Rj. Uitti et al., AMANTADINE TREATMENT IS AN INDEPENDENT PREDICTOR OF IMPROVED SURVIVALIN PARKINSONS-DISEASE, Nervenheilkunde, 16(7), 1997, pp. 417-423
Amantadine has been used for more than 20 years in the symptomatic tre
atment of Parkinson's disease (PD). Several recent discoveries suggest
that amantadine could also have a neuroprotective effect in PD. We st
udied survival in ail parkinsonism (including PD and other parkinsonia
n syndromes) patients attending a single clinic, employing standard su
rvival curves and a Cox regression model, to identify independent pred
ictive variables for survival (while taking into account factors poten
tially associated with both outcome and treatment selection). Amantadi
ne-treated patients (n = 250) were similar to the patients not treated
with amantadine (n = 586) in terms of age, gender, type of parkinsoni
sm, Hoehn and Yahr stage and dementia status at initial neurological v
isit. Amantadine use was an independent predictor of improved survival
(p < 0.01). Improved survival was also associated with a higher 10-ye
ar expected survival (based on age, gender, and birth year), absence o
f dementia, type of parkinsonism = PD, and low Hoehn and Yahr stage (I
or II) at initial neurologic visit (all p < 0.01); these additional f
actors occurred in statistically similar proportions in the groups tha
t were and were not treated with amantadine. The association of improv
ed survival with amantadine use may stem from symptomatic benefit or m
ay reflect a ''neuroprotective'' effect, mediated through N-methyl-D-a
spartate (NMDA) receptor antagonism, dopamine uptake blockade activity
, or other mechanisms. Our preliminary findings suggest that a prospec
tive, controlled, randomized trial of amantadine's effects on PD progr
ession is warranted.