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review of literature on clinical pancreatology - The Pancreapedia

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the risk <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer. It was followed the participants in the NIH-AARP Diet andHealth Study from 1995/1996 through 2003. A baseline self-administered food frequencyquesti<strong>on</strong>naire was used to assess the dietary intake and exposure informati<strong>on</strong>. A total <str<strong>on</strong>g>of</str<strong>on</strong>g>1,151 exocrine pancreatic cancer cases were identified from 482,362 participants afterexcluding first-year <str<strong>on</strong>g>of</str<strong>on</strong>g> follow-up. <strong>The</strong>re were no associati<strong>on</strong>s between glycemic index, total oravailable carbohydrates, gycemic load, and pancreatic cancer risk. Participants with high freefructose and glucose intake were at a greater risk <str<strong>on</strong>g>of</str<strong>on</strong>g> developing pancreatic cancer. <strong>The</strong>rewere no statistically significant interacti<strong>on</strong>s by body mass index, physical activity, or smokingstatus. <strong>The</strong> results do not support an associati<strong>on</strong> between glycemic index, total or availablecarbohydrate intake, and glycemic load and pancreatic cancer risk. <strong>The</strong> higher riskassociated with high free fructose intake needs further c<strong>on</strong>firmati<strong>on</strong> and elucidati<strong>on</strong> [344].FructoseUsing fructose dehydrogenase-catalyzed c<strong>on</strong>versi<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> d-fructose to 5-ket<str<strong>on</strong>g>of</str<strong>on</strong>g>ructose, followedby quantitati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> MTT [3-(4,5-dimethylthiaze-syl)-2,5-diphenyltetrazolium bromide] formazanproducti<strong>on</strong> by direct spectrophotometry, an assay to measure serum fructose c<strong>on</strong>centrati<strong>on</strong>was developed, and assay sensitivity and specificity were tested. Validity <str<strong>on</strong>g>of</str<strong>on</strong>g> the assay wasc<strong>on</strong>firmed by gas chromatography-mass spectroscopy, and the assay was tested in healthysubjects and pancreatic cancer patients. <strong>The</strong> assay was highly specific, exhibiting no crossreactivitywith other sugars. Mean serum fructose c<strong>on</strong>centrati<strong>on</strong> in fasting healthy volunteerswas 1.9 + 0.4 mM and after ingesti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> a fructose and glucose-c<strong>on</strong>taining drink rose to 16.3+ 1.2 mM at 15 minutes and peaked at 30 minutes when serum fructose was 17.2 + 1.1 mM.Mean fasting serum fructose level was significantly higher at 5.7 + 2.5 mM in patients withpancreatic cancer than those with no pancreatic cancer. <strong>The</strong> fructose dehydrogenase-basedenzymatic assay correlated highly with gas chromatography-mass spectroscopic analysis <str<strong>on</strong>g>of</str<strong>on</strong>g>serum fructose with a correlati<strong>on</strong> coefficient <str<strong>on</strong>g>of</str<strong>on</strong>g> 0.94. It was c<strong>on</strong>cluded that measurement <str<strong>on</strong>g>of</str<strong>on</strong>g>serum fructose c<strong>on</strong>centrati<strong>on</strong> may provide insight into the relati<strong>on</strong>ship between refinedfructose intake and diseases including pancreatic cancer [345].Citrus fruits<strong>The</strong> purpose <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>on</strong>e systematic <str<strong>on</strong>g>review</str<strong>on</strong>g> was to investigate the associati<strong>on</strong> between dietaryintake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrus fruits and pancreatic cancer risk. <strong>The</strong> authors searched electr<strong>on</strong>ic databasesand the reference lists <str<strong>on</strong>g>of</str<strong>on</strong>g> publicati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> studies addressing diet and pancreatic cancer up toDecember 2007. All <str<strong>on</strong>g>of</str<strong>on</strong>g> the epidemiological studies that obtained individual data <strong>on</strong> dietaryintake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrus fruits and presented risk estimates <str<strong>on</strong>g>of</str<strong>on</strong>g> the associati<strong>on</strong> between intake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrusfruits and risk <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer were identified and included. Using general variancebasedmethods, study-specific odds ratios (ORs)/relative risk and associated c<strong>on</strong>fidenceinterval (CI)/SE for highest versus lowest intake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrus fruits level were extracted from eacharticle. Nine articles including 4 case-c<strong>on</strong>trol studies and 5 cohort studies proved eligible.Overall summary OR using random effect model suggested an inverse associati<strong>on</strong> in risk <str<strong>on</strong>g>of</str<strong>on</strong>g>pancreatic caner with intake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrus fruits (summary odds ratio, 0.83) with largeheterogeneity across studies. It was c<strong>on</strong>cluded that pooled results from observati<strong>on</strong>al studiesshowed an inverse associati<strong>on</strong> between intake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrus fruits and the risk <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreaticcancer, although results vary substantially across studies, and the apparent effect isrestricted to the weaker study design (case-c<strong>on</strong>trol studies) [346].Polluti<strong>on</strong>To describe the mortality pr<str<strong>on</strong>g>of</str<strong>on</strong>g>ile <str<strong>on</strong>g>of</str<strong>on</strong>g> the populati<strong>on</strong> resident in the polluted area <str<strong>on</strong>g>of</str<strong>on</strong>g> nati<strong>on</strong>alc<strong>on</strong>cern "Laguna di Grado e Marano" Friuli-Venezia-Giulia regi<strong>on</strong>, in the period 1997-2001and to examine mortality temporal trends between 1981 and 2001 a small-areaepidemiological study based <strong>on</strong> descriptive statistics, socioec<strong>on</strong>omic deprivati<strong>on</strong> variables,

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