EMG Blind Spots: What Your Study Can Miss Disorders of the NMJ W. David Arnold, MD AAPMR 2014 Outline • Review of Prototypical NMJ Disorder, Myasthenia Gravis, and the General Approach to NMJ Disorders • Review a series of 4 Cases to Highlight Potential Pitfalls and Key Concepts in NMJ Edx studies Case 1: “Proximal Limb Weakness” • 18 year old woman presents with a progressive proximal limb weakness is sent to the EMG Lab Limb Girdle Muscular Dystrophy? • Examination: – 4 grade proximal limb weakness – Normal bulbar strength, sensation, and reflexes Case 1: NCS and EMG • Normal median sensory and motor response • EMG: short duration, small amplitude motor unit action potentials with early recruitment without fibrillations Case 1: Proximal Limb Weakness (Cont.) • EMG and NCS: Non-irritable myopathy • Diagnostic consideration was given to a possible limb girdle muscular dystrophy • Muscle Biopsy: normal • Thoughts? Case 1: Additional Studies • Repetitive ulnar nerve stimulation at 3 Hz ~50% decrement • SFEMG Increased jitter and blocking Follow up Lab testing: – Elevated acetylcholine receptor antibodies Diagnosis: acetylocholine receptor antibody positive myasthenia gravis (MG) Treatment: Excellent response to pyridostigmine and immunomodulatory treatments Clinical Pearl of Case 1: Ask the Correct Question 338 charts of patients with NMJ disorders 6 patients underwent muscle biopsy for possible myopathy 2 with coexistent inflammatory muscle dz 4 with NMJ disorders mimicking myopathy (based on normal muscle bx) Consider RNS in patients with weakness MG • MG is the most common NMJ disorder • Prevalence of 20 in 100,000 and incidence of 2 per 100,000. (Phillips Ann N Y Acad Sci. 2003) • Antibodies – Ach receptor antibodies (80%) – Muscle specific tyrosine kinase (MuSK) (10%) – Antibody negative (5%-10%) • Treated with cholinesterase inhibitors and immunomodulatory treatments NMJ Disorders: History • Weakness: proximal muscles with fatigability – Severity of involvement: Ocular>bulbar>limb>respiratory • Sensory: No sensory loss, paresthesia, or neuropathic pain • Autonomic: dry mouth, blurry vision, impotence, constipation, and difficulty with urination – Some disorders such as Lambert Eaton myasthenic syndrome (LEMS) and botulism Generalized fatigue ≠ NMJ disorder NMJ Disorders: Examination • Weakness in proximal limb, ocular, and bulbar muscles – Distal or focal weakness may occur in 12% of MG (Wirtz et al 2002) – Extraocular and bulbar weakness are early and prominent in MG and botulism – Less prominent extraocular weakness in LEMS • Reflexes are normal in postsynaptic disorders such as myasthenia gravis but characteristically absent or reduced in presynaptic NMJ d/o • Sensory function is normal • Pupillary responses are usually reduced in botulism Post-synaptic NMJ disorders • Sensory NCS -normal • Motor NCS -usually normal CMAP amplitude • EMG -Possibly short duration, low amplitude, unstable MUAP’s if severe (Jiggle) • Slow RNS (3 Hz) -decrement (60-80% of generalized MG) • CMAP with 10 sec exercise (or Rapid RNS, 20-50 Hz) -no increment • CMAP with Exercise -no increment • SFEMG -Jitter and blocking (95-98% MG) (Nl jitter in weak muscle ≠ MG) Post-synaptic NMJ disorder Pre-synaptic NMJ disorder Sensory NCS -normal Motor NCS -usually low CMAP amplitude EMG -Possibly short duration, low amplitude, unstable MUAP’s if severe -some disorders with fibrillations (botulism) Slow RNS (3 Hz) -decrement CMAP with 10 sec exercise (or Rapid RNS, 20-50 Hz) -increment 300% in one muscle or 100% in three (diagnostic for Lambert Eaton MS) SFEMG -Jitter and blocking (jitter and blocking decrease with increasing firing rate) Presynaptic NMJ Pre-exercise Post-exercise 350% increment following 10 seconds exercise Case 2: Dysarthria • 64 year old woman with symptoms of progressive dysarthria and facial weakness is sent to the EMG Lab Possible myasthenia gravis? • Examination – – – – Mild facial and moderate tongue weakness Tongue fasciculations Normal limb strength Generalized Brisk reflexes and jaw jerk Case 2: Nerve Conduction Studies Median and ulnar sensory responses are normal Median and ulnar motor responses are normal Repetitive nerve stimulation at 3 Hz -Orbicularis Oris with >20% decrement Myasthenia Gravis? Case 2: Electromyography Single Fiber EMG -Increased jitter and blocking in frontalis and extensor digitorum EMG Fibrillations/fasciculations/ dec recruitment/enlarged motor unit action potentials (mentalis and tongue) Limb muscles normal Jitter and Blocking Example: Post-synaptic NMJ disorder Case 2 Clinical Pearl of Case 2: Not all that Jitters is Myasthenia the “False Positive” test Amyotrophic Lateral Sclerosis & NMJ transmission defect • Severe decrement frequently seen on RNS (reported up to 35% of CMAP amplitude) (I have seen up to 50%) • Increased decrement correlates with faster progression and worse prognosis Daube 2004; Wang 2001 • SFEMG: increased jitter and block may be early finding, prior to denervation (also seen in early reinnervation) • Axonal Stimulation SFEMG: lack of facilitation with increasing frequency of stimulation Arimura 1995 Case 3: Seronegative MG A 58 year old woman with a 30 year history of seronegative myasthenia gravis PMH: poliomyelitis at age 6 requiring ventilation support in an iron lung for a month PE: normal CN exam, severe proximal limb weakness with fatigability, normal sensation and reflexes Case 3: Seronegative MG • 3Hz RNS with up to 70% decrement in proximal muscles • She describes dramatic improvement with pyridostigmine • Worsening with prednisone • No improvement with IVIG or PLEX • Ideas? Clinical Pearl of Case 3: Hoof beats (aka decrement)? Don’t assume it is a horse (MG) – Multiple NMJ disorders may fall within this clinical presentation • Seronegative (autoimmune) MG • Congenital Myasthenic syndromes • Other neuromuscular disorders with secondary NMJ effects or clinical patterns similar to NMJ disorders Congenital Myasthenic Syndrome • Historical points in case 3 suggesting this possibility: – No clear response to immunomodulation – Atypical phenotype (Severe disease with minimal to no bulbar involvement) – PMH of “polio” after which she states she was “normal” in every way until developing weakness in her 20’s – On more direct questions she described being a “blue baby” at birth • Electrodiagnosis of CMS Case 4: MG second opinion 45 year old man with progressive ptosis, dysphagia FH: mother with “seronegative myasthenia gravis” Examination: bilateral ptosis and extraocular muscle weakness without clear fatigability; mild proximal limb weakness Antibody testing: AChR and MuSK Antibodies (-) EMG and NCS: decrement on repetitive nerve stimulation studies Diagnosed with seronegative myasthenia gravis but then had minimal response to immune therapies and pyridostigmine? Ideas? Case 4: Repeat EMG and NCS • NCS: multiple mononeuropathies c/w the patient’s known HNPP • RNS: normal • SFEMG: mildly increased jitter in frontalis with no blocking • EMG: Short duration small amplitude motor unit action potentials with sparse fibrillations in proximal limb and facial muscles Case 4: Pre and Post Surgery Images Clinical Pearl of Case 4: When in doubt, trust your exam… double check technique Movement artifact is significant challenge in repetitive nerve stimulation and can lead to false positive tests Our patient: • Lacked clinical features of fatigability or response to treatment • Diagnosed with oculopharyngeal muscular dystrophy (OPMD) – – – – Autosomal dominant slowly progressive hereditary muscle disorder GCG repeat expansion (8-13) Often mistaken for seronegative MG Typically later/less involvement of extraocular muscles Thanks! Questions? [email protected] References 1. 2. 3. 4. 5. 6. 7. 8. Phillips LH, 2nd. The epidemiology of myasthenia gravis. 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