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.

Sunday, February 1, 2026

New scan could help millions with hard-to-treat high blood pressure

 Is your doctor and hospital up-to-date on this? Do they even have a research analyst whose job is to monitor and implement research? 

If not, YOUR BOARD OF DIRECTOIRS IS COMPLETELY FUCKING INCOMPETENT!

New scan could help millions with hard-to-treat high blood pressure

                   A speedy new scan could improve how millions of people with high blood pressure are treated, suggests a new study led by UCL researchers.

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About a quarter of people with high blood pressure have been estimated to have a problem with their adrenal glands producing too much of the hormone aldosterone, which regulates levels of salt in the body.

This problem is often missed, as the path to diagnosis is complex, involving multiple tests and, to guide treatment, an invasive procedure that is not always reliable.

The new 10-minute scan, developed at UCL and described in a research letter in the New England Journal of Medicine (NEJM), reveals overactivity in adrenal glands that was invisible with conventional tests, showing exactly where too much aldosterone is being made.

This, the researchers say, will make it easier to decide on the best treatment approach - either removal of an adrenal gland that is producing too much aldosterone, or the use of new medications that block aldosterone production, targeting the cause of high blood pressure in many patients.

Professor Bryan Williams, Chair of Medicine at UCL and clinical lead for the study, said: “We have been waiting for a test like this for many decades. This British innovation is going to transform the diagnosis of aldosterone excess as an important and previously hidden cause of hypertension in many of our patients. It offers huge potential to completely change the way we make this diagnosis and enable us to provide better targeted treatment for our patients.”

The over-production of aldosterone, which raises high blood pressure by causing the body to retain too much salt, can result in a condition called primary aldosteronism, which increases the risk of heart disease, stroke and kidney disease. However, many people who do not meet the threshold for this condition are thought to have excess aldosterone raising their blood pressure.

Currently the condition is screened with a blood test and confirmed with a second test*. To decide on treatment, two catheters are inserted in veins on either side of the groin to measure levels of aldosterone on each side of the body. This helps clinicians determine if the problem is only located in one adrenal gland or both - but the test is not always accurate and not often offered as few hospitals have the expertise to perform this complex procedure.

To better detect the condition, researchers at UCL used a PET-CT scan, which creates detailed 3D images (computed tomography, or CT) of parts of the inside of the body and maps the accumulation of a tiny amount of radioactive tracer injected into a person’s vein (position emission tomography or PET).

They built a new tracer compound designed to bind to the aldosterone-producing enzyme, aldosterone synthase. The tracer was highly selectively taken up by the parts of the adrenal gland that were over-producing aldosterone, lighting up these areas on the scan.

In their NEJM research letter, the researchers described how 17 patients were scanned in the world’s first use of this technique at UCLH. The team found the source of over-production of aldosterone in every patient and did not see any side effects.

Professor Williams added: “This is the first time we have been able to visualise this disease. We can see it light up on the scan. The intensity of the signal reflects the level of aldosterone over-production. This might allow us, in future, to more precisely target these over-producing areas.” 

PET-CT scan

The achievement builds on more than a decade’s work by Professor Erik Arstad (UCL Division of Medicine and UCL Chemistry) and colleagues, who pioneered and patented a new method to make radioactive tracers.

Using this method, they were able to repurpose a drug-like molecule that bound to the aldosterone-producing enzyme for use as a tracer, replacing a single atom with a radioactive version of that atom – meaning this molecule would light up on a PET-CT scan.

Professor Arstad said: “It is very rewarding to be able to bring laboratory innovation into the clinic for the benefit of patients with hard-to-treat hypertension.”

The study was conducted at UCL and UCLH and was funded by the MRC and the NIHR University College London Hospitals Biomedical Research Centre.

The team is now embarking on a phase 2 clinical trial to gather sufficient data for the test to be approved for routine clinical use in the NHS.

In the UK, more than 14 million people are estimated to have high blood pressure (about one in three adults).

*For instance, a salt loading test, where a person increases their intake of salt (sodium), which would be expected to suppress aldosterone levels. If aldosterone levels are still high despite this increase, that confirms a primary hyperaldosteronism diagnosis.

Brain Conductors Find Precise Connection to Target Cells via Protein Handshake

 How will your competent? doctor and hospital use this to get you recovered?

Do you prefer your doctor, hospital and board of director's incompetence NOT KNOWING? OR NOT DOING? Your choice; let them be incompetent or demand action!

Brain Conductors Find Precise Connection to Target Cells via Protein Handshake

Summary: Researchers have identified two specific proteins, gliomedin and CNTNAP4, that act as a “handshake” mechanism allowing inhibitory chandelier cells to connect precisely with excitatory pyramidal neurons. This connection is vital for maintaining electrical balance in the brain. Disruptions in this process are linked to neurological disorders such as epilepsy, schizophrenia, and autism.

Source: Ohio State University

The brain’s ability to process information relies on a delicate balance between neurons that send “go” signals and those that send “stop” signals. Now, researchers have discovered exactly how the “conductors” of this orchestra find their way to the podium.

A new study from Ohio State University reveals how chandelier cells—a class of inhibitory interneurons—link up with their target excitatory cells. The team identified two specific molecules that must be present to enable a “handshake” between the cells, allowing synapses to form.

Chandelier cells are critical for brain function. They connect to a specific location on target excitatory neurons (pyramidal cells) called the axon initial segment. By grabbing this “handle,” chandelier cells can powerfully suppress the activity of the excitatory neurons, effectively preventing runaway electrical signals.

“These inhibitory interneurons shape and balance local circuit activity – they are the modulators, coordinators, the conductors of the orchestra,” said Yasufumi Hayano, lead author and postdoctoral scholar at Ohio State University. “From our results, we’ve concluded that interaction between two specific proteins regulates the specificity of their synapse formation.”

Loss of coordination between these cell types is associated with severe neurological and psychiatric disorders, including epilepsy, depression, autism, and schizophrenia.

The Molecular Handshake

The researchers discovered that the connection relies on a precise molecular interaction. The study identified two key proteins:

  • CNTNAP4: Located on the chandelier cells (the “conductors”).
  • Gliomedin: Located on the axon initial segment of the target neurons.

When these two proteins meet, they facilitate the formation of the synapse. Using visualizations in the brains of young mice, the team observed that when the genes for gliomedin were removed, the chandelier cells failed to form adequate connections with their targets. The “handshake” was broken, leaving the “conductors” unable to control the orchestra.

Implications for Neurological Disorders

Because the axon initial segment is the exact site where neurons generate action potentials (the signals used to communicate), chandelier cells have a disproportionately strong influence on brain activity. They essentially control the “faucet” of information flow.

“This is basic neuroscience, but there might be an impact for neuronal disorders,” said Hayano. “If this process is disrupted, what happens? If we lose those genes, which neuronal disorder might occur? We still don’t know, but those possibilities should be explored.”

Senior author Hiroki Taniguchi noted that understanding these developmental mechanisms is the first step toward identifying therapeutic targets for conditions where brain circuitry is imbalanced.


About this neuroscience research news

Author: Media Relations
Source: Ohio State University
Contact: Emily Caldwell – Ohio State University
Image: The image is credited to Ohio State University

Original Research: Closed access.
“The highly localized interaction between Neurofascin-186 and Gliomedin promotes subcellular innervation by the chandelier cell” by Yasufumi Hayano et al. The Journal of Neuroscience

Ipsilesional upper limb performance in stroke individuals: relationship among outcomes of different tests used to assess hand function

 Nothing here GETS SURIVORS RECOVERED AT ALL! You need exact protocols for that!

Ipsilesional upper limb performance in stroke individuals: relationship among outcomes of different tests used to assess hand function

Bianca Pinto Cunha [a]  
Bianca Pinto Cunha [a],  
Sandra Maria Sbeghen Ferreira de Freitas, 
Viviana Van Den Berg de Menezes [b] , 
Paulo Barbosa de Freitas [a]* 
[a] Universidade Cruzeiro do Sul (UNICSUL), São Paulo, SP, Brazil 
[b] Universidade Cidade de São Paulo (UNICID), São Paulo, SP, Brazil  

Abstract  

Introduction:  
Stroke individuals have sensorimotor repercussions on their ipsilesional upper limb. Therefore, it is important to use tests that allow an adequate assessment and follow-up of such deficits. Physical and occupational therapists commonly use maximal grip strength tests to assess the functional condition of stroke individuals. However, one could ask whether a single test is able to characterize the hand function in this population. 
 
Objective: 

The aim of this study was to investigate the relationship among outcomes of different tests frequently used to describe the function of the hand in the ipsilesional upper limb of stroke individuals.  Methods:  Twenty-two stroke individuals performed four hand function tests:  maximal handgrip strength (HGSMax), maximal pinch grip strength (PGSMax), Jebsen-Taylor Hand Function Test (JTHFT) and Nine Hole Peg Test (9-HPT). All tests were performed with the ipsilesional hand. Pearson’s correlation analyses were performed.  

Results:  

The results indicated a moderate and positive relationship between HGSMax and JTHFT (r = 0.50) and between JTHFT and 9-HPT (r = 0.55). 

Conclusion:  

We conclude that the existence of only moderate relationships between test outcomes demonstrates the need to use at least two instruments to better describe the ipsilesional hand function of stroke individuals.