Spinocerebellar ataxia type 2-neuronopathy or neuropathy?


Journal

Muscle & nerve
ISSN: 1097-4598
Titre abrégé: Muscle Nerve
Pays: United States
ID NLM: 7803146

Informations de publication

Date de publication:
09 2019
Historique:
received: 21 12 2018
revised: 13 06 2019
accepted: 16 06 2019
pubmed: 23 6 2019
medline: 10 1 2020
entrez: 23 6 2019
Statut: ppublish

Résumé

Use of peripheral nerve ultrasound alongside standard electrodiagnostic tests may help to gain insight into the pathophysiology of peripheral nerve involvement in type 2 spinocerebellar ataxia (SCA2). Twenty-seven patients with SCA2 underwent ultrasound cross-sectional area (CSA) measurement of median, ulnar, sural and tibial nerves, and motor (median, ulnar, tibial) and sensory (median, ulnar, radial, sural) nerve conduction studies. Twenty patients had pathologically small-nerve CSAs, suggestive of sensory neuronopathy. In these patients, electrophysiology showed non-length-dependent sensory neuropathy (14 of 20), "possible sensory neuropathy" (1 of 20), or normal findings (5 of 20). Four different patients had length-dependent sensory neuropathy on electrophysiology, and 1 had enlarged nerve CSAs. Regression analysis showed an inverse relationship between ataxia scores and upper limb nerve CSA (P < 0.03). Our findings suggest that a majority of patients with SCA2 (74%) have a sensory neuronopathy and this correlates with disability. A minority of patients have findings consistent with axonal neuropathy (18%). Muscle Nerve, 2019.

Identifiants

pubmed: 31228263
doi: 10.1002/mus.26613
doi:

Substances chimiques

Nerve Tissue Proteins 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

271-278

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Luciana Pelosi (L)

Department of Neurology and Clinical Neurophysiology, Bay of Plenty District Health Board, Tauranga Hospital, Tauranga, New Zealand.

Rosa Iodice (R)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University Federico II, Naples, Italy.

Antonella Antenora (A)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University Federico II, Naples, Italy.

Dean Kilfoyle (D)

Department of Neurology, Auckland District Health Board, Auckland, New Zealand.

Eoin Mulroy (E)

Department of Neurology, Auckland District Health Board, Auckland, New Zealand.

Miriam Rodrigues (M)

Department of Neurology, Auckland District Health Board, Auckland, New Zealand.

Richard Roxburgh (R)

Department of Neurology, Auckland District Health Board, Auckland, New Zealand.
Centre of Brain Research Neurogenetics Research Clinic, University of Auckland, Auckland, New Zealand.

Aniello Iovino (A)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University Federico II, Naples, Italy.

Alessandro Filla (A)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University Federico II, Naples, Italy.

Fiore Manganelli (F)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University Federico II, Naples, Italy.

Lucio Santoro (L)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University Federico II, Naples, Italy.

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Classifications MeSH