[TrxR2 gene polymorphisms may not be associated with the susceptibility to Kashin-Beck disease]

Nan Fang Yi Ke Da Xue Xue Bao. 2010 Oct;30(10):2246-8.
[Article in Chinese]

Abstract

Objective: To study the association between single nucleotide polymorphisms of thioredoxin reductase-2 (TrxR2) gene and the susceptibility to Kashin-Beck disease (KBD).

Methods: Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to analyze the genotype frequencies of rs5748469 in TrxR2 gene in 84 KBD patients and 109 healthy control subjects.

Results: The genotype frequencies of A/A, A/C, and C/C in the KBD patients were 83.33%, 15.48% and 1.19%, as compared with the frequencies of 74.31%, 25.69%, and 0.00% in the healthy control, respectively, showing no significant difference in the single nucleotide polymorphisms of TrxR2 gene between the two groups (P=0.13).

Conclusion: No obvious correlation can be found between rs5748469 polymorphisms in TrxR2 gene and the susceptibility to KBD.

Publication types

  • English Abstract
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Alleles
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Kashin-Beck Disease / genetics*
  • Male
  • Middle Aged
  • Polymorphism, Restriction Fragment Length
  • Polymorphism, Single Nucleotide*
  • Thioredoxin Reductase 2 / genetics*

Substances

  • TXNRD2 protein, human
  • Thioredoxin Reductase 2