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THE STUDY OF THE RELATIONSHIP BETWEEN FGB GENE POLYMORPHISM AND PLATELET PARAMETERS IN PATIENTS WITH CORONARY HEART DISEASE, TYPE 2 DIABETES MELLITUS, AND ARTERIAL HYPERTENSION
Nazirova V.B.


DOI: 10.61775/2413-3302.v2i32.11


ABSTRACT
Genetic factors are an important contributor to the risk of ischemic heart disease (IHD), and great progress has been made in this area over the past decade. The problem of studying the genetic mechanisms of IHD is quite complex and is associated with the development of adequate approaches and methods of analysis, which is noted by many authors. One of the effective approaches to studying the role of genetic mechanisms in the development of IHD is associated with the identification of a group of genes with a potentially greatest contribution to the pathogenesis of the disease. Purpose. Study of FGB gene polymorphisms and its relationship with platelet indexes in Azerbaijani patients with ischemic heart disease, arterial hypertension, and type 2 diabetes mellitus. Material and methods. 100 patient participated in the study. Anthropometric parameters, total blood count, lipid profile, fasting blood sugar and/or HbA1C, fibrinogen gene, and electrocardiographic and echocardiographic examination were performed in each patient. Results. A statistically significant prevalence of the homozygous G/G genotype of the FGB G (-455) A fibrinogen gene was noted in the studied groups. A statistically significant difference in the frequency of the GA polymorphism of the FGB G (-455) A fibrinogen gene was found between all groups. In addition, an increase in thrombocyte indexes was observed in homozygous allele A genotype carriers, which may be an indicator of thrombosis tendency in these genotype carriers.
Keywords: ischemic heart disease, arterial hypertension, type 2 diabetes mellitus, fibrinogen gene, platelet indexes


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