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Serum transforming growth factor- beta 1 and risk of pancreatic cancer in three prospective cohort studies
Purpose: Clinically evident chronic pancreatitis is a strong risk factor for pancreatic cancer. A small Japanese cohort study previously reported that pre-diagnostic serum transforming growth factor- beta 1 (TGF- beta 1) concentration, a potential marker of subclinical pancreatic inflammation, was a...
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Published in: | Cancer causes & control 2014-09, Vol.25 (9), p.1083-1091 |
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creator | Jacobs, Eric J Newton, Christina C Silverman, Debra T Nogueira, Leticia M Albanes, Demetrius Maennisto, Satu Pollak, Michael Stolzenberg-Solomon, Rachael Z |
description | Purpose: Clinically evident chronic pancreatitis is a strong risk factor for pancreatic cancer. A small Japanese cohort study previously reported that pre-diagnostic serum transforming growth factor- beta 1 (TGF- beta 1) concentration, a potential marker of subclinical pancreatic inflammation, was associated with higher risk of pancreatic cancer. We further explored this association in a larger prospective study. Methods: Serum TGF- beta 1 concentrations were measured in pre-diagnostic samples from 729 pancreatic cancer cases and 907 matched controls from a cohort of Finnish male smokers (the Alpa-Tocopherol, Beta-Carotene (ATBC) Cancer Prevention Study) and two cohorts of US men and women, the Cancer Prevention Study-II and the Prostate Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial. Multivariable-adjusted odds ratios (ORs) were estimated using conditional logistic regression. Results: Overall, serum TGF- beta 1 concentration was not associated with a clear increase in pancreatic cancer risk (OR 1.36, 95 % confidence interval (CI) 0.98-1.88 for highest vs. lowest quintile, p trend = 0.20). However, this association differed significantly by follow-up time (p = 0.02). Serum TGF- beta 1 concentration was not associated with risk during the first 10 years of follow-up, but was associated with higher risk during follow-up after 10 years (OR 2.13, 95 % CI 1.23-3.68 for highest vs. lowest quintile, p trend = 0.001). During follow-up after 10 years, serum TGF- beta 1 was associated with higher risk only in the ATBC cohort, although most subjects were from ATBC during this time period and statistical evidence for heterogeneity across cohorts was limited (p = 0.14). Conclusions: These results suggest that high serum TGF- beta 1 may be associated with increased risk of pancreatic cancer although a long follow-up period may be needed to observe this association. |
doi_str_mv | 10.1007/s10552-014-0409-z |
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A small Japanese cohort study previously reported that pre-diagnostic serum transforming growth factor- beta 1 (TGF- beta 1) concentration, a potential marker of subclinical pancreatic inflammation, was associated with higher risk of pancreatic cancer. We further explored this association in a larger prospective study. Methods: Serum TGF- beta 1 concentrations were measured in pre-diagnostic samples from 729 pancreatic cancer cases and 907 matched controls from a cohort of Finnish male smokers (the Alpa-Tocopherol, Beta-Carotene (ATBC) Cancer Prevention Study) and two cohorts of US men and women, the Cancer Prevention Study-II and the Prostate Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial. Multivariable-adjusted odds ratios (ORs) were estimated using conditional logistic regression. Results: Overall, serum TGF- beta 1 concentration was not associated with a clear increase in pancreatic cancer risk (OR 1.36, 95 % confidence interval (CI) 0.98-1.88 for highest vs. lowest quintile, p trend = 0.20). However, this association differed significantly by follow-up time (p = 0.02). Serum TGF- beta 1 concentration was not associated with risk during the first 10 years of follow-up, but was associated with higher risk during follow-up after 10 years (OR 2.13, 95 % CI 1.23-3.68 for highest vs. lowest quintile, p trend = 0.001). During follow-up after 10 years, serum TGF- beta 1 was associated with higher risk only in the ATBC cohort, although most subjects were from ATBC during this time period and statistical evidence for heterogeneity across cohorts was limited (p = 0.14). Conclusions: These results suggest that high serum TGF- beta 1 may be associated with increased risk of pancreatic cancer although a long follow-up period may be needed to observe this association.</description><identifier>ISSN: 0957-5243</identifier><identifier>EISSN: 1573-7225</identifier><identifier>DOI: 10.1007/s10552-014-0409-z</identifier><language>eng</language><ispartof>Cancer causes & control, 2014-09, Vol.25 (9), p.1083-1091</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids></links><search><creatorcontrib>Jacobs, Eric J</creatorcontrib><creatorcontrib>Newton, Christina C</creatorcontrib><creatorcontrib>Silverman, Debra T</creatorcontrib><creatorcontrib>Nogueira, Leticia M</creatorcontrib><creatorcontrib>Albanes, Demetrius</creatorcontrib><creatorcontrib>Maennisto, Satu</creatorcontrib><creatorcontrib>Pollak, Michael</creatorcontrib><creatorcontrib>Stolzenberg-Solomon, Rachael Z</creatorcontrib><title>Serum transforming growth factor- beta 1 and risk of pancreatic cancer in three prospective cohort studies</title><title>Cancer causes & control</title><description>Purpose: Clinically evident chronic pancreatitis is a strong risk factor for pancreatic cancer. A small Japanese cohort study previously reported that pre-diagnostic serum transforming growth factor- beta 1 (TGF- beta 1) concentration, a potential marker of subclinical pancreatic inflammation, was associated with higher risk of pancreatic cancer. We further explored this association in a larger prospective study. Methods: Serum TGF- beta 1 concentrations were measured in pre-diagnostic samples from 729 pancreatic cancer cases and 907 matched controls from a cohort of Finnish male smokers (the Alpa-Tocopherol, Beta-Carotene (ATBC) Cancer Prevention Study) and two cohorts of US men and women, the Cancer Prevention Study-II and the Prostate Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial. Multivariable-adjusted odds ratios (ORs) were estimated using conditional logistic regression. Results: Overall, serum TGF- beta 1 concentration was not associated with a clear increase in pancreatic cancer risk (OR 1.36, 95 % confidence interval (CI) 0.98-1.88 for highest vs. lowest quintile, p trend = 0.20). However, this association differed significantly by follow-up time (p = 0.02). Serum TGF- beta 1 concentration was not associated with risk during the first 10 years of follow-up, but was associated with higher risk during follow-up after 10 years (OR 2.13, 95 % CI 1.23-3.68 for highest vs. lowest quintile, p trend = 0.001). During follow-up after 10 years, serum TGF- beta 1 was associated with higher risk only in the ATBC cohort, although most subjects were from ATBC during this time period and statistical evidence for heterogeneity across cohorts was limited (p = 0.14). Conclusions: These results suggest that high serum TGF- beta 1 may be associated with increased risk of pancreatic cancer although a long follow-up period may be needed to observe this association.</description><issn>0957-5243</issn><issn>1573-7225</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNotjk1LAzEURYMoWKs_wN1buonmO9OlFLVCwYW6LpnkpZ3aTsYko-Cvd0Dhwr2Lw-EScs3ZLWfM3hXOtBaUcUWZYgv6c0JmXFtJrRD6lMzYQluqhZLn5KKUPWNMG8FmZP-KeTxCza4vMeVj129hm9N33UF0vqZMocXqgIPrA-SufECKMLjeZ3S18-CniRm6HuouI8KQUxnQ1-4LwaddyhVKHUOH5ZKcRXcoePXfc_L--PC2XNH1y9Pz8n5NB86bSkNQbeQxNCYaIxrvhPVeS22Mb6LF0EapkSvjg2hVgxMghWxRWseiVcrKObn5805XPkcsdXPsisfDwfWYxrLhhk-ZhFb-AoPPXi8</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Jacobs, Eric J</creator><creator>Newton, Christina C</creator><creator>Silverman, Debra T</creator><creator>Nogueira, Leticia M</creator><creator>Albanes, Demetrius</creator><creator>Maennisto, Satu</creator><creator>Pollak, Michael</creator><creator>Stolzenberg-Solomon, Rachael Z</creator><scope>7U1</scope><scope>7U2</scope><scope>C1K</scope></search><sort><creationdate>20140901</creationdate><title>Serum transforming growth factor- beta 1 and risk of pancreatic cancer in three prospective cohort studies</title><author>Jacobs, Eric J ; Newton, Christina C ; Silverman, Debra T ; Nogueira, Leticia M ; Albanes, Demetrius ; Maennisto, Satu ; Pollak, Michael ; Stolzenberg-Solomon, Rachael Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p118t-dd4bf1fd86f6628ca27cc53566c8f7edbf35e146cd2b48e8ca323be37a0f74473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jacobs, Eric J</creatorcontrib><creatorcontrib>Newton, Christina C</creatorcontrib><creatorcontrib>Silverman, Debra T</creatorcontrib><creatorcontrib>Nogueira, Leticia M</creatorcontrib><creatorcontrib>Albanes, Demetrius</creatorcontrib><creatorcontrib>Maennisto, Satu</creatorcontrib><creatorcontrib>Pollak, Michael</creatorcontrib><creatorcontrib>Stolzenberg-Solomon, Rachael Z</creatorcontrib><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Cancer causes & control</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jacobs, Eric J</au><au>Newton, Christina C</au><au>Silverman, Debra T</au><au>Nogueira, Leticia M</au><au>Albanes, Demetrius</au><au>Maennisto, Satu</au><au>Pollak, Michael</au><au>Stolzenberg-Solomon, Rachael Z</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum transforming growth factor- beta 1 and risk of pancreatic cancer in three prospective cohort studies</atitle><jtitle>Cancer causes & control</jtitle><date>2014-09-01</date><risdate>2014</risdate><volume>25</volume><issue>9</issue><spage>1083</spage><epage>1091</epage><pages>1083-1091</pages><issn>0957-5243</issn><eissn>1573-7225</eissn><abstract>Purpose: Clinically evident chronic pancreatitis is a strong risk factor for pancreatic cancer. A small Japanese cohort study previously reported that pre-diagnostic serum transforming growth factor- beta 1 (TGF- beta 1) concentration, a potential marker of subclinical pancreatic inflammation, was associated with higher risk of pancreatic cancer. We further explored this association in a larger prospective study. Methods: Serum TGF- beta 1 concentrations were measured in pre-diagnostic samples from 729 pancreatic cancer cases and 907 matched controls from a cohort of Finnish male smokers (the Alpa-Tocopherol, Beta-Carotene (ATBC) Cancer Prevention Study) and two cohorts of US men and women, the Cancer Prevention Study-II and the Prostate Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial. Multivariable-adjusted odds ratios (ORs) were estimated using conditional logistic regression. Results: Overall, serum TGF- beta 1 concentration was not associated with a clear increase in pancreatic cancer risk (OR 1.36, 95 % confidence interval (CI) 0.98-1.88 for highest vs. lowest quintile, p trend = 0.20). However, this association differed significantly by follow-up time (p = 0.02). Serum TGF- beta 1 concentration was not associated with risk during the first 10 years of follow-up, but was associated with higher risk during follow-up after 10 years (OR 2.13, 95 % CI 1.23-3.68 for highest vs. lowest quintile, p trend = 0.001). During follow-up after 10 years, serum TGF- beta 1 was associated with higher risk only in the ATBC cohort, although most subjects were from ATBC during this time period and statistical evidence for heterogeneity across cohorts was limited (p = 0.14). Conclusions: These results suggest that high serum TGF- beta 1 may be associated with increased risk of pancreatic cancer although a long follow-up period may be needed to observe this association.</abstract><doi>10.1007/s10552-014-0409-z</doi><tpages>9</tpages></addata></record> |
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title | Serum transforming growth factor- beta 1 and risk of pancreatic cancer in three prospective cohort studies |
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