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超声心动图参数和分子生物标志物在心力衰竭中的临床影响:与超声心动图参数的相关性及多态性:一项比较研究。

Clinical impact of echocardiography parameters and molecular biomarkers in heart failure: Correlation of and polymorphisms with echocardiography parameters: A comparative study.

作者信息

Suciu-Petrescu Mălina, Truta Anamaria, Suciu Mihai Domnutiu, Trifa Adrian Pavel, Petrescu Denisa, Roșianu Horia Ștefan, Sabin Octavia, Popa Daciana Elena, Macarie Antonia Eugenia, Vesa Ștefan Cristian, Buzoianu Anca Dana

机构信息

Department of Pharmacology, Toxicology and Clinical Pharmacology, 'Iuliu Hațieganu' University of Medicine and Pharmacy, 400337 Cluj-Napoca, Romania.

Department of Cardiology, 'Regina Maria' Hospital, 400117 Cluj-Napoca, Romania.

出版信息

Exp Ther Med. 2021 Jul;22(1):686. doi: 10.3892/etm.2021.10118. Epub 2021 Apr 28.

Abstract

Heart failure is still the leading cause of hospitalization in patients over 65 years of age and is defined as a multifactorial pathology which involves environmental factors and also genetic predispositions. The aim of the present study was to evaluate a possible correlation between single nucleotide polymorphisms (SNPs) of angiotensin converting enzyme 2 () and monocyte chemoattractant protein-1 () genes and cardiac remodeling in Caucasian patients diagnosed with heart failure. Our comparative translational research study included 116 patients diagnosed with heart failure and was carried out in Cluj-Napoca, Romania between September 2017 and March 2019. Three SNPs, namely rs4646156, rs4646174 and rs1024611, were genotyped using a Taqman real-time PCR technique. Our results showed that carriers of the AA genotype for rs4646156 had a significant dilatation of the left ventricle (LV) with signs of LV hypertrophy (LVH), while TT carriers had a significant left atrial dilatation. For rs4646174, homozygotes for the C allele presented a dilated LV with signs of LVH with statistical significance and had a tendency towards a lower ejection fraction. rs1024611 AA variant carriers had a significant LVH in the dominant model. In conclusion, our study showed a strong association between echocardiographic parameters of cardiac remodeling and SNPs rs4646156, rs4646174 of and rs1024611 of .

摘要

心力衰竭仍然是65岁以上患者住院的主要原因,它被定义为一种涉及环境因素和遗传易感性的多因素病理状态。本研究的目的是评估血管紧张素转换酶2(ACE2)和单核细胞趋化蛋白-1(MCP-1)基因的单核苷酸多态性(SNP)与诊断为心力衰竭的白种人患者心脏重塑之间的可能相关性。我们的比较性转化研究纳入了116例诊断为心力衰竭的患者,于2017年9月至2019年3月在罗马尼亚克卢日-纳波卡进行。使用Taqman实时PCR技术对三个SNP,即rs4646156、rs4646174和rs1024611进行基因分型。我们的结果显示,rs4646156的AA基因型携带者左心室(LV)有明显扩张,并伴有左心室肥厚(LVH)迹象,而TT基因型携带者左心房有明显扩张。对于rs4646174,C等位基因纯合子的左心室扩张并伴有LVH迹象,具有统计学意义,且射血分数有降低趋势。rs1024611的AA变异携带者在显性模型中有明显的LVH。总之,我们的研究表明心脏重塑的超声心动图参数与ACE2的SNP rs4646156、rs4646174以及MCP-1的rs1024611之间存在密切关联。

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