Affective symptoms in multiple system atrophy and Parkinson's disease: response to levodopa therapy

Citation
V. Fetoni et al., Affective symptoms in multiple system atrophy and Parkinson's disease: response to levodopa therapy, J NE NE PSY, 66(4), 1999, pp. 541-544
Citations number
30
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
ISSN journal
00223050 → ACNP
Volume
66
Issue
4
Year of publication
1999
Pages
541 - 544
Database
ISI
SICI code
0022-3050(199904)66:4<541:ASIMSA>2.0.ZU;2-8
Abstract
The objective was to determine the extent to which psychiatric disturbances (especially mood disorders) generally considered poor prognostic factors, are present in patients with striatonigral (SND) type multiple system atrop hy (MSA) compared with patients with idiopathic Parkinson's disease (IPD). The Hamilton depression scale (HAM-D), brief psychiatric rating scale (BPRS ), and Unified Parkinson's disease rating scale (UPDRS) were administered t o clinically probable non-demented patients with SND-type MSA and patients with IPD matched for age and motor disability, at baseline and after receiv ing levodopa. At baseline total HAM-D score was greater in patients with IPD. Overall, BP RS score did not differ between the two groups; however, patients with IPD scored higher on anxiety items of the BPRS, and patients with MSA had highe r scores on the item indicating blunted affect. After levodopa, both groups improved significantly in UPDRS and HAM-D total scores (just significant f or patients with MSA). Patients with IPD improved significantly in total BP RS score but patients with MSA did not. At baseline patients with IPD were more depressed and anxious than patients with MSA who, by contrast, showed blunted affect. After levodopa, depressi on and anxiety of patients with IPD improved significantly whereas the affe ctive detachment of patients with MSA did not change. Major neuronal loss i n the caudate and ventral striatum, which are part of the lateral orbitofro ntal and limbic circuits, may be responsible for the blunted affect not res ponsive to levodopa therapy found in patients with MSA.