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

Author:

Schließer Patricia1,Struebing Felix L.23,Northoff Bernd H.4,Kurz Anna5,Rémi Jan1,Holdt Lesca4,Höglinger Günter U.16,Herms Jochen23,Koeglsperger Thomas12ORCID

Affiliation:

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

2. Department of Translational Brain Research German Centre for Neurodegenerative Diseases Munich Germany

3. Center for Neuropathology and Prion Research Ludwig Maximilian University Munich Germany

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

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

6. German Center for Neurodegenerative Diseases e.V. (DZNE) Munich Munich Germany

Abstract

ABSTRACTBackgroundBiomaterials 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.ObjectiveWe 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.MethodsHealthy 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.ResultsStatistical 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.ConclusionsOur 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.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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