Utility of stimulus induced after discharges in the evaluation of peripheral nerve hyperexcitability: Old wine in a new bottle?


Journal

Journal of the peripheral nervous system : JPNS
ISSN: 1529-8027
Titre abrégé: J Peripher Nerv Syst
Pays: United States
ID NLM: 9704532

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 04 08 2020
revised: 01 10 2020
accepted: 05 11 2020
pubmed: 13 11 2020
medline: 6 11 2021
entrez: 12 11 2020
Statut: ppublish

Résumé

Limited literature is available on stimulus induced after discharges (SIAD) in patients with peripheral nerve hyperexcitability (PNH). The aim of the study was to examine the diagnostic utility of SIAD in the diagnosis and monitoring of primary PNH disorders. In this retrospective study, we studied 26 patients who were admitted with a diagnosis of primary PNH to the department of Neurology from January 2013 to April 2019. Their clinical profile, immunological characteristics were extracted from the database and nerve conduction studies were relooked for the presence of SIAD. 76% of patients in the primary PNH cohort had SIAD with 90% of them being voltage-gated potassium channel complex antibody positive; predominantly against contactin-associated protein-2 antigen and rest being paraneoplastic. There was also resolution of SIAD following treatment indicating reversible hyperexcitability. SIAD is a sensitive marker for Primary PNH syndrome with monitoring and diagnostic implications.

Identifiants

pubmed: 33179828
doi: 10.1111/jns.12422
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

90-98

Informations de copyright

© 2020 Peripheral Nerve Society.

Références

Katirji B. Peripheral nerve hyperexcitability. Handbook of Clinical Neurology. Vol 161. Amsterdam, Netherlands: Elsevier; 2019:281-290. https://doi.org/10.1016/B978-0-444-64142-7.00054-0.
Irani SR, Alexander S, Waters P, et al. Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia. Brain. 2010;133(9):2734-2748. https://doi.org/10.1093/brain/awq213.
Hart IK. Phenotypic variants of autoimmune peripheral nerve hyperexcitability. Brain. 2002;125(8):1887-1895. https://doi.org/10.1093/brain/awf178.
Benatar M, Chapman KM, Rutkove SB. Repetitive nerve stimulation for the evaluation of peripheral nerve hyperexcitability. J Neurol Sci. 2004;221(1-2):47-52. https://doi.org/10.1016/j.jns.2004.03.025.
Niu J, Guan H, Cui L, Guan Y, Liu M. Afterdischarges following M waves in patients with voltage-gated potassium channels antibodies. Clin Neurophysiol Pract. 2017;2:72-75. https://doi.org/10.1016/j.cnp.2017.02.002.
Rubio-Agusti I, Perez-Miralles F, Sevilla T, et al. Peripheral nerve hyperexcitability: a clinical and immunologic study of 38 patients. Neurology. 2011;76(2):172-178. https://doi.org/10.1212/WNL.0b013e3182061b1e.
van Sonderen A, Ariño H, Petit-Pedrol M, et al. The clinical spectrum of Caspr2 antibody-associated disease. Neurology. 2016;87(5):521-528. https://doi.org/10.1212/WNL.0000000000002917.
Liewluck T, Klein CJ, Jones LK. Cramp-fasciculation syndrome in patients with and without neural autoantibodies: cramp-fasciculation syndrome. Muscle Nerve. 2014;49(3):351-356. https://doi.org/10.1002/mus.23935.
Preston DC, Shapiro BE. Electromyography and Neuromuscular Disorders: Clinical-Electrophysiologic Correlations. 3rd ed. Philadelphia, PA: Saunders Press; 2013.
Bodkin CL, Kennelly KD, Boylan KB, Crook JE, Heckman MG, Rubin DI. Defining normal duration for afterdischarges with repetitive nerve stimulation: a pilot study. J Clin Neurophysiol off Publ Am Electroencephalogr Soc. 2009;26(1):45-49. https://doi.org/10.1097/WNP.0b013e3181968f00.
Tankisi H, Burke D, Cui L, et al. Standards of instrumentation of EMG. Clin Neurophysiol. 2020;131(1):243-258. https://doi.org/10.1016/j.clinph.2019.07.025.
Fisher MA. H-reflex and F-response studies. Aminoff's Electrodiagnosis in Clinical Neurology. New York, NY: Churchill Livingstone; 2012:407-420. https://doi.org/10.1016/B978-1-4557-0308-1.00018-2.
Nobrega JAM, Pinheiro DS, Manzano GM, Kimura J. Various aspects of F-wave values in a healthy population. Clin Neurophysiol off J Int Fed Clin Neurophysiol. 2004;115(10):2336-2342. https://doi.org/10.1016/j.clinph.2004.05.011.
Arimura K, Arimura Y, Ng A, et al. The origin of spontaneous discharges in acquired neuromyotonia. A macro EMG study. Clin Neurophysiol. 2005;116(8):1835-1839. https://doi.org/10.1016/j.clinph.2005.03.023.
Engel AG, ed. Myasthenia Gravis and Myasthenic Disorders. Oxford, UK: Oxford University Press; 2012. https://doi.org/10.1093/med/9780199738670.001.0001.
Watanabe O. Isaacs's syndrome and associated diseases. Rinsho Shinkeigaku. 2013;53(11):1067-1070. https://doi.org/10.5692/clinicalneurol.53.1067.
Maddison P, Mills KR, Newsom-Davis J. Clinical electrophysiological characterization of the acquired neuromyotonia phenotype of autoimmune peripheral nerve hyperexcitability. Muscle Nerve. 2006;33(6):801-808. https://doi.org/10.1002/mus.20536.
Panagariya A, Kumar H, Mathew V, Sharma B. Neuromyotonia: clinical profile of twenty cases from Northwest India. Neurol India. 2006;54(4):382-386. https://doi.org/10.4103/0028-3886.28110.
Khwaja GA, Batla A, Patidar Y, et al. Clinical and electrophysiological profile of Isaac's syndrome: a report of six cases. 2015;16(3):4.
Merchut MP. Management of voltage-gated potassium channel antibody disorders. Neurol Clin. 2010;28(4):941-959. https://doi.org/10.1016/j.ncl.2010.03.024.
Tanosaki M, Baba M, Miura H, Matsunaga M, Arimura K. Reversible F-wave hyperexcitability associated with antibodies to potassium channels in Isaacs' syndrome. Eur J Neurol. 1999;6(1):95-98. https://doi.org/10.1046/j.1468-1331.1999.610095.x.

Auteurs

Aditya Vijayakrishnan Nair (AV)

Department of Neurology, Christian Medical College, Vellore, India.

Arun Mani (A)

Department of Neurology, Christian Medical College, Vellore, India.

Asish Vijayaraghavan (A)

Department of Neurology, Christian Medical College, Vellore, India.

Pullumpallil Alexander (P)

Department of Neurology, Christian Medical College, Vellore, India.

Atif Shaikh (A)

Department of Neurology, Christian Medical College, Vellore, India.

Rohit Ninan (R)

Department of Neurology, Christian Medical College, Vellore, India.

A T Prabhakar (AT)

Department of Neurology, Christian Medical College, Vellore, India.

Ajith Sivadasan (A)

Department of Neurology, Christian Medical College, Vellore, India.

Sanjit Aaron (S)

Department of Neurology, Christian Medical College, Vellore, India.

John Jude (J)

Department of Clinical Microbiology, Christian Medical College, Vellore, India.

Vivek Mathew (V)

Department of Neurology, Christian Medical College, Vellore, India.

Mathew Alexander (M)

Department of Neurology, Christian Medical College, Vellore, India.

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