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, July 22, 2020

Ten Targets for Reducing Alzheimer's Risk

Well shit, this is mostly useless. I'd much rather they analyze these. Because this stuff is way too far in the future to help us now. 

You can ask your doctor what pieces of the kitchen sink they are throwing at preventing Alzheiners/dementia before clinical stuff is proven. 

Is this earlier research enough for your doctor to use?

Can An Anti-Asthma Drug Rejuvenate the Brain? montelukast January 2016 

A Decades-Old Asthma Drug Has Reversed Brain Damage From Dementia in Mice - zileuton July 2018

 

Or is your doctor using one of these to prevent dementia? 

1.  The End of Alzheimer's: The First Program to Prevent and Reverse Cognitive Decline by Dale Bredesen 

 

2.  A Real Alzheimer's Prevention Program from The University of California

 

3. I'm a Brain Doctor, and This Is What I Do to Prevent Alzheimer's December 2018 

 

4. Reversing the Alzheimer’s Catastrophe April 2007 

You can't use mine, I'm not medically trained, your doctors' better be EXACT.

Dementia prevention 19 ways per Dean

 

The latest here:

Ten Targets for Reducing Alzheimer's Risk

Meta-analysis offers evidence-based guidance for Alzheimer's prevention

A depressed looking senior woman with her hand on her head holds her husband’s hand who has a blank stare
Ten risk factors appeared to have a significant effect on developing Alzheimer's disease, many of which could be targeted with preventive steps, a meta-analysis suggested.
From an analysis of 395 studies, 21 clinical evidence-based suggestions to reduce Alzheimer's disease risk emerged, reported Jin-Tai Yu, MS, PhD, of Fudan University in Shanghai, China, and colleagues.
The suggestions pinpointed 10 risk factors with Class 1 Level A strong evidence, they wrote in the Journal of Neurology, Neurosurgery & Psychiatry:
  • Diabetes
  • Hyperhomocysteinemia
  • Poor BMI management
  • Reduced education
  • Hypertension in midlife
  • Orthostatic hypotension
  • Head trauma
  • Less cognitive activity
  • Stress
  • Depression
Nine risk factors had Class 1 Level B weaker evidence: obesity in midlife, weight loss in late life, physical exercise, smoking, sleep, cerebrovascular disease, frailty, atrial fibrillation, and vitamin C, they added. Two interventions with Class III evidence were not recommended: estrogen replacement therapy and acetylcholinesterase inhibitors.
Evidence about Alzheimer's disease prevention is challenging to interpret "due to varying study designs with different endpoints and credibility," Yu noted.
"We worked with an international team of researchers, including several renowned neurologists, geriatricians, psychiatrists, psychologists, and epidemiologists, to review and analyze all current evidence in order to produce the first evidence-based guideline for Alzheimer's disease prevention," he told MedPage Today.
"Nearly two-thirds of these suggestions target vascular risk factors and lifestyle, strengthening the importance of keeping a good vascular condition and maintaining a healthy lifestyle for preventing Alzheimer's disease," he added.
"Evidence is building rapidly that modifiable risk factors play a key role in whether a person will develop cognitive decline and impairment as they age, whether that be due to Alzheimer's disease or any other dementia," observed Keith Fargo, PhD, director of scientific programs and outreach at the Alzheimer's Association in Chicago, who wasn't involved with the study.
"However, it can be difficult to separate the wheat from the chaff," Fargo told MedPage Today. "While no proposed intervention has been shown to be perfect -- we can reduce risk, but not yet eliminate risk altogether -- meta-analyses such as these are helping us hone in on some of the most important factors, as well as helping us steer clear of things that may not be as impactful."
The "ultimate gold standard" is a randomized, controlled clinical trial to evaluate whether lifestyle interventions that target many risk factors can protect cognition in older adults at increased risk of decline, like the ongoing U.S. POINTER study, Fargo added.
In their review, Yu and collaborators looked at data from 243 observational prospective studies and 152 randomized controlled trials, culled from electronic databases and relevant websites from inception until March 2019. A total of 104 modifiable risk factors and 11 interventions were included in their analysis.
Most studies (82%) recruited people without dementia at baseline, and 17% specifically constrained the sample population to people with normal cognition.
Bias in observational studies stemmed mainly from generalizability, attrition, and misclassification. In trials, performance bias, incomplete outcome data, inadequate allocation concealment, and selective outcome reporting were factors.
The findings are in line with other studies that have not shown a beneficial effect of menopausal hormone therapy on Alzheimer's disease, noted Tomi Mikkola, MD, of Helsinki University Hospital in Finland, who wasn't involved with the meta-analysis. "However, we have shown in various papers that menopausal hormone therapy has beneficial effects on vascular disease, including vascular dementia," he said.
"In my view, this outlines the difference of Alzheimer's disease and vascular dementia, although in many studies they have not been clearly separated and this is a challenge since, at a very old age, likely both may occur," Mikkola told MedPage Today. "It shows the importance to try to further study and understand Alzheimer's disease in more detail; it's likely we have missed 'the window of opportunity' at the time of the Alzheimer's diagnosis."
The suggestions that emerge from this meta-analysis should be particularly noted by non-demented but high-risk individuals -- people who carry APOEε4 or who have a high polygenic score, family history of dementia, or amyloid- positive evidence -- and their primary care physicians, the researchers wrote.
"Our study provides an advanced and contemporary survey of the evidence, suggesting that more high-quality observational prospective studies and randomized controlled trials are urgently needed to strengthen the evidence base for uncovering more promising approaches to preventing Alzheimer's disease," Yu said.
"Well-designed clinical trials also are needed to verify the effects on Alzheimer's disease of several promising interventions, including sleep improvement, smoking cessation, anti-depression management, and anti-diabetic agents," he added.
  • 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 study was funded by the National Key R&D Program of China, Shanghai Municipal Science and Technology Major Project, and Zhangjiang Lab.
Yu disclosed serving as associate editor-in-chief for Annals of Translational Medicine and as senior editor for Journal of Alzheimer's Disease. Other researchers disclosed relevant relationships with Ipsen, Pierre Fabre, Nestlé, Sanofi, Servier, Biogen, Nutrition Santé, Pfizer, Icon, Eli Lilly, Roche, TauRx, Lundbeck, Eisai, Affiris, Boehringer Ingelheim, Schwabe, Takeda, Toyama, Abbott, Abbvie, Amgen, Anavex, AstraZeneca, Biotie, Bristol-Myers Squibb, Cardeus, Cohbar, Elan, Genentech, Ichor, iPerian, Janssen, Medivation, NeuroPhage, Novartis, Probiodrug, Somaxon, Avid, Exonhit, MSD, Otsuka, Regenron, LPG Systems, Alzheon, and Transition Therapeutics.

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