Evidence map›Paper›PMID 38726012›Full record

ArticleFrontiers in immunology2024

Clinical characteristics of patients with autoimmune nodopathy with anti-neurofascin155 antibodies.

Jiwei Zhang, Xiaotong Hou, Liting Wei, Jinshun Liu, Shibo Li, Yifan Guo, Hongbo Liu, Yan Jiang

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Antibody-Mediated Nodo- and Paranodopathies.Journal of clinical medicine · 2024
    Review
  4. Article
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

8 authors.

Jiwei Zhang *Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Xiaotong Hou *Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Liting Wei *Department of Neurology, Luoyang Central Hospital, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang, China.
Jinshun Liu *Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Shibo Li *Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yifan Guo *Department of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Hongbo LiuDepartment of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yan JiangDepartment of Neurology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: According to the latest guidelines on chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), patients with CIDP with anti-neurofascin 155 (NF155) antibodies are referred to as autoimmune nodopathy (AN), an autoimmune disorder distinct from CIDP. We aimed to compare the clinical data of patients with AN with anti-NF155 antibodies with those of anti-NF155 antibodies-negative patients with CIDP, and to summarize the clinical characteristics of patients with AN with anti-NF155 antibodies. Methods: Nine patients with AN with anti-NF155 antibodies and 28 serologically negative patients with CIDP were included in this study. Diagnosis was made according to the diagnostic criteria in the European Academy of Neurology (EAN)/Peripheral Nerve Society (PNS) guidelines on CIDP published in 2021. Demographics, clinical manifestations, electrophysiological examination, cerebrospinal fluid (CSF) tests, and response to treatment were retrospectively analyzed. Results: Compared with serologically negative patients with CIDP, those patients with AN with anti-NF155 antibodies were younger ( Conclusions: Patients with AN with anti-NF155 antibodies differed from serologically negative patients with CIDP in terms of clinical characteristics. When AN is suspected, testing for antibodies associated with the nodes of Ranvier is essential for early diagnosis and to guide treatment.

Indexed as

AutoantibodiesCell Adhesion MoleculesNerve Growth FactorsPolyradiculoneuropathy, Chronic Inflammatory DemyelinatingAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesYoung AdultAutoantibodiesCell Adhesion MoleculesNerve Growth FactorsNFASC protein, humananti-neurofascin155 antibodiesautoimmune nodopathychronic inflammatory demyelinating polyradiculoneuropathyclinical characteristicsnodes of Ranvier

Identifiers

PMID38726012
PMCPMC11079118

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