Abstract:
Introduction: Hypertension is a multifactorial, complex and polygenic human disease that
causes significant morbidity and mortality worldwide. The World Health Organization suggests that
the number of people affected by hypertension will rise to 1.5 billion in 2020, or 29% of the total
population by 2025. In adults there is a continuous, incremental risk of cardiovascular disease,
stroke and renal disease associated with high blood pressure. Identifying risk factors for this disease
is one of the main directions of research initiated by World and European scientific community.
Among these, genetic factors have a decisive impact, role of genetic factors ranging from 31% to
68%.Monogenic and polygenic forms of hypertension have been described. Rare monogenic blood
pressure syndromes are characterized by a major gene defect, affecting a single pathway ordinarily
involving renal electrolyte balance. Thus, there is a pressing need for a greater understanding of the
pathophysiological and genetic underpinnings of blood pressure regulation and dysregulation.
Purpose and Objectives: characterization of the genetic factors involved in the production of
high blood pressure; classification of the etiopathogenetic factors that predispose to the occurrence of
hypertension; characterization of genes involved in the control of hypertension; study the distribution of
the polymorphisms II, DD, ID of the ACE gene and GG, TT, GT of the NOS gene in people affected by
essential hypertension and non-affected from the population of Republic of Moldova.
Materials and methods: The study has included 30 persons, 15 affected by essential
hypertension and 15 non-affected. Methods which have been used are DNA isolation, PCR and
electrophoresis of DNA fragments.
Results: The results of the analysis of the ACE genotype frequency in the study group
showed an increased frequency of 55% for ID genotype in compared to 25% for II and 20% for DD
genotypes. The results of the analysis of the NOS genotype frequency in the study group showed an
increased frequency of 72% for GT genotype in healthy individuals, the homozygous genotypes are
seen with greater frequency in affected individuals.
Conclusion: There is an association between ACE and NOS gene polymorphisms with
hypertension prevalence.DD genotype of ACE gene and TT genotype of NOS gene may be
associated with increased risk of hypertension.
Description:
Department of Molecular biology and Human genetics, State University of Medicine and Pharmacy “Nicolae Testemitanu”, Chisinau, Republic of Moldova