Evidence map›Paper›PMID 40913126›Full record

ReviewNature reviews. Neurology2025

The changing landscape of primary autoimmune neuropathies.

Marta Caballero-Ávila, Elba Pascual-Goñi, Cinta Lleixà, Lorena Martín-Aguilar, Roger Collet-Vidiella, Luis Querol

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
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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

6 authors.

Marta Caballero-ÁvilaNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0001-9850-8504
Elba Pascual-GoñiNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.
Cinta LleixàNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.
Lorena Martín-AguilarNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0002-1553-2224
Roger Collet-VidiellaNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID 0000-0003-1668-1018
Luis QuerolNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain. lquerol@santpau.cat.ORCID 0000-0002-4289-8264

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune neuropathies, such as Guillain-Barré syndrome (GBS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), are rare, disabling disorders. Diagnosis, follow-up and treatment of autoimmune neuropathies rely almost exclusively on clinical parameters, and the available therapies, such as intravenous immunoglobulins and corticosteroids, date from >30 years ago. The lack of therapeutic progress in autoimmune neuropathies has resulted from a combination of limited understanding of their pathophysiology, disease heterogeneity and challenges in trial design. However, advances in the past 5 years are set to change the rate of progress. The discovery of pathogenic autoantibodies that target cell-adhesion molecules at the node of Ranvier, thereby defining the new diagnostic category of autoimmune nodopathies, has provided a new perspective on disease pathophysiology. In addition, better definitions of the diagnostic criteria for GBS and CIDP, FDA approval of efgartigimod for the treatment of CIDP, promising results in trials of complement inhibitors in CIDP, GBS and multifocal motor neuropathy and the identification of biomarkers with the potential to optimize prognostication and monitoring are moving us towards targeted and precise therapeutic approaches to improve outcomes of autoimmune neuropathies. In this Review, we summarize the latest developments in autoimmune neuropathies, including discoveries in disease mechanisms, the implications of new diagnostic guidelines, identification of new biomarkers and the status of the most promising clinical trials.

Indexed as

Autoimmune Diseases of the Nervous SystemGuillain-Barre SyndromePolyradiculoneuropathy, Chronic Inflammatory DemyelinatingAutoantibodiesHumansAutoantibodies

Identifiers

What OpenQuestion holds

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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.