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.

Tuesday, December 2, 2025

Higher B12 Levels Linked to Slower Cognitive Decline

 With nothing on how to measure or what higher means: COMPLETELY FUCKING USELESS! Does no one in stroke have any brains at all?

Higher B12 Levels Linked to Slower Cognitive Decline

TOPLINE:

Higher vitamin B12 status in mid-to-late life was associated with slower declines in memory, executive function, and language compared to lower status in patients without baseline dementia, new research showed. Additionally, the associations for executive function and language — but not memory — persisted regardless of folate status.

METHODOLOGY:

  • Researchers analyzed 1994 dementia-free adults (mean age, 60 years; 54% women; 99% non-Hispanic White individuals) from the Framingham Heart Study Offspring Cohort. All had at least two assessments of vitamin B12 biomarkers and neuropsychological test scores between 1998 and 2018.
  • The participants were divided into four quartiles on the basis of the cumulative average of three vitamin B12 biomarkers: serum levels of cobalamin, methylmalonic acid, and total homocysteine, corrected for low folate levels.
  • The primary outcomes were changes in memory, executive function, and language factor scores over a mean follow-up duration of 14.2 years.
  • The analysis was adjusted for demographic, lifestyle, and medical factors, including age, education, and apolipoprotein E allele status.

TAKEAWAY:

  • Participants with a higher cumulative vitamin B12 status showed significantly slower annual cognitive decline than those with a lower B12 status in the domains of language (for trend = .003), memory (P for trend = .004), and executive function (P for trend = .03).
  • The highest B12 level was also associated with less cognitive decline (by 0.05-0.09 SD) over 10 years than the lowest level.
  • The results were consistent across folate levels, though the association between B12 status and memory was slightly stronger in those with elevated folate levels (≥ 20 ng/mL).

IN PRACTICE:

“Given that even small delays in the onset of symptoms can reduce the prevalence of cognitive impairment, efforts to manage vitamin B12 status and improve nutrition throughout the life course may help mitigate cognitive decline into older age,” the investigators wrote.

SOURCE:

The study was led by Francesca R. Marino, Boston University Chobanian and Avedisian School of Medicine, Boston. It was published online on October 21 in Alzheimer’s & Dementia.

LIMITATIONS:

The study population consisted primarily of European American participants, possibly reducing the generalizability of the findings. Neuropsychological test scores and vitamin B12 biomarkers were not measured at the same time, and different assays were used across study exams, which could introduce nondifferential error. Genetic data on polymorphisms affecting homocysteine or other B12 biomarkers were unavailable. Additionally, excluded participants were older with lower B12 or folate levels, which may have introduced selection bias.

DISCLOSURES:

The study was funded by the National Heart, Lung, and Blood Institute and the National Institute on Aging. Several investigators reported serving in advisory or editorial roles for several pharmaceutical and research organizations. Full details are provided in the original article.

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