Prospective Study of Serum Vitamin E Levels and Esophageal and Gastric Cancers
Participants in the General Population Trial, a randomized nutrition intervention trial in Linxian, China, who received a combination of selenium, β-carotene, and vitamin E supplements, had statistically significantly lower cancer mortality rates than those who did not receive the supplements. In th...
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Published in | JNCI : Journal of the National Cancer Institute Vol. 95; no. 18; pp. 1414 - 1416 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cary, NC
Oxford University Press
17.09.2003
Oxford Publishing Limited (England) |
Subjects | |
Online Access | Get full text |
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Summary: | Participants in the General Population Trial, a randomized nutrition intervention trial in Linxian, China, who received a combination of selenium, β-carotene, and vitamin E supplements, had statistically significantly lower cancer mortality rates than those who did not receive the supplements. In the current study, we used a case–cohort design to examine the association between pre-trial serum vitamin E levels and the risks of developing esophageal and gastric cancers during the trial. We measured serum α- and γ-tocopherol and cholesterol levels in 1072 case patients with incident esophageal squamous cell carcinoma (ESCC), gastric cardia cancer (GCC), or gastric noncardia cancer (GNCC) and in 1053 control subjects. The relative risks for comparisons of the highest to the lowest quartiles of serum α-tocopherol were 0.63 (95% confidence interval [CI] = 0.44 to 0.91) for ESCC, 0.84 (95% CI = 0.55 to 1.26) for GCC, and 2.05 (95% CI = 0.89 to 4.75) for GNCC. Serum γ-tocopherol level was not associated with the incidence of any of these cancers. Our findings provide support for the role of α-tocopherol in the etiology of upper gastrointestinal cancers. |
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Bibliography: | ark:/67375/HXZ-215W23LN-H Correspondence to: Philip R. Taylor, MD, ScD, Cancer Prevention Studies Branch, Center for Cancer Research, National Cancer Institute, 6116 Executive Blvd., Rm. 705, Bethesda, MD 20892–8314 (e-mail: ptaylor@mail.nih.gov). istex:8C0547CE802D83E68E98D7C7C304C2DDA69F93DE local:0951414 PII:1460-2105 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0027-8874 1460-2105 |
DOI: | 10.1093/jnci/djg044 |