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.

Tuesday, June 1, 2021

Simple Tool Predicts Individual Alzheimer's Risk

With your risk of dementia post stroke your doctor should have this test be a protocol to establish a baseline for you.

If found then your doctor needs to prescribe the dementia prevention protocols that they have already assembled. If s/he doesn't have any call the president and ask when competent people will be hired to create them.  Hopefully in time for your children and grandchildren to use.

1. A documented 33% dementia chance post-stroke from an Australian study?   May 2012.

2. Then this study came out and seems to have a range from 17-66%. December 2013.`    

3. A 20% chance in this research.   July 2013.

4. Dementia Risk Doubled in Patients Following Stroke September 2018 

The latest here:

 

Simple Tool Predicts Individual Alzheimer's Risk

Blood and quick cognitive tests boost accuracy to 90%

A computer rendering of phosphorylation of tau proteins

A simple blood test, coupled with brief memory tests, showed who will develop Alzheimer's disease in the future with a high degree of accuracy.

Combining plasma phosphorylated tau (p-tau), APOE genotype, and scores from 10-minute executive function and memory tests predicted Alzheimer's disease onset within 2 to 6 years among people with memory complaints with 90% certainty, reported Oskar Hansson, MD, PhD, and Sebastian Palmqvist, MD, PhD, both at Lund University in Sweden, and colleagues.

When dementia experts examined the same patients, they were about 71% accurate, the researchers noted in Nature Medicine.

"We show for the first time that a time- and cost-effective diagnostic algorithm clearly outperforms the clinical work-up typically done today when it comes to predicting Alzheimer's dementia," Hansson told MedPage Today.

To build their prediction algorithms, the researchers studied 340 people with mild cognitive symptoms in the Swedish BioFINDER cohort. Participants were 60 to 80 years old, had a Mini-Mental State Examination (MMSE) score of 24 to 30 points at baseline, and did not fulfill criteria for any dementia. The primary outcome was prediction of progression to Alzheimer's dementia versus to any other dementia, or to not progressing, in 4 years.

The researchers assessed demographics, APOE4 genotype, cortical thickness, cognitive measures, and plasma and cerebrospinal fluid (CSF) markers, searching first for the best fit, then omitting variables to find simpler algorithms with similar predictive power. They used data from 543 participants in the Alzheimer's Disease Neuroimaging Initiative (ADNI) as the validation cohort.

Within 4 years, plasma p-tau217 alone predicted Alzheimer's in the BioFINDER cohort with an area under the curve (AUC) of 0.83. Combining plasma p-tau 217, memory tests, executive function tests, and APOE boosted accuracy to 91% (AUC 0.91, 95% CI 0.88-0.95, P<0.001).

In ADNI, this model had a similar AUC (0.90) using plasma p-tau181 instead of p-tau217. Within 2 and 6 years, similar models had AUCs of 0.90-0.91 in both cohorts. Using CSF p-tau, amyloid beta, and neurofilament light instead of plasma biomarkers did not improve accuracy significantly.

Phosphorylated tau blood biomarkers have great potential in Alzheimer's disease, said Nicholas Ashton, PhD, of University of Gothenburg in Sweden, who wasn't involved with the study. "They offer a low-cost, less-invasive alternative to understanding what's going on molecularly in the brain," he told MedPage Today.

Blood tests will be useful both for clinicians and to recruit people into therapeutic trials for drugs specifically targeted for Alzheimer's pathology, Ashton noted.

Both p-tau217 and p-tau181 performed well in this analysis, he added. "There's been debate about which is superior, but this study shows that -- in combination with the cognitive tests and genetic tests -- it doesn't matter what type of phospho-tau biomarker you use: they both gave the same prediction power."

The algorithm is being developed for clinics without access to advanced diagnostic instruments, Palmqvist said in a statement. "In the future, the algorithm might therefore make a major difference in the diagnosis of Alzheimer's within primary healthcare," he noted.

As of now, it's been tested only on patients who have been examined in memory clinics, he added. "Our hope is that it will also be validated for use in primary healthcare as well as in developing countries with limited resources."

 

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