AUDITORY EVENT-RELATED CEREBRAL POTENTIALS (P300) IN HEPATIC-ENCEPHALOPATHY - TOPOGRAPHIC DISTRIBUTION AND CORRELATION WITH CLINICAL AND PSYCHOMETRIC ASSESSMENT
S. Hollerbach et al., AUDITORY EVENT-RELATED CEREBRAL POTENTIALS (P300) IN HEPATIC-ENCEPHALOPATHY - TOPOGRAPHIC DISTRIBUTION AND CORRELATION WITH CLINICAL AND PSYCHOMETRIC ASSESSMENT, Hepato-gastroenterology, 44(16), 1997, pp. 1002-1012
Background/Aims: Early cognitive disturbances in patients with cirrhos
is (Ci) are difficult to assess. Therefore, we evaluated the role of t
opographic auditory evoked cerebral potentials (P300-EP). Methodology:
Prospective longitudinal study. Setting: Tertiary clinical care insti
tution. Participants: 45 patients with cirrhosis were compared to 22 h
ealthy subjects. Main Outcome Measures: Hepatic Encephalopathy (HE) wa
s assessed using the clinical grading, standardized psychometric tests
, and auditory evoked P300-EP by multichannel EEG recordings. Results:
In the patients, the mean P300 peak latency teas significantly increa
sed (386.7+/-26.7 versus 318.6+/-22.2 ms in controls, p<0.00001). Even
in patients with cirrhosis but no HE (n=18) the P300 peak latency was
abnormally prolonged (>384 ms) in 8 cases (44%). In addition, P180 pe
ak latency was significantly longer in patients with liver cirrhosis a
s compared to controls (p=0.021). The maximal P300 amplitude was signi
ficantly lowered in patients with liver cirrhosis in the frontocentral
and central cortical regions (FZ: p<0.008; Cz: p<0.04). Liver functio
n and etiology of liver disease were not related to the increased peak
latencies of the P300 and P180 peaks. Conclusions: P300-EP is a sensi
tive measure to defect functional cognitive impairment in cirrhotic pa
tients with subclinical HE and clinically apparent HE. Typical changes
include latency prolongation and decreased central peak amplitude. So
me 40% of patients with no clinical evidence of HE and normal psychome
tric tests show abnormal results during P300 testing, which is likely
to reflect early impairment of cognitive function. Auditory evoked P30
0 potentials are more sensitive than psychometric testing alone.