Prediagnostic selenium status and hepatobiliary cancer risk in the European Prospective Investigation into Cancer and Nutrition cohort

0301 basic medicine Male Hepatocellular carcinoma selenoprotein P Medicine (miscellaneous) 09 Engineering 0302 clinical medicine Risk Factors HEPATOCELLULAR-CARCINOMA Odds Ratio Prospective Studies selenium BILIARY-TRACT 11 Medical and Health Sciences Nutrition and Dietetics SELENOMETHIONINE Liver Neoplasms Gallbladder CHRONIC HEPATITIS hepatocellular carcinoma Hepatobiliary cancer Middle Aged 3. Good health Europe Biliary Tract Neoplasms Liver selenium status PLASMA SELENIUM VIRUS Female Selenium status Life Sciences & Biomedicine Liver cancer SELENOPROTEIN-P EXPRESSION Carcinoma, Hepatocellular BIOMARKERS prospective cohort Nutritional Status hepatobiliary cancer liver cancer Selenium 03 medical and health sciences Selenoprotein P Journal Article Humans Aged Science & Technology Nutrition & Dietetics Carcinoma Hepatocellular LIVER-CIRRHOSIS Prospective cohort hepatobiliary cancer; hepatocellular carcinoma; liver cancer; prospective cohort; selenium; selenium status; selenoprotein P Logistic Models Case-Control Studies Bile Ducts Deficiency Diseases
DOI: 10.3945/ajcn.116.131672 Publication Date: 2016-06-30T03:33:41Z
ABSTRACT
BACKGROUND: Selenium status is suboptimal in many Europeans and may be a risk factor for the development of various cancers, including those of the liver and biliary tract. OBJECTIVE: We wished to examine whether selenium status in advance of cancer onset is associated with hepatobiliary cancers in the EPIC (European Prospective Investigation into Cancer and Nutrition) study. DESIGN: We assessed prediagnostic selenium status by measuring serum concentrations of selenium and selenoprotein P (SePP; the major circulating selenium transfer protein) and examined the association with hepatocellular carcinoma (HCC; n = 121), gallbladder and biliary tract cancers (GBTCs; n = 100), and intrahepatic bile duct cancer (IHBC; n = 40) risk in a nested case-control design within the EPIC study. Selenium was measured by total reflection X-ray fluorescence, and SePP was determined by a colorimetric sandwich ELISA. Multivariable ORs and 95% CIs were calculated by using conditional logistic regression. RESULTS: HCC and GBTC cases, but not IHBC cases, showed significantly lower circulating selenium and SePP concentrations than their matched controls. Higher circulating selenium was associated with a significantly lower HCC risk (OR per 20-μg/L increase: 0.41; 95% CI: 0.23, 0.72) but not with the risk of GBTC or IHBC. Similarly, higher SePP concentrations were associated with lowered HCC risk only in both the categorical and continuous analyses (HCC: P-trend ≤ 0.0001; OR per 1.5-mg/L increase: 0.37; 95% CI: 0.21, 0.63). CONCLUSION: These findings from a large prospective cohort provide evidence that suboptimal selenium status in Europeans may be associated with an appreciably increased risk of HCC development.
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