Evidence map›Paper›PMID 26706772›Full record

ArticleJournal of digestive diseases2016

Prostate stem cell antigen gene TT genotype and development of intestinal metaplasia in Helicobacter pylori infection.

Takahiro Uotani, Mitsushige Sugimoto, Hitomi Ichikawa, Shingo Tanaka, Hiroyuki Nagashima, Tomohisa Uchida, David Y Graham, Yoshio Yamaoka

Abstract read
In one paragraph

Article in Journal of digestive diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 5 institutions in 2 countries.

Takahiro UotaniDepartment of Gastroenterology and Hepatology, Baylor College of Medicine and Michael DeBakey Veterans Affairs Medical Center, Houston, USA.
Mitsushige SugimotoDivision of Digestive Endoscopy, Shiga University of Medical Science Hospital, Otsu.
Hitomi IchikawaFirst Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu.
Shingo TanakaDepartment of Gastroenterology and Hepatology, Baylor College of Medicine and Michael DeBakey Veterans Affairs Medical Center, Houston, USA.
Hiroyuki NagashimaGastroenterological Medicine, Rumoi City Hospital, Rumoi.
Tomohisa UchidaDepartment of Molecular Pathology, Oita University Faculty of Medicine, Yufu, Oita, Japan.
David Y GrahamDepartment of Gastroenterology and Hepatology, Baylor College of Medicine and Michael DeBakey Veterans Affairs Medical Center, Houston, USA.
Yoshio YamaokaDepartment of Gastroenterology and Hepatology, Baylor College of Medicine and Michael DeBakey Veterans Affairs Medical Center, Houston, USA.
Oita University · JPMichael E. DeBakey VA Medical Center · USHamamatsu University School of Medicine · JPIzumi City General Hospital · JPShiga University of Medical Science Hospital · 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

objectivesGastric cancer is etiologically related to interactions between Helicobacter pylori (H. pylori) infection, environmental and host factors. Gastric carcinoma is associated with a cascade of increasing atrophic gastric mucosal damage. Prostate stem cell antigen (PSCA) polymorphisms have been associated with an increased risk of gastric cancer. We aimed to examine the interaction between PSCA polymorphisms and H. pylori in the progression of H. pylori-related gastritis.

methodsThe genotypes (TT, TC and CC) of PSCA single nucleotide polymorphism rs2294008 among H. pylori infected and uninfected Bhutanese were compared with the severity of H. pylori-related gastritis [neutrophils, monocytes, atrophy scores, H. pylori density, and the presence and extent of intestinal metaplasia (IM)] using the updated Sydney system.

resultsBiopsies from 339 participants were included. The proportion of biopsies with IM was significantly (P < 0.05) greater in those with the TT genotype than in either those with the CT or CC genotype. Although no significant differences were found in inflammation or H. pylori density scores, the scores for IM at both gastric corpus and antrum among participants infected by H. pylori with the TT genotype was significantly (P < 0.05) greater than in the C allele carriers.

conclusionPSCA TT genotype is associated with a more than a threefold increase in the prevalence and the extent of gastric mucosal IM compared to C allele carriers among H. pylori-infected Bhutanese.

Indexed as

Helicobacter pyloriAdultBiopsyFemaleGastric MucosaGastroscopyGenetic Predisposition to DiseaseGenotypeHelicobacter InfectionsHumansKallikreinsMaleMetaplasiaMiddle AgedPolymorphism, Single NucleotidePrecancerous ConditionsKallikreinsKLK3 protein, humanProstate-Specific Antigengastric neoplasmsHelicobacter pyloriintestinal metaplasiaprostate stem cell antigen genesingle nucleotide polymorphism

Identifiers

PMID26706772
PMCPMC4783456
OpenAlexW2207471964

What OpenQuestion holds

Textmetadata
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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.