血管紧张素转换酶2基因多态性与肥厚性心肌病发病和预后的相关性

IF 2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sujuan Li, Xizhi Lin, Haoting Ye, Biyun Li, Siyu Zeng, Qinghua Mei, Yukai Huang, Yixuan Liu
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引用次数: 0

摘要

背景:探讨血管紧张素转换酶2 (ACE2)基因多态性与肥厚性心肌病(HCM)发病及预后的相关性,为今后早期预防和精准治疗HCM提供参考。方法:选取100例HCM患者(HCM组)和100例年龄、性别、种族匹配的健康体检者(对照组)进行病例对照研究。采用构象差异凝胶电泳方法对ACE2基因启动子区rs102312、rs102883和rs119247的单核苷酸多态性进行了分型。采用卡方检验检验ACE2基因型分布频率是否符合遗传平衡规律。同时,分析ACE2基因启动子区不同多态性及等位基因与HCM发病及预后的相关性。结果:经Hardy-Weinberg平衡分析,ACE2基因的3个多态性均符合遗传平衡规律(p < 0.05)。遗传关联分析结果显示,ACE2基因启动子区rs102312多态性及其等位基因与HCM的发生相关(p0.05)。此外,我们还发现携带rs102312多态性GG基因型的HCM患者的心功能和预后较携带TT基因型的患者差(p结论:ACE2基因启动子区rs102312多态性与HCM患者的发病有关,携带rs102312多态性GG基因型的HCM患者临床预后较差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlations of gene polymorphisms of angiotensin-converting enzyme 2 with onset and prognosis of hypertrophic cardiomyopathy.

Background: To investigate the correlations of the gene polymorphisms of angiotensin-converting enzyme 2 (ACE2) with the onset and prognosis of hypertrophic cardiomyopathy (HCM), so as to provide references for the early prevention and precise treatment of HCM in the future.

Methods: In this case-control study, a total of 100 HCM patients (HCM group) and 100 healthy people receiving physical examination who had matched age, gender and race (Control group) were collected. The single nucleotide polymorphisms (rs102312, rs102883 and rs119247) in the promoter region of ACE2 gene were genotyped by means of conformation-difference gel electrophoresis. Whether the distribution frequency of ACE2 genotypes is in agreement with the law of genetic equilibrium was examined using chi-square test. Meanwhile, the correlations of different polymorphisms and alleles in the promoter region of ACE2 gene with the onset and prognosis of HCM were analyzed.

Results: The Hardy-Weinberg equilibrium analysis showed that all the three polymorphisms of ACE2 gene were in agreement with the law of genetic equilibrium (p>0.05). According to the results of genetic association analysis, the polymorphism rs102312 and its alleles in the promoter region of ACE2 gene were correlated with the occurrence of HCM (p<0.05), while the polymorphisms rs102883 and rs119247 as well as their alleles had no associations with the occurrence of HCM (p>0.05). Furthermore, it was found that the cardiac function and prognosis of HCM patients carrying genotype GG of polymorphism rs102312 were poorer than those of patients carrying genotype TT (p<0.05).

Conclusions: The polymorphism rs102312 in the promoter region of ACE2 gene is associated with the onset of HCM in patients, and HCM patients carrying the genotype GG of polymorphism rs102312 have a poorer clinical prognosis.

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来源期刊
Journal of Medical Biochemistry
Journal of Medical Biochemistry BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.00
自引率
12.00%
发文量
60
审稿时长
>12 weeks
期刊介绍: The JOURNAL OF MEDICAL BIOCHEMISTRY (J MED BIOCHEM) is the official journal of the Society of Medical Biochemists of Serbia with international peer-review. Papers are independently reviewed by at least two reviewers selected by the Editors as Blind Peer Reviews. The Journal of Medical Biochemistry is published quarterly. The Journal publishes original scientific and specialized articles on all aspects of clinical and medical biochemistry, molecular medicine, clinical hematology and coagulation, clinical immunology and autoimmunity, clinical microbiology, virology, clinical genomics and molecular biology, genetic epidemiology, drug measurement, evaluation of diagnostic markers, new reagents and laboratory equipment, reference materials and methods, reference values, laboratory organization, automation, quality control, clinical metrology, all related scientific disciplines where chemistry, biochemistry, molecular biology and immunochemistry deal with the study of normal and pathologic processes in human beings.
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