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Can electrophysiology differentiate polyneuropathy with anti-MAG/SGPG antibodies from chronic inflammatory demyelinating polyneuropathy?

AbstractOBJECTIVES:
Patients with polyneuropathy and antibodies to myelin-associated glycoprotein (MAG) and sulphated glucuronyl paragloboside (SGPG) differ from chronic inflammatory demyelinating polyneuropathy (CIDP) because of a slower, progressive course, symmetrical and predominantly sensory involvement of legs, predominantly distal slowing of motor conductions, and poorer response to therapy. We studied whether a wide set of electrophysiologic parameters may differentiate these two neuropathies.
METHODS:
We reviewed the electrophysiological studies of 10 patients with anti-MAG/SGPG antibodies and 22 with CIDP examining: (1) motor conduction velocity and distal compound muscle action potential amplitude; (2) conduction block (CB) and temporal dispersion; (3) distal motor latency and terminal latency index (TLI); (4) F wave and proximal conduction time; and (5) sensory conduction and occurrence of abnormal median with normal sural sensory potential.
RESULTS:
Anti-MAG/SGPG neuropathies showed: (1) more severe involvement of peroneal nerves; (2) more frequent disproportionate distal slowing of motor conductions (TLI< or =0.25) and absent sural potential, and (3) no CB. However 3/22 CIDP patients also had at least two nerves with TLI< or =0.25 and no CB.
CONCLUSIONS:
Electrophysiologic findings suggest in anti-MAG/SGPG neuropathy a length-dependent process with a likely centripetal evolution. A disproportionate slowing of conduction in distal segments of motor nerves suggests the diagnosis of anti-MAG/SGPG neuropathy, although it is not pathognomonic.
AuthorsMargherita Capasso, Filomena Torrieri, Antonio Di Muzio, Maria Vittoria De Angelis, Alessandra Lugaresi, Antonino Uncini
JournalClinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology (Clin Neurophysiol) Vol. 113 Issue 3 Pg. 346-53 (Mar 2002) ISSN: 1388-2457 [Print] Netherlands
PMID11897535 (Publication Type: Journal Article)
Chemical References
  • Autoantibodies
  • Globosides
  • Myelin-Associated Glycoprotein
  • sulfate-3-glucuronyl paragloboside
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Autoantibodies (blood)
  • Diagnosis, Differential
  • Electric Stimulation
  • Electrodiagnosis (methods)
  • Electrophysiology (methods)
  • Female
  • Globosides (immunology)
  • Humans
  • Male
  • Middle Aged
  • Myelin-Associated Glycoprotein (immunology)
  • Neural Conduction
  • Peroneal Nerve (physiopathology)
  • Polyneuropathies (blood, diagnosis, immunology)
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (diagnosis)
  • Predictive Value of Tests
  • Reaction Time
  • Retrospective Studies
  • Sural Nerve (physiopathology)

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