Lai G Y, Weinstein S J, Albanes D, Taylor P R, Virtamo J, McGlynn K A, Freedman N D
1] Cancer Prevention Fellowship Program, Division of Cancer Prevention, National Cancer Institute, 9609 Medical Center Drive, Bethesda, MD 20892, USA [2] Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Room 6E316, Bethesda, MD 20892, USA.
Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Room 6E316, Bethesda, MD 20892, USA.
Br J Cancer. 2014 Nov 25;111(11):2163-71. doi: 10.1038/bjc.2014.365. Epub 2014 Oct 14.
Micronutrients may influence the development or progression of liver cancer and liver disease. We evaluated the association of serum α-tocopherol, β-carotene, and retinol with incident liver cancer and chronic liver disease (CLD) mortality in a prospective cohort of middle-aged Finnish male smokers.
Baseline and 3-year follow-up serum were available from 29,046 and 22,805 men, respectively. After 24 years of follow-up, 208 men were diagnosed with liver cancer and 237 died from CLD. Hazards ratios and 95% confidence intervals were calculated for highest vs lowest quartiles from multivariate proportional hazards models.
Higher β-carotene and retinol levels were associated with less liver cancer (β-carotene: 0.35, 0.22-0.55, P-trend <0.0001; retinol: 0.58, 0.39-0.85, P-trend=0.0009) and CLD mortality (β-carotene: 0.47, 0.30-0.75, P-trend=0.001; retinol: 0.55, 0.38-0.78, P-trend=0.0007). α-Tocopherol was associated with CLD mortality (0.63, 0.40-0.99, P-trend=0.06), but not with liver cancer (1.06, 0.64-1.74, P-trend=0.77). Participants with higher levels of β-carotene and retinol, but not α-tocopherol, at both baseline and year 3 had lower risk of each outcome than those with lower levels.
Our findings suggest that higher concentrations of β-carotene and retinol are associated with incident liver cancer and CLD. However, such data do not indicate that supplementation should be considered for these diseases.
微量营养素可能会影响肝癌和肝病的发生或发展。我们在一个芬兰中年男性吸烟者前瞻性队列中,评估了血清α-生育酚、β-胡萝卜素和视黄醇与肝癌发病及慢性肝病(CLD)死亡率之间的关联。
分别有29,046名和22,805名男性的基线血清和3年随访血清可用。经过24年的随访,208名男性被诊断为肝癌,237名死于CLD。通过多变量比例风险模型计算最高四分位数与最低四分位数的风险比及95%置信区间。
较高的β-胡萝卜素和视黄醇水平与较低的肝癌发病率(β-胡萝卜素:0.35,0.22 - 0.55,P趋势<0.0001;视黄醇:0.58,0.39 - 0.85,P趋势 = 0.0009)和CLD死亡率相关(β-胡萝卜素:0.47,0.30 - 0.75,P趋势 = 0.001;视黄醇:0.55,0.38 - 0.78,P趋势 = 0.0007)。α-生育酚与CLD死亡率相关(0.63,0.40 - 0.99,P趋势 = 0.06),但与肝癌无关(1.06,0.64 - 1.74,P趋势 = 0.77)。在基线和第3年时β-胡萝卜素和视黄醇水平较高但α-生育酚水平不高的参与者,其每种结局的风险均低于水平较低者。
我们的研究结果表明,较高浓度的β-胡萝卜素和视黄醇与肝癌发病及CLD相关。然而,这些数据并不表明对于这些疾病应考虑补充这些营养素。