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dc.contributor.authorMichael, Milou R
dc.contributor.authorWieske, Luuk
dc.contributor.authorAllen, Jeffrey A
dc.contributor.authorLunn, Michael P
dc.contributor.authorDoppler, Kathrin
dc.contributor.authorTan, Cheng-Yin
dc.contributor.authorKoike, Haruki
dc.contributor.authorMarkvardsen, Lars K
dc.contributor.authorKapoor, Mahima
dc.contributor.authorHsieh, Sung-Tsang
dc.contributor.authorNobile-Orazio, Eduardo
dc.contributor.authorJacobs, Bart C
dc.contributor.authorRajabally, Yusuf A
dc.contributor.authorBasta, Ivana
dc.contributor.authorRipellino, Paolo
dc.contributor.authorQuerol, Luis
dc.contributor.authorEftimov, Filip
dc.date.accessioned2025-01-10T12:12:48Z
dc.date.available2025-01-10T12:12:48Z
dc.date.issued2024-10-25
dc.identifier.citationMichael MR, Wieske L, Allen JA, Lunn MP, Doppler K, Tan CY, Koike H, Markvardsen LK, Kapoor M, Hsieh ST, Nobile-Orazio E, Jacobs BC, Rajabally YA, Basta I, Ripellino P, Querol L, Eftimov F; INCbase Consortium. Inflammatory Neuropathy Consortium base (INCbase): a protocol of a global prospective observational cohort study for the development of a prediction model for treatment response in chronic inflammatory demyelinating polyneuropathy. BMC Neurol. 2024 Oct 25;24(1):415. doi: 10.1186/s12883-024-03903-w.en_US
dc.identifier.eissn1471-2377
dc.identifier.doi10.1186/s12883-024-03903-w
dc.identifier.pmid39455929
dc.identifier.urihttp://hdl.handle.net/20.500.14200/6915
dc.description.abstractBackground: INCbase is an international, multicenter prospective observational study using a customizable web-based modular registry to study the clinical, biological and electrophysiological variation and boundaries of chronic inflammatory demyelinating polyneuropathy (CIDP). The primary objective of INCbase is to develop and validate a clinical prediction model for treatment response. Methods: All patients meeting clinical criteria for CIDP can be included in INCbase. Collected data include demographics, clinical history, diagnostics and various domains of clinical outcomes. Data is collected at a minimum of every 6 months for two years, and more frequently at the discretion of the investigational site to allow for assessment of unexpected changes in treatment response or clinical status. Participants can be enrolled in various sub-studies designed to capture data relevant to specific groups of interest. Data is entered directly into the web-based data entry system by local investigators and/or participants. Collection and local storage of biomaterial is optional. To develop a clinical prediction model for treatment response, newly diagnosed patients with active disease warranting start of first-line treatment will be included. The study population will be split into a development and validation cohort. Univariate and multivariate logistic regression analysis will be used to identify and combine predictors at start of treatment for treatment response at six months. Model performance will be assessed through discrimination and calibration in an external validation cohort. The externally validated prediction model will be made available to researchers and clinicians on the INCbase website. Discussion: With this study, we aim to create a clinically relevant and implementable prediction model for treatment response to first line treatments in CIDP. INCbase enrollment started in April 2021, with 29 centers across 8 countries and 303 patients participating to date. This collaborative effort between academia, patient advocacy organizations and pharmaceutical industry will deepen our understanding of how to diagnose and treat CIDP.en_US
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.relation.urlhttps://bmcneurol.biomedcentral.com/en_US
dc.rights© 2024. The Author(s).
dc.subjectDiseases & disorders of the nervous system (e.g. Parkinson's)en_US
dc.titleInflammatory Neuropathy Consortium base (INCbase): a protocol of a global prospective observational cohort study for the development of a prediction model for treatment response in chronic inflammatory demyelinating polyneuropathyen_US
dc.typeArticleen_US
dc.source.journaltitleBMC Neurologyen_US
dc.source.volume24
dc.source.issue1
dc.source.beginpage415
dc.source.endpage
dc.source.countryEngland
rioxxterms.versionNAen_US
dc.contributor.trustauthorRajabally, Yusuf A
dc.contributor.departmentNeurologyen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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