Author
Listed:
- Chris C. Tang
(The Feinstein Institutes for Medical Research)
- Yoshikazu Nakano
(The Feinstein Institutes for Medical Research)
- An Vo
(The Feinstein Institutes for Medical Research
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell)
- Nha Nguyen
(The Feinstein Institutes for Medical Research)
- Katharina A. Schindlbeck
(The Feinstein Institutes for Medical Research
LMU Munich)
- Paul J. Mattis
(The Feinstein Institutes for Medical Research
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell)
- Kathleen L. Poston
(Stanford University School of Medicine)
- Jean-François Gagnon
(Centre d’Études Avancées en Médecine du Sommeil, Hôpital du Sacré-Cœur de Montréal
Department of Psychology, Université du Québec à Montréal)
- Ronald B. Postuma
(Centre d’Études Avancées en Médecine du Sommeil, Hôpital du Sacré-Cœur de Montréal
Department of Psychology, Université du Québec à Montréal
Department of Neurology and Neurosurgery, Montreal Neurological Institute, Faculty of Medicine and Health Sciences, McGill University)
- Martin Niethammer
(The Feinstein Institutes for Medical Research
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell)
- Yilong Ma
(The Feinstein Institutes for Medical Research
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell)
- Shichun Peng
(The Feinstein Institutes for Medical Research)
- Vijay Dhawan
(The Feinstein Institutes for Medical Research
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell)
- David Eidelberg
(The Feinstein Institutes for Medical Research
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell)
Abstract
Isolated rapid eye movement sleep behavior disorder is a prodrome of α-synucleinopathies. Using positron emission tomography, we assessed changes in Parkinson’s disease-related motor and cognitive metabolic networks and caudate/putamen dopaminergic input in a 4-year longitudinal imaging study of 13 male subjects with this disorder. We also correlated times to phenoconversion with baseline network expression in an independent validation sample. Expression values of both Parkinson’s disease-related networks increased over time while dopaminergic input gradually declined in the longitudinal cohort. While abnormal functional connections were identified at baseline in both networks, others bridging these networks appeared later. These changes resulted in compromised information flow through the networks years before phenoconversion. We noted an inverse correlation between baseline network expression and times to phenoconversion to Parkinson’s disease or dementia with Lewy bodies in the validation sample. Here, we show that the rate of network progression is a useful outcome measure in disease modification trials.
Suggested Citation
Chris C. Tang & Yoshikazu Nakano & An Vo & Nha Nguyen & Katharina A. Schindlbeck & Paul J. Mattis & Kathleen L. Poston & Jean-François Gagnon & Ronald B. Postuma & Martin Niethammer & Yilong Ma & Shic, 2024.
"Longitudinal network changes and phenoconversion risk in isolated REM sleep behavior disorder,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54695-z
DOI: 10.1038/s41467-024-54695-z
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