Alcohol consumption, one-carbon metabolites, liver cancer and liver disease mortality

Excess alcohol consumption adversely affects one-carbon metabolism and increases the risk of liver disease and liver cancer. Conversely, higher folate levels have been inversely associated with liver damage. The current study investigated the effects of alcohol and one-carbon metabolite intake on li...

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Veröffentlicht in:PloS one 2013-10, Vol.8 (10), p.e78156-e78156
Hauptverfasser: Schwartz, Lauren M, Persson, E Christina, Weinstein, Stephanie J, Graubard, Barry I, Freedman, Neal D, Männistö, Satu, Albanes, Demetrius, McGlynn, Katherine A
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container_end_page e78156
container_issue 10
container_start_page e78156
container_title PloS one
container_volume 8
creator Schwartz, Lauren M
Persson, E Christina
Weinstein, Stephanie J
Graubard, Barry I
Freedman, Neal D
Männistö, Satu
Albanes, Demetrius
McGlynn, Katherine A
description Excess alcohol consumption adversely affects one-carbon metabolism and increases the risk of liver disease and liver cancer. Conversely, higher folate levels have been inversely associated with liver damage. The current study investigated the effects of alcohol and one-carbon metabolite intake on liver cancer incidence and liver disease mortality within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study. Cox proportional hazards modeling was used to calculate hazard ratios and 95% confidence intervals (CIs) in a population of 27,086 Finnish males with 194 incident liver cancers and 213 liver disease deaths. In a nested case-control subset (95 liver cancers, 103 controls), logistic regression was used to calculate odds ratios and 95% CIs for serum one-carbon metabolites in relation to liver cancer risk. Daily alcohol consumption of more than 20.44 g was associated with an increased risk of both liver cancer incidence (Hazard Ratio (HR) 1.52, 95%CI 1.06-2.18) and liver disease mortality (HR 6.68, 95%CI 4.16-10.71). These risks were unaffected by one-carbon metabolite intake. Similarly, in the case-control study, none of the serum one-carbon metabolites were associated with liver cancer. The current study provided no convincing evidence for a protective association of one-carbon metabolite intake or serum level on the risk of liver cancer or liver disease mortality.
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Conversely, higher folate levels have been inversely associated with liver damage. The current study investigated the effects of alcohol and one-carbon metabolite intake on liver cancer incidence and liver disease mortality within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study. Cox proportional hazards modeling was used to calculate hazard ratios and 95% confidence intervals (CIs) in a population of 27,086 Finnish males with 194 incident liver cancers and 213 liver disease deaths. In a nested case-control subset (95 liver cancers, 103 controls), logistic regression was used to calculate odds ratios and 95% CIs for serum one-carbon metabolites in relation to liver cancer risk. Daily alcohol consumption of more than 20.44 g was associated with an increased risk of both liver cancer incidence (Hazard Ratio (HR) 1.52, 95%CI 1.06-2.18) and liver disease mortality (HR 6.68, 95%CI 4.16-10.71). These risks were unaffected by one-carbon metabolite intake. 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subjects Alcohol Drinking - adverse effects
Alcohol Drinking - metabolism
Alcohol use
Alcoholic beverages
Cancer
Carbon
Carbon - blood
Carbon - metabolism
Carotene
Confidence intervals
Disease control
Disease prevention
Folic acid
Hazards
Health hazards
Health risk assessment
Health risks
Humans
Incidence
Liver
Liver cancer
Liver diseases
Liver Diseases - blood
Liver Diseases - metabolism
Liver Diseases - mortality
Liver Neoplasms - blood
Liver Neoplasms - metabolism
Liver Neoplasms - mortality
Males
Metabolism
Metabolites
Mortality
Proportional Hazards Models
Risk
Risk Factors
Statistical analysis
Surveys and Questionnaires
Tocopherol
title Alcohol consumption, one-carbon metabolites, liver cancer and liver disease mortality
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