Evidence map›Paper›PMID 27196462›Full record

ArticleMedicine2016

Familial Clustering of Gastric Cancer: A Retrospective Study Based on the Number of First-Degree Relatives.

Yoon Jin Choi, Nayoung Kim, Woncheol Jang, Bochang Seo, Sooyeon Oh, Cheol Min Shin, Dong Ho Lee, Hyun Chae Jung

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Genetic and Epigenetic Alterations ofPharmaceuticals (Basel, Switzerland) · 2021
    Article
  2. Promising aberrant DNA methylation marker to predict gastric cancer development in individuals with family history and long-term effects of H. pylori eradication on DNA methylation.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2021
    Article
  3. Article
  4. Association of currentUnited European gastroenterology journal · 2019
    Article
  5. Gastric cancer and family history.The Korean journal of internal medicine · 2016
    Review
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 1 institution in 1 country.

Yoon Jin ChoiFrom the Department of Internal Medicine (YJC, NK, CMS and DHL), Seoul National University Bundang Hospital, Seongnam; Department of Internal Medicine and Liver Research Institute (NK, SO, DHL and HCJ), Seoul National University College of Medicine; and Department of Statistics (WJ, BS), College of Science, Seoul National University, Seoul, South Korea.
Nayoung Kim
Woncheol Jang
Bochang Seo
Sooyeon Oh
Cheol Min Shin
Dong Ho Lee
Hyun Chae Jung
Seonam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This comprehensive cross-sectional study aimed to identify factors contributing to familial aggregation of gastric cancer (GC). A total of 1058 GC patients and 1268 controls were analyzed separately according to the presence or absence of a first-degree relative of GC (GC-relative). Logistic regression analysis adjusted for age, gender, residence during childhood, smoking, alcohol intake, monthly income, spicy food ingestion, Helicobacter pylori status and host cytokine polymorphisms was performed. Cytotoxin-associated gene A (cagA) positivity was a distinctive risk factor for GC in the family history (FH)-positive group (odds ratio [OR], 2.39; 95% confidence interval [CI], 1.42-4.00), while current/ex-smoker, moderate to strong spicy food ingestion, and non-B blood types were more closely associated with GC in the FH-negative group. Among the FH-positive group, alcohol consumption showed a synergistic carcinogenic effect in the at least 2 GC-relatives group compared to the 1 GC-relative group (1.71 vs. 9.58, P for interaction = 0.026), and this was dose-dependent. In the subjects with ≥2 GC-relatives, TGFB1-509T/T was a risk factor for GC (OR 23.74; 95% CI 1.37-410.91), as were rural residency in childhood, alcohol consumption, spicy food ingestion, and cagA positivity. These results suggest that subjects with FH may be a heterogeneous group in terms of gastric cancer susceptibility. Especially, subjects with ≥2 GC-relatives should undergo risk stratification including TGFB1-509T/T and alcohol consumption.

Indexed as

FamilyHelicobacter pyloriAdultAgedAlcohol DrinkingAntigens, BacterialBacterial ProteinsCase-Control StudiesCross-Sectional StudiesDietFemaleHelicobacter InfectionsHumansIncomeMaleMetaplasiaAntigens, BacterialBacterial ProteinscagA protein, Helicobacter pyloriTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID27196462
PMCPMC4902404
OpenAlexW2403808898

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.