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, July 25, 2024

Dementia Risk Drops With Shingrix Vaccine

 Does your competent? doctor have enough functioning neurons to ensure you get this while still in the hospital? To remove one of your dementia risks post stroke?

Oh, you don't have a competent doctor because s/he doesn't even know about this or even that you are likely to get dementia?

Your chances of getting dementia.

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:

Dementia Risk Drops With Shingrix Vaccine

Recombinant shingles vaccine tied to 164 additional days without dementia diagnosis

A photo of a woman’s hand lifting a vial of the recombinant shingles vaccine (Shingrix) from a box.

Key Takeaways

  • The recombinant zoster vaccine (Shingrix) was associated with a 17% increase in time without a dementia diagnosis, compared with the live vaccine.
  • This translated into 164 additional days without a dementia diagnosis.
  • The findings support hypotheses about shingles vaccination and dementia prevention.

The recombinant shingles vaccine (Shingrix) was associated with a larger reduction in dementia than the live shingles vaccine (Zostavax), an analysis of more than 200,000 U.S. older adults showed.

Over a 6-year follow-up period, adults who predominantly received the recombinant herpes zoster vaccine had a 17% increase in time without a dementia diagnosis (restricted mean time lost ratio 0.83, 95% CI 0.80-0.87, P<0.0001) compared with those who received the live vaccine, reported Maxime Taquet, PhD, of the University of Oxford in England, and co-authors.

This translated into 164 additional days without a dementia diagnosis, Taquet and colleagues reported in Nature Medicine. The reduction in dementia risk was present in both men and women, but greater in women.

The recombinant shingles vaccine also was tied to a lower risk of dementia compared with two other vaccines commonly used in older people -- influenza and tetanus/diphtheria/pertussis (Tdap) vaccines.

"The size and nature of this study makes these findings convincing, and should motivate further research," Taquet said in a statement.

"They support the hypothesis that vaccination against shingles might prevent dementia," he continued. "If validated in clinical trials, these findings could have significant implications for older adults, health services, and public health."

Several studies have linked viral illnesses with subsequent dementia. Human herpesvirus 6A (HHV-6A) and human herpesvirus 7 (HHV-7) have been found in postmortem tissue samplesopens in a new tab or window of people with Alzheimer's disease at levels up to twice as high as non-Alzheimer's disease samples, for example.

Researchers also have suggested that herpes simplex virus 1 (HSV-1) coupled with an APOE4 gene may raise Alzheimer's risk considerably. Based on early HSV-1 research, a trial of the antiviral drug valacyclovir (Valtrex) in mild Alzheimer's disease is currently underway.

Last year, a preprint study in Wales suggested that the live shingles vaccine may be associated with a 20% reduction in dementia risk, with the relationship stronger in women than men.

"Although previous studies have suggested immunization against herpes viruses might protect against dementia, particularly in women, this took advantage of a change in vaccine type to overcome the many confounding variables that may have provided alternative explanations," noted Robert Howard, MD, of University College London, who wasn't involved with the new Oxford study.

"The next question is how does vaccination exert this dementia protection effect?" Howard asked in a post on the U.K. Science Media Centre. "Is it through suppression of virus or is the induced immune response targeting a step in the molecular pathology of Alzheimer's disease?"

In the U.S., the recombinant shingles vaccine was approved in October 2017. In 2018, it received a preferential recommendationopens in a new tab or window by the CDC's Advisory Committee on Immunization Practices (ACIP) over the live shingles vaccine. As of November 2020, the live shingles vaccine was no longer available, according to the CDC.

Taquet and co-authors used TriNetX electronic health records in the U.S. to study 103,837 individuals ages 65 and older who received a first dose of shingles vaccine between November 2017 and October 2020; 95% received the recombinant vaccine. These older adults were propensity-score matched with 103,837 individuals who received their first dose between October 2014 and September 2017 (98% had the live vaccine). People with previous diagnoses of dementia or neurodegenerative disease were excluded from the study.

Median follow-up was 4.15 years in the recombinant vaccine group, and 6.0 years in the live vaccine group. The primary outcome was a first diagnosis of dementia from 3 months (to exclude possible pre-existing dementia) to 6 years post-vaccination in a time-to-event analysis, based on ICD-10 codes.

Associations between recombinant shingles vaccination and dementia were consistent across dementia types except frontotemporal and Lewy body dementia. Older adults vaccinated after October 2017 also were less likely to have a herpes zoster infection post-vaccination.

The study was observational and cannot show causality, the researchers acknowledged. It relied on electronic health records, which may have had errors. Being diagnosis-free does not mean participants were disease-free, they pointed out.

Nonetheless, the findings are "intriguing and encouraging," said co-author Paul Harrison, FRCPsych, also of the University of Oxford. "Anything that might reduce the risk of dementia is to be welcomed, given the large and increasing number of people affected by it."

  • Judy George covers neurology and neuroscience news for MedPage Today, writing about brain aging, Alzheimer’s, dementia, MS, rare diseases, epilepsy, autism, headache, stroke, Parkinson’s, ALS, concussion, CTE, sleep, pain, and more. Follow

Disclosures

This research was supported by the NIHR Oxford Health Biomedical Research Centre.

Taquet and Harrison had no disclosures.

One co-author was a consultant for GSK, maker of Shingrix. GSK was not aware of the study until after the manuscript had been accepted.

Howard reported no conflicts of interest.

Primary Source

Nature Medicine

Source Reference: Taquet M, et al "The recombinant shingles vaccine is associated with lower risk of dementia" Nat Med 2024; DOI: 10.1038/s41591-024-03201-5.

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