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, October 20, 2022

No association of Viagra and Cialis with reduced Alzheimer’s disease risk

 Well damn, this earlier research sounded promising, I was going ask for a Viagra prescription at my next doctor appointment, may still do it. What is the downside for me?

Can Erectile Dysfunction Drugs Reduce Dementia Risk?

The latest here:

No association of Viagra and Cialis with reduced Alzheimer’s disease risk

At a Glance

  • Researchers found no evidence that the drugs Viagra and Cialis reduce the risk of Alzheimer’s and related dementias.
  • The findings contradict those from an earlier study that suggested these drugs as possible Alzheimer’s treatments.
The study findings contradict earlier work suggesting that a class of drugs including Viagra and Cialis might be used to treat Alzheimer’s disease. Robert Kneschke / Shutterstock

Efforts to develop new drugs to treat Alzheimer’s disease (AD) haven’t yet yielded significant clinical benefits. One recent approach to developing AD treatments is to seek existing FDA-approved drugs that could potentially be repurposed.

Computational methods have suggested that a class of existing drugs called phosphodiesterase-5 (PDE5) inhibitors might be used to treat AD. These drugs include sildenafil (Viagra) and tadalafil (Cialis). Both are approved for treating erectile dysfunction and pulmonary arterial hypertension, a type of high blood pressure that affects the arteries in the lungs and heart.

An earlier NIH-funded study found that people taking sildenafil were less likely to develop AD. Sildenafil also reduced certain molecular abnormalities associated with AD in cultured nerve cells derived from AD patients.

Among those searching for existing drugs that could treat AD is a team of researchers at NIH’s National Institute on Aging (NIA) led by Dr. Madhav Thambisetty. In their new study, the team sought to verify the earlier findings on PDE5 inhibitors. Their results appeared in Brain Communications on October 4, 2022.

Both studies examined insurance claims data from Medicare beneficiaries but took different approaches. The earlier study compared people who took sildenafil for any reason to those who did not. Since most people tend to take sildenafil for erectile dysfunction, this approach might have created differences between the people in the two groups that couldn’t be corrected based on the information in medical claims.

In contrast, the current study focused on people with pulmonary arterial hypertension. The researchers compared the incidence of AD and related dementias among those treated for the condition with sildenafil or tadalafil versus those treated with a different class of drugs. This made the two comparison groups more likely to have people with similar characteristics. The study included data on more than 13,000 people.

The team did not find any significant difference in AD and related dementia risk between the two treatment groups. The researchers analyzed the data four different ways to address various possible biases in the data. None of these analyses found a significant effect of PDE5 inhibitor treatment on the risk of Alzheimer’s or related dementias.

The researchers also examined the effect of sildenafil on a range of molecular features associated with AD in cell cultures. Although sildenafil had a modest anti-inflammatory effect, no protective effects were observed on any other outcomes tested.

The results do not support the use of PDE5 inhibitors such as sildenafil for AD treatment. This is in contrast to the earlier findings. The authors of the new study attribute the discrepancy mainly to differences in the design of the two studies, particularly in the selection of the treatment and control groups.

“The combination of routinely collected healthcare data with experimental studies to test potential drug repurposing in Alzheimer’s disease is a powerful approach,” Thambisetty says. “It can help us discover promising drugs to test in rigorous clinical trials.”

—by Brian Doctrow, Ph.D.


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