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.

Wednesday, October 25, 2023

Another Study Highlights Metformin's Dementia Protection Properties

 

Well, since this has been around for years why the hell doesn't someone actually do human testing and create protocols on stroke recovery?

Earlier research has this line:The drug, which is cheaply available for just $0.16 a day, works by boosting the number of oxygen molecules released into a cell, which in turn seems to benefit the robustness and longevity of the body’s basic building blocks. (This would seem to be much easier and faster than HBOT. I'm requesting this at my next stroke, my doctor won't know what hit her when I tell her how to treat me.)

 

 

Another Study Highlights Metformin's Dementia Protection Properties

Association appeared irrespective of HbA1c level

A photo of a glucose meter laying on a box of metformin tablets

More evidence suggested that metformin may be protective against new-onset dementia in older adults with diabetes, a cohort study found.

Compared with routine metformin users, those who stopped the drug early for reasons other than kidney dysfunction saw a 21% higher risk for developing dementia (HR 1.21, 95% CI 1.12-1.30), found Sarah Ackley, PhD, of Boston University, and colleagues.

This link was largely independent of changes in HbA1c and insulin usage, they reported in JAMA Network Openopens in a new tab or window.

Mediation analysis found HbA1c level or insulin use contributed to an acceleration of dementia diagnosis by 0.07 years (95% CI 0.02-0.13 years) 1 year after metformin termination, but by the 5-year mark had zero contribution to dementia diagnosis acceleration (0.00 years, 95% CI -0.02 to 0.02 years).

"For individuals with diabetes at particularly high risk of dementia, such as carriers of APOE4 or individuals with a family history of dementia, it may be particularly beneficial to find ways to manage or mitigate gastrointestinal adverse effects (e.g., switching to slower release formulations of metformin or taking the medication with food in the evening) instead of replacing metformin with other agents, given that participants in this study remained on anti-diabetes drugs after early termination with metformin," Ackley's group advised.

These findings track with a prior meta-analysisopens in a new tab or window that found people with diabetes on metformin had 24% lower risk for developing dementia compared with patients not on metformin (HR 0.76, 95% CI 0.60-0.97). Another 2020 studyopens in a new tab or window found an 81% reduction in incident dementia risk in older metformin users (HR 0.19, 95% CI 0.04-0.85, P=0.030).

Here, 12,220 early terminators of metformin were included from the Kaiser Permanente Northern California health system, defined as any individuals with diabetes who stopped using metformin without prior history of abnormal kidney function. This sample included 46.2% women with an average age of 59.4 at the start of their first metformin prescription. About 63% were white, 14.9% were Hispanic, 13.4% were Asian, and 8.2% were Black.

They were compared with 29,126 routine users, who were patients remaining on metformin at the age when the matched early-terminator group stopped using it. This group had either not yet terminated metformin treatment or had terminated -- with or without restarting -- after their first abnormal estimated glomerular filtration rate (eGFR) measurement. They were comparable in terms of demographics. The mean HbA1c level at baseline was 8 and 7.7 for early terminators and routine users, respectively. All patients in both groups were born prior to 1955.

Routine metformin users were less likely to have cardiovascular disease at baseline (26.5% vs 33%) but were more likely to have a low eGFR at initiation of metformin (4.6% vs 1.6%).

Data on the reason behind metformin termination were not available, which was a limitation of the study.

As for next steps, the researchers noted that "[f]ormally evaluating the heterogeneity of the metformin estimate across known risk factors for dementia is an important extension of our work."

"Given considerable interest in drug repurposing for dementia, further confirmatory work would be required to extrapolate to prediabetic or nondiabetic populations," they said.

  • author['full_name']

    Kristen Monaco is a senior staff writer, focusing on endocrinology, psychiatry, and nephrology news. Based out of the New York City office, she’s worked at the company since 2015.

Disclosures

The study was funded by grants from the National Institutes of Health National Institute on Aging.

Ackley reported no disclosures. Other co-authors reported relationships with AbbVie, Gilead Sciences, CRISPR Therapeutics, Abbott Laboratories, California Department of Public Health, National Institutes of Health, the National Institute of Diabetes and Digestive and Kidney Diseases, National Institute on Aging, Biogen Healthy Climate, and Healthy Lives Scientific Advisory Council.

Primary Source

JAMA Network Open

Source Reference: opens in a new tab or windowZimmerman SC, et al "Metformin cessation and dementia incidence" JAMA Netw Open 2023; DOI: 10.1001/jamanetworkopen.2023.39723.

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