Treatment for Alzheimer's Disease: Brief summaries of research reports
This section is offshoot of my gathering of news items about memory. I am not a medical expert. My background is in psychology. The information I have gathered here should not be taken as providing any advice.
You can check out words you don't know in the glossary of terms used in Alzheimer's research
Approved drugs
Memantine
Reminyl
Aricept
Exelon
Anti-inflammatory drugs
Statins
Anti-hypertensive drugs
Pilot drug studies
Estrogen
Supplements
Vaccines
Estrogen
For women over 65, Combined Hormone
Therapy increases risk of dementia
Much to the researchers’ surprise and
disappointment, a four-year experiment involving 4,532 women at 39 medical
centers, has found that combined hormone therapy (involving both estrogen and
progestin) doubles the risk of Alzheimer's disease and other types of dementia
in women who began the treatment at age 65 or older, although the risk is still
small : for every 10,000 women 65 and older who take hormones, 23 of the
predicted 45 cases of dementia a year, will be attributable to the hormones. The
study also found that the combined hormone therapy produced no improvement in
general cognitive function, and in fact had adverse effects on cognition among
some women. This supports an earlier study suggesting that, while estrogen is
helpful to cognitive function in postmenopausal women, the benefits can be
cancelled out by progestin / progesterone. The study also confirmed previous
research showing that the combination therapy increased the risk of stroke -
previous research has indicated that risk factors for stroke are also risk
factors for cognitive decline.
The study was published in the May 28 issue of the
Journal of the American Medical Association.
Full reference
2
3
http://www.eurekalert.org/pub_releases/2003-05/wfub-chr052203.htm
Animal studies suggest why estrogen can't help after dementia has developed
Research with rats suggests that nerve cells in the brain
called cholinergic neurons are needed for estrogen to help learning and memory.
This suggests why starting estrogen after dementia has developed is ineffective.
The report appeared in the November issue of Hormones and
Behavior. Full reference
http://www.eurekalert.org/pub_releases/2002-11/uopm-asp110502.htm
October 2002
Long-term ERT in postmenopausal women with Alzheimer's may worsen memory
A study using female rats investigated the
interaction of two conditions known to exist within the brains of female
Alzheimer's patients: 1) the presence of chronic neuroinflammation, and 2)
having too much or not enough estrogen. They found that rats who had their
ovaries removed (to model the condition of post-menopausal women) performed more
poorly on a water maze task when they had chronic brain inflammation OR
long-term estrogen replacement therapy. Most significantly, those who had both
conditions performed much more poorly – beyond what would be expected by either
condition alone. That such results extend to postmenopausal women is supported
by a 2000 study involving a long term, placebo-controlled study that examined
the effects of estrogen replacement therapy on cognitive function in women with
mild to moderate Alzheimer's. The effects of ERT were initially beneficial, but
the performance of women receiving sustained ERT declined more than that of
women receiving the placebo treatment. The results of these studies suggest that
postmenopausal women with Alzheimer's disease who undergo long-term estrogen
replacement therapy may make their memory loss worse.
The study was reported in the October issue of Behavioral
Neuroscience.Full
reference
http://www.eurekalert.org/pub_releases/2002-10/apa-lei102202.htm
Full text of the article is available at
http://www.apa.org/journals/bne/press_releases/october_2002/bne1165902.html.
August 2001
Estrogen patch may improve memory for women with Alzheimer's
A new study suggests that an estrogen skin
patch given to women with mild to moderate Alzheimer's
disease can improve their memory and attention skills. The
study involved only 20 women for eight weeks, and the
results will need to be confirmed by a larger-scale study.
Research to date has been equivocal about the effects of
estrogen on women with Alzheimer's, with some finding a
memory-enhancing effect, and others finding no effect. It is
speculated that the type of estrogen might be critical. The
present study used estradiol, a type of estrogen that has
been shown to have an effect on the brain.
The study was published in the August 28 issue of
Neurology, the journal of the American Academy of
Neurology.
http://www.eurekalert.org/pub_releases/2001-08/aaon-epm082001.htm
Supplements
October 2006
Omega-3 fatty acids may slow cognitive decline in some patients with very mild Alzheimer's disease
Several studies have shown that eating fish, which is high in omega-3
fatty acids, may protect against Alzheimer's disease. A Swedish study
has now tested whether supplements could have similar effects. Patients
with mild-to-moderate Alzheimer’s who took 1.7 grams of DHA and .6g of
EPA showed the same rate of cognitive decline as those taking a placebo,
however, among a subgroup of 32 patients with very mild cognitive
impairment, those who took the fatty acids experienced less decline in
six months compared with those who took placebo. It may be that
anti-inflammatory effects are an important reason for the benefit,
potentially explaining why effects were seen only in those with very
early-stage disease, when levels of inflammation seem to be higher.
The study was published in the October issue of
Archives of Neurology.
Full reference
http://www.eurekalert.org/pub_releases/2006-10/jaaj-ofa100506.htm
April 2006
Dietary supplements offer new hope for Alzheimer's patients
A "cocktail" of dietary supplements (omega-3 fatty acids, uridine and
choline) has been found to dramatically increase the amount of membranes
that form brain cell synapses in gerbils. The treatment is now in human
clinical trials. It is hoped that such treatment may significantly delay
Alzheimer's disease. The treatment offers a different approach from the
traditional tactic of targeting amyloid plaques and tangles. Choline can be
found in meats, nuts and eggs, and omega-3 fatty acids are found in a
variety of sources, including fish, eggs, flaxseed and meat from grass-fed
animals. Uridine, which is found in RNA and produced by the liver and
kidney, is not obtained from the diet, although it is found in human breast
milk.
The study appears in the May 9 issue of Brain Research.
Full reference
http://www.eurekalert.org/pub_releases/2006-04/miot-mro042706.htm
November 2005
Compound in wine reduces levels of Alzheimer's disease-causing peptides
In cell studies, resveratrol has been found to lower levels of
amyloid-beta peptides. Resveratrol is a natural compound occurring in
abundance in grapes, berries and peanuts. The highest concentration has
been reported in wines prepared from Pinot Noir grapes. The
anti-amyloidogenic effect of resveratrol observed in cell cultures does
not however necessarily mean that the beneficial effect can result
simply from eating grapes or drinking wine. Further research aims to
develop more active and more stable compounds.
The study was published in the November 11 issue of the
Journal of Biological Chemistry.
Full reference
http://www.eurekalert.org/pub_releases/2005-11/asfb-ciw110305.htm
http://www.sciam.com/article.cfm?chanID=sa003&articleID=000581B2-EE9B-136B-AE9B83414B7F0000
April 2005
Clinical diagnosis of Alzheimer's may be delayed with donepezil
In a study of people with mild cognitive impairment,
those who took the drug donepezil were at reduced risk of
progressing to a diagnosis of Alzheimer's during the first
years of the trial, but by the end of the 3-year study there
was no benefit from the drug. Of the 769 participants, 212
developed possible or probable Alzheimer’s within the 3-year
study period; the donepezil group's risk of progression to a
diagnosis of Alzheimer’s was reduced by 58% one year into
the study, and 36% at 2 years, but no risk reduction at the
end of three years. Vitamin E was also tested in the study
and was found to have no effect at any point in the study.
The findings were reported in the April 14 online issue of
The New England Journal of Medicine, and will appear
in the June 9 print issue.
Full reference
http://www.eurekalert.org/pub_releases/2005-04/nioa-cdo041205.htm
http://www.eurekalert.org/pub_releases/2005-04/mc-dia041105.htm
December 2004
Pilot study points to healing power of turmeric
A study using genetically engineered mice has found that those mice on a diet
rich in curcumin (the yellow pigment in the curry spice turmeric) developed 85%
few Alzheimer’s plaques then the control group. Curcumin has antioxidant,
anti-inflammatory, and cholesterol lowering properties, and has long been used
in India as treatment for a variety of ailments. A human trial involving 33
Alzheimer's patients will soon commence.
The study was reported online December 7 in the
Journal of Biological Chemistry.
Full reference
A copy of the full paper can be found on the Journal of Biological
Chemistry Web site athttp://tinyurl.com/5bzbs
http://www.eurekalert.org/pub_releases/2004-12/potn-usn122804.htm
http://www.sciencentral.com/articles/view.htm3?article_id=218392455
November 2003
Dietary supplement helps Alzheimer’s
A three-month study of 55 elderly patients with mild or moderate Alzheimer’s
found that those given EV-1, a dietary supplement containing, among other
things, the putative antioxidant ingredient of red wine, showed no deterioration
during the trial. The supplement is designed to interfere with a defective
mitochondrial cycle thought to contribute to the metabolic disturbances
associated with late onset Alzheimer’s. The Krebs tricarboxylic acid cycle is
fuelled by glucose and regulates levels of reactive oxygen species in the body.
EV-1 contains glucose, a compound called malate that primes or maintains the
Krebs cycle, and resveratrol - the antioxidant component of red wine that is
thought to soak up reactive oxygen species. More studies are needed to confirm
this result.
The findings were presented in November at the annual meeting of the Society for
Neuroscience (SFN) in New Orleans.
http://gateways.bmn.com/news/story?day=031121&story=1
Related topics
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