Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Wednesday, October 23, 2024

Brain-movement relationship during upper-limb functional movements in chronic post-stroke patients

 So we finally got some research that attempts to OBJECTIVELY determine the damage from the stroke. Now if the proper followup occurs we'll get EXACT REHAB PROTOCOLS that fix such damage and get survivors 100% recovered. At least that is what proper stroke research does; it leads to survivor recovery; NOT biomarkers, predictions or descriptions of damage!

Brain-movement relationship during upper-limb functional movements in chronic post-stroke patients

Abstract

Background

Following a stroke, brain activation reorganisation, movement compensatory strategies, motor performance and their evolution through rehabilitation are matters of importance for clinicians. Two non-invasive neuroimaging methods allow for recording task-related brain activation: functional near-infrared spectroscopy (fNIRS) and electroencephalography (fEEG), respectively based on hemodynamic response and neuronal electrical activity. Their simultaneous measurement during movements could allow a better spatiotemporal mapping of brain activation, and when associated to kinematic parameters could unveil underlying mechanisms of functional upper limb (UL) recovery. This study aims to depict the motor cortical activity patterns using combined fNIRS-fEEG and their relationship to motor performance and strategies during UL functional tasks in chronic post-stroke patients.

Methods

Twenty-one healthy old adults and 21 chronic post-stroke patients were recruited and completed two standardised functional tasks of the UL: a paced-reaching task where they had to reach a target in front of them and a circular steering task where they had to displace a target using a hand-held stylus, as fast as possible inside a circular track projected on a computer screen. The activity of the bilateral motor cortices and motor performance were recorded simultaneously utilizing a fNIRS-fEEG and kinematics platform.

Results and conclusions

Kinematic analysis revealed that post-stroke patients performed worse in the circular steering task and used more trunk compensation in both tasks. Brain analysis of bilateral motor cortices revealed that stroke individuals over-activated during the paretic UL reaching task, which was associated with more trunk usage and a higher level of impairment (clinical scores). This work opens up avenues for using such combined methods to better track and understand brain-movement evolution through stroke rehabilitation.

Background

Due to its prevalence, functional non-recovery of the paretic upper limb (UL) is a critical concern in stroke rehabilitation [1]. UL functional recovery is mainly attributed to plastic reorganization within the human brain [2, 3], and post-stroke patients often demonstrate abnormal brain activation in comparison to healthy individuals. When using the paretic hand, patients with stroke show increased contralesional and ipsilesional sensorimotor network activation compared to healthy individuals [4], as well as increased activations of contralesional primary motor cortex and bilateral premotor and supplementary motor areas [5]. During the process of functional paretic arm recovery, there is a progressive evolution towards a more “normal” lateralization of the primary sensorimotor cortex [6,7,8,9,10], which underlines the potential of monitoring brain reorganization to predict patients’ responses to rehabilitation [11]. Brain reorganization is classically assessed by functional magnetic resonance imaging (fMRI), mostly in the supine position and during moderately functional tasks such as thumb-finger opposition or elbow flexion-extension [12]. To monitor brain activations under more ecological conditions, i.e., during upright, unrestrained, functional tasks, it is possible to use portable brain imagery techniques such as functional near infrared spectroscopy (fNIRS) and functional electroencephalography (fEEG).

The fNIRS method detects variations in blood-oxygen level-dependant response, as in fMRI [13], and can do so under more ecological conditions [14]. FNIRS measures both oxygenated (HbO2) and deoxygenated (HbR) hemoglobin in the cerebral cortex blood vessels, and has been previously used to measure sensorimotor network activation during UL movements in healthy young adults [15, 16], older healthy adults [16, 17] and stroke patients [18, 19]. In fully UL functional tasks, such as reaching, studies have identified a bilateral sensorimotor cortex (SM1) activation pattern [16, 20]. Nevertheless, to the best of our knowledge, only one recent study investigated SM1 activation in a stroke population using fNIRS during a reaching task under ecological conditions [18]. They found enhanced ipsi/contralesional SM1 activation in the stroke patients despite poorer motor performance in reaching and grasping.

The fEEG method detects direct variations in electrical currents at the scalp due to local electric fields produced by neuronal activity [21]. Event-related power changes within specific frequency bands (alpha-mu – 8 to 13 Hz and beta – 14 to 29 Hz) reflect the balance between excitation and inhibition in the sensorimotor network [22], classically with an event-related desynchronization (ERD, i.e. power decrease) at movement execution and an event-related synchronization (ERS, i.e. power increase) at rest [23]. In patients with stroke, a number of studies have shown a relationship between the magnitude of the ERD in the lesioned hemisphere and the paretic UL function [24,25,26].

Coupling fNIRS and fEEG could provide a better spatio-temporal view of SM1 brain activation patterns in both hemispheres [27]. However, to better understand SM1 activity during fully functional UL tasks, it is important to complement functional brain imaging with kinematic assessments [16]. During forward-reaching tasks, stroke patients often exhibit non-mandatory trunk compensation, i.e. even if they can do with their paretic UL alone, they favour trunk flexion to the detriment of arm use [28, 29]. Unfortunately, this non-use of the paretic UL [30] can lead to maladaptive brain plasticity [31] and hinder functional recovery [32]. Overall, it is now clear that non-mandatory trunk compensation and associated non-use have an impact on the plastic reorganisation of the brain (for a review, see [33]). Thus, investigating how trunk compensation affects SM1 activations during different functional UL tasks (detailed description of UL tasks in Sect. “Experimental design”) may help to understand the mechanisms underlying functional recovery [18].

The primary aim of the present study was to investigate bilateral SM1 activation during functional UL tasks in people with and without stroke. We hypothesised increased SM1 activation in the stroke cohort, both in the ipsilesional and contralesional hemispheres and particularly during performance of the paretic UL. Additionally, we investigated the effect of stroke on the relationship between brain activation patterns and motor performance. Our hypothesis was that individuals in the stroke group would perform worse when using their paretic arm, and that SM1 activation in the injured hemisphere would be positively correlated with task performance.

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