Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study

Abstract Small fiber neuropathy (SFN) has been suggested as a trigger of restless legs syndrome (RLS). An increased prevalence of peripheral neuropathy has been demonstrated in Parkinson’s disease (PD). We aimed to investigate, in a cross-sectional manner, whether SFN is overrepresented in PD patien...

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Autores principales: Mattias Andréasson, Neil Lagali, Reza A. Badian, Tor Paaske Utheim, Fabio Scarpa, Alessia Colonna, Stephan Allgeier, Andreas Bartschat, Bernd Köhler, Ralf Mikut, Klaus-Martin Reichert, Göran Solders, Kristin Samuelsson, Henrik Zetterberg, Kaj Blennow, Per Svenningsson
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:0ebc3b91d1a748528d953d2a27282feb2021-12-02T15:13:03ZParkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study10.1038/s41531-020-00148-52373-8057https://doaj.org/article/0ebc3b91d1a748528d953d2a27282feb2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41531-020-00148-5https://doaj.org/toc/2373-8057Abstract Small fiber neuropathy (SFN) has been suggested as a trigger of restless legs syndrome (RLS). An increased prevalence of peripheral neuropathy has been demonstrated in Parkinson’s disease (PD). We aimed to investigate, in a cross-sectional manner, whether SFN is overrepresented in PD patients with concurrent RLS relative to PD patients without RLS, using in vivo corneal confocal microscopy (IVCCM) and quantitative sensory testing (QST) as part of small fiber assessment. Study participants comprised of age- and sex-matched PD patients with (n = 21) and without RLS (n = 21), and controls (n = 13). Diagnosis of RLS was consolidated with the sensory suggested immobilization test. Assessments included nerve conduction studies (NCS), Utah Early Neuropathy Scale (UENS), QST, and IVCCM, with automated determination of corneal nerve fiber length (CNFL) and branch density (CNBD) from wide-area mosaics of the subbasal nerve plexus. Plasma neurofilament light (p-NfL) was determined as a measure of axonal degeneration. No significant differences were found between groups when comparing CNFL (p = 0.81), CNBD (p = 0.92), NCS (p = 0.82), and QST (minimum p = 0.54). UENS scores, however, differed significantly (p = 0.001), with post-hoc pairwise testing revealing higher scores in both PD groups relative to controls (p = 0.018 and p = 0.001). Analysis of all PD patients (n = 42) revealed a correlation between the duration of l-dopa therapy and CNBD (ρ = −0.36, p = 0.022), and p-NfL correlated with UENS (ρ = 0.35, p = 0.026) and NCS (ρ = −0.51, p = 0.001). Small and large fiber neuropathy do not appear to be associated with RLS in PD. Whether peripheral small and/or large fiber pathology associates with central neurodegeneration in PD merits further longitudinal studies.Mattias AndréassonNeil LagaliReza A. BadianTor Paaske UtheimFabio ScarpaAlessia ColonnaStephan AllgeierAndreas BartschatBernd KöhlerRalf MikutKlaus-Martin ReichertGöran SoldersKristin SamuelssonHenrik ZetterbergKaj BlennowPer SvenningssonNature PortfolioarticleNeurology. Diseases of the nervous systemRC346-429ENnpj Parkinson's Disease, Vol 7, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurology. Diseases of the nervous system
RC346-429
Mattias Andréasson
Neil Lagali
Reza A. Badian
Tor Paaske Utheim
Fabio Scarpa
Alessia Colonna
Stephan Allgeier
Andreas Bartschat
Bernd Köhler
Ralf Mikut
Klaus-Martin Reichert
Göran Solders
Kristin Samuelsson
Henrik Zetterberg
Kaj Blennow
Per Svenningsson
Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
description Abstract Small fiber neuropathy (SFN) has been suggested as a trigger of restless legs syndrome (RLS). An increased prevalence of peripheral neuropathy has been demonstrated in Parkinson’s disease (PD). We aimed to investigate, in a cross-sectional manner, whether SFN is overrepresented in PD patients with concurrent RLS relative to PD patients without RLS, using in vivo corneal confocal microscopy (IVCCM) and quantitative sensory testing (QST) as part of small fiber assessment. Study participants comprised of age- and sex-matched PD patients with (n = 21) and without RLS (n = 21), and controls (n = 13). Diagnosis of RLS was consolidated with the sensory suggested immobilization test. Assessments included nerve conduction studies (NCS), Utah Early Neuropathy Scale (UENS), QST, and IVCCM, with automated determination of corneal nerve fiber length (CNFL) and branch density (CNBD) from wide-area mosaics of the subbasal nerve plexus. Plasma neurofilament light (p-NfL) was determined as a measure of axonal degeneration. No significant differences were found between groups when comparing CNFL (p = 0.81), CNBD (p = 0.92), NCS (p = 0.82), and QST (minimum p = 0.54). UENS scores, however, differed significantly (p = 0.001), with post-hoc pairwise testing revealing higher scores in both PD groups relative to controls (p = 0.018 and p = 0.001). Analysis of all PD patients (n = 42) revealed a correlation between the duration of l-dopa therapy and CNBD (ρ = −0.36, p = 0.022), and p-NfL correlated with UENS (ρ = 0.35, p = 0.026) and NCS (ρ = −0.51, p = 0.001). Small and large fiber neuropathy do not appear to be associated with RLS in PD. Whether peripheral small and/or large fiber pathology associates with central neurodegeneration in PD merits further longitudinal studies.
format article
author Mattias Andréasson
Neil Lagali
Reza A. Badian
Tor Paaske Utheim
Fabio Scarpa
Alessia Colonna
Stephan Allgeier
Andreas Bartschat
Bernd Köhler
Ralf Mikut
Klaus-Martin Reichert
Göran Solders
Kristin Samuelsson
Henrik Zetterberg
Kaj Blennow
Per Svenningsson
author_facet Mattias Andréasson
Neil Lagali
Reza A. Badian
Tor Paaske Utheim
Fabio Scarpa
Alessia Colonna
Stephan Allgeier
Andreas Bartschat
Bernd Köhler
Ralf Mikut
Klaus-Martin Reichert
Göran Solders
Kristin Samuelsson
Henrik Zetterberg
Kaj Blennow
Per Svenningsson
author_sort Mattias Andréasson
title Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
title_short Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
title_full Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
title_fullStr Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
title_full_unstemmed Parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
title_sort parkinson’s disease with restless legs syndrome—an in vivo corneal confocal microscopy study
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/0ebc3b91d1a748528d953d2a27282feb
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