Evidence map›Paper›PMID 36789984›Full record

ArticleThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2023

The Relationship between Gastroduodenal Pathologies and Helicobacter pylori cagL (Cytotoxin-Associated Gene L) Polymorphism.

Doğukan Özbey, Süleyman Demiryas, Seher Akkuş, Nuray Kepil, Harika Öykü Dinç, Nesrin Gareayaghi, Mehmet Demirci, Enes Ali Kurt, Ömer Uysal, Suat Sarıbaş and 2 more

Open access · diamondAbstract read
In one paragraph

Article in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 4 institutions in 2 countries.

Doğukan ÖzbeyDepartment of Medical Microbiology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Süleyman DemiryasDepartment of General Surgery, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Seher AkkuşDepartment of Medical Microbiology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Nuray KepilDepartment of Medical Pathology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Harika Öykü DinçDepartment of Pharmaceutical Microbiology, Bezmialem Vakıf University Faculty of Pharmacy, İstanbul, Turkey.
Nesrin GareayaghiUniversity of Health Sciences, İstanbul Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey.
Mehmet DemirciDepartment of Medical Microbiology, Kırklareli University Faculty of Medicine, Kırklareli, Turkey.
Enes Ali KurtDivision of Gastroenterology, Department of Internal Medicine, Cerrahpaşa School of Medicine, İstanbul University-Cerrahpaşa, İstanbul, Turkey.
Ömer UysalDepartment of Biostatistics, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Suat SarıbaşDepartment of Medical Microbiology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Hrisi Bahar TokmanDepartment of Medical Microbiology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Bekir KocazeybekDepartment of Medical Microbiology, İstanbul University Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Istanbul University-Cerrahpaşa · TRAnkara University · TRBezmiâlem Vakıf Üniversitesi · TRSağlık Bilimleri Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe polymorphisms in the region between 58 and 62 amino acids of the 194-amino acid CagL protein (CagL hypervariable motif) affect the binding affinity of CagL to integrin α5β1 (ITGA5B1) receptor in host epithelial cells and have an effect on the development of various gastrointestinal diseases. We aimed to evaluate the associations of gastroduodenal pathologies, with the polymorphisms of cagL gene of Helicobacter pylori (H. pylori) and also associations between vacA genotypes and cagL polymorphisms.

methodsA total of 19 gastric cancer, 16 duodenal ulcer, and 26 non-ulcer dyspepsia patients were included in this case-control study. All cases had H. pylori. A fragment of 651 bp from gene cagL (hp0539) and cagA, vacA genes was amplified by polymerase chain reaction. Purified polymerase chain reaction products were sequenced by Sanger sequencing, and nucleotide sequences were translated into amino acid sequences.

resultsAll of the H. pylori strains had cagL and cagA genes. In the 16 (84%) gastric cancer cases, the D58 amino acid polymorphism was significant than the 4 (15.4%) duodenal ulcer cases (P = .029), and the D58/K59 amino acid polymorphism was significant in 12 (63.1%) of the gastric cancer cases than 1 (3.85%) duodenal ulcer case (P = .008). D58/K59 and DKIGQ (n = 10; 52.63%) were the most common polymorphisms in the gastric cancer and were associated with the vacA genotype s1/m2, respectively (P = .022 and P = .008). The D58/K59 amino acid polymorphism was found to have a significant Odds Ratio (OR) value of 8.9 (P = .0017) in multivariate logistic regression analysis.

conclusionsThe risk of gastric cancer development is 8.9 times higher with D58/K59 polymorphism.

Indexed as

Duodenal UlcerHelicobacter InfectionsHelicobacter pyloriStomach NeoplasmsAmino AcidsAntigens, BacterialBacterial ProteinsCase-Control StudiesGenotypeHumansAmino AcidsAntigens, BacterialBacterial Proteins

Identifiers

PMID36789984
PMCPMC10210604
OpenAlexW4320856332

What OpenQuestion holds

Textmetadata
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.