Evidence map›Paper›PMID 22279585›Full record

SynthesisPloS one2012

Helicobacter pylori iceA, clinical outcomes, and correlation with cagA: a meta-analysis.

Seiji Shiota, Masahide Watada, Osamu Matsunari, Shun Iwatani, Rumiko Suzuki, Yoshio Yamaoka

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
7.3field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Association betweenBMJ open · 2020
    Pooled it
  3. Global epidemiology ofMicrobiology spectrum · 2026
    Article
  4. Helicobacter pylori cagA, vacA, and iceA genotypes and clinical outcomes: a cross-sectional study in central Vietnam.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Article
  5. Cancers · 2024
    Article
  6. Pathogenomics of Helicobacter pylori.Current topics in microbiology and immunology · 2023
    Review
  7. Correlation analysis of gastric mucosal lesions withAnnals of translational medicine · 2022
    Article
  8. Article
  9. Cells · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Canadian journal of gastroenterology & hepatology · 2017
    Article
  15. Gene polymorphisms of pathogenicWorld journal of gastroenterology · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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 1 institution in 2 countries.

Seiji ShiotaDepartment of Environmental and Preventive Medicine, Oita University Faculty of Medicine, Hasama-machi, Yufu-City, Oita, Japan.
Masahide Watada
Osamu Matsunari
Shun Iwatani
Rumiko Suzuki
Yoshio Yamaoka
Oita University · JP

Funding

REGULATION OF CXC CHEMOKINE EXPRESSION BY H. PYLORIR01DK062813 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI YAMAOKA, YOSHIO · 2004 to 2013
$3.0M
NIDDK NIH HHS DK62813NIDDK NIH HHS R01 DK062813
6 · The paper itself

Abstract

backgroundAlthough the iceA (induced by contact with epithelium) allelic types of Helicobacter pylori have been reported to be associated with peptic ulcer, the importance of iceA on clinical outcomes based on subsequent studies is controversial. The aim of this study was to estimate the magnitude of the risk for clinical outcomes associated with iceA.

methodsA literature search was performed using the PubMed and EMBASE databases for articles published through April 2011. Published case-control studies examining the relationship between iceA and clinical outcomes (gastritis, peptic ulcer, including gastric ulcer and duodenal ulcer, and gastric cancer) were included.

resultsFifty studies with a total of 5,357 patients were identified in the search. Infection with iceA1-positive H. pylori increased the overall risk for peptic ulcer by 1.26-fold (95% confidence interval [CI], 1.09-1.45). However, the test for heterogeneity was significant among these studies. Sensitivity analysis showed that the presence of iceA1 was significantly associated with peptic ulcer (odds ratio [OR] = 1.25, 95% CI = 1.08-1.44). The presence of iceA2 was inversely associated with peptic ulcer (OR = 0.76, 95% CI = 0.65-0.89). The presence of iceA was not associated with gastric cancer. Most studies examined the cagA status; however, only 15 studies examined the correlation and only 2 showed a positive correlation between the presence of cagA and iceA1.

conclusionOur meta-analysis confirmed the importance of the presence of iceA for peptic ulcer, although the significance was marginal.

Indexed as

Antigens, BacterialBacterial ProteinsCase-Control StudiesDuodenal UlcerGastritisGene Expression Regulation, BacterialGenotypeHelicobacter InfectionsHelicobacter pyloriHumansPeptic UlcerPrognosisStomach NeoplasmsAntigens, BacterialBacterial ProteinscagA protein, Helicobacter pyloriiceA1 protein, Helicobacter pyloriIceA2 protein, Helicobacter pylori

Identifiers

PMID22279585
PMCPMC3261200
OpenAlexW1971174795

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.