[The role of Werner's syndrome gene in the genetic susceptibility to the type 2 diabetes in Chinese population]

Zhonghua Yi Xue Za Zhi. 2000 May;80(5):360-1.
[Article in Chinese]

Abstract

Objective: To test the hypothesis that Werner's syndrome gene (WRN) contributes to the genetic susceptibility to the type 2 diabetes in Chinese population.

Methods: Polymerase chain reaction-restrictive fragment length polymorphism (PCR-RFLP) method was used to test the distribution of a polymorphism (Cys1367Arg ) of the WRN gene in 241 type 2 diabetes patients and 108 normal control subjects.

Results: The frequency of "R" allele of the WRN gene in type 2 diabetes patients whose diagnosis age >/= 45 was significantly increased as compared with that in the control subjects (9.6% vs 4.6%, P = 0.04).

Conclusion: The high frequency of allele "R" of the WRN gene in early onset Chinese type 2 diabetes patients suggests that the WRN gene may contribute to the genetic susceptibility of type 2 diabetes in Chinese population through either directly causing diabetes or interacting with the diabetogenic gene.

MeSH terms

  • Adult
  • Age Factors
  • Alleles
  • Asian People / genetics*
  • China / ethnology
  • DNA Helicases / genetics*
  • Diabetes Mellitus, Type 2 / genetics*
  • Ethnicity / genetics*
  • Exodeoxyribonucleases
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Male
  • Middle Aged
  • Polymerase Chain Reaction / methods
  • Polymorphism, Restriction Fragment Length
  • RecQ Helicases
  • Werner Syndrome / genetics*
  • Werner Syndrome Helicase

Substances

  • Exodeoxyribonucleases
  • DNA Helicases
  • RecQ Helicases
  • WRN protein, human
  • Werner Syndrome Helicase