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, July 29, 2025

Combination Cardiovascular Therapies May Protect the Aging Brain

 Well, your incompetent? doctor doesn't know about all this earlier research on diabetes drugs helping other conditions. And still hasn't been fired yet! The board of directors is complicit in incompetence squared!
  • diabetes drug (6 posts to august 2017)
  • Do you prefer your doctor and hospital incompetence NOT KNOWING? OR NOT DOING?

    I have hypertension drugs and cholesterol drugs, but not diabetes and my brainpower is fantastic.

    Combination Cardiovascular Therapies May Protect the Aging Brain

    Older adults taking a combination of medications to treat high blood pressure, cholesterol, and diabetes experienced slower cognitive decline and reduced dementia-related brain pathologies than those taking fewer or no such medications, a large analysis showed.

    “In individuals simultaneously using two or three medication classes, the decline of cognition was slower, equivalent to the change in cognition of a person 3 years younger than the average age on this sample,” Roshni Biswas, MBBS, PhD, MPH, research scientist, Rush Alzheimer’s Disease Center, Chicago, told Medscape Medical News.

    “Our findings suggest that early interventions with combination therapies targeting multiple vascular metabolic risk factors could potentially delay or prevent cognitive decline and dementia,” Biswas said.

    The study was presented on July 27 at Alzheimer’s Association International Conference (AAIC) 2025.

    Heart-Brain Connections

    Hypertension, dyslipidemia, and diabetes are known risk factors for dementia. Antihypertensives, lipid-lowering, and antidiabetic medications may help reduce the risk for dementia.

    However, a few studies have examined the association of combination cardiovascular therapies with cognitive decline and dementia-related postmortem neuropathologies.

    To that end, Biswas and colleagues evaluated 4651 older adults without dementia at baseline who participated in five ongoing longitudinal studies of aging and dementia at the Rush Alzheimer’s Disease Center.

    Participants underwent at least two annual cognitive assessments for an average of 9 years. Use of antihypertensive, lipid-lowering, and antidiabetic medications was documented annually.

    In a subgroup of 1896 participants who had died and undergone autopsy, the researchers evaluated the extent of Alzheimer’s disease (AD) and other dementia-related neuropathologies.

    Synergistic Effects?

    Compared with no medication use, treatment with all three medication classes was associated with a slower decline in global cognition (P = .02), particularly semantic and working memory, the researchers found.

    Among autopsied participants, treatment with all three medication classes was associated with lower odds of atherosclerosis (odds ratio [OR], 0.47; P < .01) and arteriolosclerosis (OR, 0.53; P = .01); less global AD pathology (P < .01), specifically amyloid and tangles; and lower odds of hippocampal sclerosis (OR, 0.27; P = .03) and TDP-43 (OR, 0.46; P < .01), a protein increasingly recognized as a key player in AD pathology, particularly in its later stages.

    Even treatment with just two medication classes was associated with a slower decline in global cognition (P < .01), as well as lower odds of atherosclerosis (OR, 0.63; P < .01), less global AD pathology (P = .03) and tangles (P = .03), and lower odds of TDP-43 (OR, 0.71; P = .02).

    Use of a single class of medication was associated with more limited but still measurable benefits, especially in preserving semantic memory and reducing tangles.

    “Our study raises the possibility for increased beneficial effects of combination vascular metabolic therapies (as opposed to single therapy) in preventing cognitive decline and dementia in aging. However, further study is needed before making clinical recommendations,” Biswas told Medscape Medical News.

    Reached for comment, Courtney Kloske, PhD, director of Scientific Engagement for the Alzheimer’s Association, said this study supports the “heart-brain connection”and demonstrates that “controlling modifiable vascular risk factors could have beneficial impacts on the brain.”

    The study had no commercial funding. Biswas and Kloske had no relevant disclosures.


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