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Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population
BACKGROUND: A series of evidence suggests that genetic variation in toll-like receptor (TLR) 9 might influence the outcome of Helicobacter pylori (H. pylori) infection and play an important role in gastric carcinogenesis. METHODS: We conducted a case-control study to evaluate TLR9 polymorphisms on t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798501/ https://www.ncbi.nlm.nih.gov/pubmed/35117413 http://dx.doi.org/10.21037/tcr.2019.11.45 |
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author | Gao, Fang Qin, Jindong Wei, Xingru Tian, Xuyang Dong, Wenjie Dang, Tong Jia, Yanbin |
author_facet | Gao, Fang Qin, Jindong Wei, Xingru Tian, Xuyang Dong, Wenjie Dang, Tong Jia, Yanbin |
author_sort | Gao, Fang |
collection | PubMed |
description | BACKGROUND: A series of evidence suggests that genetic variation in toll-like receptor (TLR) 9 might influence the outcome of Helicobacter pylori (H. pylori) infection and play an important role in gastric carcinogenesis. METHODS: We conducted a case-control study to evaluate TLR9 polymorphisms on the risk of H. pylori infection and non-cardia gastric cancer (GC) in a Chinese population. We genotyped a tagging single-nucleotide polymorphism (SNP), rs164640, and a potentially functional SNP, rs187084, by TaqMan technique among 288 patients with non-cardia GC and 281 controls. Unconditional logistic regression (LR) was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for SNPs in association with H. pylori infection and non-cardia GC risk. RESULTS: Our results indicated that among normal controls, the minor allele homozygotes of both SNPs were significantly associated with a decreased risk of H. pylori infection when compared with their major allele homozygotes (for rs164640: OR =0.41, 95% CI, 0.18–0.93; for 187084: OR =0.38, 95% CI, 0.17–0.85). However, neither of the two SNPs demonstrated a significant association with non-cardia GC risk. CONCLUSIONS: Our results revealed that TLR9 polymorphisms might have effects on the risk of H. pylori infection, but they do not seem to contribute to the risk of non-cardia GC in our studied population. |
format | Online Article Text |
id | pubmed-8798501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87985012022-02-02 Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population Gao, Fang Qin, Jindong Wei, Xingru Tian, Xuyang Dong, Wenjie Dang, Tong Jia, Yanbin Transl Cancer Res Original Article BACKGROUND: A series of evidence suggests that genetic variation in toll-like receptor (TLR) 9 might influence the outcome of Helicobacter pylori (H. pylori) infection and play an important role in gastric carcinogenesis. METHODS: We conducted a case-control study to evaluate TLR9 polymorphisms on the risk of H. pylori infection and non-cardia gastric cancer (GC) in a Chinese population. We genotyped a tagging single-nucleotide polymorphism (SNP), rs164640, and a potentially functional SNP, rs187084, by TaqMan technique among 288 patients with non-cardia GC and 281 controls. Unconditional logistic regression (LR) was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for SNPs in association with H. pylori infection and non-cardia GC risk. RESULTS: Our results indicated that among normal controls, the minor allele homozygotes of both SNPs were significantly associated with a decreased risk of H. pylori infection when compared with their major allele homozygotes (for rs164640: OR =0.41, 95% CI, 0.18–0.93; for 187084: OR =0.38, 95% CI, 0.17–0.85). However, neither of the two SNPs demonstrated a significant association with non-cardia GC risk. CONCLUSIONS: Our results revealed that TLR9 polymorphisms might have effects on the risk of H. pylori infection, but they do not seem to contribute to the risk of non-cardia GC in our studied population. AME Publishing Company 2020-02 /pmc/articles/PMC8798501/ /pubmed/35117413 http://dx.doi.org/10.21037/tcr.2019.11.45 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Gao, Fang Qin, Jindong Wei, Xingru Tian, Xuyang Dong, Wenjie Dang, Tong Jia, Yanbin Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population |
title | Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population |
title_full | Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population |
title_fullStr | Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population |
title_full_unstemmed | Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population |
title_short | Polymorphisms of TLR9 gene are associated with a decreased risk of H. pylori infection in a Chinese population |
title_sort | polymorphisms of tlr9 gene are associated with a decreased risk of h. pylori infection in a chinese population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798501/ https://www.ncbi.nlm.nih.gov/pubmed/35117413 http://dx.doi.org/10.21037/tcr.2019.11.45 |
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