Alzheimer disease (AD) is one of several types of chronic and very common d
ementing disorders, affecting individuals aged 65 years or older. During th
e last five years, an enormous growth in the field has enriched our underst
anding of this complex condition. Molecular genetic studies have identified
at least three genes that, when mutated. cause the autosomal dominant, ear
ly-onset familial form of the disease. The late-onset. most common forms of
the disease are likely to be associated with various genetic susceptibilit
y factors. The application of cell biological techniques has given insight
into basic aspects of the functions of important proteins involved in disea
se progression. and transgenic animal studies have further enriched our kno
wledge of the pathophysiological aspects of the disease. More efficient the
rapeutic drugs to retard its progression have been developed, as well as te
chniques to identify the preclinical phase of the disorder. Although we are
st ill lacking the molecular basis and order of events involved in the dis
ease process, the future for AD research, as well as for AD patients, is mo
re promising than ever before.