Polymorphism of coagulation factor genes in patients with type 2 diabetes mellitus and chronic heart failure with retained ejection fraction

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM Diabetes Mellitus Pub Date : 2023-07-05 DOI:10.14341/dm13006
© Т.С. Свеклина, С.Б. Шустов, Светлана Николаевна Колюбаева, А.Н. Кучмин, В.А. Козлов, О.А. Мирошниченко, T. Sveklina, Sergey B. Shustov, Svetlana N. Kolyubayeva, Alexey N. Kuchmin, V. A. Kozlov, Olga A. Miroshnichenko
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Abstract

BACKGROUND. Patients with type 2 diabetes mellitus (DM2) have disorders of cellular and plasma hemostasis independent of the level of glycemia, increased platelet activation, combined with microvascular angiopathy. The study of the role of genetic markers of hemostasis disorders in the formation and progression of chronic heart failure (CHF) in patients with type 2 diabetes will allow for prevention, possibly optimize treatment and improve prognosis.AIM. To reveal polymorphisms of genes of the hemostasis system in patients with type 2 diabetes mellitus and chronic heart failure with preserved ejection fraction.MATERIALS AND METHODS. The frequency of coagulation factor genetic polymorphisms was studied in patients with CHF-pEF and DM2 (52 people), CHF with reduced ejection fraction (CHF-rEF) and DM2 (49) and healthy volunteers (66), mean age 69.9±10.1 years old. DNA was isolated from venous blood according to the method of the manufacturer. Genetic polymorphisms were determined by real-time polymerase chain reaction.RESULTS. The frequencies of polymorphisms rs1799963 and rs6025 of the genes of blood coagulation factors F2 (prothrombin) and F5 (factor V of blood coagulation) in all three groups were insignificant and comparable in magnitude. In patients with CHF and DM2, the frequencies of the rs6046 polymorphism of the factor F7 gene in the heterozygous form were slightly higher (by 2.6 and 1.7 times, respectively) than in the control group, but the result was not statistically significant. The CHF-pEF and CHF-rEF groups differ in the frequencies of F13 (rs5985) and fibrinogen (rs1800790) genetic polymorphisms, but are more common in patients with CHF-rEF and DM2.CONCLUSION. Based on the results of the study, it follows that the groups of CHF-pEF and CHF-rEF differ significantly in the frequencies of polymorphisms of the studied genes, both among themselves and with the control group. The highest frequency of polymorphisms of genes, the products of which are involved in the coagulation and cellular components of hemostasis, is observed in the group of patients with DM2 and CHF-rEF.
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2型糖尿病合并慢性心力衰竭伴射血分数保留患者凝血因子基因多态性研究
背景。2型糖尿病(DM2)患者存在独立于血糖水平的细胞和血浆止血障碍,血小板活化增加,并合并微血管病变。研究止血障碍遗传标记在2型糖尿病患者慢性心力衰竭(CHF)形成和进展中的作用,将有助于预防、优化治疗和改善预后。目的:探讨2型糖尿病合并慢性心力衰竭患者的止血系统基因多态性。材料和方法。研究CHF- pef合并DM2患者(52人)、CHF合并射血分数降低(CHF- ref)合并DM2患者(49人)和健康志愿者(66人)凝血因子遗传多态性频率,平均年龄69.9±10.1岁。按厂家方法从静脉血中分离DNA。实时聚合酶链反应检测遗传多态性。凝血因子F2(凝血酶原)和凝血因子V(凝血因子5)基因rs1799963和rs6025的多态性频率在三组中均不显著,且量级相当。在CHF和DM2患者中,因子F7基因的rs6046杂合子多态性频率略高于对照组(分别为2.6倍和1.7倍),但结果无统计学意义。CHF-pEF组和CHF-rEF组在F13 (rss5985)和纤维蛋白原(rs1800790)遗传多态性频率上存在差异,但在CHF-rEF和dm2患者中更为常见。根据研究结果,CHF-pEF组和CHF-rEF组之间以及与对照组的基因多态性频率存在显著差异。在DM2和CHF-rEF患者组中观察到的基因多态性频率最高,其产物与止血的凝血和细胞成分有关。
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来源期刊
Diabetes Mellitus
Diabetes Mellitus ENDOCRINOLOGY & METABOLISM-
CiteScore
1.90
自引率
40.00%
发文量
61
审稿时长
7 weeks
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