Evidence map›Paper›PMID 40207596›Full record

ArticleEuropean journal of neurology2025

Factors Distinguishing Nonsystemic Versus Systemic Vasculitic Peripheral Neuropathy: A Retrospective Cohort Study.

Edouard Berling, Thierry Maisonobe, Olivier Morassi, Andoni Echaniz-Laguna, Christian Denier, Adrien Le Guillou, Mathilde Duschene, Céline Labeyrie, Clovis Adam

Abstract read
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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

9 authors.

Edouard BerlingService de Neurologie, AP-HP, Hôpital Raymond Poincaré, Centre de référence Nord-Est-Ile-de-France, FHU PHENIX, Garches, France.
Thierry MaisonobeDépartement de Neurophysiologie Clinique, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Olivier MorassiNeurology Department and French National Reference Center for Rare Neuropathies (CERAMIC), Bicêtre University Hospital, Le Kremlin-Bicêtre, France.
Andoni Echaniz-LagunaNeurology Department and French National Reference Center for Rare Neuropathies (CERAMIC), Bicêtre University Hospital, Le Kremlin-Bicêtre, France.ORCID 0000-0003-1012-9783
Christian DenierStroke Units and Department of Neurology of Hôpital Bicêtre, Le Kremlin Bicêtre, Assistance Publique-Hôpitaux de Paris, Paris Saclay University, Paris, France.ORCID 0000-0002-2087-5563
Adrien Le GuillouDepartment of Epidemiology, Emory University, Atlanta, Georgia, USA.
Mathilde DuscheneNeurIT (Neuropathies et Innovations Thérapeutiques) UR 20218, Faculties of Medicine and Pharmacy, University of Limoges, Limoges, France.ORCID 0000-0002-5621-7335
Céline LabeyrieNeurology Department and French National Reference Center for Rare Neuropathies (CERAMIC), Bicêtre University Hospital, Le Kremlin-Bicêtre, France.ORCID 0000-0001-9765-709X
Clovis AdamAP-HP, Service D'anatomopathologie Clinique, CHU Bicêtre, Le Kremlin-Bicêtre, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrompt differentiation of nonsystemic vasculitic neuropathy (NSVN) from systemic vasculitic neuropathy (SVN) without antineutrophil cytoplasmic antibodies or organ involvement (SVN-) is challenging but crucial given the differences in management. Our primary objective was to identify predictors of SVN- versus NSVN.

methodsWe retrospectively identified patients seen at either of two centers for histologically definite or probable vasculitic neuropathy diagnosed as SVN- or NSVN. Clinical, electromyographic, laboratory, and histological data at diagnosis and last follow-up were collected.

resultsWe included 98 patients, of whom 46 (47%) had NSVN and 52 (53%) SVN-. Symptoms and neurophysiological findings did not significantly differ between the two groups. By univariate analysis, compared to the NSVN group, the SVN- group had more patients with C-reactive protein ≥ 10 mg/L (44.2% vs. 17.4%, p < 0.01), antinuclear antibodies (42.3% vs. 21.7%, p = 0.04), and low C3 or C4 (23.1% vs. 4.3%, p = 0.02). All three associations were confirmed by multivariate analysis. By multivariate analysis adjusted for symptom duration, muscle vasculitis also was associated with SVN- (OR, 8.33; 95% CI, 2.63-25.00; p < 0.01).

conclusionSimple, readily available laboratory and histological variables may help to rapidly distinguish SVN from NSVN.

Indexed as

Peripheral Nervous System DiseasesSystemic VasculitisVasculitisAdultAgedCohort StudiesC-Reactive ProteinDiagnosis, DifferentialElectromyographyFemaleHumansMaleMiddle AgedRetrospective StudiesC-Reactive Proteindiagnosisperipheral nervous system diseasesvasculitis

Identifiers

PMID40207596
PMCPMC11983150

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.