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Record W2891646477 · doi:10.1093/brain/awy232

Regional variation of Guillain-Barré syndrome

2018· article· en· W2891646477 on OpenAlexaff
Alex Y. Doets, Christine Verboon, Bianca van den Berg, Thomas Harbo, David R. Cornblath, Hugh J. Willison, Zhahirul Islam, Shahram Attarian, Fábio Barroso, Kathleen Bateman, Luana Benedetti, Peter Van den Bergh, Carlos Casasnovas, Guido Cavaletti, Govindsinh Chavada, Kristl G. Claeys, Efthimios Dardiotis, Amy Davidson, Pieter A. van Doorn, T E Feasby, Giuliana Galassi, Kenneth C. Gorson, Hans-Peter Hartung, Sung‐Tsang Hsieh, Richard AC Hughes, Isabel Illa, Badrul Islam, Susumu Kusunoki, Satoshi Kuwabara, Helmar C. Lehmann, James Miller, Quazi Deen Mohammad, Soledad Monges, Eduardo Nobile‐Orazio, Julio Pardo, Yann Péréon, Simon Rinaldi, Luís Querol, Ricardo Reisin, Nortina Shahrizaila, Søren H. Sindrup, Waqar Waheed, Bart C. Jacobs, H.‐P. Hartung, M. van Woerkom, Joyce Roodbol, Stephen Reddel, P. van den Bergh, Jean Addington, Senda Ajroud‐Driss, Henning Andersen, Giovanni Antonini, Alessandra Ariatti, Umesh A. Badrising, Alessandro Beronio, Marcelle Martim Bianco, Delphine Binda, Chiara Briani, Carina Bunschoten, Jan Bürmann, I.R. Bella, T. E. Bertoríni, Ratna Bhavaraju‐Sanka, Thomas H. Brannagan, Mark Busby, S. Butterworth, Chi‐Chao Chao, Sarentha Chetty, M E Conti, Jeremy Cosgrove, Marinos C. Dalakas, Miroslawa A Derejko, Mazen M. Dimachkie, Kathrin Doppler, Charlotta Dornonville de la Cour, Andoni Echaniz‐Laguna, Filip Eftimov, Catharina G. Faber, Raffaella Fazio, T. Fujioka, E. Fulgenzi, Tania García‐Sobrino, Martina Garnero, Marcel P.J. Garssen, C.J. Gijsbers, James M. Gilchrist, Jonathan Goldstein, Volkan Granit, Aude‐Marie Grapperon, Gerardo Gutiérrez‐Gutiérrez, Robert D. M. Hadden, Jakob Vormstrup Holbech, James K. L. Holt, Christian Homedes Pedret, M. Htut, I. Jericó Pascual, Kenichi Kaida, Summer Karafiath, Hans Katzberg, Lynette Kiers, B. C. Kieseier, Kurt Kimpinski, R. P. Kleyweg, Norito Kokubun, Noah Kolb, Krista Kuitwaard, Jing Yi Kwan, Shafeeq Ladha, Lisbeth Lassen, Victoria Lawson, David Ledingham, Luciana León Cejas, S.T. Lucy, Michael P. Lunn, Armelle Magot, Hadi Manji, Cintia Marchesoni, Girolama Alessandra Marfia, Celedonio Márquez‐Infante, Eugenia Martínez‐Hernández, Giorgia Mataluni, Christopher McDermott, Gregg Meekins, M.S. Monges, Maria C Jimeno Montero, J. Mozzoni, Caterina Nascimbene, R.J. Nowak, P. Orizaloa Balaguer, M. Osei-Bonsu, Elizabeth Pan, Mamatha Pasnoor, Yusuf A. Rajabally, Christian Ritter, Rhys Roberts, I. Rojas-Marcos, Stacy A. Rudnicki, M Ruiz, Gabriele Sachs, Johnny P.A. Samijn, L. Santoro, Angelo Schenone, Lenka Schwindling, María J. Sedano Tous, Yukari Sekiguchi, Kazim A. Sheikh, Nicholas J. Silvestri, Claudia Sommer, Beth E. Shubin Stein, Amro Stino, Alex C. Spyropoulos, Jothsana Srinivasan, Hidekazu Suzuki, Hatice Tankişi, D. Tigner, Paul Twydell, Philip Van Damme, Anneke J. van der Kooi, Gert W. van Dijk, T. van der Ree, Rinske van Koningsveld, J.D. Varrato, Frédérique H Vermeij, Leo H. Visser, M.V. Vytopil, Waquas Waheed, Michael Wilken, Cory Wilkerson, Paul W. Wirtz, Yuki Yamagishi, Lan Zhou, Saša Živković

Bibliographic record

VenueBrain · 2018
Typearticle
Languageen
FieldMedicine
TopicPeripheral Neuropathies and Disorders
Canadian institutionsUniversity of Calgary
FundersInstituto de Salud Carlos IIINational Health and Medical Research CouncilNational Institutes of HealthPrinses Beatrix SpierfondsServierUniversity of GlasgowNeurocrine BiosciencesAstellas PharmaCalithera BiosciencesIonis PharmaceuticalsJapan Blood Products OrganizationAstraZenecaCSL BehringGenentechGrifolsGBS/CIDP Foundation InternationalTeva Pharmaceutical IndustriesGlaxoSmithKlineMedical Research CouncilBiogenSanofiPfizer
KeywordsGuillain-Barre syndromeMedicinePediatricsCohort studyCohortObservational studyMiller-Fisher syndromeInternal medicine

Abstract

fetched live from OpenAlex

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 countries (n = 4/65, 6%) (P < 0.001). In all regions, patients with the axonal subtype were younger, had fewer sensory deficits, and showed a trend towards poorer recovery compared to patients with the demyelinating subtype. The proportion of patients able to walk unaided after 1 year varied between Asia (n = 31/34, 91%), Europe/Americas (n = 334/404, 83%) and Bangladesh (n = 67/97, 69%) (P = 0.003). A similar variation was seen for mortality, being higher in Bangladesh (n = 19/114, 17%) than in Europe/Americas (n = 23/486, 5%) and Asia (n = 1/45, 2%) (P < 0.001). This study showed that factors related to geography have a major influence on clinical phenotype, disease severity, electrophysiological subtype, and outcome of Guillain-Barré syndrome.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.262
Teacher spread0.245 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations330
Published2018
Admission routes1
Has abstractyes

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