Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer
Our study investigated the relationship between gastric cancer development and activity of Helicobacter pylori‐associated chronic gastritis or the resulting chronic atrophic gastritis (CAG). A cohort of 4,655 healthy asymptomatic subjects, in whom serum pepsinogen (PG) and H. pylori antibody titer h...
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Veröffentlicht in: | International journal of cancer 2014-03, Vol.134 (6), p.1445-1457 |
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creator | Yoshida, Takeichi Kato, Jun Inoue, Izumi Yoshimura, Noriko Deguchi, Hisanobu Mukoubayashi, Chizu Oka, Masashi Watanabe, Mika Enomoto, Shotaro Niwa, Toru Maekita, Takao Iguchi, Mikitaka Tamai, Hideyuki Utsunomiya, Hirotoshi Yamamichi, Nobutake Fujishiro, Mitsuhiro Iwane, Masataka Takeshita, Tatsuya Ushijima, Toshikazu Ichinose, Masao |
description | Our study investigated the relationship between gastric cancer development and activity of Helicobacter pylori‐associated chronic gastritis or the resulting chronic atrophic gastritis (CAG). A cohort of 4,655 healthy asymptomatic subjects, in whom serum pepsinogen (PG) and H. pylori antibody titer had been measured to assess the activity and stage of H. pylori‐associated chronic gastritis, was followed for up to 16 years, and cancer development was investigated. In subjects with a serologically diagnosed healthy stomach (H. pylori‐negative/CAG‐negative), cancer incidence rate was low, at 16/100,000 person‐years. With the establishment of H. pylori infection and progression of chronic gastritis, significant stepwise cancer risk elevations were seen from CAG‐free subjects (H. pylori‐positive/CAG‐negative) [hazard ratio (HR) = 8.9, 95% confidence interval (CI) = 2.7–54.7] to subjects with CAG (H. pylori‐positive/CAG‐positive) (HR = 17.7, 95% CI = 5.4–108.6) and finally to subjects with metaplastic gastritis (H. pylori‐negative/CAG‐positive) (HR = 69.7, 95% CI = 13.6–502.9). In H. pylori‐infected CAG‐free subjects, significantly elevated cancer risk was observed in the subgroup with active inflammation‐based high PG II level or potent immune response‐based high H. pylori antibody titer; the former was associated with a particularly high risk of diffuse‐type cancer, and both subgroups showed high cancer incidence rates of around 250/100,000 person‐years, comparable to that in subjects with CAG. No such risk elevation was observed in H. pylori‐infected subjects with CAG. These results clearly indicate that gastric cancer develops mainly from the gastritis‐atrophy‐metaplasia‐cancer sequence and partly from active inflammation‐based direct carcinogenesis, and that serum levels of PG and H. pylori antibody titer provide indices of cancer development in H. pylori‐infected subjects.
What's new?
Infection with the bacteria H. pylori is the most common risk factor for developing gastric cancer. The infection causes chronic inflammation leading to a sequence of gastritis, atrophy, metaplasia, dysplasia, cancer. This study follows up a cohort of 6,000 men after 16 years and showed that cancer risk increased with the progression of inflammation and atrophy, which can be measured by serum tests. These tests, the authors suggest, would be useful in assessing risk among people infected with H. pylori. |
doi_str_mv | 10.1002/ijc.28470 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1492643725</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1492643725</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5170-cae2f6c026510e74310dcae25976f0c1e94018db947af5e5c8b50b3ab3143c6d3</originalsourceid><addsrcrecordid>eNp10dGK1DAUBuAiijuuXvgCEhBBL7p70qZNcynD6q4seKPXJU1PZzOkSc1pV_o8vuhmdkYFwavAycd_DvxZ9prDBQcoLu3eXBSNkPAk23BQMoeCV0-zTfqDXPKyPsteEO0BOK9APM_OCgGgeKk22a-t9gYj6_EeXZhG9DPrNGHPgmfmLgZvDdNmtvfIdprmaGdLTPueRaTFzdbvTvPE5himu5XpBIiQDindygjjMjJ3WEAsDGzCiawPO_SPOdforAld2pHOmFYXok3z2XahX9ls0_Rl9mzQjvDV6T3Pvn-6-ra9zm-_fr7ZfrzNTcUl5EZjMdQGirrigFKUHPrDrFKyHsBwVAJ403dKSD1UWJmmq6ArdVdyUZq6L8-z98fcKYYfC9LcjpYMOqc9hoVaLlRRi1IWVaJv_6H7sESfrktKCs4bBTKpD0dlYiCKOLRTtKOOa8uhPTTXpubax-aSfXNKXLoR-z_yd1UJvDsBTUa7IabiLP11DVdKNSK5y6P7aR2u_9_Y3nzZHlc_AJCosjI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1474118907</pqid></control><display><type>article</type><title>Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Yoshida, Takeichi ; Kato, Jun ; Inoue, Izumi ; Yoshimura, Noriko ; Deguchi, Hisanobu ; Mukoubayashi, Chizu ; Oka, Masashi ; Watanabe, Mika ; Enomoto, Shotaro ; Niwa, Toru ; Maekita, Takao ; Iguchi, Mikitaka ; Tamai, Hideyuki ; Utsunomiya, Hirotoshi ; Yamamichi, Nobutake ; Fujishiro, Mitsuhiro ; Iwane, Masataka ; Takeshita, Tatsuya ; Ushijima, Toshikazu ; Ichinose, Masao</creator><creatorcontrib>Yoshida, Takeichi ; Kato, Jun ; Inoue, Izumi ; Yoshimura, Noriko ; Deguchi, Hisanobu ; Mukoubayashi, Chizu ; Oka, Masashi ; Watanabe, Mika ; Enomoto, Shotaro ; Niwa, Toru ; Maekita, Takao ; Iguchi, Mikitaka ; Tamai, Hideyuki ; Utsunomiya, Hirotoshi ; Yamamichi, Nobutake ; Fujishiro, Mitsuhiro ; Iwane, Masataka ; Takeshita, Tatsuya ; Ushijima, Toshikazu ; Ichinose, Masao</creatorcontrib><description>Our study investigated the relationship between gastric cancer development and activity of Helicobacter pylori‐associated chronic gastritis or the resulting chronic atrophic gastritis (CAG). A cohort of 4,655 healthy asymptomatic subjects, in whom serum pepsinogen (PG) and H. pylori antibody titer had been measured to assess the activity and stage of H. pylori‐associated chronic gastritis, was followed for up to 16 years, and cancer development was investigated. In subjects with a serologically diagnosed healthy stomach (H. pylori‐negative/CAG‐negative), cancer incidence rate was low, at 16/100,000 person‐years. With the establishment of H. pylori infection and progression of chronic gastritis, significant stepwise cancer risk elevations were seen from CAG‐free subjects (H. pylori‐positive/CAG‐negative) [hazard ratio (HR) = 8.9, 95% confidence interval (CI) = 2.7–54.7] to subjects with CAG (H. pylori‐positive/CAG‐positive) (HR = 17.7, 95% CI = 5.4–108.6) and finally to subjects with metaplastic gastritis (H. pylori‐negative/CAG‐positive) (HR = 69.7, 95% CI = 13.6–502.9). In H. pylori‐infected CAG‐free subjects, significantly elevated cancer risk was observed in the subgroup with active inflammation‐based high PG II level or potent immune response‐based high H. pylori antibody titer; the former was associated with a particularly high risk of diffuse‐type cancer, and both subgroups showed high cancer incidence rates of around 250/100,000 person‐years, comparable to that in subjects with CAG. No such risk elevation was observed in H. pylori‐infected subjects with CAG. These results clearly indicate that gastric cancer develops mainly from the gastritis‐atrophy‐metaplasia‐cancer sequence and partly from active inflammation‐based direct carcinogenesis, and that serum levels of PG and H. pylori antibody titer provide indices of cancer development in H. pylori‐infected subjects.
What's new?
Infection with the bacteria H. pylori is the most common risk factor for developing gastric cancer. The infection causes chronic inflammation leading to a sequence of gastritis, atrophy, metaplasia, dysplasia, cancer. This study follows up a cohort of 6,000 men after 16 years and showed that cancer risk increased with the progression of inflammation and atrophy, which can be measured by serum tests. These tests, the authors suggest, would be useful in assessing risk among people infected with H. pylori.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.28470</identifier><identifier>PMID: 24009139</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken, NJ: Wiley-Blackwell</publisher><subject>Antibodies, Bacterial - blood ; Antibodies, Bacterial - immunology ; atrophic gastritis ; Biological and medical sciences ; Biomarkers, Tumor - blood ; Biomarkers, Tumor - immunology ; Cancer ; cancer high‐risk ; Cohort Studies ; cohort study ; Confidence intervals ; Disease Progression ; Enzyme-Linked Immunosorbent Assay ; Follow-Up Studies ; Gastric cancer ; Gastritis, Atrophic - blood ; Gastritis, Atrophic - diagnosis ; Gastritis, Atrophic - etiology ; Gastroenterology. Liver. Pancreas. Abdomen ; Helicobacter Infections - complications ; Helicobacter Infections - immunology ; Helicobacter Infections - microbiology ; Helicobacter pylori ; Helicobacter pylori - immunology ; Helicobacter pylori - pathogenicity ; Humans ; Infections ; Inflammation - blood ; Inflammation - diagnosis ; Inflammation - etiology ; Male ; Medical research ; Medical sciences ; Metaplasia - blood ; Metaplasia - diagnosis ; Metaplasia - etiology ; Middle Aged ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Other diseases. Semiology ; pepsinogen ; Pepsinogen A - blood ; Pepsinogen C - blood ; Prognosis ; Radioimmunoassay ; Risk Factors ; Stomach - pathology ; Stomach - virology ; Stomach Neoplasms - blood ; Stomach Neoplasms - diagnosis ; Stomach Neoplasms - etiology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors ; Ulcers</subject><ispartof>International journal of cancer, 2014-03, Vol.134 (6), p.1445-1457</ispartof><rights>2013 UICC</rights><rights>2015 INIST-CNRS</rights><rights>2013 UICC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5170-cae2f6c026510e74310dcae25976f0c1e94018db947af5e5c8b50b3ab3143c6d3</citedby><cites>FETCH-LOGICAL-c5170-cae2f6c026510e74310dcae25976f0c1e94018db947af5e5c8b50b3ab3143c6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.28470$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.28470$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28199984$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24009139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoshida, Takeichi</creatorcontrib><creatorcontrib>Kato, Jun</creatorcontrib><creatorcontrib>Inoue, Izumi</creatorcontrib><creatorcontrib>Yoshimura, Noriko</creatorcontrib><creatorcontrib>Deguchi, Hisanobu</creatorcontrib><creatorcontrib>Mukoubayashi, Chizu</creatorcontrib><creatorcontrib>Oka, Masashi</creatorcontrib><creatorcontrib>Watanabe, Mika</creatorcontrib><creatorcontrib>Enomoto, Shotaro</creatorcontrib><creatorcontrib>Niwa, Toru</creatorcontrib><creatorcontrib>Maekita, Takao</creatorcontrib><creatorcontrib>Iguchi, Mikitaka</creatorcontrib><creatorcontrib>Tamai, Hideyuki</creatorcontrib><creatorcontrib>Utsunomiya, Hirotoshi</creatorcontrib><creatorcontrib>Yamamichi, Nobutake</creatorcontrib><creatorcontrib>Fujishiro, Mitsuhiro</creatorcontrib><creatorcontrib>Iwane, Masataka</creatorcontrib><creatorcontrib>Takeshita, Tatsuya</creatorcontrib><creatorcontrib>Ushijima, Toshikazu</creatorcontrib><creatorcontrib>Ichinose, Masao</creatorcontrib><title>Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Our study investigated the relationship between gastric cancer development and activity of Helicobacter pylori‐associated chronic gastritis or the resulting chronic atrophic gastritis (CAG). A cohort of 4,655 healthy asymptomatic subjects, in whom serum pepsinogen (PG) and H. pylori antibody titer had been measured to assess the activity and stage of H. pylori‐associated chronic gastritis, was followed for up to 16 years, and cancer development was investigated. In subjects with a serologically diagnosed healthy stomach (H. pylori‐negative/CAG‐negative), cancer incidence rate was low, at 16/100,000 person‐years. With the establishment of H. pylori infection and progression of chronic gastritis, significant stepwise cancer risk elevations were seen from CAG‐free subjects (H. pylori‐positive/CAG‐negative) [hazard ratio (HR) = 8.9, 95% confidence interval (CI) = 2.7–54.7] to subjects with CAG (H. pylori‐positive/CAG‐positive) (HR = 17.7, 95% CI = 5.4–108.6) and finally to subjects with metaplastic gastritis (H. pylori‐negative/CAG‐positive) (HR = 69.7, 95% CI = 13.6–502.9). In H. pylori‐infected CAG‐free subjects, significantly elevated cancer risk was observed in the subgroup with active inflammation‐based high PG II level or potent immune response‐based high H. pylori antibody titer; the former was associated with a particularly high risk of diffuse‐type cancer, and both subgroups showed high cancer incidence rates of around 250/100,000 person‐years, comparable to that in subjects with CAG. No such risk elevation was observed in H. pylori‐infected subjects with CAG. These results clearly indicate that gastric cancer develops mainly from the gastritis‐atrophy‐metaplasia‐cancer sequence and partly from active inflammation‐based direct carcinogenesis, and that serum levels of PG and H. pylori antibody titer provide indices of cancer development in H. pylori‐infected subjects.
What's new?
Infection with the bacteria H. pylori is the most common risk factor for developing gastric cancer. The infection causes chronic inflammation leading to a sequence of gastritis, atrophy, metaplasia, dysplasia, cancer. This study follows up a cohort of 6,000 men after 16 years and showed that cancer risk increased with the progression of inflammation and atrophy, which can be measured by serum tests. These tests, the authors suggest, would be useful in assessing risk among people infected with H. pylori.</description><subject>Antibodies, Bacterial - blood</subject><subject>Antibodies, Bacterial - immunology</subject><subject>atrophic gastritis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - blood</subject><subject>Biomarkers, Tumor - immunology</subject><subject>Cancer</subject><subject>cancer high‐risk</subject><subject>Cohort Studies</subject><subject>cohort study</subject><subject>Confidence intervals</subject><subject>Disease Progression</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Follow-Up Studies</subject><subject>Gastric cancer</subject><subject>Gastritis, Atrophic - blood</subject><subject>Gastritis, Atrophic - diagnosis</subject><subject>Gastritis, Atrophic - etiology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Helicobacter Infections - complications</subject><subject>Helicobacter Infections - immunology</subject><subject>Helicobacter Infections - microbiology</subject><subject>Helicobacter pylori</subject><subject>Helicobacter pylori - immunology</subject><subject>Helicobacter pylori - pathogenicity</subject><subject>Humans</subject><subject>Infections</subject><subject>Inflammation - blood</subject><subject>Inflammation - diagnosis</subject><subject>Inflammation - etiology</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Metaplasia - blood</subject><subject>Metaplasia - diagnosis</subject><subject>Metaplasia - etiology</subject><subject>Middle Aged</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Other diseases. Semiology</subject><subject>pepsinogen</subject><subject>Pepsinogen A - blood</subject><subject>Pepsinogen C - blood</subject><subject>Prognosis</subject><subject>Radioimmunoassay</subject><subject>Risk Factors</subject><subject>Stomach - pathology</subject><subject>Stomach - virology</subject><subject>Stomach Neoplasms - blood</subject><subject>Stomach Neoplasms - diagnosis</subject><subject>Stomach Neoplasms - etiology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><subject>Ulcers</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10dGK1DAUBuAiijuuXvgCEhBBL7p70qZNcynD6q4seKPXJU1PZzOkSc1pV_o8vuhmdkYFwavAycd_DvxZ9prDBQcoLu3eXBSNkPAk23BQMoeCV0-zTfqDXPKyPsteEO0BOK9APM_OCgGgeKk22a-t9gYj6_EeXZhG9DPrNGHPgmfmLgZvDdNmtvfIdprmaGdLTPueRaTFzdbvTvPE5himu5XpBIiQDindygjjMjJ3WEAsDGzCiawPO_SPOdforAld2pHOmFYXok3z2XahX9ls0_Rl9mzQjvDV6T3Pvn-6-ra9zm-_fr7ZfrzNTcUl5EZjMdQGirrigFKUHPrDrFKyHsBwVAJ403dKSD1UWJmmq6ArdVdyUZq6L8-z98fcKYYfC9LcjpYMOqc9hoVaLlRRi1IWVaJv_6H7sESfrktKCs4bBTKpD0dlYiCKOLRTtKOOa8uhPTTXpubax-aSfXNKXLoR-z_yd1UJvDsBTUa7IabiLP11DVdKNSK5y6P7aR2u_9_Y3nzZHlc_AJCosjI</recordid><startdate>20140315</startdate><enddate>20140315</enddate><creator>Yoshida, Takeichi</creator><creator>Kato, Jun</creator><creator>Inoue, Izumi</creator><creator>Yoshimura, Noriko</creator><creator>Deguchi, Hisanobu</creator><creator>Mukoubayashi, Chizu</creator><creator>Oka, Masashi</creator><creator>Watanabe, Mika</creator><creator>Enomoto, Shotaro</creator><creator>Niwa, Toru</creator><creator>Maekita, Takao</creator><creator>Iguchi, Mikitaka</creator><creator>Tamai, Hideyuki</creator><creator>Utsunomiya, Hirotoshi</creator><creator>Yamamichi, Nobutake</creator><creator>Fujishiro, Mitsuhiro</creator><creator>Iwane, Masataka</creator><creator>Takeshita, Tatsuya</creator><creator>Ushijima, Toshikazu</creator><creator>Ichinose, Masao</creator><general>Wiley-Blackwell</general><general>Wiley Subscription Services, Inc</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>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7QL</scope><scope>7T2</scope><scope>7U1</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20140315</creationdate><title>Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer</title><author>Yoshida, Takeichi ; Kato, Jun ; Inoue, Izumi ; Yoshimura, Noriko ; Deguchi, Hisanobu ; Mukoubayashi, Chizu ; Oka, Masashi ; Watanabe, Mika ; Enomoto, Shotaro ; Niwa, Toru ; Maekita, Takao ; Iguchi, Mikitaka ; Tamai, Hideyuki ; Utsunomiya, Hirotoshi ; Yamamichi, Nobutake ; Fujishiro, Mitsuhiro ; Iwane, Masataka ; Takeshita, Tatsuya ; Ushijima, Toshikazu ; Ichinose, Masao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5170-cae2f6c026510e74310dcae25976f0c1e94018db947af5e5c8b50b3ab3143c6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antibodies, Bacterial - blood</topic><topic>Antibodies, Bacterial - immunology</topic><topic>atrophic gastritis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - blood</topic><topic>Biomarkers, Tumor - immunology</topic><topic>Cancer</topic><topic>cancer high‐risk</topic><topic>Cohort Studies</topic><topic>cohort study</topic><topic>Confidence intervals</topic><topic>Disease Progression</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Follow-Up Studies</topic><topic>Gastric cancer</topic><topic>Gastritis, Atrophic - blood</topic><topic>Gastritis, Atrophic - diagnosis</topic><topic>Gastritis, Atrophic - etiology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Helicobacter Infections - complications</topic><topic>Helicobacter Infections - immunology</topic><topic>Helicobacter Infections - microbiology</topic><topic>Helicobacter pylori</topic><topic>Helicobacter pylori - immunology</topic><topic>Helicobacter pylori - pathogenicity</topic><topic>Humans</topic><topic>Infections</topic><topic>Inflammation - blood</topic><topic>Inflammation - diagnosis</topic><topic>Inflammation - etiology</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Metaplasia - blood</topic><topic>Metaplasia - diagnosis</topic><topic>Metaplasia - etiology</topic><topic>Middle Aged</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Other diseases. Semiology</topic><topic>pepsinogen</topic><topic>Pepsinogen A - blood</topic><topic>Pepsinogen C - blood</topic><topic>Prognosis</topic><topic>Radioimmunoassay</topic><topic>Risk Factors</topic><topic>Stomach - pathology</topic><topic>Stomach - virology</topic><topic>Stomach Neoplasms - blood</topic><topic>Stomach Neoplasms - diagnosis</topic><topic>Stomach Neoplasms - etiology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshida, Takeichi</creatorcontrib><creatorcontrib>Kato, Jun</creatorcontrib><creatorcontrib>Inoue, Izumi</creatorcontrib><creatorcontrib>Yoshimura, Noriko</creatorcontrib><creatorcontrib>Deguchi, Hisanobu</creatorcontrib><creatorcontrib>Mukoubayashi, Chizu</creatorcontrib><creatorcontrib>Oka, Masashi</creatorcontrib><creatorcontrib>Watanabe, Mika</creatorcontrib><creatorcontrib>Enomoto, Shotaro</creatorcontrib><creatorcontrib>Niwa, Toru</creatorcontrib><creatorcontrib>Maekita, Takao</creatorcontrib><creatorcontrib>Iguchi, Mikitaka</creatorcontrib><creatorcontrib>Tamai, Hideyuki</creatorcontrib><creatorcontrib>Utsunomiya, Hirotoshi</creatorcontrib><creatorcontrib>Yamamichi, Nobutake</creatorcontrib><creatorcontrib>Fujishiro, Mitsuhiro</creatorcontrib><creatorcontrib>Iwane, Masataka</creatorcontrib><creatorcontrib>Takeshita, Tatsuya</creatorcontrib><creatorcontrib>Ushijima, Toshikazu</creatorcontrib><creatorcontrib>Ichinose, Masao</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>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshida, Takeichi</au><au>Kato, Jun</au><au>Inoue, Izumi</au><au>Yoshimura, Noriko</au><au>Deguchi, Hisanobu</au><au>Mukoubayashi, Chizu</au><au>Oka, Masashi</au><au>Watanabe, Mika</au><au>Enomoto, Shotaro</au><au>Niwa, Toru</au><au>Maekita, Takao</au><au>Iguchi, Mikitaka</au><au>Tamai, Hideyuki</au><au>Utsunomiya, Hirotoshi</au><au>Yamamichi, Nobutake</au><au>Fujishiro, Mitsuhiro</au><au>Iwane, Masataka</au><au>Takeshita, Tatsuya</au><au>Ushijima, Toshikazu</au><au>Ichinose, Masao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2014-03-15</date><risdate>2014</risdate><volume>134</volume><issue>6</issue><spage>1445</spage><epage>1457</epage><pages>1445-1457</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Our study investigated the relationship between gastric cancer development and activity of Helicobacter pylori‐associated chronic gastritis or the resulting chronic atrophic gastritis (CAG). A cohort of 4,655 healthy asymptomatic subjects, in whom serum pepsinogen (PG) and H. pylori antibody titer had been measured to assess the activity and stage of H. pylori‐associated chronic gastritis, was followed for up to 16 years, and cancer development was investigated. In subjects with a serologically diagnosed healthy stomach (H. pylori‐negative/CAG‐negative), cancer incidence rate was low, at 16/100,000 person‐years. With the establishment of H. pylori infection and progression of chronic gastritis, significant stepwise cancer risk elevations were seen from CAG‐free subjects (H. pylori‐positive/CAG‐negative) [hazard ratio (HR) = 8.9, 95% confidence interval (CI) = 2.7–54.7] to subjects with CAG (H. pylori‐positive/CAG‐positive) (HR = 17.7, 95% CI = 5.4–108.6) and finally to subjects with metaplastic gastritis (H. pylori‐negative/CAG‐positive) (HR = 69.7, 95% CI = 13.6–502.9). In H. pylori‐infected CAG‐free subjects, significantly elevated cancer risk was observed in the subgroup with active inflammation‐based high PG II level or potent immune response‐based high H. pylori antibody titer; the former was associated with a particularly high risk of diffuse‐type cancer, and both subgroups showed high cancer incidence rates of around 250/100,000 person‐years, comparable to that in subjects with CAG. No such risk elevation was observed in H. pylori‐infected subjects with CAG. These results clearly indicate that gastric cancer develops mainly from the gastritis‐atrophy‐metaplasia‐cancer sequence and partly from active inflammation‐based direct carcinogenesis, and that serum levels of PG and H. pylori antibody titer provide indices of cancer development in H. pylori‐infected subjects.
What's new?
Infection with the bacteria H. pylori is the most common risk factor for developing gastric cancer. The infection causes chronic inflammation leading to a sequence of gastritis, atrophy, metaplasia, dysplasia, cancer. This study follows up a cohort of 6,000 men after 16 years and showed that cancer risk increased with the progression of inflammation and atrophy, which can be measured by serum tests. These tests, the authors suggest, would be useful in assessing risk among people infected with H. pylori.</abstract><cop>Hoboken, NJ</cop><pub>Wiley-Blackwell</pub><pmid>24009139</pmid><doi>10.1002/ijc.28470</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0020-7136 |
ispartof | International journal of cancer, 2014-03, Vol.134 (6), p.1445-1457 |
issn | 0020-7136 1097-0215 |
language | eng |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Antibodies, Bacterial - blood Antibodies, Bacterial - immunology atrophic gastritis Biological and medical sciences Biomarkers, Tumor - blood Biomarkers, Tumor - immunology Cancer cancer high‐risk Cohort Studies cohort study Confidence intervals Disease Progression Enzyme-Linked Immunosorbent Assay Follow-Up Studies Gastric cancer Gastritis, Atrophic - blood Gastritis, Atrophic - diagnosis Gastritis, Atrophic - etiology Gastroenterology. Liver. Pancreas. Abdomen Helicobacter Infections - complications Helicobacter Infections - immunology Helicobacter Infections - microbiology Helicobacter pylori Helicobacter pylori - immunology Helicobacter pylori - pathogenicity Humans Infections Inflammation - blood Inflammation - diagnosis Inflammation - etiology Male Medical research Medical sciences Metaplasia - blood Metaplasia - diagnosis Metaplasia - etiology Middle Aged Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Other diseases. Semiology pepsinogen Pepsinogen A - blood Pepsinogen C - blood Prognosis Radioimmunoassay Risk Factors Stomach - pathology Stomach - virology Stomach Neoplasms - blood Stomach Neoplasms - diagnosis Stomach Neoplasms - etiology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors Ulcers |
title | Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer |
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