The association between dilated cardiomyopathy and RTN4 3'UTR insertion/deletion polymorphisms

Clin Chim Acta. 2009 Feb;400(1-2):21-4. doi: 10.1016/j.cca.2008.09.028. Epub 2008 Oct 8.

Abstract

Background: The Nogo isoforms A, B and C are members of the reticulon family of proteins. Nogo-B is found in most tissues, especially highly expressed in endothelial and smooth muscle cells of the vessel wall, and Nogo-B is a regulator of cell migration in vitro and vascular remodeling in vivo. The TATC and CAA 3'UTR insertion/deletion polymorphisms of the RTN4, the gene encoding Nogo isoforms A, B and C, have been linked to schizophrenia and depression, but data were inconsistent. However, it is unclear whether these polymorphisms are associated with dilated cardiomyopathy (DCM).

Methods: A total of 159 DCM patients and 215 control subjects were recruited in this study. The RTN4 TATC and CAA insertion/deletion genotypes were determined using PCR-polyacrylamide gel electrophoresis.

Results: Frequencies of (TATC)(2) allele and (TATC)(2)/(TATC)(2) genotype were significantly different from that in healthy controls (P = 0.045, OR = 1.356, 95% CI = 1.006-1.827 and P = 0.021, OR = 2.094, 95% CI = 1.113-3.940, respectively). No significant differences in CAA insertion/deletion genotype and allele frequencies were observed between the DCM and controls.

Conclusion: These data provide evidence that RTN4 allele (TATC)(2) and (TATC)(2)/(TATC)(2) genotype are associated with DCM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics*
  • Adolescent
  • Adult
  • Aged
  • Cardiomyopathy, Dilated / genetics*
  • Child
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • INDEL Mutation*
  • Male
  • Middle Aged
  • Myelin Proteins / genetics*
  • Nogo Proteins
  • Polymorphism, Genetic*

Substances

  • 3' Untranslated Regions
  • Myelin Proteins
  • Nogo Proteins
  • RTN4 protein, human