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 17, 2025

Shingles, RSV vaccines may lower dementia risk

 Didn't your competent? doctor get you the newer shingles vaccine a while ago? I've had both. 

  • Shingrix vaccine (4 posts to October 2017)
  • Shingles, RSV vaccines may lower dementia risk


    Older adults who had received AS01-adjuvanted shingles and RSV vaccines may have a reduced risk of dementia over the next 18 months, according to a study published in npj Vaccines.

    Using electronic health records from 436,788 individuals, researchers led by Maxime Taquet,  University of Oxford, Oxford, United Kingdom, investigated whether AS01-adjuvanted vaccines affect dementia risk. The study included recipients of shingles vaccine (Shingrix; n = 103,798), RSV vaccine (Arexvy; n = 35,938), or both vaccines (n = 78,658), with matched influenza vaccine recipients serving as the comparison group.

    All groups were balanced across key demographic and clinical characteristics (standardised mean differences < 0.1). The mean age of the cohorts ranged from 69.20 to 72.91 years. 

    Over an 18-month follow-up period, individuals who had received RSV vaccine and shingles vaccine had a 29% (ratio of restricted mean time lost [RMTL] = 0.71; 95% confidence interval [CI], 0.61-0.83; P = 2.8 x 10⁻⁵) and 18% (RMTL: 0.82, 95% CI 0.74-0.91; P = .00027) lower risk of dementia, respectively, while those who had received both vaccines had a 37% lower risk (RMTL = 0.63; 95% CI, 0.55-0.72; P = 4.7 x 10⁻¹²), compared with those who had received influenza vaccines. These findings corresponded to an additional 87, 53, and 113 days free of dementia diagnosis within the 18-month period, respectively.

    No significant difference in dementia risk was observed between individuals who received either AS01-adjuvanted vaccines and those who received both vaccines. The reduction in risk was consistent across sexes and remained robust when including individuals diagnosed with dementia within the first 3 months of follow-up. A similar protective association was also seen for the composite outcome of dementia or death.

    “It is likely that both the AS01 shingles and RSV vaccines provide some protection against dementia,” the authors remarked. “The mechanisms underpinning this protection remain to be determined. Our data provide support for the hypothesis that, besides protection against their target infection, these vaccines could well protect against dementia via the action of the AS01 components through specific immunological pathways.”

    Given the implications for ageing populations, the authors called for further clinical and mechanistic studies to validate and elucidate the durability and pathways of this observed protective effect.

    Source: npj Vaccines

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