[Clinicogenetic aspects of carbohydrate metabolism disorders and efficacy of their correction with moxonidine and metformine in patients with arterial hypertension]

Ter Arkh. 2005;77(1):46-51.
[Article in Russian]

Abstract

Aim: To study effects of monotherapy with moxonidine and metformine on metabolic parameters in hypertensive patients with carbohydrate dysbolism (CD) regarding polymorphic markers of genes PPARalpha, PPARgamma and IRS type 1 and 2.

Material and methods: A total of 83 patients (31 male and 52 female patients aged 40-75 years) with untreated arterial hypertension stage I, obesity and CD (by glucose tolerance test) entered the trial. The patients were randomized into two groups. Patients of group I (n=42) received moxonidin in a dose 0.4 mg/day, of group 2 (n=41)--metformin in a dose 1000 mg/day. Measurement of arterial pressure, blood count and biochemistry, oral test for glucose tolerance with glucose and insulin measurement before meal and 1, 2 and 3 hours later was made initially and on the treatment week 16 Genotypes of polymorphic markers of genes PPARA, PPARG2, IRS1 and IRS2 were defined in all the patients.

Results: Changes in basic hemodynamic and metabolic indices in therapy with moxonidine depending on polymorphic markers of genes PPARA, PPARG2, IRS1 and IRS2 in patients with AH and CD showed that G allele PPARG2 is associated with greater weight loss, G allele PPARA--with weight loss, C allele PPARA--with maximal fall of diastolic blood pressure.

Conclusion: Genetic factors participate in development of metabolic disturbances in hypertensive patients, obesity and CD and determine treatment efficacy in each individual patient.

Publication types

  • Clinical Trial
  • Comparative Study
  • English Abstract
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Antihypertensive Agents / therapeutic use*
  • Blood Pressure / drug effects
  • Blood Pressure / physiology
  • Carbohydrate Metabolism*
  • DNA / drug effects
  • DNA / genetics
  • Female
  • Follow-Up Studies
  • Genetic Markers / drug effects
  • Genetic Markers / genetics
  • Glucose Metabolism Disorders / blood
  • Glucose Metabolism Disorders / complications
  • Glucose Metabolism Disorders / drug therapy
  • Glucose Metabolism Disorders / genetics*
  • Humans
  • Hypertension / blood
  • Hypertension / complications
  • Hypertension / genetics*
  • Hypoglycemic Agents / therapeutic use*
  • Imidazoles / therapeutic use*
  • Insulin / blood
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Metformin / therapeutic use*
  • Middle Aged
  • PPAR alpha / blood
  • PPAR alpha / drug effects
  • PPAR alpha / genetics
  • PPAR gamma / blood
  • PPAR gamma / drug effects
  • PPAR gamma / genetics
  • Phosphoproteins / blood
  • Phosphoproteins / drug effects
  • Phosphoproteins / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / drug effects
  • Polymorphism, Genetic / genetics*
  • Treatment Outcome

Substances

  • Antihypertensive Agents
  • Genetic Markers
  • Hypoglycemic Agents
  • IRS1 protein, human
  • IRS2 protein, human
  • Imidazoles
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • PPAR alpha
  • PPAR gamma
  • Phosphoproteins
  • DNA
  • Metformin
  • moxonidine