Memory changes cause concern to many patients as they grow older. Gary Small
provides reassurance and gives a strategy forassessing age related
memory loss and protecting brain health
As doctors and scientists have focused more attention on Alzheimer's disease
and related dementias, patients are expressinggreater concern about
their common, age related memory changes.When results of new
research on early detection and preventionreach a wider audience,
our patients often come to the officewith questions about what they
can do to preserve their memoryabilities as they age. Many of
today's doctors trained duringa time when minimal information was
provided on these topics duringtheir medical training. This paper
will provide a practical strategyfor assessing age related memory
loss and will discuss interventionsthat may or may not protect brain
health.
Summary points
Patients with mild memory loss are common in clinical practice; if
their symptoms warrant a diagnosis of dementia, treatment with
cholinesterase inhibitor drugs is needed
Doctors need to be cautious about unproved treatments for slowing brain
ageing because of potential side effects
Lifestyle choices may protect people with mild forms of age related
memory loss from future decline: essentially, what is healthy for the body
is healthy for the brain
The risks of these interventions are minimal and are not likely to
outweigh the many
benefits
The viewpoints presented were based on my clinical experience and a databased
literature review. I selected articles withMedline searches using
key words relevant to the theme of thisreview, emphasising peer
reviewed journals and data from controlledclinical trials or
methodologically sound epidemiological studieswhen
available.
With age comes the increasing likelihood of developing memory loss. The
mildest form, age associated memory impairment, ischaracterised by
self perception of memory loss and a standardisedmemory test score
showing a decline in objective memory performancecompared with
younger adults.1 About 40% of people aged 65or
older have age associated memory impairmentin
the United States,about 16 million people. Only about 1% of them
will progress todementia eachyear.
Mild cognitive impairment represents a more severe form of memory loss and is
often defined by important memory deficits withoutfunctional
impairments. Although patients with mild cognitiveimpairment are
able to continue to live independently, they showobjective memory
impairments similar to those seen in people withvery mild
Alzheimer's disease.2 About 10% of people aged 65years
or older have mild cognitive impairment, and nearly 15%of them
develop Alzheimer's disease each year. Studies of drugsto treat mild
cognitive impairment in order to delay the onsetof Alzheimer's
disease are currently inprogress.
As people live longer, the risk for developing Alzheimer's disease increases
dramatically. Although it is the most commoncause of late life
dementia, other causes, particularly vasculardisease, contribute to
the occurrence of dementia, often definedas impairment in several
cognitive domains including memory tothe extent that it interferes
with daily life.3
Because age related memory change may signal treatable medical conditions, it
is important to take any complaint seriously.Risk factors that
should trigger a memory screen include age olderthan 65 years,
illnesses that increase the possibility of a diagnosisof dementia
(diabetes, Parkinson's disease, stroke disease, etc),or a family
history of dementia. A simple screening question askingabout the
patient's memory ability is ofteninformative.
The first assessment step is to determine if the patient falls into one of
the three main categories of memory loss: age associatedmemory
impairment, mild cognitive impairment, or dementia. Itis helpful to
obtain a standardised score of cognitive abilityusing rating scales
like the mini-mental state examination, whichconsists of 30 items
that rate memory, orientation, attention,calculation, language, and
visual skills.4 The test takes only
about 10 minutes, but is limited because it will not detect subtle
memory losses, particularly in college graduates. More detailed
memory assessments, known as neuropsychological tests, will providea
better idea about subtle memory deficits. In the memory clinicat
University of California, Los Angeles, doctors ask patientsto
perform a task involving delayed recall (for example, givingthe
patient a list of words (box 1) and testing them 20 minuteslater) to identify subtle memory loss in educated people. Such
tests have been standardised and can provide a preliminary diagnosis
of mild cognitive impairment. In the United States, positron emission
tomography is sometimes used to help in the diagnosis of dementia
because it has high diagnostic accuracy and sensitivity for detecting
Alzheimer's disease early in its course.5
Ask the patient to study the following
words for up to one minute:
Dirt
Gallery
Lemon
Vest
Ambassador
Snake
Lump
Mantle
Elbow
Kettle
When the minute is up, reset the timer for a 20 minute break.
After the 20 minutes, ask the patient to write down as many of the
words as possible. Recalling fewer than five words could indicate a
problem with delayed recall
The evaluation of memory loss (box 2) should include
review of the onset and course of symptoms, a physical examination, andlaboratory assessment to rule out treatable medical conditions
that could affect memory. An inventory of the patient's drugswill
help sort out possible drug toxicity as a cause of memoryloss.
Screening for depression can often be done through a standardised
questionnaire while the patient is in the waiting room. Laboratory
assessments should at least include some blood tests to screenout
thyroid disease, vitamin B-12 deficiency, anaemia, liver disease,and
various metabolic disturbances, which could possibly causememory
change.
Box 2: Assessing age
related memory loss
Screen patients with such risk factors as older age, concerns
about memory loss, or family history of dementia
Get a history about the nature of the memory symptoms, their
onset, and their course
Take a medication inventory
Use a standard memory assessment tool
Screen for depression
Obtain laboratory tests to rule out medical conditions that
can affect memory ability
If the memory loss is severe enough to warrant a diagnosis of dementia, then
cholinesterase inhibitor therapy would be indicated.3In the United States, many physicians also recommend vitamin E
because of findings that high doses (2000 units daily) delay functionaldecline in patients compared with placebo treatment.3
For milderforms of memory loss, drug treatments have not beenapproved.
Not everyone is destined to develop Alzheimer's disease, and genetic
predisposition explains only some of the risk for thedisease. Thus,
lifestyle choices may be important in disease riskand prevention.7
Recent findings about possible non-geneticfactors contributing to
brain health suggest several practicalstrategies that may decelerate
brain ageing and delay onset ofdementia (but see box
3). For my patients with age associatedmemory impairment and
related conditions, I briefly review thesepossible strategies and
discuss the potential benefits and risksof each.
Box 3: Some
treatments under investigation but not proved to prevent Alzheimer's
disease
Ginkgo biloba
Cholinesterase inhibitor drugs
Anti-inflammatory drugs
DHEA (dehydropeindrosterone)
Oestrogen
Testosterone
Risk factors and protective factors for
brain ageing
Research during the last decade found a major genetic risk for Alzheimer's
disease, the apolipoprotein E-4 allele.3 Thisallele has a dose related effect on increasing risk and loweringthe age of onset of Alzheimer's disease. A test of the apolipoproteinE genotype, either alone or in combination with other tests, is
not considered a useful predictor of future cognitive declinein
people without dementia.8
Studies of monozygotic twins show concordance rates of approximately 50% for
Alzheimer's disease, indicating that non-geneticfactors contribute
to development of the disease. While severehead trauma and lower
educational achievement seem to increasethe risk for Alzheimer's
disease, other factors may be protective.Unproved but possible
protective factors include use of non-steroidalanti-inflammatory
drugs, postmenopausal oestrogen in women, anti-oxidantvitamins, and
cholesterol-lowering statin drugs; low fat diet;and aerobic
conditioning.6
Stress reduction
Chronic stress may be detrimental to brainhealth and memory
performance. Animal studies show that prolongedexposure to stress
hormones has an adverse effect on the hippocampus,a brain region
involved in memory and learning.9 Human
investigationsindicate that several days of exposure to high levels
of the stresshormone cortisol can impair memory.10
Chronic stress can contributeto depression and anxiety disorders,
which often interfere withnormal memory processing, particularly as
people age. Taken together,these findings suggest that minimising
stress may have a beneficialimpact on brainhealth.
Physical activity
When laboratory animals exercise regularlythey develop new neurones
in the hippocampus compared with inactiveanimals.11
The physical exercise may increase cerebral bloodflow, which in turn
promotes nerve cell growth. Studies of peoplewho have been
physically active between the ages of 20 and 60show that they have a
lower risk for Alzheimer's disease laterin life.12
A recent study of healthy adults between ages 60and 75 found that
mental tasks involved in executive controlmonitoring,scheduling, planning, inhibition, and memoryimproved
in a grouptaking aerobic exercise but not in a control group.13
(Credit: GARY ISAACS/PHOTONICA)
Healthy diet
People with excess body fat have a greaterrisk for such illnesses as
diabetes and hypertension. These obesityrelated conditions increase
the risk for cerebrovascular disease,which often leads to memory
decline and dementia. Epidemiologicalstudies show that lower fat
diets in young and middle aged adultsmay reduce the risk for
Alzheimer's disease decades later. Somefats, however, may benefit
brain health. A recent investigationfound that a Mediterranean diet
high in olive oil is protectiveagainst age related cognitive
decline.14
Antioxidant vitamins may also protect the brain. In people with mild memory
complaints, vitamins E and C may protect brainhealth, but at what
dose is not known.15
Nutritional scientists have developed methods to determine the degree of
antioxidant potency of various foods, and such antioxidanteffects
may protect brain health as we age. Fruits such as blueberries,
strawberries, and tomatoes, as well as vegetables such as broccoli,
have relatively high antioxidant capacity.16
A diet rich in carbohydrates with high glycaemic indices (pretzels, French
fries, etc) can increase the risk for diabetes,which can lead to
stroke disease and vascular dementia,17 butdietary changes can reverse such effects. A recent study found
that the combination of weight loss, eating a healthy diet, and
exercising regularly can reduce the risk for developing type 2diabetes
by more than 50%.18
Mental activity
The risk of developing Alzheimer's diseaseis lower in people who
have been intellectually active than inthose who have not.12
Studies also indicate that higher mentalfunction in one's 20s
predicts better cognitive function latein life. People who spend
time reading and who have mentally stimulatingjobs or educational
experiences maintain their memories betterand longer as they age.
Other studies have shown that collegegraduates have a lower risk of
eventually developing Alzheimer'sdisease than people with less
educational achievement.19
Animal studies have shown that enriched environments lead to more neurones in
hippocampal memory centres.20 Additional researchsupports the idea that continual, life long mental stimulation
is healthy for human brains as well. People with advanced education
and professional accomplishments tend to have greater densityof
neuronal connections in brain areas involved in complex reasoning.19
These discoveries point to the conclusion that mental stimulation, or
exerting our brains in various ways intellectually,may not only
improve memory performance but may stave off futurecognitive
decline.
Stress reductionprepare
ahead, balance work and leisure, set realistic expectations, and
take relaxation breaks at regular intervals
Mental activitydo
crosswords, puzzles, read, or challenge yourself intellectually
Healthy brain dietdrink
six glasses of water each day, eat low fat foods and plenty of
fruits and vegetables, avoid fried foods, and take the antioxidant
vitamins E and C
Regular physical exercise, including an adequate aerobic
workout
Sports and activities with low risk for head trauma
Avoidance of tobacco and excessive use of alcohol
Activities that have personal meaning
Other lifestyle choices
People with a history of head trauma withloss of consciousness for
an hour or more have double the riskfor developing Alzheimer's
disease later in life.21 A study
comparing amateur soccer players in their mid-20s and swimmersand
runners (who were less likely to incur head injuries) of thesame age
found that over 30% of the soccer players had memoryimpairments,
compared with less than 10% of the swimmers and runners.22Avoiding head trauma seems to be an important strategy to keepingthe brain healthy throughoutlife.
Smoking is another risk for memory loss as we age. One study found that
smokers had double the risk of getting Alzheimer'sdisease of people
who never smoked.23 However, when people quitsmoking, at whatever age, they are able to reduce their risk.
Additional educational
resources
Gary Small's book, The Memory Bible: An Innovative Strategy for
Keeping the Brain Young (London: Penguin, 2002), updates readers on the
latest research and practical approaches to age related memory loss. This
book could be recommended to patients with mild memory complaints and their
families
John Rowe and Robert Kahn summarise the MacArthur findings in their book,
Successful Aging (New York: Pantheon, 1998) and show that several
lifestyle choices determine physical and mental health as we age
Arthur Kramer and colleagues describe how physical conditioning
influences cognitive vitality in"Exercise, aging and cognition: healthy
body, healthy mind?" in Fisk AD, Rogers W, eds. Human Factors
Interventions for the Health Care of Older Adults. (Hillsdale, NJ:
Erlbaum, 2001)
A balanced review of complementary medicines can be found in Spencer JW,
Jacobbs JJ, eds. Complementary/ Alternative Medicine: An Evidence-Based
Approach. (St Louis: Mosby-Year Book, 1999)
Websites
The Natural Pharmacist (www.tnp.com)
provides a database of information on nutritional products
Alzheimer's Society (www.alzheimers.org.uk)UK's
leading care and research charity for people with all forms of dementia and
their carers
British Geriatrics Society (www.bgs.org.uk)the
national professional organisation that works to restore an ill and disabled
person to a level of maximum ability and wherever possible return the person
to an independent life at home
Association of British Neurologists (www.theabn.org)the
national professional organisation that supports research, education, and
clinical care
Royal College of Psychiatrists (www.rcpsych.ac.uk)the
national professional organisation that provides public information about
mental health and illness
An eight year long epidemiological investigation found that mild to moderate
alcohol consumptiondefined
as one to four drinkseach dayactually
lowered a person's risk for developing severememory loss compared
with non-drinkers or heavy drinkers.24
Similar studies of moderate wine drinkers indicate lower risksfor
Alzheimer's disease compared with heavy drinkers and non-drinkers.
Exactly how alcohol might protect the brain or heart is not fully
known, but it may involve an antiplatelet effect that lowers the
blood's tendency to clot and cause tissuedamage.
The MacArthur study of successful ageing also found that staying in close
contact with people and remaining involved in meaningfulactivities
predicted successful ageing.25 Because a large
componentof the study's definition for successful ageing was
cognitivesuccess, such activities will likely promote brain health
aswell.
Footnotes
Funding: Supported by the Fran and Ray Stark Foundation Fund for
Alzheimer's Diseaseresearch.
Competing interests: GWS has served as a consultant and speaker for Janssen,
Eisai, Merck, Lilly, Pfizer, Abbott, Novartis,Forest, and Organon
and has received research grants from Pfizer,Lilly, and
Forest.
Small GW, Rabins PV, Barry PP, Buckholtz NS, DeKosky ST,
Ferris SH, et al. Diagnosis and treatment of Alzheimer disease and related
disorders: consensus statement of the American Association for Geriatric
Psychiatry, the Alzheimer's Association, and the American Geriatrics
Society. JAMA 1997; 278: 1363-1371[Medline].
Folstein M, Folstein S, McHugh P. "Mini-mental state": a
practical method for grading the cognitive state of patients for the
clinician. J Psychiatr Res 1975; 12: 189-198[Medline].
Silverman DHS, Small GW, Chang CY, Lu CV, Kung de Aburto
MA, Chen W, et al. Positron emission tomography in evaluation of dementia:
regional brain metabolism and long-term clinical outcome. JAMA 2001;
286: 2120-2127[Medline].
Relkin NR, Tanzi R, Breitner J, Farrer L, Gandy S, Haines
J, et al. Apolipoprotein E genotyping in Alzheimer's disease: position
statement of the National Institute on Aging/Alzheimer's Association Working
Group. Lancet 1996; 347: 1091-1095[Medline].
Friedland RP, Fritsch T, Smyth KA, Koss E, Lerner AJ, Chen
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Kramer AF, Hahn S, McAuley E, Cohen NJ, Banich MT, Harrison
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Fisk AD, Rogers W, eds. Human factors interventions for the health care
of older adults. Hillsdale, NJ: Erlbaum, 2001.
Solfrizzi V, Panza F, Torres F, Mastroianni F, Del Parigi
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Morris MC, Beckett LA, Scherr PA, Herbert LE, Bennett DA,
Field TS, et al. Vitamin E and vitamin C supplement use and risk of incident
Alzheimer disease. Alzheim Dis Assoc Disord 1998; 12: 121-126.
Del Ser T, Hachinski V, Merskey H, Munoz DG. An
autopsy-verified study of the effect of education on degenerative dementia.
Brain 1999; 122: 2309-2319[Abstract/Full
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Mayeux R. Gene-environment interaction in late-onset
Alzheimer disease: the role of apolipoprotein-epsilon4. Alzheimer Dis
Assoc Disord 1998; 12(suppl 3): S10-S15[Medline].
Merchant C, Tang MX, Albert S, Manly J, Stern Y, Mayeux R.
The influence of smoking on the risk of Alzheimer's disease. Neurology
1999; 52: 1408-1412[Abstract/Full
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Ruitenberg A, van Swieten JC, Witteman JC, Mehta KM, van
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Rotterdam study. Lancet 2002; 359: 281-286[Medline].
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