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.

Thursday, November 2, 2017

Inflammation in Middle Age May Be Tied to Brain Shrinkage Decades Later

What is your doctors protocol to counteract this problem? NO excuses.
Inflammation in Middle Age May Be Tied to Brain Shrinkage Decades Later

MINNEAPOLIS, Minn -- November 1, 2017 -- People who have biomarkers tied to inflammation in their blood in their 40s and 50s may have more brain shrinkage decades later than people without the biomarkers, according to a study published in the November 1, 2017, online issue of Neurology.
The brain cell loss was found especially in areas of the brain that are affected by Alzheimer’s disease.
“These results suggest that inflammation in midlife may be an early contributor to the brain changes that are associated with Alzheimer’s disease and other forms of dementia,” said Keenan Walker, PhD, Johns Hopkins University School of Medicine, Baltimore, Maryland. “Because the processes that lead to brain cell loss begin decades before people start showing any symptoms, it is vital that we figure out how these processes that happen in middle age affect people many years later.”
People with the inflammation markers and brain shrinkage also had lower scores on average on a memory test.
For the study, the researchers tested the levels of 5 markers of inflammation in the blood, including the white blood cell count, in 1,633 people with an average age of 53 years. An average of 24 years later, the participants took a memory test and had brain scans to measure the volume of several areas of the brain.
The participants were divided into 3 groups based on how many elevated levels of inflammation they had among the 5 biomarkers.
Compared with the people with no elevated levels, people with elevated levels on 3 or more biomarkers had on average 5% lower volume in the hippocampus and other areas of the brain associated with Alzheimer’s disease.
Dr. Walker said that the effect of one standard deviation increase in the overall inflammation score in midlife on brain volume decades later was similar to the effect associated with having 1 copy of the apolipoprotein E (APOE) e4 gene that increases the risk of Alzheimer’s disease.
Every standard deviation increase in the inflammation score was also associated with a hippocampus volume that was 110 cubic millimeters smaller and the volume of other areas affected by Alzheimer’s disease was 532 cubic millimeters smaller.
On the memory test, where people were asked to remember a list of 10 words, the people with no elevated markers remembered an average of about 5.5 words, while those with 3 or more elevated markers remembered an average of about 5 words.
Limitations of the study include that the biomarkers were measured only once. Dr. Walker said it’s not clear whether a single measurement can adequately determine that people have chronic inflammation.
SOURCE: American Academy of Neurology

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