TRIB3 functional Q84R polymorphism is a risk factor for metabolic syndrome and carotid atherosclerosis

Diabetes Care. 2009 Jul;32(7):1311-3. doi: 10.2337/dc09-0061. Epub 2009 Apr 23.

Abstract

Objective: To determine the association of TRIB3 Q84R polymorphism with metabolic syndrome (MetS) and carotid atherosclerosis.

Research design and methods: A case-control study enrolled 513 Chinese subjects in three groups: control, MetS, and obese. The functional TRIB3 Q84R polymorphism was genotyped among subjects undergoing carotid ultrasonography. The clinical and biochemical characteristics were determined.

Results: For individuals with the TRIB3 R84 allele, the odds ratio for developing MetS was 2.349 (P = 0.018), abdominal obesity 2.351 (P = 0.012), hypertriglyceridemia 2.314 (P = 0.00003), and insulin resistance 1.697 (P = 0.023). Likewise, the odds ratio for individuals with the TRIB3 R84 allele to develop thickened intima-media thickness was 2.208 (P = 0.040).

Conclusions: Individuals with the functional TRIB3 Q84R polymorphism are at risk for MetS. The TRIB3 R84 allele especially predisposes to carotid atherosclerosis in part through the effects of abdominal obesity, hypertriglyceridemia, and insulin resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdomen / anatomy & histology
  • Adult
  • Aged
  • Aged, 80 and over
  • Amino Acid Substitution*
  • Carotid Artery Diseases / epidemiology
  • Carotid Artery Diseases / genetics*
  • Case-Control Studies
  • Cell Cycle Proteins / genetics*
  • China
  • Genotype
  • Humans
  • Insulin Resistance / genetics
  • Metabolic Syndrome / epidemiology
  • Metabolic Syndrome / genetics*
  • Middle Aged
  • Obesity / epidemiology
  • Obesity / genetics
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Protein Serine-Threonine Kinases / genetics*
  • Repressor Proteins / genetics*
  • Tunica Media / pathology
  • Young Adult

Substances

  • Cell Cycle Proteins
  • Repressor Proteins
  • TRIB3 protein, human
  • Protein Serine-Threonine Kinases