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Published on: June 3, 2020
Evolution of clinical features in possible DLB depending on FP-CIT SPECT result
Zuzana Walker1, Emilio Moreno2, Alan Thomas2
1From University College London (Z.W.); North Essex Partnership University NHS Foundation Trust (Z.W., T.S., T.W.), Braintree; GE Healthcare (E.M.), Buckinghamshire; Newcastle University (A.T.), Newcastle upon Tyne; Glasgow Memory Clinic Ltd. (F.I.); Brighton and Sussex Medical School (N.T.), Brighton, UK; Centre for Age-Related Diseases (D.A.), Stavanger University Hospital; Department of Geriatric Psychiatry (D.A.), Akershus University Hospital, Oslo, Norway; Department of Neurobiology, (D.A.) Care Sciences and Society Division of Alzheimer's Disease Research Centre, Karolinska Institutet, Stockholm, Sweden; Karl Landsteiner Institut für Gedächtnis und Alzheimerforschung Wien (M.R.), Austria; and University of Brescia (A.P.), Italy. z.walker@ucl.ac.uk.
Objective:
To test the hypothesis that core and suggestive features in possible dementia with Lewy bodies (DLB) would vary in their ability to predict an abnormal dopamine transporter scan and therefore a follow-up diagnosis of probable DLB. A further objective was to assess the evolution of core and suggestive features in patients with possible DLB over time depending on the (123)I-FP-CIT SPECT scan result.
Methods:
A total of 187 patients with possible DLB (dementia plus one core or one suggestive feature) were randomized to have dopamine transporter imaging or to follow-up without scan. DLB features were compared at baseline and at 6-month follow-up according to imaging results and follow-up diagnosis.
Results:
For the whole cohort, the baseline frequency of parkinsonism was 30%, fluctuations 29%, visual hallucinations 24%, and REM sleep behavior disorder 17%. Clinician-rated presence of parkinsonism at baseline was significantly (p = 0.001) more frequent and Unified Parkinson's Disease Rating Scale (UPDRS) score at baseline was significantly higher (p = 0.02) in patients with abnormal imaging. There was a significant increase in UPDRS score in the abnormal scan group over time (p < 0.01). There was relatively little evolution of the rest of the DLB features regardless of the imaging result.
Conclusions:
In patients with possible DLB, apart from UPDRS score, there was no difference in the evolution of DLB clinical features over 6 months between cases with normal and abnormal imaging. Only parkinsonism and dopamine transporter imaging helped to differentiate DLB from non-DLB dementia.
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