Plasma Metabolomic Signatures of H. pylori Infection, Alcohol Drinking, Smoking, and Risk of Gastric Cancer
Circulating metabolic profiles have shown promising potential in identifying high-risk populations for various diseases, while metabolic perturbation plays an important role in gastric cancer. In this study, we conducted a cross-sectional study with 1800 participants to identify plasma metabolite si...
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creator | Yu, Yuhui Zheng, Zhonghua Gao, Xinxiang Gu, Yuanliang Zhang, Min Hu, Beiping Gao, Qian Li, Zhe Chen, Yan Li, Qian Shen, Fang Zhu, Meng Hang, Dong Zhan, Qiang Wang, Lu Shen, Chong Lu, Xiangfeng Gu, Dongfeng Ma, Hongxia Shen, Hongbing Jin, Guangfu Yan, Caiwang |
description | Circulating metabolic profiles have shown promising potential in identifying high-risk populations for various diseases, while metabolic perturbation plays an important role in gastric cancer. In this study, we conducted a cross-sectional study with 1800 participants to identify plasma metabolite signatures associated with environmental risk factors of gastric cancer. Subsequently, we evaluated the association between these signatures and gastric cancer risk in a nested case-control study involving 326 gastric cancer cases and 326 matched cancer-free controls. We conducted mediation analyses to elucidate the potential impact of metabolites on the association between environmental factors and gastric cancer. In the cross-sectional study, we identified 46 metabolites associated with Helicobacter pylori (H. pylori) infection, 365 with alcohol drinking, and 154 with smoking status. In the nested case-control study, 60 plasma metabolites, comprising 30 lipids, 15 amino acids, 6 xenobiotics, 3 nucleotides, 2 cofactors and vitamins, 2 carbohydrate, 1 energy, and 1 peptide, were associated with gastric cancer risk. A one-standard deviation increment in the H. pylori infection-related metabolomic signature was associated with an increased risk of gastric cancer (OR = 1.66, 95% CI: 1.32-2.09, p = 1.62 × 10
). Furthermore, the effect of H. pylori infection on gastric cancer was partially mediated by the metabolomic signature (23.28%, 95% CI: 0.09-0.56) or adenine (13.69%, 95% CI: 0.05-0.31). In conclusion, we have identified metabolites associated with environmental factors and demonstrated the association between the H. pylori infection signature and gastric cancer risk. The findings provide novel insights into characterizing high-risk population for gastric cancer. |
doi_str_mv | 10.1002/mc.23851 |
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). Furthermore, the effect of H. pylori infection on gastric cancer was partially mediated by the metabolomic signature (23.28%, 95% CI: 0.09-0.56) or adenine (13.69%, 95% CI: 0.05-0.31). In conclusion, we have identified metabolites associated with environmental factors and demonstrated the association between the H. pylori infection signature and gastric cancer risk. The findings provide novel insights into characterizing high-risk population for gastric cancer.</description><identifier>ISSN: 0899-1987</identifier><identifier>ISSN: 1098-2744</identifier><identifier>EISSN: 1098-2744</identifier><identifier>DOI: 10.1002/mc.23851</identifier><identifier>PMID: 39630052</identifier><language>eng</language><publisher>United States</publisher><ispartof>Molecular carcinogenesis, 2024-12</ispartof><rights>2024 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c174t-c79c581ce948f91be64b779f4f405cc99e3474c5a47dfacb68153236997b0f343</cites><orcidid>0000-0002-2581-5906 ; 0000-0001-6944-0459 ; 0000-0002-9821-6955 ; 0000-0003-0249-5337</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39630052$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Yuhui</creatorcontrib><creatorcontrib>Zheng, Zhonghua</creatorcontrib><creatorcontrib>Gao, Xinxiang</creatorcontrib><creatorcontrib>Gu, Yuanliang</creatorcontrib><creatorcontrib>Zhang, Min</creatorcontrib><creatorcontrib>Hu, Beiping</creatorcontrib><creatorcontrib>Gao, Qian</creatorcontrib><creatorcontrib>Li, Zhe</creatorcontrib><creatorcontrib>Chen, Yan</creatorcontrib><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Shen, Fang</creatorcontrib><creatorcontrib>Zhu, Meng</creatorcontrib><creatorcontrib>Hang, Dong</creatorcontrib><creatorcontrib>Zhan, Qiang</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Shen, Chong</creatorcontrib><creatorcontrib>Lu, Xiangfeng</creatorcontrib><creatorcontrib>Gu, Dongfeng</creatorcontrib><creatorcontrib>Ma, Hongxia</creatorcontrib><creatorcontrib>Shen, Hongbing</creatorcontrib><creatorcontrib>Jin, Guangfu</creatorcontrib><creatorcontrib>Yan, Caiwang</creatorcontrib><title>Plasma Metabolomic Signatures of H. pylori Infection, Alcohol Drinking, Smoking, and Risk of Gastric Cancer</title><title>Molecular carcinogenesis</title><addtitle>Mol Carcinog</addtitle><description>Circulating metabolic profiles have shown promising potential in identifying high-risk populations for various diseases, while metabolic perturbation plays an important role in gastric cancer. In this study, we conducted a cross-sectional study with 1800 participants to identify plasma metabolite signatures associated with environmental risk factors of gastric cancer. Subsequently, we evaluated the association between these signatures and gastric cancer risk in a nested case-control study involving 326 gastric cancer cases and 326 matched cancer-free controls. We conducted mediation analyses to elucidate the potential impact of metabolites on the association between environmental factors and gastric cancer. In the cross-sectional study, we identified 46 metabolites associated with Helicobacter pylori (H. pylori) infection, 365 with alcohol drinking, and 154 with smoking status. In the nested case-control study, 60 plasma metabolites, comprising 30 lipids, 15 amino acids, 6 xenobiotics, 3 nucleotides, 2 cofactors and vitamins, 2 carbohydrate, 1 energy, and 1 peptide, were associated with gastric cancer risk. A one-standard deviation increment in the H. pylori infection-related metabolomic signature was associated with an increased risk of gastric cancer (OR = 1.66, 95% CI: 1.32-2.09, p = 1.62 × 10
). Furthermore, the effect of H. pylori infection on gastric cancer was partially mediated by the metabolomic signature (23.28%, 95% CI: 0.09-0.56) or adenine (13.69%, 95% CI: 0.05-0.31). In conclusion, we have identified metabolites associated with environmental factors and demonstrated the association between the H. pylori infection signature and gastric cancer risk. The findings provide novel insights into characterizing high-risk population for gastric cancer.</description><issn>0899-1987</issn><issn>1098-2744</issn><issn>1098-2744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpFkM1OAjEURhujEUQTn8B06YLBdtqZTpcEFUgwGtH1pFNarPQH22HB2wuCurp3cb6zOABcYzTACOV3Tg5yUhX4BHQx4lWWM0pPQRdVnGeYV6wDLlL6RAhjVqBz0CG8JAgVeResXqxITsAn1Yom2OCMhHOz9KLdRJVg0HAygOutDdHAqddKtib4PhxaGT6ChffR-JXxyz6cu3B4hF_AV5NW--1YpDbujCPhpYqX4EwLm9TV8fbA--PD22iSzZ7H09FwlknMaJtJxmVRYak4rTTHjSppwxjXVFNUSMm5IpRRWQjKFlrIpqxwQXJScs4apAklPXB78K5j-Nqo1NbOJKmsFV6FTaoJpogTVDL0j8oYUopK1-tonIjbGqN6n7Z2sv5Ju0NvjtZN49TiD_xtSb4BEkVytw</recordid><startdate>20241204</startdate><enddate>20241204</enddate><creator>Yu, Yuhui</creator><creator>Zheng, Zhonghua</creator><creator>Gao, Xinxiang</creator><creator>Gu, Yuanliang</creator><creator>Zhang, Min</creator><creator>Hu, Beiping</creator><creator>Gao, Qian</creator><creator>Li, Zhe</creator><creator>Chen, Yan</creator><creator>Li, Qian</creator><creator>Shen, Fang</creator><creator>Zhu, Meng</creator><creator>Hang, Dong</creator><creator>Zhan, Qiang</creator><creator>Wang, Lu</creator><creator>Shen, Chong</creator><creator>Lu, Xiangfeng</creator><creator>Gu, Dongfeng</creator><creator>Ma, Hongxia</creator><creator>Shen, Hongbing</creator><creator>Jin, Guangfu</creator><creator>Yan, Caiwang</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2581-5906</orcidid><orcidid>https://orcid.org/0000-0001-6944-0459</orcidid><orcidid>https://orcid.org/0000-0002-9821-6955</orcidid><orcidid>https://orcid.org/0000-0003-0249-5337</orcidid></search><sort><creationdate>20241204</creationdate><title>Plasma Metabolomic Signatures of H. pylori Infection, Alcohol Drinking, Smoking, and Risk of Gastric Cancer</title><author>Yu, Yuhui ; Zheng, Zhonghua ; Gao, Xinxiang ; Gu, Yuanliang ; Zhang, Min ; Hu, Beiping ; Gao, Qian ; Li, Zhe ; Chen, Yan ; Li, Qian ; Shen, Fang ; Zhu, Meng ; Hang, Dong ; Zhan, Qiang ; Wang, Lu ; Shen, Chong ; Lu, Xiangfeng ; Gu, Dongfeng ; Ma, Hongxia ; Shen, Hongbing ; Jin, Guangfu ; Yan, Caiwang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c174t-c79c581ce948f91be64b779f4f405cc99e3474c5a47dfacb68153236997b0f343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Yuhui</creatorcontrib><creatorcontrib>Zheng, Zhonghua</creatorcontrib><creatorcontrib>Gao, Xinxiang</creatorcontrib><creatorcontrib>Gu, Yuanliang</creatorcontrib><creatorcontrib>Zhang, Min</creatorcontrib><creatorcontrib>Hu, Beiping</creatorcontrib><creatorcontrib>Gao, Qian</creatorcontrib><creatorcontrib>Li, Zhe</creatorcontrib><creatorcontrib>Chen, Yan</creatorcontrib><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Shen, Fang</creatorcontrib><creatorcontrib>Zhu, Meng</creatorcontrib><creatorcontrib>Hang, Dong</creatorcontrib><creatorcontrib>Zhan, Qiang</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Shen, Chong</creatorcontrib><creatorcontrib>Lu, Xiangfeng</creatorcontrib><creatorcontrib>Gu, Dongfeng</creatorcontrib><creatorcontrib>Ma, Hongxia</creatorcontrib><creatorcontrib>Shen, Hongbing</creatorcontrib><creatorcontrib>Jin, Guangfu</creatorcontrib><creatorcontrib>Yan, Caiwang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular carcinogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Yuhui</au><au>Zheng, Zhonghua</au><au>Gao, Xinxiang</au><au>Gu, Yuanliang</au><au>Zhang, Min</au><au>Hu, Beiping</au><au>Gao, Qian</au><au>Li, Zhe</au><au>Chen, Yan</au><au>Li, Qian</au><au>Shen, Fang</au><au>Zhu, Meng</au><au>Hang, Dong</au><au>Zhan, Qiang</au><au>Wang, Lu</au><au>Shen, Chong</au><au>Lu, Xiangfeng</au><au>Gu, Dongfeng</au><au>Ma, Hongxia</au><au>Shen, Hongbing</au><au>Jin, Guangfu</au><au>Yan, Caiwang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma Metabolomic Signatures of H. pylori Infection, Alcohol Drinking, Smoking, and Risk of Gastric Cancer</atitle><jtitle>Molecular carcinogenesis</jtitle><addtitle>Mol Carcinog</addtitle><date>2024-12-04</date><risdate>2024</risdate><issn>0899-1987</issn><issn>1098-2744</issn><eissn>1098-2744</eissn><abstract>Circulating metabolic profiles have shown promising potential in identifying high-risk populations for various diseases, while metabolic perturbation plays an important role in gastric cancer. In this study, we conducted a cross-sectional study with 1800 participants to identify plasma metabolite signatures associated with environmental risk factors of gastric cancer. Subsequently, we evaluated the association between these signatures and gastric cancer risk in a nested case-control study involving 326 gastric cancer cases and 326 matched cancer-free controls. We conducted mediation analyses to elucidate the potential impact of metabolites on the association between environmental factors and gastric cancer. In the cross-sectional study, we identified 46 metabolites associated with Helicobacter pylori (H. pylori) infection, 365 with alcohol drinking, and 154 with smoking status. In the nested case-control study, 60 plasma metabolites, comprising 30 lipids, 15 amino acids, 6 xenobiotics, 3 nucleotides, 2 cofactors and vitamins, 2 carbohydrate, 1 energy, and 1 peptide, were associated with gastric cancer risk. A one-standard deviation increment in the H. pylori infection-related metabolomic signature was associated with an increased risk of gastric cancer (OR = 1.66, 95% CI: 1.32-2.09, p = 1.62 × 10
). Furthermore, the effect of H. pylori infection on gastric cancer was partially mediated by the metabolomic signature (23.28%, 95% CI: 0.09-0.56) or adenine (13.69%, 95% CI: 0.05-0.31). In conclusion, we have identified metabolites associated with environmental factors and demonstrated the association between the H. pylori infection signature and gastric cancer risk. The findings provide novel insights into characterizing high-risk population for gastric cancer.</abstract><cop>United States</cop><pmid>39630052</pmid><doi>10.1002/mc.23851</doi><orcidid>https://orcid.org/0000-0002-2581-5906</orcidid><orcidid>https://orcid.org/0000-0001-6944-0459</orcidid><orcidid>https://orcid.org/0000-0002-9821-6955</orcidid><orcidid>https://orcid.org/0000-0003-0249-5337</orcidid></addata></record> |
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title | Plasma Metabolomic Signatures of H. pylori Infection, Alcohol Drinking, Smoking, and Risk of Gastric Cancer |
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