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Cardiac noradrenergic deficiency revealed by 18F-dopamine positron emission tomography identifies preclinical central Lewy body diseases
David S. Goldstein, … , Tianxia Wu, Yehonatan Sharabi
David S. Goldstein, … , Tianxia Wu, Yehonatan Sharabi
Published October 26, 2023
Citation Information: J Clin Invest. 2024;134(1):e172460. https://doi.org/10.1172/JCI172460.
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Clinical Research and Public Health Neuroscience Article has an altmetric score of 181

Cardiac noradrenergic deficiency revealed by 18F-dopamine positron emission tomography identifies preclinical central Lewy body diseases

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Abstract

BACKGROUND. In Lewy body diseases (LBDs) Parkinson disease (PD), and dementia with Lewy bodies (DLB), by the time parkinsonism or cognitive dysfunction manifests clinically, substantial neurodegeneration has already occurred. Biomarkers are needed to identify central LBDs in a preclinical phase, when neurorescue strategies might forestall symptomatic disease. This phase may involve catecholamine deficiency in the autonomic nervous system. We analyzed data from the prospective, observational, long-term PDRisk study to assess the predictive value of low versus normal cardiac 18F-dopamine positron emission tomography (PET), an index of myocardial content of the sympathetic neurotransmitter norepinephrine, in at-risk individuals. METHODS. Participants self-reported risk factor information (genetics, olfactory dysfunction, dream enactment behavior, and orthostatic intolerance or hypotension) at a protocol-specific website. Thirty-four with 3 or more confirmed risk factors underwent serial cardiac 18F-dopamine PET at 1.5-year intervals for up to 7.5 years or until PD was diagnosed. RESULTS. Nine participants had low initial myocardial 18F-dopamine–derived radioactivity (<6,000 nCi-kg/cc-mCi) and 25 had normal radioactivity. At 7 years of follow-up, 8 of 9 with low initial radioactivity and 1 of 11 with normal radioactivity were diagnosed with a central LBD (LBD+) (P = 0.0009 by Fisher’s exact test). Conversely, all 9 LBD+ participants had low 18F-dopamine–derived radioactivity before or at the time of diagnosis of a central LBD, whereas among 25 participants without a central LBD only 1 (4%) had persistently low radioactivity (P < 0.0001 by Fisher’s exact test). CONCLUSION. Cardiac 18F-dopamine PET highly efficiently distinguishes at-risk individuals who are diagnosed subsequently with a central LBD from those who are not. TRIAL REGISTRATION. ClinicalTrials.gov NCT00775853. FUNDING. Division of Intramural Research, NIH, NINDS.

Authors

David S. Goldstein, Courtney Holmes, Patti Sullivan, Grisel Lopez, Janna Gelsomino, Sarah Moore, Risa Isonaka, Tianxia Wu, Yehonatan Sharabi

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Figure 3

Individual and mean (±SEM) values for cardiac PET data and biomarkers of central dopaminergic innervation in at-risk individuals who subsequently were diagnosed with a central Lewy body disease (LBD+) or were not diagnosed with a central Lewy body disease (LBD–) and concurrently studied healthy volunteers (HVs).

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Individual and mean (±SEM) values for cardiac PET data and biomarkers of...
(A) 18F-dopamine–derived (18F-DA–derived) radioactivity in the dynamic PET frame with the midpoint 8 minutes after initiation of intravenous administration of the tracer. (B) Mono-exponential slope of decline in 18F-DA–derived radioactivity across the time points from the maximum value to the value in the dynamic frame with the midpoint 25 minutes after initiation of infusion of the tracer (kMax–25′). (C) 13N-ammonia–derived (13NH3-derived) radioactivity in the dynamic PET frame with the midpoint 8 minutes after initiation of intravenous administration of the tracer. (D) Cerebrospinal fluid concentration of 3,4-dihydroxyphenylacetic acid (DOPAC). (E) Putamen/occipital (PUT/OCC) cortex ratios of 18F-DOPA–derived radioactivity. (F) Percentage decrease in putamen 18F-DOPA–derived radioactivity between the 15-minute static scan beginning 30 minutes after intravenous administration of the tracer and the 15-minute static scan ending 120 minutes after administration of the tracer. Statistical testing was 1-way ANOVA with Tukey’s post hoc test for multiple comparisons.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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