Evidence map›Paper›PMID 39455929›Full record

Observational studyBMC neurology2024

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.

Milou R Michael, Luuk Wieske, Jeffrey A Allen, Michael P Lunn, Kathrin Doppler, Cheng-Yin Tan, Haruki Koike, Lars K Markvardsen, Mahima Kapoor, Sung-Tsang Hsieh and 8 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in BMC neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Milou R MichaelDepartment of Neurology and Neurophysiology, Location AMC, Amsterdam Neuroscience, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Luuk WieskeDepartment of Neurology and Neurophysiology, Location AMC, Amsterdam Neuroscience, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Jeffrey A AllenDepartment of Neurology, University of Minnesota, Minneapolis, USA.
Michael P LunnCentre for Neuromuscular Disease, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Kathrin DopplerDepartment of Neurology, University Hospital Würzburg, Würzburg, Germany.
Cheng-Yin TanDivision of Neurology, Department of Medicine, University of Malaya, Kuala Lumpur, 50603, Malaysia.
Haruki KoikeDivision of Neurology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Lars K MarkvardsenDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmark.
Mahima KapoorNeurology Department, Alfred Hospital, Melbourne, VIC, Australia.
Sung-Tsang HsiehDepartment of Neurology, National Taiwan University Hospital, Taipei City, Taiwan.
Eduardo Nobile-OrazioNeuromuscular and Neuroimmunology Service, Department of Medical Biotechnology and Translational Medicine, IRCCS Humanitas Research Institute, University of Milan, Milan, Italy.
Bart C JacobsDepartment of Neurology and Immunology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Yusuf A RajaballyNeuromuscular Service, Neurology, Queen Elizabeth Hospital Birmingham, Birmingham, UK.
Ivana BastaNeurology Clinic, Medical faculty, University Clinical Center of Serbia, University of Belgrade, Belgrade, Serbia.
Paolo RipellinoDepartment of Neurology, Neurocenter of Southern Switzerland EOC, Lugano, CH, Switzerland.
Luis QuerolDepartment of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Filip EftimovDepartment of Neurology and Neurophysiology, Location AMC, Amsterdam Neuroscience, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands. f.eftimov@amsterdamumc.nl.
INCbase Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundINCbase 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.

methodsAll 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.

Indexed as

Polyradiculoneuropathy, Chronic Inflammatory DemyelinatingCohort StudiesFemaleHumansMaleProspective StudiesRegistriesTreatment OutcomeBiomarkersChronic inflammatory demyelinating polyneuropathyClinimetricsDiagnosisOutcomePrediction modelPrognosisTreatment

Identifiers

PMID39455929
PMCPMC11515301

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.