4.6 Article

Circulating 25-Hydroxyvitamin D and Risk of Esophageal and Gastric Cancer

Journal

AMERICAN JOURNAL OF EPIDEMIOLOGY
Volume 172, Issue 1, Pages 94-106

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/aje/kwq121

Keywords

case-control studies; cohort studies; esophageal neoplasms; prospective studies; stomach neoplasms; vitamin D

Funding

  1. National Institutes of Health, Division of Cancer Control and Population Sciences, National Cancer Institute (NCI) (Bethesda, Maryland)
  2. National Institutes of Health, Division of Cancer Epidemiology and Genetics, NCI
  3. NCI [R01 CA098661, R37 CA54281, P01 CA33619, R01 CA063464, N01-PC35137, R01 CA82729, R37 CA70867, N02-CP11010-66, N01-CN-25514, N01-CN-25522, N01-CN-25513, NO1-CN-25516, N01-CN25511, N01-CN-25524, N01-CN-25518, NO1-CN-75022, N01-CN-25476]

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Upper gastrointestinal (GI) cancers of the stomach and esophagus have high incidence and mortality worldwide, but they are uncommon in Western countries. Little information exists on the association between vitamin D and risk of upper GI cancers. This study examined the association between circulating 25-hydroxyvitamin D (25(OH)D) and upper GI cancer risk in the Cohort Consortium Vitamin D Pooling Project of Rarer Cancers. Concentrations of 25(OH)D were measured from 1,065 upper GI cancer cases and 1,066 age-, sex-, race-, and season-of blood draw-matched controls from 8 prospective cohort studies. In multivariate-adjusted models, circulating 25(OH)D concentration was not significantly associated with upper GI cancer risk. Subgroup analysis by race showed that among Asians, but not Caucasians, lower concentrations of 25(OH)D (< 25 nmol/L) were associated with a statistically significant decreased risk of upper GI cancer (reference: 50-< 75 nmol/L) (odds ratio = 0.53, 95% confidence interval: 0.31, 0.91; P trend = 0.003). Never smokers with concentrations of < 25 nmol/L showed a lower risk of upper GI cancers (odds ratio = 0.55, 95% confidence interval: 0.31, 0.96). Subgroup analyses by alcohol consumption produced opposing trends. Results do not support the hypothesis that interventions aimed at increasing vitamin D status would lead to a lower risk of these highly fatal cancers.

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