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.

Friday, December 9, 2022

Brain Vitamin D Tied to Cognitive Function

FYI. This does not suggest endorsing supplementation.

Brain Vitamin D Tied to Cognitive Function

No links seen with Alzheimer's or dementia pathology, however

A computer rendering of the molecular model of calcifediol over a human brain.

Vitamin D levels in post-mortem brain tissue were linked with cognitive function, an autopsy study showed.

Higher concentrations of 25(OH)D3 -- the main form of vitamin D assessed in the study -- in four areas of the brain were tied to 25% to 33% lower odds of dementia or mild cognitive impairment, according to Sarah Booth, PhD, of Tufts University in Boston, and colleagues.

However, brain concentrations of vitamin D were not associated with any neuropathology or biomarker outcome, Booth and co-authors reported in Alzheimer's & Dementia.

Relationships between vitamin D and cognition have been investigated previously with mixed results, noted Claire Sexton, DPhil, senior director of scientific programs and outreach at the Alzheimer's Association in Chicago, in an email to MedPage Today. "Some studies found a connection; some did not."

While "an interesting possible connection," Sexton observed, "this study, because it is an observational study and not an intervention, cannot establish that the vitamin D levels cause the lower risk, only that there is a connection to lower risk. More research is needed to answer those questions."

"Finding an association between vitamin levels and reduced risk is not the same as endorsing supplementation," Sexton pointed out. "Previous clinical trials of vitamin D supplementation to reduce dementia risk found mixed and varying results and had side effects. It is not recommended to start vitamin D supplementation to reduce dementia risk."

The study aimed to analyze brain concentrations of vitamin D and determine whether associations with cognitive measures and neuropathology outcomes existed.

"Many studies have implicated dietary or nutritional factors in cognitive performance or function in older adults, including many studies of vitamin D, but all of them are based on either dietary intakes or blood measures of vitamin D," said coauthor M. Kyla Shea, PhD, also of Tufts, in a statement. "We wanted to know if vitamin D is even present in the brain, and if it is, how those concentrations are linked to cognitive decline."

The researchers evaluated 25(OH)D3 and other vitamin D forms in four brain regions -- mid-frontal and mid-temporal cortex, cerebellum, and anterior watershed -- in post-mortem tissue of 290 deceased participants in the Rush Memory and Aging Project. Decedents whose brains were stored for more than 6 years were excluded.

Global Alzheimer's pathology included counts of neuritic plaques, diffuse plaques, and neurofibrillary tangles. Macroscopic and microscopic cerebral infarctions were identified as were Lewy bodies.

Participants had a mean age of 92 at death. Most were female (77%) and had at least 12 years of education (72%).

Cognitive evaluations were performed annually. At their last clinic visit, 40% of participants had diagnosed dementia, 24% had mild cognitive impairment, and 36% had no cognitive impairment.

Odds of having dementia or mild cognitive impairment at the last visit were 25%-33% lower per doubling of 25(OH)D3 in the four brain regions (OR 0.669-0.754, P≤0.031 for all). Brain vitamin D concentrations were correlated across the regions (intra-class correlation coefficient 0.87) but were not associated with any neuropathology outcome evaluated.

Plasma total 25(OH)D3 and free 25(OH)D were moderately correlated with brain 25(OH)D3 (r 0.32-0.39, P≤0.0001), but free 25(OH)D was not significantly associated with cognitive function.

Other forms of vitamin D were below the lower limit of detection in over half of the brains analyzed, limiting the ability to evaluate associations of 1,25(OH)2D3 -- the biologically active form of vitamin D -- with cognition or pathology, the researchers acknowledged. Most decedents were white and results may not apply to others, they added. Residual confounding also may have occurred.

"We now know that vitamin D is present in reasonable amounts in human brains, and it seems to be correlated with less decline in cognitive function," Shea said. "But we need to do more research to identify the neuropathology that vitamin D is linked to in the brain before we start designing future interventions."

  • 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

The research was supported by National Institute on Aging and the USDA Agricultural Research Service.

Booth reported relationships with NIH and USDA. Co-authors had relationships with NIH, USDA, and industry.

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