دورية أكاديمية
Regional variation of Guillain-Barré syndrome
| العنوان: | Regional variation of Guillain-Barré syndrome |
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| المؤلفون: | Doets A. Y., Verboon C., van den Berg B., Harbo T., Cornblath D. R., Willison H. J., Islam Z., Attarian S., Barroso F. A., Bateman K., Benedetti L., van den Bergh P., Casasnovas C., Cavaletti G., Chavada G., Claeys K. G., Dardiotis E., Davidson A., van Doorn P. A., Feasby T. E., Galassi G., Gorson K. C., Hartung H. -P., Hsieh S. -T., Hughes R. A. C., Illa I., Islam B., Kusunoki S., Kuwabara S., Lehmann H. C., Miller J. A. L., Mohammad Q. D., Monges S., Nobile Orazio E., Pardo J., Pereon Y., Rinaldi S., Querol L., Reddel S. W., Reisin R. C., Shahrizaila N., Sindrup S. H., Waqar W., Jacobs B. C., van Woerkom M., Roodbol J., Addington J. M., Ajroud-Driss S., Andersen H., Antonini G., Ariatti A., Badrising U. A., Beronio A., Bianco M., Binda D., Briani C., Bunschoten C., Burmann J., Bella I. R., Bertorini T. E., Bhavaraju-Sanka R., Brannagan T. H., Busby M., Butterworth S., Chao C. C., Chetty S., Conti M. E., Cosgrove J. S., Dalakas M. C., Derejko M. A., Dimachkie M. M., Doppler K., Dornonville de la Cour C., Echaniz-Laguna A., Eftimov F., Faber C. G., Fazio R., Fujioka T., Fulgenzi E. A., Garcia-Sobrino T., Garnero M., Garssen M. P. J., Gijsbers C. J., Gilchrist J. M., Goldstein J. M., Granit V., Grapperon A., Gutierrez G., Hadden R. D. M., Holbech J. V., Holt J. K. L., Homedes Pedret C., Htut M., Jerico Pascual I., Kaida K., Karafiath S., Katzberg H. D., Kiers L., Kieseier B. C., Kimpinski K., Kleyweg R. P., Kokubun N., Kolb N. A., Kuitwaard K., Kwan J. Y., Ladha S. S., Landschoff Lassen L., Lawson V., Ledingham D., Leon Cejas L., Lucy S. T., Lunn M. P. T., Magot A., Manji H., Marchesoni C., Marfia G. A., Marquez Infante C., Martinez Hernandez E., Mataluni G., McDermott C. J., Meekins G. D., Monges M. S., Montero M. C. J., Moris de la Tassa G., Mozzoni J., Nascimbene C., Nowak R. J., Orizaloa Balaguer P., Osei-Bonsu M., Lee Pan E. B., Pasnoor M., Rajabally Y. A., Ritter C., Roberts R. C., Rojas-Marcos I., Rudnicki S. A., Ruiz M., Sachs G. M., Samijn J. P. A., Santoro L., Schenone A., Schwindling L., Sedano Tous M. J., Sekiguchi Y., Sheikh K. A., Silvestri N. J., Sommer C. L., Stein B., Stino A. M., Spyropoulos A., Srinivasan J., Suzuki H., Tankisi H., Tigner D., Twydell P. T., van Damme P., van der Kooi A. J., van Dijk G. W., van der Ree T., van Koningsveld R., Varrato J. D., Vermeij F. H., Visser L. H., Vytopil M. V., Waheed W., Wilken M., Wilkerson C., Wirtz P. W., Yamagishi Y., Zhou L., Zivkovic S. |
| المساهمون: | Doets, A. Y., Verboon, C., van den Berg, B., Harbo, T., Cornblath, D. R., Willison, H. J., Islam, Z., Attarian, S., Barroso, F. A., Bateman, K., Benedetti, L., van den Bergh, P., Casasnovas, C., Cavaletti, G., Chavada, G., Claeys, K. G., Dardiotis, E., Davidson, A., van Doorn, P. A., Feasby, T. E., Galassi, G., Gorson, K. C., Hartung, H. -P., Hsieh, S. -T., Hughes, R. A. C., Illa, I., Islam, B., Kusunoki, S., Kuwabara, S., Lehmann, H. C., Miller, J. A. L., Mohammad, Q. D., Monges, S., Nobile Orazio, E., Pardo, J., Pereon, Y., Rinaldi, S., Querol, L., Reddel, S. W., Reisin, R. C., Shahrizaila, N., Sindrup, S. H., Waqar, W., Jacobs, B. C., van Woerkom, M., Roodbol, J., Addington, J. M., Ajroud-Driss, S., Andersen, H., Antonini, G., Ariatti, A., Badrising, U. A., Beronio, A., Bianco, M., Binda, D., Briani, C., Bunschoten, C., Burmann, J., Bella, I. R., Bertorini, T. E., Bhavaraju-Sanka, R., Brannagan, T. H., Busby, M., Butterworth, S., Chao, C. C., Chetty, S., Conti, M. E., Cosgrove, J. S., Dalakas, M. C., Derejko, M. A., Dimachkie, M. M., Doppler, K., Dornonville de la Cour, C., Echaniz-Laguna, A., Eftimov, F., Faber, C. G., Fazio, R., Fujioka, T., Fulgenzi, E. A., Garcia-Sobrino, T., Garnero, M., Garssen, M. P. J., Gijsbers, C. J., Gilchrist, J. M., Goldstein, J. M., Granit, V., Grapperon, A., Gutierrez, G., Hadden, R. D. M., Holbech, J. V., Holt, J. K. L., Homedes Pedret, C., Htut, M., Jerico Pascual, I., Kaida, K., Karafiath, S., Katzberg, H. D., Kiers, L., Kieseier, B. C. |
| بيانات النشر: | GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND Oxford University Press |
| سنة النشر: | 2018 |
| المجموعة: | Università degli Studi di Genova: CINECA IRIS |
| مصطلحات موضوعية: | axonal degeneration, clinical course, demyelination, outcome, polyradiculoneuropathy |
| الوصف: | Guillain-Barré syndrome is a heterogeneous disorder regarding the clinical presentation, electrophysiological subtype and outcome. Previous single country reports indicate that Guillain-Barré syndrome may differ among regions, but no systematic comparative studies have been conducted. Comparative studies are required to identify factors determining disease susceptibility, variation and prognosis, and to improve diagnostic criteria. The International Guillain-Barré Syndrome Outcome Study is a prospective, observational cohort study including all patients within the diagnostic spectrum, aiming to describe the heterogeneity of Guillain-Barré syndrome worldwide. The current study was based on the first 1000 inclusions with a follow-up of at least 1 year and confirmed the variation in clinical presentation, course and outcome between patients. The full clinical spectrum of Guillain-Barré syndrome was observed in patients from all countries participating in the International Guillain-Barré Syndrome Outcome Study, but the frequency of variants differed between regions. We compared three regions based on geography, income and previous reports of Guillain-Barré syndrome subtypes: Europe/Americas', Asia' (without Bangladesh), and Bangladesh'. We excluded 75 (8%) patients because of alternative diagnoses, protocol violations, or missing data. The predominant clinical variant was sensorimotor in Europe/Americas (n = 387/562, 69%) and Asia (n = 27/63, 43%), and pure motor in Bangladesh (n = 74/107, 69%). Miller Fisher syndrome and Miller Fisher-Guillain-Barré overlap syndrome were more common in Asia (n = 14/63, 22%) than in the other two regions (Europe/Americas: n = 64/562, 11%; Bangladesh: n = 1/107, 1%) (P < 0.001). The predominant electrophysiological subtype was demyelinating in all regions (Europe/Americas: n = 312/573, 55%; Asia: n = 29/65, 45%; Bangladesh: n = 38/94, 40%). The axonal subtype occurred more often in Bangladesh (n = 34/94, 36%) than in Europe/Americas (n = 33/573, 6%) and other Asian ... |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | ELETTRONICO |
| اللغة: | English |
| العلاقة: | info:eu-repo/semantics/altIdentifier/pmid/30247567; info:eu-repo/semantics/altIdentifier/wos/WOS:000446548400013; volume:141; firstpage:2866; lastpage:2877; numberofpages:12; journal:BRAIN; http://hdl.handle.net/11567/998129Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85054687956 |
| DOI: | 10.1093/brain/awy232 |
| الإتاحة: | https://doi.org/10.1093/brain/awy232Test http://hdl.handle.net/11567/998129Test |
| حقوق: | info:eu-repo/semantics/closedAccess |
| رقم الانضمام: | edsbas.DD78D8E2 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1093/brain/awy232 |
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