Detection of a Parkinson's Disease-Specific MicroRNA Signature in Nasal and Oral Swabs.


Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
09 2023
Historique:
revised: 11 05 2023
received: 17 02 2023
accepted: 31 05 2023
medline: 19 9 2023
pubmed: 29 6 2023
entrez: 29 6 2023
Statut: ppublish

Résumé

Biomaterials from oral and nasal swabs provide, in theory, a potential resource for biomarker development. However, their diagnostic value has not yet been investigated in the context of Parkinson's disease (PD) and associated conditions. We have previously identified a PD-specific microRNA (miRNA) signature in gut biopsies. In this work, we aimed to investigate the expression of miRNAs in routine buccal (oral) and nasal swabs obtained from cases with idiopathic PD and isolated rapid eye movement sleep behavior disorder (iRBD), a prodromal symptom that often precedes α-synucleinopathies. We aimed to address their value as a diagnostic biomarker for PD and their mechanistic contribution to PD onset and progression. Healthy control cases (n = 28), cases with PD (n = 29), and cases with iRBD (n = 8) were prospectively recruited to undergo routine buccal and nasal swabs. Total RNA was extracted from the swab material, and the expression of a predefined set of miRNAs was quantified by quantitative real-time polymerase chain reaction. Statistical analysis revealed a significantly increased expression of hsa-miR-1260a in cases who had PD. Interestingly, hsa-miR-1260a expression levels correlated with diseases severity, as well as olfactory function, in the PD and iRBD cohorts. Mechanistically, hsa-miR-1260a segregated to Golgi-associated cellular processes with a potential role in mucosal plasma cells. Predicted hsa-miR-1260a target gene expression was reduced in iRBD and PD groups. Our work demonstrates oral and nasal swabs as a valuable biomarker pool in PD and associated neurodegenerative conditions. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND
Biomaterials from oral and nasal swabs provide, in theory, a potential resource for biomarker development. However, their diagnostic value has not yet been investigated in the context of Parkinson's disease (PD) and associated conditions.
OBJECTIVE
We have previously identified a PD-specific microRNA (miRNA) signature in gut biopsies. In this work, we aimed to investigate the expression of miRNAs in routine buccal (oral) and nasal swabs obtained from cases with idiopathic PD and isolated rapid eye movement sleep behavior disorder (iRBD), a prodromal symptom that often precedes α-synucleinopathies. We aimed to address their value as a diagnostic biomarker for PD and their mechanistic contribution to PD onset and progression.
METHODS
Healthy control cases (n = 28), cases with PD (n = 29), and cases with iRBD (n = 8) were prospectively recruited to undergo routine buccal and nasal swabs. Total RNA was extracted from the swab material, and the expression of a predefined set of miRNAs was quantified by quantitative real-time polymerase chain reaction.
RESULTS
Statistical analysis revealed a significantly increased expression of hsa-miR-1260a in cases who had PD. Interestingly, hsa-miR-1260a expression levels correlated with diseases severity, as well as olfactory function, in the PD and iRBD cohorts. Mechanistically, hsa-miR-1260a segregated to Golgi-associated cellular processes with a potential role in mucosal plasma cells. Predicted hsa-miR-1260a target gene expression was reduced in iRBD and PD groups.
CONCLUSIONS
Our work demonstrates oral and nasal swabs as a valuable biomarker pool in PD and associated neurodegenerative conditions. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 37382573
doi: 10.1002/mds.29515
doi:

Substances chimiques

MicroRNAs 0
Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1706-1715

Informations de copyright

© 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Auteurs

Patricia Schließer (P)

Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.

Felix L Struebing (FL)

Department of Translational Brain Research, German Centre for Neurodegenerative Diseases, Munich, Germany.
Center for Neuropathology and Prion Research, Ludwig Maximilian University, Munich, Germany.

Bernd H Northoff (BH)

Institute of Laboratory Medicine, LMU University Hospital, LMU Munich, Munich, Germany.

Anna Kurz (A)

Department of Gynaecology and Obstetrics, Klinikum Landsberg am Lech, Landsberg, Germany.

Jan Rémi (J)

Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.

Lesca Holdt (L)

Institute of Laboratory Medicine, LMU University Hospital, LMU Munich, Munich, Germany.

Günter U Höglinger (GU)

Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
German Center for Neurodegenerative Diseases e.V. (DZNE) Munich, Munich, Germany.

Jochen Herms (J)

Department of Translational Brain Research, German Centre for Neurodegenerative Diseases, Munich, Germany.
Center for Neuropathology and Prion Research, Ludwig Maximilian University, Munich, Germany.

Thomas Koeglsperger (T)

Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
Department of Translational Brain Research, German Centre for Neurodegenerative Diseases, Munich, Germany.

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