GST M1/T1 and MTHFR polymorphisms as risk factors for hypertension

Biochem Biophys Res Commun. 2007 Feb 9;353(2):344-50. doi: 10.1016/j.bbrc.2006.12.019. Epub 2006 Dec 11.

Abstract

The aim of this study is to investigate GSTM1, GSTT1 and MTHFR genetic polymorphisms and its relation with total plasma glutathione (tGSH) levels in hypertension. Genotype distributions of GSTM1 and GSTT1 deletion polymorphisms and C677T variant of MTHFR were examined in a sample of 94 hypertensive patients with congestive heart failure and 207 healthy unrelated Portuguese individuals using PCR techniques. Plasma GST activity was determined spectrophotometrically. The antioxidant status was evaluated by fluorometric assays of tGSH. Genotype distributions of GSTT1 (chi2 test; p < 0.01) and MTHFR (chi2 test; p < 0.01) differ significantly between control and hypertensive patients with a greater prevalence of "non-null GSTT1/M1" and CT (heterozygous) genotypes. Moreover, GST activity and tGSH were markedly decreased in hypertension but there is no correlation with the studied polymorphisms. GSH depletion confirmed the possible involvement of oxidative stress in this pathology. Deletion of GSTT1 gene might be considered as protective factor for hypertension.

Publication types

  • Multicenter Study

MeSH terms

  • 5,10-Methylenetetrahydrofolate Reductase (FADH2) / genetics*
  • DNA Mutational Analysis
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Genetic Testing / methods*
  • Glutathione Transferase / genetics*
  • Humans
  • Hypertension / epidemiology*
  • Hypertension / genetics*
  • Male
  • Middle Aged
  • New York / epidemiology
  • Polymorphism, Single Nucleotide / genetics
  • Portugal / epidemiology
  • Prevalence
  • Risk Assessment / methods*
  • Risk Factors

Substances

  • 5,10-Methylenetetrahydrofolate Reductase (FADH2)
  • glutathione S-transferase T1
  • Glutathione Transferase
  • glutathione S-transferase M1