Carotenoid intake and esophageal cancer risk: a meta-analysis.

Asian Pac J Cancer Prev

Department of Medical Oncology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

Published: January 2014

AI Article Synopsis

  • The meta-analysis evaluated the connection between carotenoid intake and esophageal cancer risk, analyzing data from ten studies with nearly 2,000 cancer cases and over 4,500 controls.
  • Higher consumption of carotenoids like beta-carotene and lycopene was linked to a significant reduction in esophageal cancer risk.
  • It was suggested that more extensive studies are needed to understand how carotenoids may protect against various types of esophageal cancer.

Article Abstract

This meta-analysis was conducted to evaluate the association between intake of carotenoids and risk of esophageal cancer. A systematic search using PubMed, Cochrane Library, Web of Science, Scopus, CNKI, and CBM (updated to 6 May 2012) identified ten articles meeting the inclusion criteria with 1,958 cases of esophageal cancer and 4,529 controls. Higher intake of beta-carotene, alpha-carotene, lycopene, beta-cryptoxanthin, lutein, and zeaxanthin reduced esophageal cancer risk with pooled ORs of 0.58 (95% CI 0.44, 0.77), 0.81 (95% CI 0.70, 0.94), 0.75 (95% CI 0.64, 0.86), 0.80 (95% CI 0.66, 0.97), and 0.71 (95% CI 0.59, 0.87), respectively. In subgroup analyses, beta-carotene showed protective effects against esophageal adenocarcinoma in studies located in Europe and North America. Alpha-carotene, lycopene, and beta-cryptoxanthin showed protection against esophageal squamous cell cancer. This meta-analysis suggested that higher intake of carotenoids (beta-carotene, alpha- carotene, lycopene, beta-cryptoxanthin, lutein, and zeaxanthin) is associated with lower risk of esophageal cancer. Further research with large-sample studies need to be conducted to better clarify the potentially protective mechanisms of carotenoid associations risk of different types of esophageal cancer.

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Source
http://dx.doi.org/10.7314/apjcp.2013.14.3.1911DOI Listing

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