某些基因多态性在腹主动脉瘤患者中的作用和意义

E. Kalmykov, I. Suchkov, R. Kalinin, Okildyhon Ne’matzoda, J. Dodkhoev
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引用次数: 0

摘要

迄今为止,许多影响腹主动脉瘤(AAA)风险和病程的因素尚未得到研究。一些遗传多态性的存在在AAA的病因和发展中具有越来越重要的意义,其中许多遗传多态性的作用也未得到研究。目的:分析腹主动脉瘤与某些基因多态性(gp)的相关性。材料与方法:分析20例AAA患者的基因多态性(研究组,SG);男性18例(90%),女性2例(10%),平均年龄68.1 ~ 7.3岁,无AAA患者5例(对照组,CG;男性4例(80%),女性1例(20%),平均年龄64.2 ~ 7.2岁。测定AAA伴发疾病的频率及危险因素。研究了以下gp:: EDN1基因中的Lys198Asn;NOS3基因中的C-786T;APOE基因中的Leu28Pro;SLC01B1基因中的Val174Ala;SELP基因中的Thr715Pro;ITGA2基因中的C807T;LpL基因Ser447Ter;AGT基因中的Thr174Met;AGT基因中的Met235Thr。统计学分析采用IBM SPSS Statistics 21,相关性分析-根据Pearson。p < 0.05认为结果有统计学意义。结果:在SG中,LpL基因的Ser447Ter多态性存在相关关系:与Lys198Asn多态性直接相关(r = 0.63;EDN1基因,Leu28Pro基因(r = 0.70;APOE基因和Thr715Pro (r = 0.63;SELP基因为0.001);与С786Т多态性呈负相关(r = -0.35;NOS3基因的差异为0.006)。在APOE基因的Leu28Pro多态性中也发现了同样数量的关系:除了与LpL基因的Ser447Ter有直接关系外,还与Lys198Asn有直接关系(r = 0.70;EDN1基因和Thr715Pro基因的差异(r = 0.63;SELP基因为0.001);与С786Т呈负相关(r = -0.35;NOS3基因的差异为0.006)。SELP基因的Thr715Pro多态性,以及与Ser447Ter的关系(r = 0.63;LpL基因中的Leu28Pro和APOE基因中的Leu28Pro与Lys198Asn有直接关系(r = 0.55;EDN1基因的差异为0.001)。AGT基因Thr174Met多态性与Leu28Pro呈负相关(r = -0.35;与Val174Ala有直接关系(r = 0.40;在SLC01B1基因中,r = 0.002)。由此可见,AGT基因Met235Thr多态性与Val174Ala有直接关系(r = 0.33;p = 0.011),与ITGA2基因中C807T呈负相关。结论:腹主动脉瘤患者中某些基因多态性存在直接相关性,提示其可能在该病理的发生发展中发挥作用,可作为确定其发生可能性的筛选试验。
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The Role and Significance of Polymorphisms of Certain Genes in Patients with Abdominal Aortic Aneurysm
INTRODUCTION: To date, many factors that influence the risk and course of abdominal aortic aneurysm (AAA) are not studied. Increasing significance in the etiology and development of AAA is assigned to the existence of some genetic polymorphisms, the role of many of them is not studied either. AIM: To analyze the existence of association of the abdominal aortic aneurysm with some gene polymorphisms (GPs). MATERIALS AND METHODS: Gene polymorphisms were analyzed in 20 patients with AAA (study group, SG); 18 men (90%) and 2 women (10%), the mean age 68.1 7.3 years), and in 5 patients without AAA (control group, CG; 4 men (80%) and 1 woman (20%), the mean age 64.2 7.2 years). The frequency of concomitant diseases and risk factors for AAA were determined. The following GPs were studied: : Lys198Asn in the EDN1 gene; C-786T in the NOS3 gene; Leu28Pro in the APOE gene; Val174Ala in the SLC01B1 gene; Thr715Pro in the SELP gene; C807T in the ITGA2 gene; Ser447Ter in the LpL gene; Thr174Met in the AGT gene; Met235Thr in the AGT gene. Statistical analysis was performed using IBM SPSS Statistics 21, correlation analysis ― according to Pearson. The results were considered statistically significant at p 0.05. RESULTS: In the SG, correlation relationships were identified in Ser447Ter polymorphism in the LpL gene: direct relationships with Lys198Asn polymorphism (r = 0.63; р 0.001) in the EDN1 gene, Leu28Pro (r = 0.70; р 0.001) in the APOE gene and Thr715Pro (r = 0.63; р 0.001) in the SELP gene; a reverse relationship with С786Т polymorphism (r = -0.35; р = 0.006) in the NOS3 gene. The same amount of relationships were found in Leu28Pro polymorphism in the APOE gene: besides with Ser447Ter in the LpL gene, there is also a direct relationship with Lys198Asn (r = 0.70; р 0.001) in the EDN1 gene and Thr715Pro (r = 0.63; р 0.001) in the SELP gene; a reverse relationship with С786Т (r = -0.35; р = 0.006) in the NOS3 gene. Thr715Pro polymorphism in the SELP gene, along with relationships with Ser447Ter (r = 0.63; р 0.001) in the LpL gene and Leu28Pro in the APOE gene, has an additional direct relationship with Lys198Asn (r = 0.55; р 0.001) in the EDN1 gene. Thr174Met polymorphism in the AGT gene has a reverse relationship with Leu28Pro (r = -0.35; р = 0.006) in the APOE gene and direct relationship with Val174Ala (r = 0.40; р = 0.002) in the SLC01B1 gene. With this, Met235Thr polymorphism in the AGT gene has a direct relationship with Val174Ala (r = 0.33; p = 0.011) in the SLC01B1 gene and reverse relationship with C807T in the ITGA2 gene. CONCLUSION: The existence of direct correlations of some gene polymorphisms in patients with abdominal aortic aneurysm has been established, which indicates their probable role in the development of this pathology and may be used as a screening test for determination of the likelihood for its development.
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