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
AUTHORS (43)
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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