Mov Disord. 2012 May 3. doi: 10.1002/mds.24978. [Epub ahead of print]
Paumier KL, Siderowf AD, Auinger P, Oakes D, Madhavan L, Espay AJ, Revilla FJ, Collier TJ; for the Parkinson Study Group Genetics Epidemiology Working Group.
Abstract
This
study examined whether antidepressants delay the need for dopaminergic
therapy or change the degree of motor impairment and disability in a
population of early Parkinson's disease (PD) patients. Preclinical
studies have indicated that antidepressants modulate signaling pathways
involved in cell survival and plasticity, suggesting they may serve to
both treat PD-associated depression and slow disease progression. A
patient-level meta-analysis included 2064 patients from the treatment
and placebo arms of the following trials: FS1, FS-TOO, ELLDOPA, QE2,
TEMPO, and PRECEPT. Depression severity was determined at baseline, and
antidepressant use was reported in a medication log each visit.
Kaplan-Meier curves and time-dependent Cox proportional hazards models
determined associations between depression severity and antidepressant
use with the primary outcome, time to initiation of dopaminergic
therapy. ANCOVAs determined associations with the secondary outcome,
degree of motor impairment and disability, reported as annualized
change in UPDRS scores from baseline to final visit. When controlling
for baseline depression, the initiation of dopaminergic therapy was
delayed for subjects taking tricyclic antidepressants compared with
those not taking antidepressants. No significant differences were found
in UPDRS scores for subjects taking antidepressants compared with those
not taking antidepressants. Tricyclic antidepressants are associated
with a delay in reaching the end point of need to start dopaminergic
therapy. The lack of change in overall UPDRS scores suggests the delay
was not attributable to symptomatic effects.
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