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.

Monday, April 1, 2019

Association Between CSF Beta-Amyloid and Apathy in Early-Stage Alzheimer Disease

You likely need to know about this and your doctors' protocol to counteract apathy.  I don't give a shit that no treatments exist for apathy. It is your doctors responsibility to initiate research that finds a treatment. Or don't you care that you have an incompetent doctor? My dad in the midst of parkinsons dementia had apathy, I couldn't help him with any of my suggestions because of that. 

You will need this.

Your chances of getting dementia.
1. 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.

Association Between CSF Beta-Amyloid and Apathy in Early-Stage Alzheimer Disease 

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First Published March 26, 2019 Research Article










Apathetic syndrome is a common clinical feature in patients with Alzheimer diseases (AD), from preclinical phases to late dementia stages, and it is strongly related to major disease outcomes. Unfortunately, no specific pharmacological treatments for apathy have been accomplished so far. Translational evidences have previously shown that a link between apathy and hallmarks of AD-related pathophysiological, that is, β-amyloid (Aβ) plaques, and neurofibrillary pathology exists. However, only few studies investigated the association between cerebrospinal fluid (CSF) core biomarkers of AD and apathy scores, finding conflicting results.

Thirty-seven patients were identified as having AD dementia according to National Institute on Aging–Alzheimer Association 2011 criteria. All participants underwent an extensive diagnostic workup including CSF assessment to assess the concentrations of the core biomarkers of AD pathophysiology, that is, Aβ42, t-tau, and pTau181. To follow, they were stratified as apathy absence, apathy mild, and apathy severe according the score of the Neuro Psychiatric Inventory-apathy item. We investigated for potential associations between apathy scores and CSF core biomarkers concentrations as well as for differences in terms of clinical and CSF biomarkers data across the 3 apathy groups.

The CSF Aβ42 values were negatively correlated with apathy scores. In addition, patients with severe apathy had significantly lower Aβ42 levels compared to nonapathetic ones.

Based on our results, we encourage further studies to untangle the potential association between the complex pathophysiological dynamics of AD and apathy. Apathy may represent an innovative reliable clinical outcome measure to use in clinical trials, investigating treatments with either a symptomatic or a disease-modifying effect.

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