About 25% of adults over 50 take a supple... - Cure Parkinson's
About 25% of adults over 50 take a supplement to improve brain health. But does it actually help?
I think they would like to take away our right to try.
" Forget about those over-the-counter products that promise better memory.
A recent survey found that about 25% of adults over age 50 take a supplement to improve their brain health with the promise of enhanced memory and sharper attention and focus.
The problem? There’s no solid proof any of them work.
The main issue with all over-the-counter supplements is lack of regulation. The FDA doesn’t oversee product testing or ingredient accuracy — they just look out for supplements that make health claims related to the treatment of specific diseases.
In terms of brain health, this means a supplement manufacturer can claim a product helps with mental alertness or memory loss — but not that it protects against or improves dementia or Alzheimer’s disease. This way manufacturers don’t have to back up any claim that their product is effective."
I think this meta analysis of RCTs says they are 100% wrong :
ncbi.nlm.nih.gov/pmc/articl...
A relevant quote from this meta analysis of RCTs using melatonin for cognitive decline :
' The current work is the first study using the NMA statistics technique to provide a view of the potential benefits of melatonin for Alzheimer’s dementia compared to the other FDA-approved dementia-managing medications. In the current NMA, we found medium-term low-dose melatonin (MLT) to be associated with the highest post-treatment MMSE among all of the investigated medications in the participants with Alzheimer’s dementia. This finding did not change after focusing on RCTs with medium-term treatment duration. Furthermore, the significantly beneficial effects on cognition of MLT were still found when focusing on RCTs that excluded concomitant medications. MLT was also associated with the highest post-treatment quality of life in the participants with Alzheimer’s dementia. All of the investigated exogenous melatonin supplements were associated with similar acceptability with respect to the drop-out rate or rate of any adverse events reported, as was the placebo. '
Based on this meta analysis, I think whoever wrote that article has it backwards as this MA shows that melatonin out performed all of the investigated medications. They should be ashamed for publishing such an article!
This post I put up last month clearly shows that Benfotiamine is beneficial for dementia :
healthunlocked.com/cure-par...
Here is a relevant quote from the study I discussed in that post :
' The trial tested whether a twelve-month treatment with benfotiamine would delay clinical decline in amyloid positron emission tomography (PET)- positive patients with amnestic mild cognitive impairment MCI (MMSE ≥ 26) or mild AD (26>MMSE>21) compared to placebo (52). The primary clinical outcome was Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog-11) and secondary outcomes were the clinical dementia rating (CDR) score and brain glucose uptake measured by fluorodeoxyglucose (FDG)-PET. The trial showed that benfotiamine at a dose of 600 mg per day is safe and very well tolerated in patients with early AD. The treatment delivery achieved a 161-fold mean increase in blood thiamine. In the intent to treat population(ITT), the benfotiamine arm showed 43% reduction in the ADAS -Cog decline of the placebo group (p = 0.125), with a larger effect size in the CDR where the benfotiamine arm was 79.2% less than the decline in the placebo arm (P = 0.0129) (66). '
' Plasma measures from study participants revealed multiple metabolites/lipids as novel potential biomarkers that might be pharmacologically responsive to benfotiamine treatment. Two dozen biomarker candidates including thiamine, tyrosine, tryptophan, lysine, and 22 lipid species, mostly belonging to phosphatidylcholines reflected reversal of changes related to AD progression. The results suggest potential mechanistic pathways that underlie the benefit of benfotiamine in AD (71). '
Here is a study for Citicoline that further shows how wrong they are with their ridiculous article and exactly how shameless they are :
ncbi.nlm.nih.gov/pmc/articl....
Here is a relevant study quote :
' Citicoline is able to potentiate neuroplasticity and is a natural precursor of phospholipid synthesis, or rather serves as a choline source in the metabolic pathways for biosynthesis of acetylcholine. Several studies have shown that it can have beneficial effects both in degenerative and in vascular cognitive decline. '
Compare that to the current meds they have for AD, Donepezil, Galantamine and Rivastigmine. To add insult to injury, these are the side effects for Donepezil :
WARNING : It will take awhile to review this list of side effects associated with use of Donepezil. When you get done reviewing this list, go look up the side effects for melatonin, citicoline and benfotiamine.
More common
Diarrhea
loss of appetite
muscle cramps
nausea
trouble in sleeping
unusual tiredness or weakness
vomiting
Less common
Abnormal dreams
constipation
dizziness
drowsiness
fainting
frequent urination
headache
joint pain, stiffness, or swelling
mental depression
pain
unusual bleeding or bruising
weight loss
Rare
Black, tarry stools
bloating
bloody or cloudy urine
blurred vision
burning, prickling, or tingling sensations
cataract
chills
clumsiness or unsteadiness
confusion
cough
decreased urination
difficult or painful urination
dryness of mouth
eye irritation
fever
flushing of skin
frequent urge to urinate
high or low blood pressure
hives
hot flashes
increase in sexual desire or performance
increased heart rate and breathing
increased sweating
increased urge to urinate during the night
irregular heartbeat
itching
loss of bladder control
loss of bowel control
mood or mental changes, including abnormal crying, aggression, agitation, delusions, irritability, nervousness, or restlessness
nasal congestion
pain in chest, upper stomach, or throat
problems with speech
runny nose
severe thirst
shortness of breath
sneezing
sore throat
sunken eyes
tightness in chest
tremor
troubled breathing
wheezing
wrinkled skin
Incidence not known
Back, leg, or stomach pains
bleeding gums
chest pain or discomfort
coma
convulsions
dark urine
difficulty breathing
fast or irregular heartbeat
fatigue
general body swelling
general tiredness and weakness
high fever
increased thirst
indigestion
light-colored stools
muscle pain or cramps
nausea and vomiting
nosebleeds
pains in stomach, side, or abdomen, possibly radiating to the back
pale skin
rash
seeing, hearing, or feeling things that are not there
seizures
severe muscle stiffness
severe nausea
slow or irregular heartbeat
stomach pain
sweating
swelling of face, ankles, or hands
tiredness
unusually pale skin
upper right abdominal or stomach pain
yellow eyes and skin
Symptoms of overdose
Convulsions (seizures)
increased sweating
increased watering of mouth
increasing muscle weakness
low blood pressure
severe nausea
severe vomiting
slow heartbeat
troubled breathing
Art
Art, would one take all three of these together or choose one?
I didn't post that to promote those for people to take, just to show the sheer stupidity of the article that clearly said there is no reason to consider supplements because there is no scientific proof that they help with memory or cognitive function.
As far as your question, it would depend on what you are trying to do. If you are trying to improve memory, you may find this interesting :
healthunlocked.com/cure-par...
Btw, this is still working very well in this person!
Art
Very interesting- and encouraging! Thank you for sharing!
You're welcome!
In case you didn't read part two, I deleted Amla extract because it was mainly being used for other health issues relevant to the lady that I was writing about and not so much for memory, and I replaced it with Citicoline because studies are stronger for Citicoline for memory. If you have any questions about that post, please post them in that thread so that we don't hijack this thread.
Art