Evidence map›Paper›PMID 33216288›Full record

ArticleJournal of molecular neuroscience : MN2021

A First Step for the Molecular Characterization of Neurological Involvement of Behçet Syndrome: an Italian Pivotal Study.

Maria Carmela Padula, Pietro Leccese, Nancy Lascaro, Angela Anna Padula, Teresa Carbone, Giuseppe Martelli, Salvatore D'Angelo

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2021. 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
0.3field-weighted citation impact, top 40% of its field
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, 2 citations in OpenAlex.

  1. Article
  2. Journal of personalized medicine · 2023
    Article
  3. Genetics in Behcet's Disease: An Update Review.Frontiers in ophthalmology · 2022
    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

7 authors at 1 institution in 1 country.

Maria Carmela PadulaRheumatology Institute of Lucania (IReL), San Carlo Hospital, Potenza, 85100, Italy. mcpadula25@gmail.com.ORCID http://orcid.org/0000-0003-0726-7085
Pietro LecceseRheumatology Institute of Lucania (IReL), San Carlo Hospital, Potenza, 85100, Italy.
Nancy LascaroRheumatology Institute of Lucania (IReL), San Carlo Hospital, Potenza, 85100, Italy.
Angela Anna PadulaRheumatology Institute of Lucania (IReL), San Carlo Hospital, Potenza, 85100, Italy.
Teresa CarboneRheumatology Institute of Lucania (IReL), San Carlo Hospital, Potenza, 85100, Italy.
Giuseppe MartelliDepartment of Science, University of Basilicata, Potenza, 85100, Italy.
Salvatore D'AngeloRheumatology Institute of Lucania (IReL), San Carlo Hospital, Potenza, 85100, Italy.
University of Basilicata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Behçet syndrome (BS) is a vasculitis characterized by several clinical manifestations including the rare neurological involvement (neuro-BS, NBS). The aim of our pivotal study was to investigate the mutational status of several inflammation-related genes in a cohort of Italian patients with and without the neurological involvement (20 NBS vs 40 no-NBS patients). The preliminary in silico single nucleotide polymorphism (SNP) selection and primer design were performed by NCBI Primer-Blast tool. Genomic DNA was isolated and amplified using PCR. PCR amplicons were sequenced and bioinformatically analysed. Twelve tagSNPs were selected and genotyped: ERAP1 rs30187, rs17482078, and rs27044; IL10 rs1800872 and rs1518111, IL12A rs17810546, IL23R rs17375018, IL23R-IL12RB2 rs924080, STAT4 rs7572482, CCR1 rs7616215, KLRC4 rs2617170, and UBAC2 rs3825427. ERAP1 and IL23R SNPs showed statistically significant higher frequencies in NBS group than no-NBS. ERAP1 rs30187 AA was more common in no-NBS patients (20.0% NBS vs 47.5% no-NBS; p < 0.05), while rs17482078 GA frequency was higher in NBS patients (55.0% NBS vs 22.5% no-NBS; p < 0.05, OR: 4.21). IL23R rs17375018 GG was more frequent in NBS group (65.0% NBS vs 40.0% no-NBS; p < 0.05), according to a previous finding. No other statistically significant differences were found. In conclusion, ERAP1 and IL23R SNPs were found associated with neurological involvement of BS. Additional and larger analyses were required to verify our preliminary findings.

Indexed as

Polymorphism, Single NucleotideAdultAminopeptidasesBehcet SyndromeFemaleHumansInterleukinsMaleMiddle AgedMinor Histocompatibility AntigensNK Cell Lectin-Like Receptor Subfamily CReceptors, CCR1STAT4 Transcription FactorUbiquitin-Activating EnzymesAminopeptidasesCCR1 protein, humanERAP1 protein, humanInterleukinsKLRC4 protein, humanMinor Histocompatibility AntigensNK Cell Lectin-Like Receptor Subfamily CReceptors, CCR1STAT4 protein, humanSTAT4 Transcription FactorUBA2 protein, humanUbiquitin-Activating EnzymesBehçet syndromeERAP1IL23RNeuro-Behçet syndromeSusceptibility

Identifiers

PMID33216288
OpenAlexW3098676937

What OpenQuestion holds

Textmetadata
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.