Tumour necrosis factor beta alleles and hyperinsulinaemia in coronary artery disease

Eur J Clin Invest. 1998 Jul;28(7):538-42. doi: 10.1046/j.1365-2362.1998.00334.x.

Abstract

Background: Hyperinsulinaemia and dyslipoproteinaemia are markers and risk factors for coronary artery disease (CAD) and non-insulin-dependent diabetes mellitus (NIDDM). We investigated the influence of a tumour necrosis factor beta (TNF-beta) gene polymorphism on serum parameters related to these metabolic disorders in patients with CAD.

Methods: A total of 199 patients with CAD and 81 control subjects with angiographically normal coronary arteries were studied. A digestion of amplified DNA with NcoI revealed three fragment patterns: homozygosity for TNF-beta *1 or TNF-beta *2 and heterozygosity (TNF-beta *1/*2).

Results: Patients with CAD who had increased serum insulin or C-peptide (fasting and after glucose load) were predominantly heterozygous for TNF-beta (72% vs. 47%) and less frequently homozygous for TNF-beta *2 (22% vs. 43%, P = 0 x 0.03).

Conclusion: This study demonstrates an association of TNF-beta alleles with the risk factor hyperinsulinaemia in CAD. Genomic variants of TNF-beta may therefore contribute to the complex susceptibility for the metabolic syndrome in patients with CAD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • C-Peptide / blood
  • Coronary Disease / blood
  • Coronary Disease / genetics*
  • Gene Frequency
  • Glucose Tolerance Test
  • Heart Valve Diseases / genetics
  • Heterozygote
  • Homozygote
  • Humans
  • Hyperinsulinism / blood
  • Hyperinsulinism / genetics*
  • Insulin / blood
  • Lymphotoxin-alpha / genetics*
  • Male
  • Middle Aged
  • Polymorphism, Genetic*

Substances

  • C-Peptide
  • Insulin
  • Lymphotoxin-alpha