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Disorders of the Neuromuscular Junction

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Electrodiagnostic Medicine

Abstract

The neuromuscular junction (NMJ) may be considered simply a connection between the nerve and muscle fiber. However, it is a specialized synapse which includes complex structures such as the presynaptic nerve terminal, synaptic cleft and a postsynaptic muscle fiber endplate. With the aid of these structures, the NMJ serves as a site for conversion of nerve impulse into an action potential which is required for contraction of skeletal muscle. The NMJ is particularly vulnerable to damage from auto-antibodies (due to lack of blood-nerve barrier) and certain toxins [1]. Genetic disorders that can specifically impair the neuromuscular transmission can result in fatigable weakness which serves as a hallmark feature for NMJ disorders. In this chapter, we will be focusing on the most common disorders of neuromuscular junction transmission such as Myasthenia Gravis (including Congenital Myasthenia Gravis), and Lambert-Eaton Syndrome.

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References

  1. Lang B, Vincent A. Autoimmune disorders of the neuromuscular junction. Curr Opin Pharmacol. 2009 Jun;9(3):336–40.

    Article  CAS  PubMed  Google Scholar 

  2. Nishimune H, Shigemoto K. Practical Anatomy of the Neuromuscular Junction in Health and Disease. Neurol Clin. 2018 May;36(2):231–40.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Ganong WF. Review of medical physiology. 23rd ed. New York: McGraw-Hill Medical; 2010.

    Google Scholar 

  4. Guyton AC. Textbook of medical physiology. 11th ed. Philadelphia: Elsevier Saunders; 2006.

    Google Scholar 

  5. Khurana I Textbook of medical physiology. Elsevier, India; 2015.

    Google Scholar 

  6. Gilhus NE, Verschuuren JJ. Myasthenia gravis: subgroup classification andtherapeutic strategies. Lancet Neurol. 2015 Oct;14(10):1023–36.

    Article  CAS  PubMed  Google Scholar 

  7. Pakzad Z, Aziz T, Oger J. Increasing incidence of myasthenia gravis amongelderly in British Columbia. Canada Neurol. 2011 Apr 26;76(17):1526–8.

    Article  Google Scholar 

  8. Nicolle MW. Myasthenia gravis and lambert-eaton myasthenic syndrome. Continuum (Minneap Minn). 2016 Dec;22 (6, Muscle and Neuromuscular Junction Disorders):1978–2005. Review.

    Google Scholar 

  9. Renton AE, Pliner HA, Provenzano C, Evoli A, Ricciardi R, Nalls MA, et al. A genome-wideassociation study of myasthenia gravis. JAMA Neurol. 2015 Apr;72(4):396–404.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Meriggioli MN, Sanders DB. Autoimmune myasthenia gravis: emerging clinical and biological heterogeneity. Lancet Neurol. 2009;8:475–99.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Querol L, Illa I. Myasthenia and the neuromuscular junction. Curr Opin Neurol. 2013;26:459–65.

    Article  PubMed  Google Scholar 

  12. Skeie GO, Apostolski S, Evoli A, et al. Guidelines for treatment of autoimmune neuromuscular transmission disorders. Eur J Neurol. 2010;17:893–902.

    Article  CAS  PubMed  Google Scholar 

  13. Rodolico C, Toscano A, Autunno M, et al. Limb-girdle myasthenia; clinical, electrophysiological and morphological features in familial and autoimmune cases. Neuromuscul Disord. 2002;12:964–9.

    Article  CAS  PubMed  Google Scholar 

  14. Zhang B, Tzartos JS, Viegas S, et al. Autoantibodies to lipoprotein-related protein 4 in patients with double-negative myasthenia gravis. Arch Neurol. 2012;69:445–51.

    Article  PubMed  Google Scholar 

  15. Leite MI, Jacob S, Viegas S, et al. IgG1 antibodies to acetylcholine receptors in “seronegative” myasthenia gravis. Brain. 2008;131:1940–52.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Jacob S, Viega S, Leite MI. Presence and pathogenic relevance of antibodies to clustered acetylcholine receptor in ocular and generalized myasthenia gravis. Arch Neurol. 2012;69:994–1001.

    Article  PubMed  Google Scholar 

  17. Gasperi C, Melms A, Schoser B, et al. Anti-agrin autoantibodies in myasthenia gravis. Neurology. 2014;82:1976–83.

    Article  CAS  PubMed  Google Scholar 

  18. Gallardo E, Martinez-Hernandez E, Titulaer MJ, et al. Cortactin autoantibodies in myasthenia gravis. Autoimmun Rev. 2014;13:1003–7.

    Article  CAS  PubMed  Google Scholar 

  19. Kerty E, Elsais A, Argov Z, Evoli A, Gilhus NE. EFNS/ENS guidelines for the treatment of ocular myasthenia gravis. Eur J Neurol. 2014;21:687–93.

    Article  CAS  PubMed  Google Scholar 

  20. Chatzistefanou KI, Kouris T, Iliakis E, Piaditis G, Tagaris G, Katsikeris N, Kaltsas G, Apostolopoulos M. The ice pack test in the differential diagnosis ofmyasthenic diplopia. Ophthalmology. 2009 Nov;116(11):2236–43.

    Article  PubMed  Google Scholar 

  21. Oh SJ, Cho HK. Edrophonium responsiveness not necessarily diagnostic of myasthenia gravis. Muscle Nerve. 1990 Mar;13(3):187–91.

    Article  CAS  PubMed  Google Scholar 

  22. Pasnoor M, Dimachkie M, Farmakidis’s C, Barohn R. Diagnosis of myasthenia gravis. Neurol Clin. 2018;36(2):261–74.

    Article  PubMed  Google Scholar 

  23. Albuquerque EX, Rash JE, Mayer RF, Satterfield JR. An electrophysiological andmorphological study of the neuromuscular junction in patients with myastheniagravis. Exp Neurol. 1976 Jun;51(3):536–63.

    Article  CAS  PubMed  Google Scholar 

  24. Albuquerque EX, Warnick JE, Mayer RF, Eldefrawi AT, Eldefrawi ME. Recentadvances in the molecular mechanisms of human and animal models of myastheniagravis. Ann N Y Acad Sci. 1981;377:496–518.

    Article  CAS  PubMed  Google Scholar 

  25. Preston DC, Shapiro BE. Electromyography and neuromuscular disorders e-book: clinical-electrophysiologic correlations (expert consult-online). Elsevier Health Sciences; 2012 Nov 1.

    Google Scholar 

  26. AAEM Quality Assurance Committee. American Association of Electrodiagnostic Medicine. Practice parameter for repetitive nerve stimulation and single fiber EMG evaluation of adults with suspected myasthenia gravis or Lambert-Eaton myasthenic syndrome: summary statement. Muscle Nerve. 2001 Sep;24(9):1236–8.

    Article  Google Scholar 

  27. Litchy WJ, Albers JW Repetitive stimulation an AANEM workshop. https://www.aanem.org/mxonline/resources/downloads/products/REPS.pdf Used on 07/25/2018

  28. Costa J, Evangelista T, Conceição I, de Carvalho M. Repetitive nerve stimulation in myasthenia gravis--relative sensitivity of different muscles. ClinNeurophysiol. 2004 Dec;115(12):2776–82.

    Google Scholar 

  29. Chiou-Tan FY. Electromyographic approach to neuromuscular junction disordersrepetitive nerve stimulation and single-fiber electromyography. Phys Med Rehabil Clin N Am. 2003 May;14(2):387–401. Review

    Google Scholar 

  30. Sarrigiannis PG, Kennett RP, Read S, Farrugia ME. Single-fiber EMG with aconcentric needle electrode: validation in myasthenia gravis. Muscle Nerve. 2006 Jan;33(1):61–5.

    Article  PubMed  Google Scholar 

  31. Srivastava A, Kalita J, Misra UK. A comparative study of single fiberelectromyography and repetitive nerve stimulation in consecutive patients withmyasthenia gravis. Electromyogr Clin Neurophysiol. 2007 Mar-Apr;47(2):93–6.

    CAS  PubMed  Google Scholar 

  32. Gilhus NE. Myasthenia gravis. N Engl J Med. 2016 Dec 29;375(26):2570–81.

    Article  CAS  PubMed  Google Scholar 

  33. Kim JY, Park KD, Richman DP. Treatment of myasthenia gravis based on its immunopathogenesis. J Clin Neurol. 2011 Dec 1;7(4):173–83.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Kesner VG, Oh SJ, Dimachkie MM, Barohn RJ. Lambert-eaton myasthenic syndrome. Neurol Clin. 2018 May 31;36(2):379–94.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Tarr TB, Wipf P, Meriney SD. Synaptic pathophysiology and treatment of Lambert-Eaton myasthenic syndrome. Mol Neurobiol. 2015 Aug 1;52(1):456–63.

    Article  CAS  PubMed  Google Scholar 

  36. Nicole S, Azuma Y, Bauché S, Eymard B, Lochmüller H, Slater C. Congenital Myasthenic syndromes or inherited disorders of neuromuscular transmission: recent discoveries and open questions. J Neuromuscul Dis. 2017;(Preprint):1–6.

    Google Scholar 

  37. Titulaer MJ, Verschuuren JJ. Lambert–Eaton myasthenic syndrome. Ann N Y Acad Sci. 2008 Jun 1;1132(1):129–34.

    Article  PubMed  Google Scholar 

  38. O’Neill JH, Murray NM, Newsom-Davis J. The Lambert-Eaton myasthenic syndrome. A review of 50 cases. Brain. 1988 Jun;111(Pt 3):577–96.

    Article  PubMed  Google Scholar 

  39. Wirtz PW, Willcox N, van der Slik AR, Lang B, Maddison P, Koeleman BP, Giphart MJ, Wintzen AR, Roep BO, Verschuuren JJ. HLA and smoking in prediction and prognosis of small cell lung cancer in autoimmune Lambert-Eaton myasthenic syndrome. J Neuroimmunol. 2005 Feb;159(1–2):230–7.

    Article  CAS  PubMed  Google Scholar 

  40. Wirtz PW, Smallegange TM, Wintzen AR, Verschuuren JJ. Differences in clinical features between the Lambert-Eaton myasthenic syndrome with and without cancer: an analysis of 227 published cases. Clin Neurol Neurosurg. 2002 Sep;104(4):359–63.

    Article  PubMed  Google Scholar 

  41. Payne M, Bradbury P, Lang B, Vincent A, Han C, Newsom-Davis J, Talbot D. Prospective study into the incidence of Lambert Eaton myasthenic syndrome in small cell lung cancer. J Thorac Oncol. 2010 Jan 1;5(1):34–8.

    Article  PubMed  Google Scholar 

  42. Titulaer MJ, Maddison P, Sont JK, et al. Clinical dutch-english lambert-eaton myasthenic syndrome (LEMS) tumor association prediction score accurately predicts small-cell lung cancer in the LEMS. J Clin Oncol. 2011 Mar 1;29(7):902–8.

    Article  PubMed  Google Scholar 

  43. Lennon VA, Kryzer TJ, Griesmann GE, O’Suilleabhain PE, Windebank AJ, Woppmann A, Miljanich GP, Lambert EH. Calcium-channel antibodies in the Lambert-Eatonsyndrome and other paraneoplastic syndromes. N Engl J Med. 1995;332(22):1467–74.

    Article  CAS  PubMed  Google Scholar 

  44. Titulaer MJ, Lang B, Verschuuren JJ. Lambert-Eaton myasthenic syndrome: fromclinical characteristics to therapeutic strategies. Lancet Neurol. 2011 Dec;10(12):1098–107.

    Article  PubMed  Google Scholar 

  45. Titulaer MJ, Lang B, Verschuuren JJ. Lambert-Eaton myasthenic syndrome: fromclinical characteristics to therapeutic strategies. Lancet Neurol. 2011 Dec;10(12):1098–107.

    Article  PubMed  Google Scholar 

  46. Oh SJ, Kurokawa K, Claussen GC, Ryan HF Jr. Electrophysiological diagnosticcriteria of Lambert-Eaton myasthenic syndrome. Muscle Nerve. 2005 Oct;32(4):515–20.

    Article  PubMed  Google Scholar 

  47. Motomura M, Lang B, Johnston I, Palace J, Vincent A, Newsom-Davis J. Incidence of serum anti-P/O-type and anti-N-type calcium channel autoantibodies in theLambert-Eaton myasthenic syndrome. J Neurol Sci. 1997 Mar 20;147(1):35–42.

    Article  CAS  PubMed  Google Scholar 

  48. Sabater L, Titulaer M, Saiz A, Verschuuren J, Güre AO, Graus F. SOX1 antibodies are markers of paraneoplastic Lambert-Eaton myasthenic syndrome. Neurology. 2008 Mar 18;70(12):924–8.

    Article  CAS  PubMed  Google Scholar 

  49. Tim RW, Massey JM, Sanders DB. Lambert-Eaton myasthenic syndrome: electrodiagnostic findings and response to treatment. Neurology. 2000 Jun 13;54(11):2176–8.

    Article  CAS  PubMed  Google Scholar 

  50. Oh SJ, Kim DS, Head TC, Claussen GC. Low-dose guanidine and pyridostigmine: relatively safe and effective long-term symptomatic therapy in Lambert-Eaton myasthenic syndrome. Muscle Nerve. 1997 Sep;20(9):1146–52.

    Article  CAS  PubMed  Google Scholar 

  51. Bain PG, Motomura M, Newsom-Davis J, Misbah SA, et al. Effects of intravenous immunoglobulin on muscle weakness andcalcium-channel autoantibodies in the Lambert-Eaton myasthenic syndrome. Neurology. 1996 Sep;47(3):678–83.

    Article  CAS  PubMed  Google Scholar 

  52. Beeson D, Hantai D, Lochmuller H, Engel AG. 126th international workshop: congenital myasthenic syndromes, 24–26 September 2004, Naarden, The Netherlands. Neuromuscul Disord. 2005;15:498–512.

    Article  PubMed  Google Scholar 

  53. Kinali M, Beeson D, Pitt MC, et al. Congenitalmyasthenic syndromesin childhood: Diagnostic and management challenges. J Neuroimmunol. 2008;201:6e12.

    Google Scholar 

  54. Beeson D, Webster R, Cossins J, et al. Congenital myasthenic syndromes and the formation of the neuromuscular junction. Ann N Y Acad Sci. 2008;1132:99e103.

    Article  CAS  Google Scholar 

  55. Engel AG. The therapy of congenital myasthenic syndromes. Neurotherapeutics. 2007 Apr 1;4(2):252–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Barišić N, Chaouch A, Müller JS, Lochmüller H. Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes. Eur J Paediatr Neurol. 2011 May 1;15(3):189–96.

    Article  PubMed  Google Scholar 

  57. Shieh PB, Oh SJ. Congenital Myasthenic Syndromes. Neurol Clin. 2018 May 31;36(2):367–78.

    Article  PubMed  Google Scholar 

  58. Lorenzoni PJ, Scola RH, Kay CS, Werneck LC. Congenital myasthenic syndrome: a brief review. Pediatr Neurol. 2012 Mar 1;46(3):141–8.

    Article  PubMed  Google Scholar 

  59. Ohno K, Tsujino A, Brengman JM, Harper CM, Bajzer Z, Udd B, Beyring R, Robb S, Kirkham FJ, Engel AG. Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans. Proc Natl Acad Sci. 2001 Feb 13;98(4):2017–22.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Byring RF, Pihko H, Tsujino A, Shen XM, Gustafsson B, Hackman P, Ohno K, Engel AG, Udd B. Congenital myasthenic syndrome associated with episodic apnea and sudden infant death. Neuromuscul Disord. 2002 Aug 1;12(6):548–53.

    Article  CAS  PubMed  Google Scholar 

  61. Maselli RA, Chen D, Mo D, Bowe C, Fenton G, Wollmann RL. Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Muscle Nerve: Official Journal of the American Association of Electrodiagnostic Medicine. 2003 Feb;27(2):180–7.

    Article  CAS  Google Scholar 

  62. Schara U, Christen HJ, Durmus H, Hietala M, Krabetz K, Rodolico C, Schreiber G, Topaloglu H, Talim B, Voss W, Pihko H. Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Eur J Paediatr Neurol. 2010 Jul 1;14(4):326–33.

    Article  PubMed  Google Scholar 

  63. Donger C, Krejci E, Serradell AP, Eymard B, et al. Mutation in the humanacetylcholinesterase-associated collagen gene, COLQ, is responsible forcongenital myasthenic syndrome with end-plate acetylcholinesterase deficiency(Type Ic). Am J Hum Genet. 1998 Oct;63(4):967–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Aldunate R, Casar JC, Brandan E, Inestrosa NC. Structural and functional organization of synaptic acetylcholinesterase. Brain Res Rev. 2004 Dec 1;47(1–3):96–104.

    Article  CAS  PubMed  Google Scholar 

  65. Bestue-Cardiel M, de Cabezón-Alvarez AS, Capablo-Liesa JL, López-Pisón J, Peña-Segura JL, Martin-Martinez J, Engel AG. Congenital endplate acetylcholinesterase deficiency responsive to ephedrine. Neurology. 2005 Jul 12;65(1):144–6.

    Article  CAS  PubMed  Google Scholar 

  66. Unwin N. Structure and action of the nicotinic acetylcholine receptor explored by electron microscopy. FEBS Lett. 2003 Nov 27;555(1):91–5.

    Article  CAS  PubMed  Google Scholar 

  67. Palace J, Beeson D. The congenital myasthenic syndromes. J Neuroimmunol. 2008 Sep 15;201–202:2–5.

    Article  PubMed  CAS  Google Scholar 

  68. Liewluck T, Selcen D, Engel AG. Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok-7 myasthenia. Muscle Nerve. 2011 Nov;44(5):789–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Harper CM, Engel AG. Quinidine sulfate therapy for the slow-channel congenitalmyasthenic syndrome. Ann Neurol. 1998 Apr;43(4):480–4.

    Article  CAS  PubMed  Google Scholar 

  70. Engel AG, Shen XM, Selcen D, Sine SM. What have we learned from the congenital myasthenic syndromes. J Mol Neurosci. 2010 Jan;40(1–2):143–53.

    Article  CAS  PubMed  Google Scholar 

  71. Selcen D, Milone M, Shen XM, Harper CM, Stans AA, Wieben ED, Engel AG. Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients. Ann Neurol: Official Journal of the American Neurological Association and the Child Neurology Society. 2008 Jul;64(1):71–87.

    Article  CAS  Google Scholar 

  72. Schara U, Barisic N, Deschauer M, Lindberg C, Straub V, Strigl-Pill N, Wendt M, Abicht A, Müller JS, Lochmüller H. Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations. Neuromuscul Disord. 2009 Dec 1;19(12):828–32.

    Article  CAS  PubMed  Google Scholar 

  73. Ohno K, Engel AG, Shen XM, Selcen D, Brengman J, Harper CM, Tsujino A, Milone M. Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome. Am J Hum Genet. 2002 Apr 1;70(4):875–85.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  74. Habbout K, Poulin H, Rivier F, Giuliano S, Sternberg D, Fontaine B, Eymard B, Morales RJ, Echenne B, King L, Hanna MG. A recessive Nav1. 4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology. 2016 Jan 12;86(2):161–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Huzé C, Bauché S, Richard P, Chevessier F, Goillot E, Gaudon K, Ammar AB, Chaboud A, Grosjean I, Lecuyer HA, Bernard V. Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. Am J Hum Genet. 2009 Aug 14;85(2):155–67.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  76. Gibbs EM, Clarke NF, Rose K, Oates EC, Webster R, Feldman EL, Dowling JJ. Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy. J Mol Med. 2013 Jun 1;91(6):727–37.

    Article  CAS  PubMed  Google Scholar 

  77. Claeys KG, Maisonobe T, Böhm J, Laporte J, Hezode M, Romero NB, Brochier G, Bitoun M, Carlier RY, Stojkovic T. Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation. Neurology. 2010 Feb 9;74(6):519–21.

    Article  CAS  PubMed  Google Scholar 

  78. Robb SA, Sewry CA, Dowling JJ, Feng L, Cullup T, Lillis S, Abbs S, Lees MM, Laporte J, Manzur AY, Knight RK. Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies. Neuromuscul Disord. 2011 Jun 1;21(6):379–86.

    Article  PubMed  Google Scholar 

Suggested Reading

  • Selvan VA. Single-fiber EMG: a review. Ann Indian Acad Neurol. 2011 Jan;14(1):64.

    Article  PubMed  PubMed Central  Google Scholar 

  • Liveson JA, Ma DM. Laboratory reference for clinical neurophysiology. Oxford: Oxford University Press; 1992.

    Google Scholar 

  • Jabre JF, Chirico-Post J, Weiner M. Stimulation SFEMG in myasthenia gravis. Muscle Nerve: Official Journal of the American Association of Electrodiagnostic Medicine. 1989 Jan;12(1):38–42.

    Article  CAS  Google Scholar 

  • Sanders DB. Clinical impact of single-fiber electromyography. Muscle Nerve. 2002;Suppl 11:S15–20.

    Article  Google Scholar 

  • Bromberg MB, Scott DM. Single fiber EMG reference values: reformatted in tabular form. AD HOC Committee of the AAEM Single Fiber Special Interest Group. Muscle Nerve. 1994;17(7):820–1.

    Article  CAS  PubMed  Google Scholar 

  • Howard JF Jr. Electrodiagnosis of disorders of neuromuscular transmission. Phys Med Rehabil Clin N Am. 2013 Feb;24(1):169–92.

    Article  PubMed  Google Scholar 

  • Titulaer MJ, Klooster R, Potman M, et al. SOX antibodies in small-cell lung cancer and Lambert-Eaton myasthenic syndrome: frequency and relation with survival. J Clin Oncol. 2009 Sep 10;27(26):4260–7.

    Article  CAS  PubMed  Google Scholar 

  • Molgó J, Lundh H, Thesleff S. Potency of 3,4-diaminopyridine and4-aminopyridine on mammalian neuromuscular transmission and the effect of pHchanges. Eur J Pharmacol. 1980 Jan 11;61(1):25–34.

    Article  PubMed  Google Scholar 

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Govindarajan, R., Nagarajan, E. (2021). Disorders of the Neuromuscular Junction. In: Galvez-Jimenez, N., Soriano, A., Morren, J.A. (eds) Electrodiagnostic Medicine. Springer, Cham. https://doi.org/10.1007/978-3-030-74997-2_10

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