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review of literature on clinical pancreatology - The Pancreapedia

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c<strong>on</strong>ducted a cohort analysis <str<strong>on</strong>g>of</str<strong>on</strong>g> prediagnostic vitamin E intake (4 tocopherols, 4 tocotrienols),serum alpha-tocopherol c<strong>on</strong>centrati<strong>on</strong>s, and pancreatic cancer in the Alpha-Tocopherol,Beta-Carotene Cancer Preventi<strong>on</strong> (ATBC) Study <str<strong>on</strong>g>of</str<strong>on</strong>g> male Finnish smokers aged 50-69 yearsat baseline. During follow-up from 1985 to 2004 (maximum: 19 years; median: 16 yeras), 318incident cases were diagnosed am<strong>on</strong>g cohort participants with complete serum samples(n=29,092); 306 cases had complete dietary data (n=27,111). Higher alpha-tocopherolc<strong>on</strong>centrati<strong>on</strong>s were associated with signifikant lower pancreatic cancer risk.Polyunsaturated fat, a putative prooxidant nutrient, modified the associati<strong>on</strong> such that theinverse alpha-tocopherol associati<strong>on</strong> was most pr<strong>on</strong>ounced in subjects with a highpolyunsaturated fat intake. No associati<strong>on</strong>s were observed for dietary tocopherols andtocotrienols. <strong>The</strong> results support the hypothesis that higher alpha-tocopherol c<strong>on</strong>centrati<strong>on</strong>smay play a protective role in pancreatic carcinogenesis in male smokers [350].Nitrate in drinking waterA matched case-c<strong>on</strong>trol and nitrate ecology study was used to investigate the associati<strong>on</strong>between mortality attributed to pancreatic cancer and nitrate exposure from Taiwan's drinkingwater. All pancreatic cancer deaths <str<strong>on</strong>g>of</str<strong>on</strong>g> Taiwan residents from 2000 through 2006 wereobtained from the Bureau <str<strong>on</strong>g>of</str<strong>on</strong>g> Vital Statistics <str<strong>on</strong>g>of</str<strong>on</strong>g> the Taiwan Provincial Department <str<strong>on</strong>g>of</str<strong>on</strong>g> Health.C<strong>on</strong>trols were deaths from other causes and were pair-matched to the cases by gender, year<str<strong>on</strong>g>of</str<strong>on</strong>g> birth, and year <str<strong>on</strong>g>of</str<strong>on</strong>g> death. Each matched c<strong>on</strong>trol was selected randomly from the set <str<strong>on</strong>g>of</str<strong>on</strong>g>possible c<strong>on</strong>trols for each case. Data <strong>on</strong> nitrate-nitrogen (NO 3 -N) levels <str<strong>on</strong>g>of</str<strong>on</strong>g> drinking waterthroughout Taiwan were collected from Taiwan Water Supply Corporati<strong>on</strong>. <strong>The</strong> municipality<str<strong>on</strong>g>of</str<strong>on</strong>g> residence for cancer cases and c<strong>on</strong>trols was assumed to be the source <str<strong>on</strong>g>of</str<strong>on</strong>g> the subject'snitrate exposure via drinking water. <strong>The</strong> adjusted odds ratios and c<strong>on</strong>fidence limits forpancreatic cancer death for those with high nitrate levels in their drinking water, as comparedto the lowest tertile, were 1.03 (0.9-1.18) and 1.1 (0.96-1.27), respectively. <strong>The</strong> results <str<strong>on</strong>g>of</str<strong>on</strong>g> thepresent study show that there was no statistically significant associati<strong>on</strong> between the levels<str<strong>on</strong>g>of</str<strong>on</strong>g> nitrate in drinking water and increased risk <str<strong>on</strong>g>of</str<strong>on</strong>g> death from pancreatic cancer [351].PerfluorooctanoatePerfluorooctanoate and perfluorooctanesulf<strong>on</strong>ate are used in many industrial products andhave been widely detected in human blood. Both chemicals are associated with tumordevelopment in animal studies, but data <strong>on</strong> carcinogenic potential in humans are sparse. Itwas investigated the associati<strong>on</strong> between plasma levels <str<strong>on</strong>g>of</str<strong>on</strong>g> perfluorooctanoate andperfluorooctanesulf<strong>on</strong>ate and cancer risk within a prospective Danish cohort <str<strong>on</strong>g>of</str<strong>on</strong>g> participantswith no previous cancer diagnosis at enrollment. From enrollment, between 1993 and 1997,and through, 2006, it was identified 713 participants with prostate cancer, 332 with bladdercancer, 128 with pancreatic cancer, and 67 with liver cancer in the entire cohort and it wasselected a comparis<strong>on</strong> subcohort <str<strong>on</strong>g>of</str<strong>on</strong>g> 772. Plasma c<strong>on</strong>centrati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> perfluorooctanoate andperfluorooctanesulf<strong>on</strong>ate were measured in each participant by use <str<strong>on</strong>g>of</str<strong>on</strong>g> high-pressure liquidchromatography coupled to tandem mass spectrometry. It was found no clear differences inincidence rate ratios for these cancers in relati<strong>on</strong> to plasma c<strong>on</strong>centrati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g>perfluorooctanoate or perfluorooctanesulf<strong>on</strong>ate. A 30-40 percent increase in risk estimatesfor prostate cancer was observed for the three upper quartiles <str<strong>on</strong>g>of</str<strong>on</strong>g> perfluorooctanesulf<strong>on</strong>atec<strong>on</strong>centrati<strong>on</strong> compared with the lowest quartile. Plasma c<strong>on</strong>centrati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g>perfluorooctanoate and perfluorooctanesulf<strong>on</strong>ate in the general Danish populati<strong>on</strong> appearnot to be associated with risk <str<strong>on</strong>g>of</str<strong>on</strong>g> prostate, bladder, pancreatic, or liver cancer [352].PsoriasisIt was examined overall and specific cancer risks am<strong>on</strong>g Swedish subjects who had beenhospitalised <strong>on</strong>e or more times for psoriasis. A database was created by identifying such

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