Abstract

The circulating levels of β-carotene are modulated not only by sex, but also by autosomal gene variations and fruit intake. The aim of this study was to investigate the interactions between β-carotene metabolism-related gene single nucleotide polymorphisms (SNPs; genetic factors) and nutrient intake (environmental factors) relating to their effects on circulating β-carotene. The serum concentrations of β-carotene and the habitual food intake of 92 healthy Japanese adults were examined. All subjects were genotyped for three common SNPs: rs6564851 in the β-carotene 15,15′-oxygenase 1 (BCO1) gene, rs2278986 in the scavenger receptor class B member 1 (SCARB1) gene and rs362090 in the intestine-specific homeobox (ISX) gene. Univariate analysis revealed that the circulating β-carotene levels were significantly higher in rs6564851 GG homozygotes (p = 0.003). Additionally, the daily intake of β-cryptoxanthin was positively associated with the circulating β-carotene levels in female GG homozygotes of rs6564851 (p = 0.023), and the daily intake of α- and β-carotenes, and β-cryptoxanthin was significantly lower in female rs6564851 T allele carries than in female GG homozygotes (p = 0.009, 0.008, 0.009, respectively). The present study apparently indicates that higher circulating β-carotene levels in female rs6564851 GG homozygotes depend on carotenoid intake.

Highlights

  • More than 25 years ago, Dr Cutler found a significant positive correlation between the potential maximal lifespan of different primate species including humans and the concentration of carotenoids in their serum [1]

  • We evaluated the effects of three single nucleotide polymorphisms (SNPs) and the dietary intake of carotenoids on serum carotenoid levels in 92 Japanese adult volunteers (63 men and 29 women)

  • In the present study on a healthy adult Japanese population, we confirmed two previous findings: the serum concentration of β-carotene is higher in females than in males [4], and a regulatory SNP of the BCO1 gene significantly affects the circulating levels of βcarotene, which were higher in the GG homozygotes than in the T allele carriers [13]

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Summary

Introduction

More than 25 years ago, Dr Cutler found a significant positive correlation between the potential maximal lifespan of different primate species including humans and the concentration of carotenoids in their serum [1]. Rs6564851 in the BCO1 Gene Affects Carotenoid Daily Intake in Japanese performed [6], suggesting that circulating carotenoid levels depend on the amount of carotenoid intake prior to blood collection. Oxidative stress such as smoking is known to decrease the circulating level of β-carotene [7]. As shown in the literature, the circulating level of β-carotene in humans is influenced by several environmental factors

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