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多态性在内皮稳态和维生素D代谢基因在冠状动脉疾病严重程度中的作用。

The Role of Polymorphism in the Endothelial Homeostasis and Vitamin D Metabolism Genes in the Severity of Coronary Artery Disease.

作者信息

Ponasenko Anastasia, Sinitskaya Anna, Sinitsky Maxim, Khutornaya Maria, Barbarash Olga

机构信息

Research Institute for Complex Issues of Cardiovascular Diseases, 650002 Kemerovo, Russia.

出版信息

Biomedicines. 2023 Aug 25;11(9):2382. doi: 10.3390/biomedicines11092382.

Abstract

Coronary artery disease (CAD) remains one of the leading causes of cardiovascular morbidity and mortality worldwide. The maintenance of endothelial homeostasis and vitamin D metabolism play an important role in CAD pathogenesis. This study aimed to determine the association of endothelial homeostasis and vitamin D metabolism gene polymorphism with CAD severity. A total of 224 low-risk patients (SYNTAX score ≤ 31) and 36 high-risk patients (SYNTAX score > 31) were recruited for this study. The serum level of E-, L- and P-selectins; endothelin; eNOS; 25OH; and 1.25-dihydroxy vitamin D was measured using an enzyme-linked immunosorbent assay (ELISA). Polymorphic variants in , , , , , and were analyzed using a polymerase chain reaction (PCR). We found no differences in the serum levels of the studied markers between high- and low-risk patients. Three polymorphic variants associated with CAD severity were discovered: rs3087459, rs5370 and rs2298849 in the log-additive model. Moreover, we discovered a significantly decreased serum level of 1.25-dihydroxy vitamin D in high-risk CAD patients with the A/A-A/G genotypes of the rs2228570 polymorphism of the gene, the A/A genotype of the rs7041 polymorphism of the gene and the A/A genotype of the rs2298849 polymorphism of the gene.

摘要

冠状动脉疾病(CAD)仍然是全球心血管疾病发病率和死亡率的主要原因之一。内皮稳态的维持和维生素D代谢在CAD发病机制中起重要作用。本研究旨在确定内皮稳态和维生素D代谢基因多态性与CAD严重程度之间的关联。本研究共招募了224例低风险患者(SYNTAX评分≤31)和36例高风险患者(SYNTAX评分>31)。使用酶联免疫吸附测定(ELISA)测量血清E-、L-和P-选择素、内皮素、eNOS、25OH和1,25-二羟基维生素D的水平。使用聚合酶链反应(PCR)分析、、、、、和中的多态性变体。我们发现高风险和低风险患者之间所研究标志物的血清水平没有差异。在对数加性模型中发现了三个与CAD严重程度相关的多态性变体:rs3087459、rs5370和rs2298849。此外,我们发现,对于基因rs2228570多态性的A/A-A/G基因型、基因rs7041多态性的A/A基因型和基因rs2298849多态性的A/A基因型的高风险CAD患者,其血清1,25-二羟基维生素D水平显著降低。

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本文引用的文献

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