Abnormal dopamine transporter imaging in pure autonomic failure: a potential biomarker of central nervous system involvement

Author:

Alnasser Alsukhni Rana1ORCID,Vichayanrat Ekawat1,Koay Shiwen1,Davis Laura May2,Ingle Gordon1,McNamara Patricia1,Panicker Jalesh N.34,Bhatia Kailash P.5,Mathias Christopher3,Bomanji Jamshed2,Iodice Valeria13

Affiliation:

1. Autonomic Unit National Hospital for Neurology and Neurosurgery London UK

2. Institute of Nuclear Medicine UCLH NHS Foundation Trust London UK

3. UCL Queen Square Institute of Neurology, Faculty of Brain Sciences University College London London UK

4. Department of Uro‐Neurology National Hospital for Neurology and Neurosurgery London UK

5. Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology University College London London UK

Abstract

AbstractBackground and purposePure autonomic failure (PAF) is a rare progressive neurodegenerative disease characterized by neurogenic orthostatic hypotension at presentation, without other neurological abnormalities. Some patients may develop other central neurological features indicative of multiple system atrophy or a Lewy body disorder. There are currently no biomarkers to assess possible central nervous system involvement in probable PAF at an early stage. A possibility is to evaluate the nigrostriatal dopaminergic degeneration by imaging of dopamine transporter with DaTscan brain imaging. The objective was to evaluate subclinical central nervous system involvement using DaTscan in PAF.MethodsWe retreospectively reviewed pure autonomic failure patients who were evaluated at the Autonomic Unit between January 2015 and August 2021 and underwent comprehensive autonomic assessment, neurological examination, brain magnetic resonance imaging and DaTscan imaging. DaTscan imaging was performed if patients presented with atypical features which did not meet the criteria for Parkinson's disease or multiple system atrophy or other atypical parkinsonism.ResultsIn this cohort, the median age was 49.5 years at disease onset, 57.5 years at presentation, and the median disease duration was 7.5 years. Five of 10 patients had an abnormal DaTscan without neurological features meeting the criteria of an alternative diagnosis. Patients with abnormal DaTscan were predominantly males, had shorter disease duration and had more severe genitourinary symptoms.DiscussionDegeneration of nigrostriatal dopaminergic neurons measured using DaTscan imaging can present in patients with PAF without concurrent signs indicating progression to widespread α‐synucleinopathy. It is advocated that DaTscan imaging should be considered as part of the workup of patients with emerging autonomic failure who are considered to have PAF.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. An update on multiple system atrophy;Current Opinion in Neurology;2024-06-03

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