Evidence map›Paper›PMID 26632999›Full record

ArticleGenes and immunity

Association of inflammatory cytokine gene polymorphisms with inflammatory bowel disease in a Moroccan cohort.

N Senhaji, A Serrano, W Badre, N Serbati, M Karkouri, Y Zaid, S Nadifi, J Martin

Abstract read
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In one paragraph

Article in Genes and immunity. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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  5. Turmeric and Curcumin-Health-Promoting Properties in Humans versus Dogs.International journal of molecular sciences · 2023
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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

8 authors at 5 institutions in 3 countries.

N SenhajiFaculty of Medicine and Pharmacy, Laboratory of Genetics and Molecular Pathology, University Hassan II, Casablanca, Morocco.
A SerranoInstituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas, P.T.S., Granada, Spain.
W BadreGastroenterology Department, CHU Ibn Rochd, Casablanca, Morocco.
N SerbatiFaculty of Medicine and Pharmacy, Laboratory of Genetics and Molecular Pathology, University Hassan II, Casablanca, Morocco.
M KarkouriPathology Department, CHU Ibn Rochd, Casablanca, Morocco.
Y ZaidLaboratory of Thrombosis and Hemostasis, Montreal Heart Institute, Montreal, Quebec, Canada.
S NadifiFaculty of Medicine and Pharmacy, Laboratory of Genetics and Molecular Pathology, University Hassan II, Casablanca, Morocco.
J MartinInstituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas, P.T.S., Granada, Spain.
University of Hassan II Casablanca · MACentre Hospitalier Universitaire Ibn Rochd · MAConsejo Superior de Investigaciones Científicas · ESInstituto de Parasitología y Biomedicina "López - Neyra" · ESMontreal Heart Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to investigate whether common variants in inflammatory and immune response genes influence inflammatory bowel disease (IBD) risk among Moroccan patients. Using a candidate gene approach, 10 single-nucleotide polymorphisms mapping on six genes (MIF_rs755622, TNFA_rs1800629, IL6_rs2069840, IL6R_rs2228145, IL6ST_rs2228044, IL17A (rs2275913, rs4711998, rs7747909, rs8193036, rs3819024)) were assessed in 510 subjects grouped in 199 IBD and 311 healthy controls. Genotyping was performed with the TaqMan allelic discrimination technology. The results were analyzed using PLINK software. The frequency of allele A for TNFA rs1800629 was significantly higher in ulcerative colitis (UC) patients compared with controls (30.16 vs 16.72%; P=0.0005; odds ratio (OR)=2.15; 95% confidence interval (CI)=1.39-3.32). Statistically significant association to UC was also found under dominant AA+AG vs GG (OR=1.85, 95% CI=1.07-3.21; P=0.02) and recessive models (OR=8.38; 95% CI=2.86-24.53; P=0.0001). In the same way, an association of TNFA rs1800629 variant was observed with IBD under recessive model AA vs AG+GG (OR=4.10; 95% CI=1.56-10.76; P=0.004). No evidence of significant associations was found for the remaining investigated polymorphisms. Our data suggest that TNFA gene promoter polymorphism participates in determining IBD susceptibility in Moroccan patients.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedColitis, UlcerativeCrohn DiseaseCytokinesFemaleHumansInflammatory Bowel DiseasesMaleMiddle AgedMoroccoReceptors, CytokineTumor Necrosis Factor-alphaYoung AdultCytokinesReceptors, CytokineTumor Necrosis Factor-alpha

Identifiers

PMID26632999
OpenAlexW2278582688

What OpenQuestion holds

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Registered trials

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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.