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.

Saturday, August 17, 2024

Expert Panel: Target These 14 Factors to Cut Dementia Incidence by Nearly Half

Oh god, more useless generalities!  Hopefully your doctor doesn't give this crapola, if your doctor even knows about dementia risk from your stroke!

Your chances of getting dementia. YOUR DOCTOR IS RESPONSIBLE FOR PREVENTING THIS!

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:

Expert Panel: Target These 14 Factors to Cut Dementia Incidence by Nearly Half

Update from Lancet Commission adds vision loss, high LDL to previous list

PHILADELPHIA -- The Lancet Commission on dementia prevention, intervention, and care has raised the number of modifiable risk factors definitively linked to cognitive loss to 14, based on research conducted since its last update in 2020.

Vision loss and high levels of low-density lipoprotein (LDL) cholesterol are now added to the commission's list, which stood at 12 in the previous version. The new 57-page update, from Gill Livingston, MD, of University College London in England, and colleagues, was published Wednesday in The Lancet and presented simultaneously at the Alzheimer Association International Conference here.

The 14 factors include:

  • Education
  • Hearing loss
  • Depression
  • Head trauma from sports and bike riding
  • Physical activity
  • Smoking
  • Hypertension
  • Obesity
  • Type 2 diabetes
  • Alcohol drinking
  • Social isolation
  • Air pollution
  • Vision loss
  • High LDL

If all of these were fully addressed -- providing higher education to everyone, ending obesity, making helmet use mandatory for youth, eliminating air pollution, etc. -- worldwide risk for dementia would fall by 45%, the commission found in its review of nearly 600 scientific publications.

About 7% of dementia risk can be attributed to high LDL, according to the report, making it one of the most powerful risk factors. Also accounting for 7% is unaddressed hearing loss; social isolation and low education are tied for third on the list, at 5% of the population-attributable risk each. Other factors account for 3% or less (the authors put the effect of untreated vision loss at 2%).

The commission also examined a number of other factors with research linking them to dementia risk, including diet, reduced sleep, and neuropsychiatric conditions such as bipolar and psychotic disorders. Ultimately the authors found that the research was insufficient to establish population-attributable risks for them. Nor is there solid evidence that interventions targeting these factors do indeed reduce dementia risk.

As well, the review took on the difficult question of direct interventions -- including diagnostic screens and scans, symptomatic treatments such as anticholinesterase inhibitors, and anti-amyloid biologic drugs -- though mainly in narrative rather than quantitative terms. The commission looked favorably on current symptomatic treatments, citing "short-term, modest positive effects and that stopping this treatment is associated with worse outcomes in the long term."

But the authors were not especially enthusiastic for anti-amyloid drugs such as donanemab (Kisunla) and lecanemab (Leqembi). "Currently, the effects of all [anti-amyloid] drugs are small. The resources required to support early biomarker-based diagnosis, supervision of administration and safety, and buying the drugs will mean that roll-outs into many health systems will be slow or non-existent in some," they wrote. (Motivated at least partly by these considerations, as well as the potential for adverse effects, the European Medicines Agency recently rejected lecanemab for European approval.)

Several of the same authors, including Livingston, helped author a separate report, published at the same time in The Lancet Healthy Longevity, on a cost-benefit analysis of policies addressing six risk factors as applied to England. These included drinking, dietary salt and sugar, pollution from automobiles, smoking, and youth head trauma. The analysis then examined interventions already tested in various settings: i.e., raising alcohol and cigarette prices, reducing salt and sugar in commercial foods, banning cars from certain areas, and mandating use of bike helmets. The authors then estimated the monetary costs and associated quality-adjusted life years (QALYs) gained if implemented in the English population.

So, for example, raising the price of alcohol by an amount that, in Scotland, cut weekly consumption by 1-2 units on average would lead to some 15,000 fewer Britons age 45 subsequently developing dementia linked to drinking. Overall costs over time would decline by £280 million ($360 million), and 4,767 QALYs would be gained.

The most dramatic effect was seen with reduction in salt intake. The authors modeled a policy that would cut mean daily intake by 1.68 g per person, with an accompanying decrease of 1.59 mm Hg in systolic blood pressure. Given the relationship previously found between hypertension and dementia risk, Livingston's group estimated that more than 43,000 people age 45 would not suffer dementia later on, and the associated cost saving would reach £2.37 billion ($3.04 billion); QALYs gained would top 39,000.

Acknowledging the real-world political landscape, "[i]t is possible that policy makers are hesitant to put these interventions into place given the long lead time before the benefits of cognitive decline could be expected," the investigators wrote.

"However, given the effect of these interventions on vascular or brain health in general, benefits in terms of other non-communicable diseases would be expected sooner. Our analysis further strengthens the argument for implementation of effective population-level policies as soon as practicably possible."

Similarly, Livingston and colleagues on the commission argued that "policy makers should prioritize resources to enable risk reduction to prevent or delay dementia and interventions to improve symptoms and life for people with dementia and their families."

  • author['full_name']

    John Gever was Managing Editor from 2014 to 2021; he is now a regular contributor.

Disclosures

The commission's work was supported by the Alzheimer's Society, the Economic and Social Research Council, and Alzheimer's Research U.K. Authors reported a wide variety of government and foundation grants, as well as extensive relationships with industry.

The England modeling study was funded by the UK National Institute for Health and Care Research. Livingston reported receiving U.K. and Norwegian government and noncommercial organization grants. Other authors declared they had no relevant financial interests.

Primary Source

The Lancet

Source Reference: Livingston G, et al "Dementia prevention, intervention, and care: 2024 report of the Lancet standing Commission" Lancet 2024; DOI: 10.1016/S0140-6736(24)01296-0.

Secondary Source

The Lancet Healthy Longevity

Source Reference: Mukadam N, et al "Benefits of population-level interventions for dementia risk factors: an economic modelling study for England" Lancet Healthy Longev 2024; DOI: 10.1016/S2666-7568(24)00117-X.

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