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, February 4, 2026

Abstract DP070: Ipsi-lesional Thalamus Atrophy after Stroke Predicts Functional Outcomes

 

Predictions DO NOTHING FOR STROKE RECOVERY, and with NO protocols written, COMPLETELY FUCKING USELESS! You're fired! All the mentors and senior researchers need to be fired for not having an objective of writing EXACT rehab protocols from research!

Abstract DP070: Ipsi-lesional Thalamus Atrophy after Stroke Predicts Functional Outcomes

Naomi Layne, BS, BA, Clara Glassman, Data Scientist, and Lisa Krishnamurthy, BS, PhD
Author Info & Affiliations 

Abstract

 The thalamus serves as the brain's relay station, processing information and facilitating communication between almost all regions of the nervous system. In our previous cross-sectional study focused on the chronic stages of stroke, we identified key demographic factors contributing to the decrease in thalamus volume, such as age and intracortical volume. We have built on these findings by analyzing a longitudinal imaging dataset that tracks stroke patients from the acute to chronic stages. This longitudinal dataset not only confirms our previous findings but also demonstrates a correlation between the volume of the ipsilesional thalamus and motor function over time.
After conducting quality control, we analyzed T1-weighted and T2-weighted MRI scans from 62 stroke patients, each with three time points: 2 weeks (A), 3 months (C), and 12 months (C2) following their stroke. The data were processed using Freesurfer’s longitudinal pipeline, and thalamic segmentation was refined with Freesurfer’s Iglesias thalamic nuclei segmentation. We modeled thalamus volume using ANOVA in JMP Pro 17, incorporating factors such as 'time since stroke,' 'lesion volume,' 'age,' 'intracranial volume,' and 'gender' to explain the observed decrease in thalamus volume. Motor function was assessed using Motricity Index scores, and the correlation between thalamus volume and motor function was analyzed with a mixed model approach in JMP Pro 17. All statistical results are presented with F or t values and their associated p-values.
Our findings indicate that the ipsilesional thalamus decreases over time, whereas the contralesional thalamus remains unchanged. Significant covariates affecting the change in ipsilesional thalamus volume include estimated intracranial volume, lesion volume, time since stroke, and the interaction of age with lesion volume. Additionally, we confirm a significant correlation between ipsilesional thalamus volume and motor function across the three time points. Patients with a greater preserved [LK1] ipsilesional thalamus volume tend to have better motor function outcomes.
After a stroke, the ipsilesional thalamus shrinks while the contralesional thalamus remains stable. An interaction between age and disease severity was observed, suggesting the thalamus could be a biomarker for assessing stroke impact on motor function. Understanding aging's relationship with disease can help personalize treatment and rehabilitation to improve outcomes and reduce disabilities.
This diagram provides a comprehensive overview of the motor control pathway, illustrating how different brain regions, including the thalamus, interact with one another to regulate motor function (Cambridge University Press).
Leverage plots and statistical values of the covariates that affect the volume of the patients' thalamus. The top row shows the covariates affecting the ipsi-lesional thalamus. The bottom row shows the factors affecting the contra-lesional thalamus.
Relationship between longitudinal ipsi-lesional thalamus and motor function in the more affected (top row) and less affected (bottom row) lower extremities across sessions.

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