Literature DB >> 26296515

Salbutamol and ephedrine in the treatment of severe AChR deficiency syndromes.

Pedro M Rodríguez Cruz, Jacqueline Palace, Hayley Ramjattan, Sandeep Jayawant, Stephanie A Robb, David Beeson.   

Abstract

OBJECTIVE: To evaluate the response to salbutamol and ephedrine in the treatment of congenital myasthenic syndromes due to CHRNE mutations causing severe acetylcholine receptor (AChR)deficiency.
METHODS: A cohort study of 6 patients with severe AChR deficiency, symptomatic despite optimal therapy with anticholinesterase and 3,4-diaminopyridine, were analyzed for their response to the addition of salbutamol or ephedrine to their medication. Baseline quantitative myasthenia gravis (QMG) (severity) scores were worse than 15 of 39. Patients were assessed in clinic with QMG and mobility scores. Pretreatment and 6- to 8-month follow-up scores were evaluated.
RESULTS: All 6 patients tolerated treatment well and reported no side effects. There was a strong positive response to treatment over the 6- to 8-month assessment period with significant improvement in QMG (p = 0.027) and mobility scores. The analysis of subcomponents of the QMG score revealed marked improvement in upper (p = 0.028) and lower (p = 0.028) limb raise times. All patients reported enhanced activities of daily living at 6 to 8 months.
CONCLUSIONS: Oral salbutamol and ephedrine appear to be effective treatments in severe cases ofAChR deficiency on pyridostigmine. They are well tolerated and improvement in strength can be dramatic. Classification of evidence: This study provides Class IV evidence that salbutamol or ephedrine improves muscle strength in patients with congenital myasthenia from severe AChR deficiency.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26296515      PMCID: PMC4603597          DOI: 10.1212/WNL.0000000000001952

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  20 in total

1.  Agrin acts via a MuSK receptor complex.

Authors:  D J Glass; D C Bowen; T N Stitt; C Radziejewski; J Bruno; T E Ryan; D R Gies; S Shah; K Mattsson; S J Burden; P S DiStefano; D M Valenzuela; T M DeChiara; G D Yancopoulos
Journal:  Cell       Date:  1996-05-17       Impact factor: 41.582

2.  Congenital endplate acetylcholinesterase deficiency responsive to ephedrine.

Authors:  M Bestue-Cardiel; A Sáenz de Cabezón-Alvarez; J L Capablo-Liesa; J López-Pisón; J L Peña-Segura; J Martin-Martinez; A G Engel
Journal:  Neurology       Date:  2005-07-12       Impact factor: 9.910

3.  Study of long-term anticholinesterase therapy. Effects on neuromuscular transmission and on motor end-plate fine structure.

Authors:  A G Engel; E H Lambert; T Santa
Journal:  Neurology       Date:  1973-12       Impact factor: 9.910

4.  Effects of neostigmine and pyridostigmine at the neuromuscular junction.

Authors:  J D Gillies; J Allen
Journal:  Clin Exp Neurol       Date:  1977

Review 5.  Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America.

Authors:  A Jaretzki; R J Barohn; R M Ernstoff; H J Kaminski; J C Keesey; A S Penn; D B Sanders
Journal:  Neurology       Date:  2000-07-12       Impact factor: 9.910

6.  Congenital myasthenia: end-plate acetylcholine receptors and electrophysiology in five cases.

Authors:  A Vincent; S G Cull-Candy; J Newsom-Davis; A Trautmann; P C Molenaar; R L Polak
Journal:  Muscle Nerve       Date:  1981 Jul-Aug       Impact factor: 3.217

7.  3,4-Diaminopyridine in the treatment of congenital (hereditary) myasthenia.

Authors:  J Palace; C M Wiles; J Newsom-Davis
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-12       Impact factor: 10.154

8.  Influence of chronic neostigmine treatment on the number of acetylcholine receptors and the release of acetylcholine from the rat diaphragm.

Authors:  C C Chang; T F Chen; S T Chuang
Journal:  J Physiol       Date:  1973-05       Impact factor: 5.182

Review 9.  The therapy of congenital myasthenic syndromes.

Authors:  Andrew G Engel
Journal:  Neurotherapeutics       Date:  2007-04       Impact factor: 7.620

10.  Distinct phenotypes of congenital acetylcholine receptor deficiency.

Authors:  G Burke; J Cossins; S Maxwell; S Robb; M Nicolle; A Vincent; J Newsom-Davis; J Palace; D Beeson
Journal:  Neuromuscul Disord       Date:  2004-06       Impact factor: 4.296

View more
  17 in total

1.  Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome.

Authors:  Grace M McMacken; Sally Spendiff; Roger G Whittaker; Emily O'Connor; Rachel M Howarth; Veronika Boczonadi; Rita Horvath; Clarke R Slater; Hanns Lochmüller
Journal:  Hum Mol Genet       Date:  2019-07-15       Impact factor: 6.150

2.  Drug treatment for spinal muscular atrophy types II and III.

Authors:  Renske I Wadman; W Ludo van der Pol; Wendy Mj Bosboom; Fay-Lynn Asselman; Leonard H van den Berg; Susan T Iannaccone; Alexander Fje Vrancken
Journal:  Cochrane Database Syst Rev       Date:  2020-01-06

3.  A Novel Missense Variant in the AGRN Gene; Congenital Myasthenic Syndrome Presenting With Head Drop.

Authors:  Mert Karakaya; Ozge Ceyhan-Birsoy; Alan H Beggs; Haluk Topaloglu
Journal:  J Clin Neuromuscul Dis       Date:  2017-03

Review 4.  Congenital Myasthenic Syndromes: a Clinical and Treatment Approach.

Authors:  Constantine Farmakidis; Mamatha Pasnoor; Richard J Barohn; Mazen M Dimachkie
Journal:  Curr Treat Options Neurol       Date:  2018-07-21       Impact factor: 3.598

5.  A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome.

Authors:  Eduardo de Paula Estephan; Cláudia Ferreira da Rosa Sobreira; André Clériston José Dos Santos; Pedro José Tomaselli; Wilson Marques; Roberta Paiva Magalhães Ortega; Marcela Câmara Machado Costa; André Macedo Serafim da Silva; Rodrigo Holanda Mendonça; Vitor Marques Caldas; Antonio Alberto Zambon; Osório Abath Neto; Paulo Eurípedes Marchiori; Carlos Otto Heise; Umbertina Conti Reed; Yoshiteru Azuma; Ana Töpf; Hanns Lochmüller; Edmar Zanoteli
Journal:  J Neurol       Date:  2018-01-30       Impact factor: 4.849

6.  A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report.

Authors:  Thashi Chang; Judith Cossins; David Beeson
Journal:  BMC Neurol       Date:  2016-10-07       Impact factor: 2.474

Review 7.  Treating pediatric neuromuscular disorders: The future is now.

Authors:  James J Dowling; Hernan D Gonorazky; Ronald D Cohn; Craig Campbell
Journal:  Am J Med Genet A       Date:  2017-09-10       Impact factor: 2.802

8.  Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey.

Authors:  Christopher Cy Mak; Gordon Kc Leung; Gary Tk Mok; Kit San Yeung; Wanling Yang; Cheuk-Wing Fung; Sophelia Hs Chan; So-Lun Lee; Ni-Chung Lee; Rolph Pfundt; Yu-Lung Lau; Brian Hy Chung
Journal:  NPJ Genom Med       Date:  2018-08-06       Impact factor: 8.617

9.  Beta-2 Adrenergic Receptor Agonists Enhance AChR Clustering in C2C12 Myotubes: Implications for Therapy of Myasthenic Disorders.

Authors:  Lisa Clausen; Judith Cossins; David Beeson
Journal:  J Neuromuscul Dis       Date:  2018

Review 10.  The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic Syndromes.

Authors:  Pedro M Rodríguez Cruz; Jacqueline Palace; David Beeson
Journal:  Int J Mol Sci       Date:  2018-06-05       Impact factor: 5.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.