4.7 Article

One-carbon metabolism-related micronutrients intake and risk for hepatocellular carcinoma: A prospective cohort study

期刊

INTERNATIONAL JOURNAL OF CANCER
卷 147, 期 8, 页码 2075-2090

出版社

WILEY
DOI: 10.1002/ijc.33007

关键词

cancer; HCC; hepatocellular carcinoma; micronutrients; one-carbon metabolism; risk

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资金

  1. Division of Cancer Prevention, National Cancer Institute
  2. NIH/NCI [K01 CA237875]
  3. NATIONAL CANCER INSTITUTE [ZIACP010158] Funding Source: NIH RePORTER

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Deficient intake of micronutrients involved in one-carbon metabolism (eg, choline, methionine, vitamin B-12 and folic acid) leads to hepatocellular carcinoma (HCC) development in rodents, but is under-investigated in humans. We investigated the association between one-carbon metabolism-related micronutrient intake and HCC risk in a prospective cohort of 494 860 participants with 16 years of follow-up in the NIH-AARP study. Dietary intakes and supplement use were ascertained at baseline using a food-frequency questionnaire. Total intake (diet plus supplements) of the following one-carbon metabolism-related micronutrients were calculated: folate, methionine and vitamins B-2 (riboflavin), B-3 (niacin), B-6 and B-12. These micronutrients were examined both individually and simultaneously, with adjustment for covariates. Cox proportional hazard models were used to calculate hazard ratios (HRs) and 95% confidence intervals (CIs). Over the 16-year follow-up period, 647 incident HCC cases were diagnosed. When examined individually, higher total vitamin B-3 intake was associated with a lower HCC risk (HRQ5 vs Q1 = 0.60; 95% CI = 0.42-0.85; P-trend = .008), and the association remained significant when all six micronutrients were examined simultaneously (HRQ5 vs Q1 = 0.32; 95% CI = 0.18-0.55; P-trend < .0001). Among participants with >3 years of follow-up, higher total vitamin B-3 intake was again associated with lower risk (HRQ5 vs Q1 = 0.37; 95% CI = 0.20-0.68; P-trend = .001), whereas higher total vitamin B-6 intake was associated with higher risk (HRQ5 vs Q1 = 2.04; 95% CI = 1.02-4.07; P-trend = .04). Restricted cubic spline analyses showed a dose-response inverse association between total vitamin B-3 intake and HCC risk, and dose-response positive association between total vitamin B-6 intake and HCC risk. The study suggests that higher vitamin B-3 intake is associated with lower HCC risk, whereas higher vitamin B-6 intake is associated with increased risk.

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