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Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP.

Abstract
To identify clinical and electrophysiologic features related to IV immunoglobulin (IVIg) responsiveness in chronic inflammatory demyelinating polyneuropathy (CIDP), the authors conducted a multicenter study on 312 patients with CIDP (199 responders and 113 nonresponders). Muscle atrophy and decreased compound muscle action potential were pronounced in nonresponders of IVIg. Male gender, longer disease duration, and slow progression of symptoms were also associated with IVIg unresponsiveness. Features suggesting axonal dysfunction in peripheral nerves indicated IVIg unresponsiveness in CIDP.
AuthorsM Iijima, M Yamamoto, M Hirayama, F Tanaka, M Katsuno, K Mori, H Koike, N Hattori, K Arimura, M Nakagawa, H Yoshikawa, K Hayasaka, O Onodera, M Baba, H Yasuda, T Saito, M Nakazato, K Nakashima, J Kira, R Kaji, N Oka, G Sobue
JournalNeurology (Neurology) Vol. 64 Issue 8 Pg. 1471-5 (Apr 26 2005) ISSN: 1526-632X [Electronic] United States
PMID15851750 (Publication Type: Clinical Trial, Journal Article, Multicenter Study)
Chemical References
  • Immunoglobulins, Intravenous
Topics
  • Adult
  • Age of Onset
  • Aged
  • Axons (drug effects, immunology, pathology)
  • Disease Progression
  • Drug Resistance (immunology)
  • Female
  • Humans
  • Immunoglobulins, Intravenous (pharmacology, therapeutic use)
  • Male
  • Middle Aged
  • Motor Neurons (drug effects, immunology, pathology)
  • Muscular Atrophy (drug therapy, immunology, physiopathology)
  • Neural Conduction (drug effects, immunology)
  • Neurons, Afferent (drug effects, immunology, pathology)
  • Peripheral Nerves (drug effects, immunology, physiopathology)
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (drug therapy, immunology, physiopathology)
  • Sex Factors
  • Treatment Outcome

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