Literature DB >> 28719826

The terminal latency of the phrenic nerve correlates with respiratory symptoms in amyotrophic lateral sclerosis.

Jin-Sung Park1, Donghwi Park2.   

Abstract

OBJECTIVE: The aim of the study was to investigate the electrophysiological parameters in phrenic nerve conduction studies (NCS) that sensitively reflect latent respiratory insufficiency present in amyotrophic lateral sclerosis (ALS).
METHOD: Forty-nine patients with ALS were examined, and after exclusion, 21 patients with ALS and their phrenic NCS results were reviewed. The patients were divided into two groups according to their respiratory sub-score in the ALS functional rating scale - revised (Group A, sub-score 12vs. Group B, sub-score 11). We compared the parameters of phrenic NCS between the two groups.
RESULTS: There were no significant differences in the clinical characteristics between the two groups. Using a multivariate model, we found that the terminal latency of the phrenic nerve was the only parameter that was associated with early symptoms of respiratory insufficiency (p<0.05). The optimal cutoff value for the terminal latency of the phrenic nerve was 7.65ms (sensitivity 80%, specificity 68.2%).
CONCLUSION: The significantly prolonged terminal latency of the phrenic nerve in our study may reflect a profound distal motor axonal dysfunction of the phrenic nerve in patients with ALS in the early stage of respiratory insufficiency that can be used as a sensitive electrophysiological marker reflecting respiratory symptoms in ALS. SIGNIFICANCE: The terminal latency of the phrenic nerve is useful for early detection of respiratory insufficiency in patients with ALS.
Copyright © 2017. Published by Elsevier B.V.

Entities:  

Keywords:  ALSFRS-R; Amyotrophic lateral sclerosis; Distal axonopathy; Phrenic nerve; Terminal latency

Mesh:

Year:  2017        PMID: 28719826     DOI: 10.1016/j.clinph.2017.06.039

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  3 in total

1.  Under-recognized primary spontaneous pneumothorax in ALS: a multicenter retrospective study.

Authors:  Jin-Sung Park; Young Woo Do; Jin-Mo Park; Hung Youl Seok; Donghwi Park
Journal:  Neurol Sci       Date:  2019-07-02       Impact factor: 3.307

2.  Complexity Measures of Heart-Rate Variability in Amyotrophic Lateral Sclerosis with Alternative Pulmonary Capacities.

Authors:  Renata M M Pimentel; Celso Ferreira; Vitor Valenti; David M Garner; Hugo Macedo; Acary S Bulle Oliveira; Francisco Naildo Cardoso Leitão; Luiz Carlos de Abreu
Journal:  Entropy (Basel)       Date:  2021-01-28       Impact factor: 2.524

3.  Multiparametric Analysis of Sniff Nasal Inspiratory Pressure Test in Middle Stage Amyotrophic Lateral Sclerosis.

Authors:  Antonio Sarmento; Andrea Aliverti; Layana Marques; Francesca Pennati; Mario Emílio Dourado-Júnior; Guilherme Fregonezi; Vanessa Resqueti
Journal:  Front Neurol       Date:  2018-05-02       Impact factor: 4.003

  3 in total

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