Abstract

Objectives: Bipolar disorder (BD) has been suggested to be a risk factor for the development of Parkinson's disease (PD). Standard treatment of BD includes drugs that are known to induce drug-induced parkinsonism (DIP). Clinical differentiation between PD and DIP is crucial and might be aided by functional neuroimaging of the dopaminergic nigrostriatal pathway.Methods: Twenty consecutive BD patients with parkinsonism were clinically assessed and underwent 123I-ioflupane dopamine transporter single-photon emission computer tomography (SPECT). Imaging data of BD patients with pathological scans were further compared to a population of 40 de novo PD patients.Results: Four BD patients had abnormal scans, but their clinical features and cumulative exposure to both antipsychotic drugs and lithium were similar to those of BD patients with normal dopamine transporter imaging. BD patients with pathological scans had putaminal binding ratio and putamen-to-caudate ratios higher than those of PD patients despite a similar motor symptom burden.Conclusions: Up to 20% of BD patients with parkinsonism might have an underlying dopaminergic deficit, which would not be due to cumulative exposure to offending drugs and is ostensibly higher than expected in the general population. This supports the evidence that BD represents a risk factor for subsequent development of neurodegenerative parkinsonism, the nature of which needs to be elucidated.

Highlights

  • Bipolar disorder (BD) is a chronic mood disorder with onset in early adulthood, and it is characterized by recurrent episodes of mania (BD type 1), hypomania (BD type 2), and depression [1, 2]

  • We primarily aimed to explore the functional integrity of the dopaminergic nigrostriatal pathway with the use of DaTSCAN in consecutive BD patients with parkinsonism

  • Two BD+ patients were started on L-3,4-dihydroxyphenylalanine (L-DOPA) (300 mg/day) and displayed an Movement Disorders Society (MDS)–UPDRS-III reduction of 12.5 and 35.3%

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Summary

Introduction

Bipolar disorder (BD) is a chronic mood disorder with onset in early adulthood, and it is characterized by recurrent episodes of mania (BD type 1), hypomania (BD type 2), and depression [1, 2]. BD treatment includes lithium, antipsychotics, and antiepileptic drugs (AEDs), all of which can cause drug-induced parkinsonism (DIP) [5]; overestimation of the presence of PD in BD could have been possible since the individual studies included in the meta-analysis might not have differentiated PD from DIP [6]. In this context, functional neuroimaging of the dopaminergic nigrostriatal pathway is of particular interest. At variance with DIP, PD presents with a significantly reduced DaT striatal specific binding ratio (SBR), which is indicative of nigrostriatal degeneration [7]

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