Prevalence of Anti-Ganglioside Antibodies and Their Clinical Correlates with Guillain-Barré Syndrome in Korea: A Nationwide Multicenter Study
2
조회
0
다운로드
23
인용
0
참고문헌
키워드
초록
Background and Purpose No previous studies have investigated the relationship betweenvarious anti-ganglioside antibodies and the clinical characteristics of Guillain-Barré syndrome(GBS) in Korea. The aim of this study was to determine the prevalence and types of anti-ganglioside antibodies in Korean GBS patients, and to identify their clinical significance. Methods Serum was collected from patients during the acute phase of GBS at 20 universitybased hospitals in Korea. The clinical and laboratory findings were reviewed and compared withthe detected types of anti-ganglioside antibody. Results Among 119 patients, 60 were positive for immunoglobulin G (IgG) or immunoglobulin M antibodies against any type of ganglioside (50%). The most frequent type was IgG anti-GM1 antibody (47%), followed by IgG anti-GT1a (38%), IgG anti-GD1a (25%), and IgG anti-GQ1b (8%) antibodies. Anti-GM1-antibody positivity was strongly correlated with the presenceof preceding gastrointestinal infection, absence of sensory symptoms or signs, and absence ofcranial nerve involvement. Patients with anti-GD1a antibody were younger, predominantlymale, and had more facial nerve involvement than the antibody-negative group. Anti-GT1a-antibody positivity was more frequently associated with bulbar weakness and was highly associated with ophthalmoplegia when coupled with the coexisting anti-GQ1b antibody. Despite the presence of clinical features of acute motor axonal neuropathy (AMAN), 68% of anti-GM1- oranti-GD1a-antibody-positive cases of GBS were diagnosed with acute inflammatory demyelinating polyradiculoneuropathy (AIDP) by a single electrophysiological study. Conclusions Anti-ganglioside antibodies were frequently found in the serum of KoreanGBS patients, and each antibody was correlated strongly with the various clinical manifestations. Nevertheless, without an anti-ganglioside antibody assay, in Korea AMAN is frequentlymisdiagnosed as AIDP by single electrophysiological studies.
Abstract
Background and Purpose No previous studies have investigated the relationship betweenvarious anti-ganglioside antibodies and the clinical characteristics of Guillain-Barré syndrome(GBS) in Korea. The aim of this study was to determine the prevalence and types of anti-ganglioside antibodies in Korean GBS patients, and to identify their clinical significance. Methods Serum was collected from patients during the acute phase of GBS at 20 universitybased hospitals in Korea. The clinical and laboratory findings were reviewed and compared withthe detected types of anti-ganglioside antibody. Results Among 119 patients, 60 were positive for immunoglobulin G (IgG) or immunoglobulin M antibodies against any type of ganglioside (50%). The most frequent type was IgG anti-GM1 antibody (47%), followed by IgG anti-GT1a (38%), IgG anti-GD1a (25%), and IgG anti-GQ1b (8%) antibodies. Anti-GM1-antibody positivity was strongly correlated with the presenceof preceding gastrointestinal infection, absence of sensory symptoms or signs, and absence ofcranial nerve involvement. Patients with anti-GD1a antibody were younger, predominantlymale, and had more facial nerve involvement than the antibody-negative group. Anti-GT1a-antibody positivity was more frequently associated with bulbar weakness and was highly associated with ophthalmoplegia when coupled with the coexisting anti-GQ1b antibody. Despite the presence of clinical features of acute motor axonal neuropathy (AMAN), 68% of anti-GM1- oranti-GD1a-antibody-positive cases of GBS were diagnosed with acute inflammatory demyelinating polyradiculoneuropathy (AIDP) by a single electrophysiological study. Conclusions Anti-ganglioside antibodies were frequently found in the serum of KoreanGBS patients, and each antibody was correlated strongly with the various clinical manifestations. Nevertheless, without an anti-ganglioside antibody assay, in Korea AMAN is frequentlymisdiagnosed as AIDP by single electrophysiological studies.
참고문헌 (36)
- Asbury AK, "Assessment of current diagnostic criteria for Guillain-Barré syndrome", Ann Neurol, 27(Suppl), pp.S21~S24 (1990)
- Hughes RA, "Guillain-Barré syndrome", Lancet, 66, pp.1653~1666 (2005)
- Kusunoki S, "Experimental sensory neuropathy induced by sensitization with ganglioside GD1b", Ann Neurol, 39, pp.424~431 (1996)
- Yuki N, "Animal model of axonal Guillain-Barré syndrome induced by sensitization with GM1 ganglioside", Ann Neurol, 49, pp.712~720 (2001)
- Yuki N., "Ganglioside mimicry and peripheral nerve disease", Muscle Nerve, 35, pp.691~711 (2007)
- Sekiguchi Y, "Antiganglioside antibodies are associated with axonal Guillain-Barrésyndrome: a Japanese-Italian collaborative study", J Neurol Neurosurg Psychiatry, 83, pp.23~28 (2012)
- Uncini A, "Pitfalls in electrodiagnosis of Guillain-Barré syndrome subtypes", J Neurol Neurosurg Psychiatry, 81, pp.1157~1163 (2010)
- Lee SH, "Acute ophthalmoplegia (without ataxia) associated with anti-GQ1b antibody", Neurology, 71, pp.426~429 (2008)
- Nagashima T, "Clinical correlates of serum anti-GT1a IgG antibodies", J Neurol Sci, 219, pp.139~145 (2004)
- Miyazaki T, "Guillain-Barré syndrome associated with IgG monospecific to ganglioside GD1b", Neurology, 56, pp.1227~1229 (2001)
- Kusunoki S, "Nacetylgalactosaminyl GD1a is a target molecule for serum antibody in Guillain-Barré syndrome", Ann Neurol, 35, pp.570~576 (1994)
- Nagashima T, "Continuous spectrum of pharyngeal-cervical-brachial variant of Guillain-Barré syndrome", Arch Neurol, 64, pp.1519~1523 (2007)
- Koga M, "Antiganglioside antibody in patients with Guillain-Barré syndrome who show bulbar palsy as an initial symptom", J Neurol Neurosurg Psychiatry, 66, pp.513~516 (1999)
- Paparounas K, "Anti-GQ1b ganglioside antibody in peripheral nervous system disorders: pathophysiologic role and clinical relevance", Arch Neurol, 61, pp.1013~1016 (2004)
- Odaka M, "Anti-GQ1b IgG antibody syndrome:clinical and immunological range", J Neurol Neurosurg Psychiatry, 70, pp.50~55 (2001)
- Chiba A, "Serum IgG antibody to ganglioside GQ1b is a possible marker of Miller Fisher syndrome", Ann Neurol, 31, pp.677~679 (1992)
- Willison HJ, "Peripheral neuropathies and anti-glycolipid antibodies", Brain, 125(Pt 12), pp.2591~2625 (2002)
- Hughes RA, "Controlled trial prednisolone in acute polyneuropathy", Lancet, 2, pp.750~753 (1978)
- Hadden RD, "Electrophysiological classification of Guillain-Barrésyndrome: clinical associations and outcome. Plasma Exchange", Sandoglobulin Guillain-Barré Syndrome Trial Group, 1998, pp.44, 780~788
- Ho TW, "Guillain-Barré syndrome in northern China. Relationship to Campylobacter jejuni infection and anti-glycolipid antibodies", Brain, 118(Pt 3), pp.597~605 (1995)
- Oh SJ, "What is the best diagnostic index of conduction block and temporal dispersion?", Muscle Nerve, 17, pp.489~493 (1994)
- Ogawara K, "Axonal Guillain-Barré syndrome: relation to anti-ganglioside antibodies and Campylobacter jejuni infection in Japan", Ann Neurol, 48, pp.624~631 (2000)
- Odaka M, "Antibodies to GD1alpha and to GQ1beta in Guillain-Barré syndrome and the related disorders", J Neurol Sci, 165, pp.126~132 (1999)
- Ho TW, "Anti-GD1a antibody is associated with axonal but not demyelinating forms of Guillain-Barré syndrome", Ann Neurol, 45, pp.168~173 (1999)
- Willison HJ, "Gangliosides as targets for autoimmune injury to the nervous system", J Neurochem, 103(Suppl 1), pp.143~149 (2007)
- Susuki K, "Anti-GM1 antibodies cause complement-mediated disruption of sodium channel clusters in peripheral motor nerve fibers", J Neurosci, 27, pp.3956~3967 (2007)
- Susuki K, "Gangliosides contribute to stability of paranodal junctions and ion channel clusters in myelinated nerve fibers", Glia, 55, pp.746~757 (2007)
- Kashihara K, "IgG anti-GT1a antibodies which do not cross react with GQ1b ganglioside in a pharyngeal-cervical-brachial variant of Guillain-Barré syndrome", J Neurol Neurosurg Psychiatry, 65, pp.799~ (1998)
- Koga M, "Is IgG anti-GT1a antibody associated with pharyngeal-cervical-brachial weakness or oropharyngeal palsy in Guillain-Barré syndrome?", J Neuroimmunol, 86, pp.74~79 (1998)
- Susuki K, "A Guillain-Barré syndrome variant with prominent facial diplegia", J Neurol, 256, pp.1899~1905 (2009)
- Gong Y, "Localization of major gangliosides in the PNS: implications for immune neuropathies", Brain, 125(Pt 11), pp.2491~2506 (2002)
- Galassi G, "Post-infectious acute ataxia and facial diplegia associated with anti-GD1a IgG antibody", Eur J Neurol, 11, pp.790~791 (2004)
- Kim SY, "Polycranial neuropathy and sensory ataxia with IgG anti-GD1a antibody as a variant of Guillain-Barré syndrome", J Clin Neurosci, 20, pp.473~475 (2013)
- Kuwabara S, "IgG anti-GM1 antibody is associated with reversible conduction failure and axonal degeneration in Guillain-Barré syndrome", Ann Neurol, 44, pp.202~208 (1998)
- Kim JK, "Acute pure motor demyelinating neuropathy with hyperreflexia and anti-GalNAc-GD1a antibodies.", Clin Neurol Neurosurg, 114, pp.1345~1347 (2012)
- Hong YH, "Axonal conduction block at intermediate nerve segments in pure motor Guillain-Barré syndrome.", J Peripher Nerv Syst, 16, pp.37~46 (2011)
