Event-related P300 potentials are closely reflecting cognitive functio
ns such as stimulus evaluation time (P300 latency) and task relevance
(P300 amplitude). Hence, both their potential clinical application for
detecting slight cognitive disturbances and an increasing interest in
the aging of cognitive human brain functions resulted in a growing nu
mber of studies on age-related P300 changes. Although there are conver
ging lines of evidence that aging results in prolongations of P300 lat
encies, reductions of P300 amplitudes and a more equipotential P300 sc
alp distribution, the amount of these changes and the best fit for the
P300-age interactions, respectively, remain still controversial. In g
eneral, these P300 alterations obviously reflect only minor cognitive
changes during normal aging. For their clinical application, however,
it is necessary to obtain an age-matched normative database. Furthermo
re, the increased P300 variability in the elderly has to be reduced -
as far as possible - by appropriate simple P300 paradigms which should
be preferentially applied in longitudinal analyses to differentiate n
ormal from pathological aging of cognitive functions. Finally, additio
nal cross-correlational analyses between the P300 and morphological as
well as neurobiochemical data are needed. By these means, our knowled
ge about age-related changes of cognitive brain functions should be co
nsiderably enlarged.