Evidence map›Paper›PMID 26504356›Full record

ArticleMediators of inflammation2015

Polymorphisms of Tumor Necrosis Factor Alpha in Moroccan Patients with Gastric Pathology: New Single-Nucleotide Polymorphisms in TNF-α(-193) (G/A).

A Essadik, H Jouhadi, T Rhouda, S Nadifiyine, A Kettani, F Maachi

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. CytokineInternational journal of medical sciences · 2021
    Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. Frequency ofMediators of inflammation · 2016
    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

6 authors at 3 institutions in 1 country.

A EssadikLaboratory of Pathology-Digestif-Oncology, Pasteur Institute of Morocco, 20360 Casablanca, Morocco ; Laboratory of Biology and Health, Molecular Modeling and Quality Control Team, Faculty of Sciences Ben M'sik, University Hassan II, 7955 Casablanca, Morocco.
H JouhadiDepartment of Radiotherapy Oncology, Ibn Rochd University Hospital, 20000 Casablanca, Morocco.
T RhoudaLaboratory of Molecular Genetics and Pathophysiology, Faculty of Sciences Ben M'sik, University Hassan II, 7955 Casablanca, Morocco.
S NadifiyineLaboratory of Pathology-Digestif-Oncology, Pasteur Institute of Morocco, 20360 Casablanca, Morocco.
A KettaniLaboratory of Biology and Health, Molecular Modeling and Quality Control Team, Faculty of Sciences Ben M'sik, University Hassan II, 7955 Casablanca, Morocco.
F MaachiLaboratory of Pathology-Digestif-Oncology, Pasteur Institute of Morocco, 20360 Casablanca, Morocco.
Institut Pasteur du Maroc · MAUniversity of Hassan II Casablanca · MACentre Hospitalier Universitaire Ibn Rochd · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymorphisms in tumor necrosis factor alpha (TNF-α) gene are emerging as key determinants of gastric diseases. The TNF-α(-308) (G/A) and TNF-α(-238) (G/A) single-nucleotide polymorphisms SNPs are the most extensively studied. However, all these studies are conducted in Caucasian and Asian populations. Thus, for the first time in Africa, we sought to investigate whether polymorphisms in TNF-α gene were associated with the development of gastric pathology in Morocco. Two SNPs located in the promoter region (positions -308 and -238) in TNF-α gene were genotyped in 244 individuals (170 patients and 74 healthy controls). Odds ratios (ORs) and 95% confidence intervals (CI) were estimated using logistic regression analysis. The TNF-α(-238) (G/A) genotype was significantly associated with a high risk of gastritis and gastric cancer (GC) (P = 0.001 and P = 0.002, resp.). Furthermore, a new polymorphism located in the promoter region at position -193 in TNF-α gene was identified. The distribution of this SNP was markedly different in patients suffering from ulcers. The association between TNF-α(-193) (G/A) genotype and high risk of ulcer was significant (P = 0.03). These results suggest that the TNF-α(-193) (G/A) allele has a protective function against gastric cancer by developing ulcer.

Indexed as

Polymorphism, Single NucleotideCase-Control StudiesGastritisGene FrequencyGenetic Predisposition to DiseaseGenotypeHealthy VolunteersHumansMoroccoOdds RatioRegression AnalysisStomach NeoplasmsStomach UlcerTumor Necrosis Factor-alphaTNF protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID26504356
PMCPMC4609487
OpenAlexW1837487677

What OpenQuestion holds

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LicenceCC BY
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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.