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Conclusions
The past twenty years have seen an explosion of knowledge
in our understanding of the human brain, especially in the
field of neurodegenerative illnesses such as Alzheimer's.
We are now in a position to describe accurately the pathology
of the brain and in many instances relate this to abnormal
biochemical and molecular reactions. This understanding has
been enhanced and further clarified by advances in human genetics
which have pinpointed gene mutations that strongly predispose
carriers to early-onset Alzheimer's and increase the risk
of the development of Alzheimer's in old age. Screens for
the identification of carriers of these genes will enable
preventive strategies to be appropriately applied once disease-modifying
medicines become available.
The search for effective medicines has benefited enormously
from this new knowledge. The approaches reviewed in this booklet
demonstrate impressive scientific creativity and a bewildering
diversity of approaches. So rapid has progress been that it
is hard to believe that the first medicine introduced specifically
for Alzheimer's became available as recently as 1993. Since
then, further products that act to conserve acetylcholine
have become available and have been shown to stabilise or,
in some cases, to reduce mental decline.
Of course, such medicines are only a first step and not the
final goal, and newer treatments are now being researched.
The ultimate aim must be to develop medicines that prevent
the brain changes that seem to underlie the functional decline.
Among these are compounds that can protect the brain from
damage by reactive oxygen or inflammation, can stimulate nerve
regeneration, or even ameliorate the formation of neurofibrillary
tangles or amyloid plaques. There are now strong grounds for
believing that compounds that act to prevent or remove amyloid
plaque will modify the progression of the condition and retain
a better quality of life for a longer time for thousands of
elderly and not-so-elderly people. In the next few years,
several such medicines should enter clinical trials, but only
then and with extended experience will we know if we have
reached the beginning of the end for Alzheimer's as a scourge
of older people, or merely the end of the beginning.
Perhaps the most exciting research over the past two to three
years has related to a potential Alzheimer's vaccine. Using
specially bred mice which carry a human gene causing them
to develop amyloid plaque and show memory and learning problems,
it has been shown that vaccination can substantially prevent
plaque formation and improve mental processes. This is now
in the early stages of assessment in humans, but by the very
nature of Alzheimer's, it will be some years before a final
answer is available. If the results are positive, we would
be justified in believing that this awful illness might be
truly preventable.
In the meantime, it is important to recognise the great demands
placed on everyone trying to cope with Alzheimer's and to
improve the coordination, access and range of services available
to them. If that is done, a substantial burden of human misery
can be lifted while we eagerly await the outcome of current
medical research.
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