Cylindrical spirals and other concentric structures of skeletal muscle in patients with neurological diseases.

Concentric cristae Concentric laminated bodies Cylindrical spirals Mitochondria Neurogenic myopathy Neuromuscular disorders

Journal

Journal of the neurological sciences
ISSN: 1878-5883
Titre abrégé: J Neurol Sci
Pays: Netherlands
ID NLM: 0375403

Informations de publication

Date de publication:
15 08 2023
Historique:
received: 30 03 2023
revised: 07 07 2023
accepted: 11 07 2023
medline: 4 8 2023
pubmed: 22 7 2023
entrez: 21 7 2023
Statut: ppublish

Résumé

Cylindrical spirals (CSs) are ultrastructurally distinct, intracytoplasmic inclusions characterized by concentrically wrapped lamellae, which are rarely found in skeletal muscle biopsies on electron microscopy (EM). CSs are often confused with other EM concentric structures including concentric laminated bodies and mitochondrial concentric cristae (MCC), due to similarities in these ultrastructures. In this study, we found CSs in 9 muscle biopsies from 9 patients, accounting for 0.5% of the biopsies examined routinely by EM. The frequency of CSs in these muscles varied from sparse and segregated to focally frequent and aggregated. CS-associated features included muscle fiber denervation atrophy in all 9 cases, fiber type grouping in 7/8 cases, tubular aggregates in 3/9 cases, and MCC in 2/9 cases. We also compared the concentric structures and highlighted their differences to distinguish CSs from other similar structures. Clinically, 8 out of 9 patients were adults aged 41-74 years and only one patient was 17 month-old. CSs were associated with several neurological diseases including Huntington's disease, amyotrophic lateral sclerosis, Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes, and other complex neurological disorders with neuropathy/encephalopathy, as well as anti-MDA5+ dermatomyositis. Eight of nine patients had genetic findings such as trinucleotide repeat expansion of huntingtin gene, ALS2 variant, MT-TL1 m.3243A > G mutation, and PMP 22 gene deletion. These results suggest that CSs may be highly variable in frequency and likely are under-reported/under-detected; they may be associated with neurogenic myopathy or central/peripheral nervous system disorders including some genetic neurological/neuromuscular diseases. Our findings of more CS-associated neurological diseases and an association of CSs with muscle neurogenic features may contribute to a better understanding of the clinico-pathological significance of CSs.

Identifiants

pubmed: 37478793
pii: S0022-510X(23)00195-8
doi: 10.1016/j.jns.2023.120734
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

120734

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Dr. Mark A. Tarnopolsky is the CEO of Exerkine Corporation and the company is working on therapies that target mitochondrial dysfunction. The remaining authors declare no conflicts of interest.

Auteurs

Jeffrey E Fournier (JE)

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

Gloria Mak (G)

Department of Medicine/Neurology, McMaster University, Hamilton, Ontario, Canada.

Katerina Gordon (K)

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

Judah Glogauer (J)

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

Faiha Fareez (F)

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

John Provias (J)

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

Mark A Tarnopolsky (MA)

Department of Medicine/Neurology, McMaster University, Hamilton, Ontario, Canada; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.

Jian-Qiang Lu (JQ)

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada. Electronic address: luj85@mcmaster.ca.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH