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, August 12, 2022

Most of the risk factors associated with Alzheimer’s disease from observational studies are likely wrong

Well shit, WHOM is going to solve the problem? So we know how to prevent Alzheimers.  Maybe you want to take a fluid intelligence test from your doctor.

How is fluid intelligence tested and measured? There are several different ways that fluid intelligence can be measured, this includes the Woodcock-Johnson Test of Cognitive Abilities, Raven's Progressive Matrices and Wesschler Intelligence Scale for Children.

Most of the risk factors associated with Alzheimer’s disease from observational studies are likely wrong

Interesting article from Korologou-Linden et al 2022, “The causes and consequences of Alzheimer’s disease: phenome-wide evidence from Mendelian randomization”.

In this study, the authors used a Mendelian randomization approach to examine the causal relationships between various risk factors and Alzheimer’s disease. They used the UK Biobank, which has a massive sample size of >300,000 participants.

They found that genetic variation at one gene — APOE — is far and away the main mediator of Alzheimer’s disease genetic risk. This replicates why Alzheimer’s has been called a quasi-monogenic disease — APOE has that large of an effect.

They don’t hold anything back in the discussion, basically arguing that their study disagrees with observational studies because their methodology is better and observational studies are wrong, because observational studies can’t identify causality.

Instead, they suggest that associations with Alzheimer’s disease in observational studies are due to reverse causation (i.e. they are symptoms of early/prodromal Alzheimer’s disease, rather than causes) or simply due to selection bias.

This means that the things often associated with Alzheimer’s disease in observational studies — body mass index, blood pressure, and physical activity — might not actually increase the risk of disease. Interestingly, Alzheimer’s genetic risk in this study is actually associated with a lower body mass index and body fat in people 53-72 years old.

They also found that Alzheimer’s disease risk is associated with a lower fluid intelligence score, with no causal effect on educational attainment.

One caveat I have with the study is that I’d like to learn about the associations of these risk factors with other forms of cognitive impairment. Laypeople often use the term “Alzheimer’s” to refer to dementia or age-related cognitive impairment in general.

For example, does a higher genetic risk for elevated blood pressure or body mass index causally affect the risk for vascular-associated cognitive impairment? My guess is that they might, which might cause this study to be a bit misleading if the results were taken in the wrong way.

That said, there seems to be a real effect of APOE on the risk of cognitive impairment that is independent of classical risk factors body mass index, blood pressure, and physical activity. And this study helps to parse out how that might be occurring, which will hopefully help to develop better preventive approaches and treatments.


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