Evidence map›Paper›PMID 38365575›Full record

SynthesisBMC gastroenterology2024

The pertinence of gastric cancer and interleukin 10-819 single nucleotide polymorphisms: a meta-analysis and systematic review.

Qianqian Mao, Yanwen Liu, Xi Chen, Cheng Jiang Liu

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in BMC gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Qianqian MaoMedical School of Southeast University, 210000, Nanjing, China.
Yanwen LiuDepartment of Oncology, Zhongda Hospital, Medical School of Southeast University, 210000, Nanjing, China. lyw0171@163.com.
Xi ChenSchool of health, Brooks College (Sunnyvale) the United States of America, Department of epidemiology and statistics, School of public health, Medical College, Zhejiang University, 310000, Hangzhou, China.
Cheng Jiang LiuDepartment of General Medicine, Affiliated Anqing First People's Hospital of Anhui Medical University, 246000, Anqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCytokines regulate the interaction between the immune system and malignant tumors. Among them, interleukin-10 (IL-10) is a multifunctional anti-inflammatory cytokine mainly produced by immune cells. The correlation between gastric cancer and T/C single nucleotide polymorphism (SNP) of interleukin-10 (IL-10) promoter-819(rs1800871)was opaque and remained to be determined. We aim to explore the pertinence of gastric cancer and SNP of interleukin 10-819 by meta-analysis via five statistical models.

methodsDatabases including PubMed, Cochrane Library, Embase, the Scopus, and Google Scholars were comprehensively retrieved for the eligible studies on the related topic from inception to March 2022. Odds ratios (ORs) were generated for dichotomous variants by meta-analysis in each model via STATA 17.0 MP. The statistical models comprised recessive model, over-dominant model, allele model, co-dominant model and dominant model. Subgroup analysis was performed to investigate the difference across races as well as the source of heterogeneity if necessary.

resultsEventually a total of 15 articles reporting 7779 patients were enrolled in our study. There were 2383 patients and 5396 controls, collectively. There was no correlation between gastric cancer and IL-10 819 in recessive model, co-dominant model or dominant model, and subgroup analysis showed that Asian, Latin American and Caucasian had no correlation with the risk of gastric cancer. In the allelic model, there was significant correlation between gastric cancer and IL-10 819 (OR = 3.96%, 95%CI: 3.28 to 3.78). In the over-dominant model, there is no correlation between gastric cancer and IL-10 819, but subgroup analysis uncovered significant vulnerability of Asian people with regard to gastric cancer.

conclusionsIn our study, both Asians, Latin Americans, and Europeans showed an increased risk of gastric cancer in the allelic model, whereas only Asians showed significant susceptibility in the super dominant model. Of course, more large cohort studies are needed to confirm our results.

Indexed as

Polymorphism, Single NucleotideStomach NeoplasmsGenetic Predisposition to DiseaseHumansInterleukin-10Risk FactorsIL10 protein, humanInterleukin-10AssociationGastric cancerGeneIL-10 819Single nucleotide polymorphism

Identifiers

PMID38365575
PMCPMC10874039

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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.