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Substantial Memory Improvement Documented Without Exotic Drugs

memory cognitive decline

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#1 Hebbeh

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Posted 30 September 2014 - 11:38 PM


Cover all the basics first and the rest will fall into line...

 

http://www.scienceda...40930143446.htm

Memory loss associated with Alzheimer's reversed: Small trial succeeds using systems approach to memory disorders

University of California, Los Angeles (UCLA), Health Sciences

 

In the case of Alzheimer's disease, Bredesen notes, there is not one drug that has been developed that stops or even slows the disease's progression, and drugs have only had modest effects on symptoms. "In the past decade alone, hundreds of clinical trials have been conducted for Alzheimer's at an aggregate cost of over a billion dollars, without success," he said.

 

Patient one had two years of progressive memory loss. She was considering quitting her job, which involved analyzing data and writing reports, she got disoriented driving, and mixed up the names of her pets. Patient two kept forgetting once familiar faces at work, forgot his gym locker combination, and had to have his assistants constantly remind him of his work schedule. Patient three's memory was so bad she used an iPad to record everything, then forgot her password. Her children noticed she commonly lost her train of thought in mid-sentence, and often asked them if they had carried out the tasks that she mistakenly thought she had asked them to do.

 

Since its first description over 100 years ago, Alzheimer's disease has been without effective treatment. That may finally be about to change: in the first, small study of a novel, personalized and comprehensive program to reverse memory loss, nine of 10 participants, including the ones above, displayed subjective or objective improvement in their memories beginning within three to six months after the program's start. Of the six patients who had to discontinue working or were struggling with their jobs at the time they joined the study, all were able to return to work or continue working with improved performance. Improvements have been sustained, and as of this writing the longest patient follow-up is two and one-half years from initial treatment. These first ten included patients with memory loss associated with Alzheimer's disease (AD), amnestic mild cognitive impairment (aMCI), or subjective cognitive impairment (SCI; when a patient reports cognitive problems). One patient, diagnosed with late stage Alzheimer's, did not improve.

 

The study, which comes jointly from the UCLA Mary S. Easton Center for Alzheimer's Disease Research and the Buck Institute for Research on Aging, is the first to suggest that memory loss in patients may be reversed, and improvement sustained, using a complex, 36-point therapeutic program that involves comprehensive changes in diet, brain stimulation, exercise, optimization of sleep, specific pharmaceuticals and vitamins, and multiple additional steps that affect brain chemistry.

 

The findings, published in the current online edition of the journal Aging, "are very encouraging. However, at the current time the results are anecdotal, and therefore a more extensive, controlled clinical trial is warranted," said Dale Bredesen, the Augustus Rose Professor of Neurology and Director of the Easton Center at UCLA, a professor at the Buck Institute, and the author of the paper.

 

In the case of Alzheimer's disease, Bredesen notes, there is not one drug that has been developed that stops or even slows the disease's progression, and drugs have only had modest effects on symptoms. "In the past decade alone, hundreds of clinical trials have been conducted for Alzheimer's at an aggregate cost of over a billion dollars, without success," he said.

 

Other chronic illnesses such as cardiovascular disease, cancer, and HIV, have been improved through the use of combination therapies, he noted. Yet in the case of Alzheimer's and other memory disorders, comprehensive combination therapies have not been explored. Yet over the past few decades, genetic and biochemical research has revealed an extensive network of molecular interactions involved in AD pathogenesis. "That suggested that a broader-based therapeutics approach, rather than a single drug that aims at a single target, may be feasible and potentially more effective for the treatment of cognitive decline due to Alzheimer's," said Bredesen.

 

While extensive preclinical studies from numerous laboratories have identified single pathogenetic targets for potential intervention, in human studies, such single target therapeutic approaches have not borne out. But, said Bredesen, it's possible addressing multiple targets within the network underlying AD may be successful even when each target is affected in a relatively modest way. "In other words," he said, "the effects of the various targets may be additive, or even synergistic."

 

The uniform failure of drug trials in Alzheimer's influenced Bredesen's research to get a better understanding of the fundamental nature of the disease. His laboratory has found evidence that Alzheimer's disease stems from an imbalance in nerve cell signaling: in the normal brain, specific signals foster nerve connections and memory making, while balancing signals support memory loss, allowing irrelevant information to be forgotten. But in Alzheimer's disease, the balance of these opposing signals is disturbed, nerve connections are suppressed, and memories are lost.

The model of multiple targets and an imbalance in signaling runs contrary to the popular dogma that Alzheimer's is a disease of toxicity, caused by the accumulation of sticky plaques in the brain. Bredesen believes the amyloid beta peptide, the source of the plaques, has a normal function in the brain -- as part of a larger set of molecules that promotes signals that cause nerve connections to lapse. Thus the increase in the peptide that occurs in Alzheimer's disease shifts the memory-making vs. memory-breaking balance in favor of memory loss.

 

Given all this, Bredesen thought that rather than a single targeted agent, the solution might be a systems type approach, the kind that is in line with the approach taken with other chronic illnesses -- a multiple-component system.

 

"The existing Alzheimer's drugs affect a single target, but Alzheimer's disease is more complex. Imagine having a roof with 36 holes in it, and your drug patched one hole very well -- the drug may have worked, a single "hole" may have been fixed, but you still have 35 other leaks, and so the underlying process may not be affected much."

 

Bredesen's approach is personalized to the patient, based on extensive testing to determine what is affecting the plasticity signaling network of the brain. As one example, in the case of the patient with the demanding job who was forgetting her way home, her therapeutic program consisted of some, but not all of the components involved with Bredesen's therapeutic program, and included:

 

(1) eliminating all simple carbohydrates, leading to a weight loss of 20 pounds;

(2) eliminating gluten and processed food from her diet, with increased vegetables, fruits, and non-farmed fish;

(3) to reduce stress, she began yoga;

(4) as a second measure to reduce the stress of her job, she began to meditate for 20 minutes twice per day;

(5) she took melatonin each night;

(6) she increased her sleep from 4-5 hours per night to 7-8 hours per night;

(7) she took methylcobalamin each day;

(8) she took vitamin D3 each day;

(9) fish oil each day;

(10) CoQ10 each day;

(11) she optimized her oral hygiene using an electric flosser and electric toothbrush;

(12) following discussion with her primary care provider, she reinstated hormone replacement therapy that had been discontinued;

(13) she fasted for a minimum of 12 hours between dinner and breakfast, and for a minimum of three hours between dinner and bedtime;

(14) she exercised for a minimum of 30 minutes, 4-6 days per week.

 

The results for nine of the 10 patients reported in the paper suggest that memory loss may be reversed, and improvement sustained with this therapeutic program, said Bredesen. "This is the first successful demonstration," he noted, but he cautioned that the results are anecdotal, and therefore a more extensive, controlled clinical trial is needed.

 

The downside to this program is its complexity. It is not easy to follow, with the burden falling on the patients and caregivers, and none of the patients were able to stick to the entire protocol. The significant diet and lifestyle changes, and multiple pills required each day, were the two most common complaints. The good news, though, said Bredesen, are the side effects: "It is noteworthy that the major side effect of this therapeutic system is improved health and an optimal body mass index, a stark contrast to the side effects of many drugs."

 

The results for nine of the 10 patients reported in the paper suggest that memory loss may be reversed, and improvement sustained with this therapeutic program, said Bredesen. "This is the first successful demonstration," he noted, but he cautioned that the results need to be replicated. "The current, anecdotal results require a larger trial, not only to confirm or refute the results reported here, but also to address key questions raised, such as the degree of improvement that can be achieved routinely, how late in the course of cognitive decline reversal can be effected, whether such an approach may be effective in patients with familial Alzheimer's disease, and last, how long improvement can be sustained," he said.

 

Cognitive decline is a major concern of the aging population. Already, Alzheimer's disease affects approximately 5.4 million Americans and 30 million people globally. Without effective prevention and treatment, the prospects for the future are bleak. By 2050, it's estimated that 160 million people globally will have the disease, including 13 million Americans, leading to potential bankruptcy of the Medicare system. Unlike several other chronic illnesses, Alzheimer's disease is on the rise--recent estimates suggest that AD has become the third leading cause of death in the United States behind cardiovascular disease and cancer.

 

Story Source:

The above story is based on materials provided by University of California, Los Angeles (UCLA), Health Sciences. Note: Materials may be edited for content and length.

Journal Reference:

  1. Dale E. Bredesen. Reversal of cognitive decline: A novel therapeutic program. Aging, September 2014

 


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#2 Nemo888

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Posted 01 October 2014 - 12:59 AM

She seems to have no idea of the cause or etiology of the disease. Eat well and exercise is not a novel therapeutic approach.
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#3 Hebbeh

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Posted 01 October 2014 - 02:15 AM

She seems to have no idea of the cause or etiology of the disease. Eat well and exercise is not a novel therapeutic approach.

 

Do you have proof it's not a lifestyle disease?  No expert has found the etiology or let alone cure or even treatment yet and as such, this is ground breaking.  And the fact you fail to comprehend this speaks volumes.  As the study said...

 

In the case of Alzheimer's disease, Bredesen notes, there is not one drug that has been developed that stops or even slows the disease's progression, and drugs have only had modest effects on symptoms. "In the past decade alone, hundreds of clinical trials have been conducted for Alzheimer's at an aggregate cost of over a billion dollars, without success," he said.

 

 

I'm sure this study has implications for all of us in pursuing our goals.  And BTW, Dale is not a she...and I doubt you have anything over on....

 

Dale Bredesen, the Augustus Rose Professor of Neurology and Director of the Easton Center at UCLA, a professor at the Buck Institute, and the author of the paper.

 

 

There's much to take home here rather than petty ignorant snide comments.  If you think you're intelligent...then start by acting as such.


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#4 Nemo888

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Posted 01 October 2014 - 09:28 AM

The regimen in the article is anti-aging, not anti-Alzheimer's. I am already doing everything on that list except for the electric flosser, so I was a bit let down and short on time. Alzheimer's is not the only amyloidosis. There are a number like Huntington's or Parkinson's that are quite well known. Some of the less well know ones have perfectly understood etiologies. Familial amyloid neuropathy(FAN) can be "cured" by a liver transplant or treated with Tafamidis or Vyndaqel. Gelsolin's amyloidosis has a new treatment being trialed to remove the amyloid plaques that involves a monoclonal antibody and a unique compound to dissolve the plaques.

 

Most amyloid diseases are genetic defects compounded by the effects of aging. Young bodies can compensate for the defect and remove the malformed proteins before they harden into plaques. An anit-aging regimen did not seem like a very creative solution IMO. At best it would slow down the disease process until a proper treatment or even cure could be found. Which is still pretty damn cool.

 

So, we good?

 


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#5 Hebbeh

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Posted 01 October 2014 - 12:14 PM

I am already doing everything on that list

 

And if you continue, you very well may live a long and healthy life while avoiding dementia.  No other treatment has shown reversal of memory loss before.  And I'm sure if it shows reversal, it will be even more powerful at preventing the issues beforehand.  Few actually walk the walk and live a healthy lifestyle....and that is the take home message.  Prevention is worth a pound of cure.


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#6 Nemo888

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Posted 01 October 2014 - 12:30 PM

I know patients who follow all those recommendations and it only slows their amyloidosis. The defects in protein synthesis are not affected by lifestyle. Only the compensatory mechanisms.
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#7 tunt01

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Posted 01 October 2014 - 05:04 PM

See Table 1 for interventions.  This researcher (Bredesen) is also working on a small molecule intervention.  But I would think these lifestyle/diet/supplement interventions are sufficient in the early stages of the AD process.

 

 


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#8 Plasticperson

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Posted 01 October 2014 - 07:14 PM

wait living the perfect life style will make me smarter... can't be true



#9 Hebbeh

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Posted 02 October 2014 - 02:41 AM

Thanks prophets!  Perhaps I should of posted the entire study in the thread....but Table 1 certainly is worthwhile posting for review...

 

Formatting sucks on here....attached as a file

 

Attached File  Table 1.docx   17.55KB   20 downloads

 

PDF version here...

 

Attached File  Reversal of cognitive decline_ A novel therapeutic program - AGING Journal.pdf   78.7KB   30 downloads

 

 


Edited by Hebbeh, 02 October 2014 - 03:39 AM.

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#10 xEva

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Posted 02 October 2014 - 05:53 AM

Alzheimer's is not the only amyloidosis. There are a number like Huntington's or Parkinson's that are quite well known. Some of the less well know ones have perfectly understood etiologies. Familial amyloid neuropathy(FAN) can be "cured" by a liver transplant or treated with Tafamidis or Vyndaqel. Gelsolin's amyloidosis has a new treatment being trialed to remove the amyloid plaques that involves a monoclonal antibody and a unique compound to dissolve the plaques.
 
Most amyloid diseases are genetic defects compounded by the effects of aging. Young bodies can compensate for the defect and remove the malformed proteins before they harden into plaques.

 
I'm curious how young bodies "compensate for malformed proteins before they harden into plaques".

I've been interested in amyloidoses lately, having been reminded that some form of systemic amyloidosis is "a norm" in people over 80 and that most supercentenarians die of it -- like if cancer or heart disease won't get you, amyloidosis certainly will. Could it be that aging is due to accumulating misfolded proteins? A sort of a slow-acting prion disease.

Recently I read that autophagy is what clears the misfolded proteins out of a cell -- which brings on fasting and CR. But is there anything that would generally help proteins to fold correctly? Like some chaperone substance maybe?
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#11 ceridwen

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Posted 02 October 2014 - 07:54 PM

I don't believe the report it sounds like a scam. I too am doing most of those things. It doesn't work
I don't believe the report it sounds like a scam. I too am doing most of those things. It doesn't work
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#12 Nemo888

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Posted 03 October 2014 - 12:42 PM

 

Alzheimer's is not the only amyloidosis. There are a number like Huntington's or Parkinson's that are quite well known. Some of the less well know ones have perfectly understood etiologies. Familial amyloid neuropathy(FAN) can be "cured" by a liver transplant or treated with Tafamidis or Vyndaqel. Gelsolin's amyloidosis has a new treatment being trialed to remove the amyloid plaques that involves a monoclonal antibody and a unique compound to dissolve the plaques.
 
Most amyloid diseases are genetic defects compounded by the effects of aging. Young bodies can compensate for the defect and remove the malformed proteins before they harden into plaques.

 
I'm curious how young bodies "compensate for malformed proteins before they harden into plaques".

I've been interested in amyloidoses lately, having been reminded that some form of systemic amyloidosis is "a norm" in people over 80 and that most supercentenarians die of it -- like if cancer or heart disease won't get you, amyloidosis certainly will. Could it be that aging is due to accumulating misfolded proteins? A sort of a slow-acting prion disease.

Recently I read that autophagy is what clears the misfolded proteins out of a cell -- which brings on fasting and CR. But is there anything that would generally help proteins to fold correctly? Like some chaperone substance maybe?

 

 

That is the million dollar question, literally. There is so much speculation. In regards to aging, glycation end products accelerate formation of amyloid proteins. Glucose levels directly affect glycation so a low carb diet may help slow the process. Also protein crystallization rates depends of concentration. Keeping the concentration below a certain level could theoretically prevent a cascade of protein aggregation that would overwhelm the cell. (like when you added salt to water in chem class till a crystal formed) Hopefully we can get the atteniton of one of the more educated since this science is exploding right now.

 

That is merely prevention, the best science is now removing the plaques that have already formed. I think they may need additional regenerative and anti-apototic peptides to prevent cell death during the removal process. Very promising.


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#13 xEva

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Posted 04 October 2014 - 12:29 AM

That is merely prevention, the best science is now removing the plaques that have already formed. I think they may need additional regenerative and anti-apototic peptides to prevent cell death during the removal process. Very promising.

 

 

That sounds interesting. What is this removal process called?  (so I can google it)  ..better yet, could recommend some papers?



#14 Nemo888

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Posted 04 October 2014 - 08:18 PM

The doc in London made a deal with GSK. Not on the internet yet as far as I know. Basically a monoclonal antibody for the amyloid and a unique agent to dissolve the plaques as well. He is pretty tight lipped about the second agent and won't even tell me how it works let alone give the recipe. It's in phase 1 trials currently.


Edited by Nemo888, 04 October 2014 - 08:23 PM.


#15 StephCThomp

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Posted 05 October 2014 - 05:13 AM

What's interesting is that the total amount of plaque in a person's brain does not correlate well with severity of Alzheimer's symptoms.  Only when a person has a larger than normal amount of plaque for their age do symptoms appear. 

 

Not certain what to make of that, but at the very least it means it's not just about the plaque.  So it will be interesting to see if dissolving it shows any benefit, or whether that proves similar to artificially lowering blood Cholesterol - chemical fiddling with a correlated symptom that turns out to have little meaningful impact on disease outcome for most people.  We'll see.

 

Bredesen's protocol really appears to be in essence "Eat healthy food (replace sugar/carbs with protein/veg), add a few straightforward supplements, do a little exercise, learn to relax, and get adequate sleep".  It is not exactly world changing.  It's the bleedin' obvious, somewhat organised.


Edited by Finley, 05 October 2014 - 05:15 AM.


#16 Kalliste

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Posted 05 October 2014 - 05:24 AM

As FA said they should redo the trial with only fasting and excersize.

Edited by Cosmicalstorm, 05 October 2014 - 05:25 AM.


#17 ceridwen

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Posted 05 October 2014 - 07:07 AM

What are the 36 points? They sad there were 36 points not 14



#18 ceridwen

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Posted 05 October 2014 - 11:00 AM

Found the link but sadly I am  already doing those things and it is getting worse



#19 Hebbeh

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Posted 06 October 2014 - 03:37 AM

I am already doing everything on that list except for the electric flosser,

 


Found the link but sadly I am  already doing those things and it is getting worse

 

You know, I seriously doubt either one of you are even close to doing everything in the protocol.  Can either one of you explain the entire protocol and how you have been following every facet of it?  And I will even give you the flosser nemo.  The protocol evolves an in-depth dietary, lifestyle, and supplemention protocols just to touch the tip of the iceberg.  A quote briefly mentioning just some of the supplementation from the discussion here... http://www.longecity...ent-bunk/page-2

 

 

If you scroll down to Table 1 in the full study, they did prescribe Me-B12, thiamine, pantothenic acid, TMG, P5P, along with mixed tocopherols and tocotrienols.....along with a laundry list of other nutraceuticals including but not limited to D3, K2, ascorbate, resveratrol, curcumin, ALCAR, citicoline, a-lipoic acid, NAC, DHA/EPA, CoQ-10, ashwagandha, bacopa, PQQ, blueberries, selenium, and zinc (while optimizing Zn:fCu ratio = limit free copper) in addition to chelation therapy for heavy metals (which would include iron)....for starters.

 

So if reading the study and protocol....they did cover all the bases you mentioned and a ton more.

 

EDIT: So is the consensus this entails a "complex dietary supplement" or "combination supplement" which is the central point to the only study to date showing not only REVERSAL of memory loss in alzheimer's but allowing a significant percentage of the patients to RETURN to work....amazing IMHO.  And this result will most certainly result in life extension for these individuals.  Am I the only one excited and amazed by this.....and not even a fucked up mouse study.

 

Double Edit: The take home message for me is if every one of us adopted the protocol guidelines early enough, most (if not all) would very likely avoid dementia and live a longer healthier life.  Longer health span AND lifespan for many of us. The proof is in the pudding.....dementia and aging is highly affected by all facets of lifestyle and can be controlled if wanting to make the effort.

 

To further put this in the amazing context that it is....quote:

 

In the case of Alzheimer's disease, Bredesen notes, there is not one drug that has been developed that stops or even slows the disease's progression, and drugs have only had modest effects on symptoms. "In the past decade alone, hundreds of clinical trials have been conducted for Alzheimer's at an aggregate cost of over a billion dollars, without success," he said.

 

 

 

 

 

Now granted, this is just a brief overview of some of the supplements used and not touching on all the other facets including but not limited to fasting, ketogenesis, low carb, low grain diet and much, much more.  And nemo, even if you have been following the protocol, do you have alzheimer's?  And if not, how can you discount it than?  And even if you know individuals with alzheimer's, it's highly unlikely that they would of been following this extensive protocol.

 

And remember, this protocol is the ONLY study to date not only showing a REVERSAL of memory loss but allowing a number of the patients not only to RETURN to work but work at high level positions.....amazing IMHO.  I know where I'm hedging my bets but good luck waiting for that pie in the sky drug to come along.


Edited by Hebbeh, 06 October 2014 - 03:45 AM.

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#20 Nemo888

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Posted 06 October 2014 - 10:12 AM

You really don't understand cellular biology Hebbeh. Good luck with eat well and exercise.


Edited by Nemo888, 06 October 2014 - 10:13 AM.

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#21 blood

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Posted 06 October 2014 - 11:50 AM

10 patients followed the protocol.

 

9 patients improved, however one continued to deteriorate.

 

Note that the patient who experienced no improvements & continued to deteriorate had the most severe memory deficits with a diagnosis of "late stage Alzheimer's"... whereas the 9 patients who demonstrated improvements were less "far gone" (most of them had a diagnosis of "subjective cognitive impairment" or "mild cognitive impairment").

 

Perhaps once a certain level of damage is achieved, "there is no going back".

 


Edited by blood, 06 October 2014 - 11:57 AM.

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#22 Hebbeh

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Posted 06 October 2014 - 12:01 PM

More on what the theory of the protocol was based on courtesy of trance....

 

 

The same author in an earlier paper:

 

Rather than focusing on monotherapeutics, the optimal approaches may involve systems of therapeutics, which include both pharmacological and non-pharmacological components. For example, if synaptic reconstruction and maintenance form parts of the optimal treatment for AD, and inflammation is to be minimized, autophagy activated (periodically, perhaps), neurotrophic factors normalized, stress minimized, Aβ oligomerization inhibited, Aβ clearance increased, ApoE4-mediated signals reduced, tau phosphorylation reduced, prionic tau amplification blocked, memory loss reversed, cholinergic neurotransmission restored and overall network balance restored; then multiple factors may require normalization, enhancement, or administration, such as hormonal balance, vitamin D3, C-reactive protein (and other inflammation-related markers), homocysteine, sleep and melatonin, citicoline (citidine-5-diphosphocholine), specific antioxidants, diet (including specific periods of fasting, avoidance of high glycemic index foods and saturated fats, etc.), exercise, stress, omega-3 fatty acids and resolvins (Mizwicki et al, 2013) and other network components.

 

Most of the factors of which such a system is comprised have already been shown to exert modest effects (trends that often have not reached statistical significance) on AD or animal models of AD, but there has been little evaluation of such a complete system. However, one of the interesting potential outcomes of including such a therapeutic system approach is that it may allow drug candidates that failed in monotherapeutic clinical trials to demonstrate beneficial effects when used as part of the system.

 

Full text:  Next generation therapeutics for Alzheimer's disease

 

.

 

 


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#23 Kalliste

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Posted 06 October 2014 - 02:10 PM

I glad that one researcher has gotten this multfactorial bit at least.

#24 Kalliste

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Posted 06 October 2014 - 03:32 PM

10 patients followed the protocol.

 

9 patients improved, however one continued to deteriorate.

 

Note that the patient who experienced no improvements & continued to deteriorate had the most severe memory deficits with a diagnosis of "late stage Alzheimer's"... whereas the 9 patients who demonstrated improvements were less "far gone" (most of them had a diagnosis of "subjective cognitive impairment" or "mild cognitive impairment").

 

Perhaps once a certain level of damage is achieved, "there is no going back".

 

The last sentence is an understatement to say the least. The fact that this was possible is very encouraging. It is definitely a big push forward for the "Brain-Diabetes" renaming initiative. Once you are in dementia-land I would have thought there is no going back at all, if you asked me a week ago if this result was possible I would have replied "Once the cascade has moved this far it is impossible to reverse it, that is why all drugs tried so far have failed miserably..."



#25 lourdaud

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Posted 06 October 2014 - 08:02 PM

I might as well post this in this thread:

My grandmother's health and cognition has started to decline rapidly. She's had IBS and autoimmune problems for a long time - probably caused/aggravated by poor diet. I'm trying to get her to stop eating grains at least but getting her to change her habits is hard. Meanwhile I'm thinking of getting her:

 

Curcumin (potent anti-inflammatory and supposedly good for dementia) 

C60oo 
Coconut oil (energy/metabolism + good for infections, candida etc)

 

Also thinking of CoQ10 but I wonder if it's wise to not throw in too many anti-oxidants?

Anyone got any input/other suggestions?



#26 blood

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Posted 07 October 2014 - 05:04 AM

Anyone got any input/other suggestions?

 
Here's the protocol from the study being discussed:
 
Attached File  protocol.png   200.1KB   7 downloads
 
Tinkering with just one or two supplements might not be enough (if you believe the results of the paper) - from the paper:
 

http://www.impactagi...ull/100690.html

2) Based on the hypothesis that AD results from an imbalance in an extensive plasticity network, the therapy should address as many of the network components as possible, with the idea that a combination may create an effect that is more than the sum of the effects of many monotherapeutics.

3) Just as for other chronic illnesses such as osteoporosis, cancer, and cardiovascular disease, the underlying network features a threshold effect, such that, once enough of the network components have been impacted, the pathogenetic process would be halted or reversed. Therefore, even though it is not expected that most patients will be able to follow every single step of the protocol, as long as enough steps are followed to exceed the threshold, that should be sufficient.


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#27 Kalliste

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Posted 07 October 2014 - 05:09 AM

That is a great summary and the reasoning resonates with my idea about health. It is incredibly depressing it took until 2014 for someone to run this down. At this rate it will be another century until some tenative scientist try a repair based approach to aging.
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#28 mindpatch

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Posted 16 February 2015 - 03:47 AM

She seems to have no idea of the cause or etiology of the disease. Eat well and exercise is not a novel therapeutic approach.

It might not be novel, but it very well may be efficacious.  Isn't that the important thing?  If Pritikin or Dean Ornish can REVERSE heart disease through diet and lifestyle interventions, why not brain disease?



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#29 3mp0w3r

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Posted 16 February 2015 - 03:15 PM

 

She seems to have no idea of the cause or etiology of the disease. Eat well and exercise is not a novel therapeutic approach.

It might not be novel, but it very well may be efficacious.  Isn't that the important thing?  If Pritikin or Dean Ornish can REVERSE heart disease through diet and lifestyle interventions, why not brain disease?

 

 

Got to agree with Nemo.  As a journal article, this carries no scientific weight.  It is basically a few case studies grouped together with no details on selection criteria, methods or even specifics about what they measured to conclude that there was a positive effect.  Instead of a methods section, there is an extended introduction which has several questionable paragraphs.  The discussion is vague and self promoting.

 

That's not to say the approach doesn't work.  Maybe it does.  But as scientific research, the article is of no use for any evidence based decision.

 

Maybe in 10 years, after several randomized control studies come out, the original idea will be proven.  But I have my doubts. 


Edited by 3mp0w3r, 16 February 2015 - 03:18 PM.


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