Patients with Alzheimer's disease (AD) have pathologic involvement of
several important components of the primary auditory pathway, includin
g the inferior colliculus, medial geniculate body, primary auditory co
rtex, and secondary auditory cortex. The main components of the brains
tem auditory evoked response (BAER) and middle latency response (MLR)
reflect the function of portions of the primary auditory pathway, incl
uding those affected pathologically in AD, The amplitude of the P1 com
ponent of the MLR reflects the degree of neuronal activity of midbrain
portions of the ascending reticular activating system (ARAS) with cor
tical cholinergic projections. To determine whether there is dysfuncti
on of the primary auditory pathway and ARAS in AD, we compared simulta
neous BAER and MLR component latency and amplitude measurements in pat
ients with mild-moderate AD (n = 35) and age-matched healthy elderly c
ontrols (n = 34). There were significant latency delays in brainstem t
ransmission time (BAER I-V interpeak latency; p < 0.05) and in primary
auditory cortex evoked potential generation (MLR Pa latency; p < 0.05
) in the AD group compared with controls. In addition, there was a sig
nificant reduction in the P1 component amplitude of the MLR in the AD
group (p < 0.01). These results indicate dysfunction of the primary au
ditory pathway and ARAS in patients with mild-moderate AD and support
the hypothesis that impairment of auditory function and of arousal are
intrinsic features of AD.