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.

Friday, April 1, 2022

'Younger' Brain Associated With Lower Risk of Post-Stroke Cognitive Disorders

 This doesn't matter at all. Your doctor is still responsible to get you 100% recovered regardless of your cognitive status.  Don't let your doctor weasel their way out of this responsibility by quoting the craptastic saying: 'All strokes are different, all stroke recoveries are different.' That quote means they know nothing about stroke and are out-of-date on research.  You don't want them treating you.

'Younger' Brain Associated With Lower Risk of Post-Stroke Cognitive Disorders

 

Dawn Elliott Knapp, PA-C, for Medscape

March 30, 2022

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The study covered in this summary was published on MedRxiv.org as a preprint and has not yet been peer reviewed.

Key Takeaways

  • Patients with greater brain age gaps (BAG, the difference between predicted and chronological brain age) were more likely to have developed neurocognitive disorders (NCD) post-stroke.

  • "Younger" brains (lower BAG) appear to be more resilient to injury and are associated with lower risk for NCD up to 36 months after a stroke.

  • As BAG is sensitive to cognitive impairment after stroke, it may be used in order to predict cognitive outcome in stroke patients.

Why This Matters

  • Long-lasting mild to major cognitive impairments affect 35%–50% of stroke survivors and may not improve over time, a significant source of disability.

  • Brain age calculation could help identify which patients are particularly at risk for post-stroke NCD and could be used to guide treatment and rehabilitation to minimize impairment. 

Study Design

  • MRIs from 269 stroke survivors (55.4% women, mean age, 71 years) from the Nor-COAST study were assessed. MRIs were performed at baseline, 18 months, and 36 months post-stroke.

  • Neuropsychological data was collected at baseline, 3, 18, and 36 months post-stroke, consisting of standardized cognitive testing, Global Deterioration Scale, and classification of NCD using the DSM-5.

  • Predicted brain age was measured via machine learning models based on cortical thickness, surface area, and gray matter/white matter volume. Associations between cognitive status and longitudinal brain age were assessed using linear mixed effects models and survival analysis.

  • Statistical analyses were performed using R v. 3.3.3 and Stata v. 16 to test three hypotheses: 1) whether brain structural characteristics are associated with post-stroke NCD; 2) if a younger appearing brain among patients showing normal cognitive function at baseline is associated with lower risk of NCD at 18- and 36- months follow-up, and 3) whether patients showing preserved cognitive function from baseline onward show less evidence of brain aging over time compared with patients showing cognitive decline.

Key Results

  • "Older" brains (higher BAG) were associated with post-stroke cognitive impairment at 18 and 36 months, confirming that a “younger" brain may confer protective factors against cognitive decline after stroke.

  • There was no significant difference in BAG between the group with preserved brain function vs the group with NCD from baseline and across follow-up times.

  • Pre-stroke BAG may be a more reliable predictor for future cognitive decline than post-stroke BAG.

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