Long-term trends in myocardial sympathetic innervation and function in synucleinopathies.

Guillaume Lamotte, Courtney Holmes, Tianxia Wu, David S Goldstein

Journal: Parkinsonism & related disorders 2020;67():27-33

PMID: 31621602

Abstract

INTRODUCTION

Parkinson disease (PD), pure autonomic failure (PAF), and multiple system atrophy (MSA) are characterized by intra-cerebral deposition of the protein alpha-synuclein and are termed synucleinopathies. Lewy body synucleinopathies involve decreased cardiac sympathetic innervation and functional abnormalities in residual noradrenergic terminals. This observational, retrospective, cohort study describes long-term trends in indices of cardiac sympathetic innervation and function in synucleinopathies.

METHODS

Patients with PD (N = 31), PAF (N = 9), or MSA (N = 9) underwent repeated F-dopamine positron emission tomography (median follow-up 3.5 years). Interventricular septal F-dopamine-derived radioactivity 8 min after tracer injection (8' Radioactivity) was used as an index of sympathetic innervation and the slope of mono-exponential decline of radioactivity between 8 and 25 min (k) as an index of intraneuronal vesicular storage. Healthy volunteers (HVs) (N = 33) and individuals at high risk of PD (N = 15) were controls.

RESULTS

Upon initial evaluation the groups with PD and orthostatic hypotension (OH), PAF, or PD and no OH had low mean 8' Radioactivity compared to HVs (p < 0.0001, p = 0.0002, p = 0.006) and had elevated k (p = 0.0007, p = 0.007, p = 0.06). There was no significant difference between MSA and HVs. In PD 8' Radioactivity decreased by a median of 4% per year and did not decrease in MSA. k values did not change during follow-up in any group.

CONCLUSIONS

Neuroimaging evidence of decreased vesicular uptake in cardiac sympathetic nerves is present upon initial evaluation of patients with Lewy body synucleinopathies and may provide a biomarker of catecholaminergic dysfunction early in the disease process.

Published by Elsevier Ltd.

Address: Clinical Neurosciences Program (CNP), Division of Intramural Research (CNP), National Institute of Neurological Disorders and Stroke (NINDS), 9000 Rockville Pike 10/8C260, Bethesda, MD, 20892, USA; Clinical Neurocardiology Section, CNP/DIR/NINDS/NIH, 9000 Rockville Pike 10/8C260, Bethesda, MD, 20892, USA. Electronic address: [email protected]/.; Clinical Neurocardiology Section, CNP/DIR/NINDS/NIH, 9000 Rockville Pike 10/8C260, Bethesda, MD, 20892, USA. Electronic address: [email protected].; Clinical Trials Unit, NINDS, 9000 Rockville Pike 10/2A23B, Bethesda, MD, 20892, USA. Electronic address: [email protected].; Clinical Neurocardiology Section, CNP/DIR/NINDS/NIH, 9000 Rockville Pike 10/8C260, Bethesda, MD, 20892, USA. Electronic address: [email protected].
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