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Association between a pro-inflammatory genetic profile and the risk of chronic atrophic gastritis among older adults from Germany
Abstract Background Pro-inflammatory polymorphisms have been suggested to explain part of the individual diversity in susceptibility to gastric carcinogenesis. We aimed to assess their impact on the risk of chronic atrophic gastritis (CAG) in a population-based study. Methods Among 9953 older adults...
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Published in: | European journal of cancer (1990) 2009-02, Vol.45 (3), p.428-434 |
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description | Abstract Background Pro-inflammatory polymorphisms have been suggested to explain part of the individual diversity in susceptibility to gastric carcinogenesis. We aimed to assess their impact on the risk of chronic atrophic gastritis (CAG) in a population-based study. Methods Among 9953 older adults from Saarland/Germany, eight single nucleotide polymorphisms (SNPs) were assessed for 534 cases with serologically defined CAG and 534 age- and sex-matched controls at baseline examination. Results Of the 8 SNPs, only IL10 T-819C showed a borderline significant association with CAG risk (odds ratio for CC versus TT: 1.67 (95% confidence interval: 1.01–2.76)). No significant differences were observed for the distribution of inferred haplotypes between cases and controls. However, joint evaluation of several cytokine variants suggested an increased risk of CAG among individuals carrying several pro-inflammatory genotypes. Conclusions Our findings suggest that a pro-inflammatory genetic profile may contribute to inter-individual variation in gastric cancer risk by increasing the susceptibility to the development of CAG. |
doi_str_mv | 10.1016/j.ejca.2008.09.019 |
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We aimed to assess their impact on the risk of chronic atrophic gastritis (CAG) in a population-based study. Methods Among 9953 older adults from Saarland/Germany, eight single nucleotide polymorphisms (SNPs) were assessed for 534 cases with serologically defined CAG and 534 age- and sex-matched controls at baseline examination. Results Of the 8 SNPs, only IL10 T-819C showed a borderline significant association with CAG risk (odds ratio for CC versus TT: 1.67 (95% confidence interval: 1.01–2.76)). No significant differences were observed for the distribution of inferred haplotypes between cases and controls. However, joint evaluation of several cytokine variants suggested an increased risk of CAG among individuals carrying several pro-inflammatory genotypes. Conclusions Our findings suggest that a pro-inflammatory genetic profile may contribute to inter-individual variation in gastric cancer risk by increasing the susceptibility to the development of CAG.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2008.09.019</identifier><identifier>PMID: 19013788</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Aged ; Biological and medical sciences ; Chronic atrophic gastritis ; Cytokines - genetics ; Female ; Gastritis, Atrophic - epidemiology ; Gastritis, Atrophic - genetics ; Gene Expression Profiling ; Genetic Predisposition to Disease - epidemiology ; Genetic Predisposition to Disease - genetics ; Germany - epidemiology ; Hematology, Oncology and Palliative Medicine ; Humans ; Interleukin-10 ; Male ; Medical sciences ; Middle Aged ; Odds Ratio ; Pharmacology. Drug treatments ; Polymorphism ; Polymorphism, Single Nucleotide - genetics ; Pro-inflammatory ; Risk Factors ; Stomach Neoplasms - epidemiology ; Stomach Neoplasms - genetics ; Susceptibility ; Tumors</subject><ispartof>European journal of cancer (1990), 2009-02, Vol.45 (3), p.428-434</ispartof><rights>Elsevier Ltd</rights><rights>2008 Elsevier Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-9a6835c38c2c4d116c1b61f6d8e1d4cd933fe8e1437a5aeb385af93a5b7e7f8b3</citedby><cites>FETCH-LOGICAL-c470t-9a6835c38c2c4d116c1b61f6d8e1d4cd933fe8e1437a5aeb385af93a5b7e7f8b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21181136$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19013788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Lei</creatorcontrib><creatorcontrib>Weck, Melanie N</creatorcontrib><creatorcontrib>Nieters, Alexandra</creatorcontrib><creatorcontrib>Brenner, Hermann</creatorcontrib><title>Association between a pro-inflammatory genetic profile and the risk of chronic atrophic gastritis among older adults from Germany</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Abstract Background Pro-inflammatory polymorphisms have been suggested to explain part of the individual diversity in susceptibility to gastric carcinogenesis. We aimed to assess their impact on the risk of chronic atrophic gastritis (CAG) in a population-based study. Methods Among 9953 older adults from Saarland/Germany, eight single nucleotide polymorphisms (SNPs) were assessed for 534 cases with serologically defined CAG and 534 age- and sex-matched controls at baseline examination. Results Of the 8 SNPs, only IL10 T-819C showed a borderline significant association with CAG risk (odds ratio for CC versus TT: 1.67 (95% confidence interval: 1.01–2.76)). No significant differences were observed for the distribution of inferred haplotypes between cases and controls. However, joint evaluation of several cytokine variants suggested an increased risk of CAG among individuals carrying several pro-inflammatory genotypes. Conclusions Our findings suggest that a pro-inflammatory genetic profile may contribute to inter-individual variation in gastric cancer risk by increasing the susceptibility to the development of CAG.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Chronic atrophic gastritis</subject><subject>Cytokines - genetics</subject><subject>Female</subject><subject>Gastritis, Atrophic - epidemiology</subject><subject>Gastritis, Atrophic - genetics</subject><subject>Gene Expression Profiling</subject><subject>Genetic Predisposition to Disease - epidemiology</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Germany - epidemiology</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Interleukin-10</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Odds Ratio</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Pro-inflammatory</subject><subject>Risk Factors</subject><subject>Stomach Neoplasms - epidemiology</subject><subject>Stomach Neoplasms - genetics</subject><subject>Susceptibility</subject><subject>Tumors</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kk2LFDEQQBtR3NnVP-BBctFbj0mnPxIQYVl0FRY8qOdQna7MpLc7GZP0LnP0n5tmBgUPnlJQryqVlyqKV4xuGWXtu3GLo4ZtRanYUrmlTD4pNkx0sqSiqZ4WGyobWQpay4viMsaRUtqJmj4vLpikjHdCbIpf1zF6bSFZ70iP6RHRESCH4EvrzATzDMmHI9mhw2T1mjB2QgJuIGmPJNh4T7wheh-8y3lIwR_2OdhBTMEmGwnM3u2InwYMBIZlSpGY4Gdyi2EGd3xRPDMwRXx5Pq-KH58-fr_5XN59vf1yc31X6rqjqZTQCt5oLnSl64GxVrO-ZaYdBLKh1oPk3GCOa95BA9hz0YCRHJq-w86Inl8Vb0998xN-LhiTmm3UOE3g0C9RVbTmQjKWweoE6uBjDGjUIdgZwlExqlbxalSreLWKV1SqLD4XvT53X_oZh78lZ9MZeHMGIGqYTACnbfzDVYyJfHebufcnDrOLB4tBRW3RaRxsQJ3U4O3_5_jwT7mebP4YmO7xiHH0S3DZsmIqVoqqb-uKrBtCRV6OhnP-G4O1uQs</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Gao, Lei</creator><creator>Weck, Melanie N</creator><creator>Nieters, Alexandra</creator><creator>Brenner, Hermann</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20090201</creationdate><title>Association between a pro-inflammatory genetic profile and the risk of chronic atrophic gastritis among older adults from Germany</title><author>Gao, Lei ; Weck, Melanie N ; Nieters, Alexandra ; Brenner, Hermann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-9a6835c38c2c4d116c1b61f6d8e1d4cd933fe8e1437a5aeb385af93a5b7e7f8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Chronic atrophic gastritis</topic><topic>Cytokines - genetics</topic><topic>Female</topic><topic>Gastritis, Atrophic - epidemiology</topic><topic>Gastritis, Atrophic - genetics</topic><topic>Gene Expression Profiling</topic><topic>Genetic Predisposition to Disease - epidemiology</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Germany - epidemiology</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Interleukin-10</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Odds Ratio</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Pro-inflammatory</topic><topic>Risk Factors</topic><topic>Stomach Neoplasms - epidemiology</topic><topic>Stomach Neoplasms - genetics</topic><topic>Susceptibility</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Lei</creatorcontrib><creatorcontrib>Weck, Melanie N</creatorcontrib><creatorcontrib>Nieters, Alexandra</creatorcontrib><creatorcontrib>Brenner, Hermann</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Lei</au><au>Weck, Melanie N</au><au>Nieters, Alexandra</au><au>Brenner, Hermann</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between a pro-inflammatory genetic profile and the risk of chronic atrophic gastritis among older adults from Germany</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>45</volume><issue>3</issue><spage>428</spage><epage>434</epage><pages>428-434</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Abstract Background Pro-inflammatory polymorphisms have been suggested to explain part of the individual diversity in susceptibility to gastric carcinogenesis. We aimed to assess their impact on the risk of chronic atrophic gastritis (CAG) in a population-based study. Methods Among 9953 older adults from Saarland/Germany, eight single nucleotide polymorphisms (SNPs) were assessed for 534 cases with serologically defined CAG and 534 age- and sex-matched controls at baseline examination. Results Of the 8 SNPs, only IL10 T-819C showed a borderline significant association with CAG risk (odds ratio for CC versus TT: 1.67 (95% confidence interval: 1.01–2.76)). No significant differences were observed for the distribution of inferred haplotypes between cases and controls. However, joint evaluation of several cytokine variants suggested an increased risk of CAG among individuals carrying several pro-inflammatory genotypes. Conclusions Our findings suggest that a pro-inflammatory genetic profile may contribute to inter-individual variation in gastric cancer risk by increasing the susceptibility to the development of CAG.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>19013788</pmid><doi>10.1016/j.ejca.2008.09.019</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Biological and medical sciences Chronic atrophic gastritis Cytokines - genetics Female Gastritis, Atrophic - epidemiology Gastritis, Atrophic - genetics Gene Expression Profiling Genetic Predisposition to Disease - epidemiology Genetic Predisposition to Disease - genetics Germany - epidemiology Hematology, Oncology and Palliative Medicine Humans Interleukin-10 Male Medical sciences Middle Aged Odds Ratio Pharmacology. Drug treatments Polymorphism Polymorphism, Single Nucleotide - genetics Pro-inflammatory Risk Factors Stomach Neoplasms - epidemiology Stomach Neoplasms - genetics Susceptibility Tumors |
title | Association between a pro-inflammatory genetic profile and the risk of chronic atrophic gastritis among older adults from Germany |
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