Evidence map›Paper›PMID 22057474›Full record

ArticleFamilial cancer2012

First degree relatives and familial aggregation of gastric cancer: who to choose for control in case-control studies?

Ricardo Marcos-Pinto, Mário Dinis-Ribeiro, Fátima Carneiro, José Carlos Machado, Ceu Figueiredo, Celso A Reis, José Ferreira, Jorge Areias

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Article in Familial cancer, 2012. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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.

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4 · The record

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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.

Ricardo Marcos-PintoInstitute of Biomedical Sciences, University of Porto (ICBAS/UP), Porto, Portugal. ricardomarcospinto@sapo.pt
Mário Dinis-Ribeiro
Fátima Carneiro
José Carlos Machado
Ceu Figueiredo
Celso A Reis
José Ferreira
Jorge Areias

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric carcinogenesis is a multifactorial process involving host gene and environmental interactions. Diverse case-control studies using different types of controls addressed the familial aggregation role for gastric cancer development. Our aim is to discuss the advantages and expected bias according to the different type of eligible controls. A PubMed search of papers on a query on first degree relatives of gastric cancer patients was conducted. The retrieved studies were evaluated regarding quality based on STROBE checklist. Data concerning risk of premalignant lesions and Helicobacter pylori infection was retrieved as the type of controls used on each study. Nine case-control studies were selected. A variety of controls were used ranging from general population to dyspeptic patients and spouses of the cases. We have observed that, independently of the type of control, the risk for the prevalence of premalignant lesions and H. pylori infection was higher for the cases. However, all of the evaluated case-control studies were average quality studies (mean 28 out of 45), with a small number of cases and controls (range from 39 to 300). Furthermore, concerning gene-environment interaction, each of the discussed type of control (general population, dyspeptic, spouse and neighbor) has potential advantages and disadvantages. The current data suggests that selection of any type of the aforementioned controls is feasible and seems to be mainly related to the feasibility of recruitment more than the genetic or environmental backgrounds. General population and dyspeptic patients would be equally appropriate for studies on familial aggregation of gastric cancer. Nevertheless, high-quality cohort studies are needed to validate this assumption.

Indexed as

Epidemiologic Research DesignGenetic Predisposition to DiseaseCase-Control StudiesFamilyGene-Environment InteractionHelicobacter InfectionsHelicobacter pyloriHumansPortugalPrecancerous ConditionsPrevalenceStomach Neoplasms

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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.