been greatly helpful in this connection. A shift in protein analysis has been observed over the past decade, driven by advancements in bioinformatics databases, tools, software, and web servers.
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Department of Anthropology and Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, USA.
Language is central to the cognitive and sociocultural traits that distinguish humans, yet the evolutionary emergence of this capacity is far from fully understood. This review explores how the study of the brains of language-trained apes (LTAs) offers a unique and valuable opportunity to tease apart the relative contribution of evolved species differences, behavior, and environment in the emergence of complex communication abilities. For example, when raised in sociolinguistically rich and interactive environments, LTAs show communicative competencies that parallel aspects of early human language acquisition and exhibit altered neuroanatomy, including increased connectivity and laterization in regions associated with language.
View Article and Find Full Text PDFNucleic Acids Res
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Division of Chromatin Regulation, National Institute for Basic Biology, Okazaki 444-8585, Japan.
Methylation of histone H3 at lysine 9 (H3K9me), a hallmark of heterochromatin, is catalyzed by Clr4/Suv39. Clr4/Suv39 contains two conserved domains-an N-terminal chromodomain and a C-terminal catalytic domain-connected by an intrinsically disordered region (IDR). Several mechanisms have been proposed to regulate Clr4/Suv39 activity, but how it is regulated under physiological conditions remains largely unknown.
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