Evidence map›Paper›PMID 20634952›Full record

ArticlePloS one2010

CD40: novel association with Crohn's disease and replication in multiple sclerosis susceptibility.

Fiona Blanco-Kelly, Fuencisla Matesanz, Antonio Alcina, María Teruel, Lina M Díaz-Gallo, María Gómez-García, Miguel A López-Nevot, Luis Rodrigo, Antonio Nieto, Carlos Cardeña and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. TheBioMed research international · 2018
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  8. IgA Vasculitis: Influence ofJournal of clinical medicine · 2022
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

17 authors at 8 institutions in 1 country.

Fiona Blanco-KellyDepartment of Clinical Immunology, Hospital Clínico San Carlos, Madrid, Spain.
Fuencisla Matesanz
Antonio Alcina
María Teruel
Lina M Díaz-Gallo
María Gómez-García
Miguel A López-Nevot
Luis Rodrigo
Antonio Nieto
Carlos Cardeña
Guillermo Alcain
Manuel Díaz-Rubio
Emilio G de la Concha
Oscar Fernandez
Rafael Arroyo
Javier Martín
Elena Urcelay
Instituto de Parasitología y Biomedicina "López - Neyra" · ESHospital Clínico San Carlos · ESSpanish Multiple Sclerosis Network · ESHospital Universitario Virgen de las Nieves · ESHospital Clínico Universitario Virgen de la Victoria · ESHospital Universitario Central de Asturias · ESHospital Universitario Puerta del Mar · ESInstituto de Investigación Biosanitaria de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA functional polymorphism located at -1 from the start codon of the CD40 gene, rs1883832, was previously reported to disrupt a Kozak sequence essential for translation. It has been consistently associated with Graves' disease risk in populations of different ethnicity and genetic proxies of this variant evaluated in genome-wide association studies have shown evidence of an effect in rheumatoid arthritis and multiple sclerosis (MS) susceptibility. However, the protective allele associated with Graves' disease or rheumatoid arthritis has shown a risk role in MS, an effect that we aimed to replicate in the present work. We hypothesized that this functional polymorphism might also show an association with other complex autoimmune condition such as inflammatory bowel disease, given the CD40 overexpression previously observed in Crohn's disease (CD) lesions. METHODOLOGY: Genotyping of rs1883832C>T was performed in 1564 MS, 1102 CD and 969 ulcerative colitis (UC) Spanish patients and in 2948 ethnically matched controls by TaqMan chemistry. PRINCIPAL

findingsThe observed effect of the minor allele rs1883832T was replicated in our independent Spanish MS cohort [p = 0.025; OR (95% CI) = 1.12 (1.01-1.23)]. The frequency of the minor allele was also significantly higher in CD patients than in controls [p = 0.002; OR (95% CI) = 1.19 (1.06-1.33)]. This increased predisposition was not detected in UC patients [p = 0.5; OR (95% CI) = 1.04 (0.93-1.17)].

conclusionThe impact of CD40 rs1883832 on MS and CD risk points to a common signaling shared by these autoimmune conditions.

Indexed as

AdultAllelesCD40 AntigensColitis, UlcerativeCrohn DiseaseGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansMultiple SclerosisPolymorphism, GeneticYoung AdultCD40 Antigens

Identifiers

PMID20634952
PMCPMC2902513
OpenAlexW1968739010

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.