A novel Zip2 Gln/Arg/Leu codon 2 polymorphism is associated with carotid artery disease in aging

Rejuvenation Res. 2008 Apr;11(2):297-300. doi: 10.1089/rej.2008.0671.

Abstract

Zinc deficiency represents a risk factor for carotid stenosis (CS) development. In mammals, members of the ZIP family regulate zinc uptake, and hZip2 is a human zinc importer upregulated by zinc depletion. The purpose of this study was to investigate the association of a novel Zip2 Gln/Arg/Leu codon 2 polymorphism with CS, analyzing 250 CS patients and 259 elderly controls. CS patients showed an increased GG genotype frequency (60% vs. 47.5%), and a reduced TT frequency (6% vs. 10%) (p < 0.05 by chi(2) test). In conclusion, Zip2 Gln/Arg/Leu polymorphism plays a role in the susceptibility to carotid artery disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aging / genetics*
  • Amino Acids / genetics*
  • Carotid Artery Diseases / genetics*
  • Case-Control Studies
  • Cation Transport Proteins / genetics*
  • Codon / genetics*
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Polymorphism, Genetic*

Substances

  • Amino Acids
  • Cation Transport Proteins
  • Codon
  • SLC39A2 protein, human