Patients with isolated rapid-eye-movement sleep behaviour disorder (RBD) are commonly regarded as being in the early stages of a progressive neurodegenerative disease involving α-synuclein pathology, such as Parkinson's disease, dementia with Lewy bodies, or multiple system atrophy. Abnormal α-synuclein deposition occurs early in the neurodegenerative process across the central and peripheral nervous systems and might precede the appearance of motor symptoms and cognitive decline by several decades. These findings provide the rationale to develop reliable biomarkers that can better predict conversion to clinically manifest α-synucleinopathies. In addition, biomarkers of disease progression will be essential to monitor treatment response once disease-modifying therapies become available, and biomarkers of disease subtype will be essential to enable prediction of which subtype of α-synucleinopathy patients with isolated RBD might develop.

Biomarkers of conversion to α-synucleinopathy in isolated rapid-eye-movement sleep behaviour disorder / Miglis, M. G.; Adler, C. H.; Antelmi, E.; Arnaldi, D.; Baldelli, L.; Boeve, B. F.; Cesari, M.; Dall'Antonia, I.; Diederich, N. J.; Doppler, K.; Dusek, P.; Ferri, R.; Gagnon, J. -F.; Gan-Or, Z.; Hermann, W.; Hogl, B.; Hu, M. T.; Iranzo, A.; Janzen, A.; Kuzkina, A.; Lee, J. -Y.; Leenders, K. L.; Lewis, S. J. G.; Liguori, C.; Liu, J.; Lo, C.; Ehgoetz Martens, K. A.; Nepozitek, J.; Plazzi, G.; Provini, F.; Puligheddu, M.; Rolinski, M.; Rusz, J.; Stefani, A.; Summers, R. L. S.; Yoo, D.; Zitser, J.; Oertel, W. H.. - In: LANCET NEUROLOGY. - ISSN 1474-4422. - 20:8(2021), pp. 671-684. [10.1016/S1474-4422(21)00176-9]

Biomarkers of conversion to α-synucleinopathy in isolated rapid-eye-movement sleep behaviour disorder

Ferri R.;Lo C.;Plazzi G.;
2021

Abstract

Patients with isolated rapid-eye-movement sleep behaviour disorder (RBD) are commonly regarded as being in the early stages of a progressive neurodegenerative disease involving α-synuclein pathology, such as Parkinson's disease, dementia with Lewy bodies, or multiple system atrophy. Abnormal α-synuclein deposition occurs early in the neurodegenerative process across the central and peripheral nervous systems and might precede the appearance of motor symptoms and cognitive decline by several decades. These findings provide the rationale to develop reliable biomarkers that can better predict conversion to clinically manifest α-synucleinopathies. In addition, biomarkers of disease progression will be essential to monitor treatment response once disease-modifying therapies become available, and biomarkers of disease subtype will be essential to enable prediction of which subtype of α-synucleinopathy patients with isolated RBD might develop.
2021
20
8
671
684
Biomarkers of conversion to α-synucleinopathy in isolated rapid-eye-movement sleep behaviour disorder / Miglis, M. G.; Adler, C. H.; Antelmi, E.; Arnaldi, D.; Baldelli, L.; Boeve, B. F.; Cesari, M.; Dall'Antonia, I.; Diederich, N. J.; Doppler, K.; Dusek, P.; Ferri, R.; Gagnon, J. -F.; Gan-Or, Z.; Hermann, W.; Hogl, B.; Hu, M. T.; Iranzo, A.; Janzen, A.; Kuzkina, A.; Lee, J. -Y.; Leenders, K. L.; Lewis, S. J. G.; Liguori, C.; Liu, J.; Lo, C.; Ehgoetz Martens, K. A.; Nepozitek, J.; Plazzi, G.; Provini, F.; Puligheddu, M.; Rolinski, M.; Rusz, J.; Stefani, A.; Summers, R. L. S.; Yoo, D.; Zitser, J.; Oertel, W. H.. - In: LANCET NEUROLOGY. - ISSN 1474-4422. - 20:8(2021), pp. 671-684. [10.1016/S1474-4422(21)00176-9]
Miglis, M. G.; Adler, C. H.; Antelmi, E.; Arnaldi, D.; Baldelli, L.; Boeve, B. F.; Cesari, M.; Dall'Antonia, I.; Diederich, N. J.; Doppler, K.; Dusek, P.; Ferri, R.; Gagnon, J. -F.; Gan-Or, Z.; Hermann, W.; Hogl, B.; Hu, M. T.; Iranzo, A.; Janzen, A.; Kuzkina, A.; Lee, J. -Y.; Leenders, K. L.; Lewis, S. J. G.; Liguori, C.; Liu, J.; Lo, C.; Ehgoetz Martens, K. A.; Nepozitek, J.; Plazzi, G.; Provini, F.; Puligheddu, M.; Rolinski, M.; Rusz, J.; Stefani, A.; Summers, R. L. S.; Yoo, D.; Zitser, J.; Oertel, W. H.
File in questo prodotto:
File Dimensione Formato  
1-s2.0-S1474442221001769-main.pdf

Accesso riservato

Tipologia: Versione pubblicata dall'editore
Dimensione 2.41 MB
Formato Adobe PDF
2.41 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1251553
Citazioni
  • ???jsp.display-item.citation.pmc??? 11
  • Scopus 103
  • ???jsp.display-item.citation.isi??? 101
social impact