Striatal dopamine transporter function in dementia with Lewy bodies and Parkinson's disease

Citation
G. Ransmayr et al., Striatal dopamine transporter function in dementia with Lewy bodies and Parkinson's disease, EUR J NUCL, 28(10), 2001, pp. 1523-1528
Citations number
35
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
EUROPEAN JOURNAL OF NUCLEAR MEDICINE
ISSN journal
03406997 → ACNP
Volume
28
Issue
10
Year of publication
2001
Pages
1523 - 1528
Database
ISI
SICI code
0340-6997(200110)28:10<1523:SDTFID>2.0.ZU;2-C
Abstract
The aim of this study was to compare parkinsonian features and loss of stri atal dopamine transporter (DAT) function in patients with dementia with Lew y bodies (DLB) and Parkinson's disease (PD), matched for age and disease du ration. Twenty patients with DLB. 24 PD patients and 10 matched controls we re examined with SPET using a dual-head camera and the dopamine-transporter ligand I-123-beta -CIT (148 MBq). Moreover, in a subgroup of patients (16 DLB and 20 PD patients), subscores of the Unified Parkinson's Disease Ratin g Scale (UPDRS) - motor examination (ME) subscale were obtained during "pra ctical off", i.e. 12 h following withdrawal of antiparkinsonian therapy. Co mpared with controls, striatal/cerebellar (S/C) ratios of DAT binding were significantly reduced in both DLB and PD, deficits being more marked in DLB patients (controls 7.2 +/-1.2. DLB 3.3 +/-1, PD 4.2 +/-1.4;, means +/- SD) . The side-to-side differences in the S/C ratios were lower in the DLB grou p and the controls than in PD patients (0.4 +/-0.4, 0.2 +/-0.2 and 0.6 +/-0 .3., respectively, P <0.05). The total UPDRS-ME scores during practical-off were significantly higher in the DLB than in the PD group (41.2 +/- 12.7 v s 26.6 +/- 15.3, P <0.01). The side-to-side differences of the summed UPDRS extremity subscores were smaller in the DLB than in the PD group (2.2 +/-2 .3 vs 7.4 +/-3.9, P <0.0001). Our findings suggest that parkinsonism evolve s largely symmetrically and progresses more rapidly with more severe loss o f striatal dopamine transporter function in DLB compared to PD. Whether the se findings are helpful in the differential diagnosis of DLB and PD needs t o be examined in further studies.