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[河南Brugada综合征患者DSG2、TTN及GATA4基因变异分析]

[Analysis of DSG2, TTN and GATA4 gene variants in patients with Brugada syndrome from Henan].

作者信息

Han Hongqiang, Wang Yan, Zhou Fan, Chen Xianjie

机构信息

Second Department of Cardiology, Xinxiang Central Hospital, Xinxiang, Henan 453000, China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 May 10;38(5):488-491. doi: 10.3760/cma.j.cn511374-20200416-00275.

Abstract

OBJECTIVE

To explore the correlation between DSG2, TTN and GATA4 genes and Brugada syndrome in Henan Province of China.

METHODS

From February 2017 to February 2019, 100 patients with Brugada syndrome and 100 healthy individuals were selected as the study and the control groups, respectively. Electrocardiogram and echocardiography were carried out, and peripheral blood samples was collected. Coding regions of DSG2, TTN and GATA4 genes were amplified by PCR and sequenced. The results were compared with standard sequences from GenBank.

RESULTS

Electrocardiogram showed that all patients from the study group had ventricular arrhythmia, 87 cases (87%) presented ventricular tachycardia (VT), 84 cases (84%) presented T wave inversion, and 51 cases (51%) presented Epsilon wave. Echocardiography showed that the right ventricle in the study group was enlarged with the inner diameter of the right ventricle being (40.0±13.3) mm, and the right ventricle showed various degree of abnormal systolic function. The enlargement of right atrium accounted for 64%, and the involvement of the left ventricle accounted for 27%. The right ventricular diameter and left ventricular diastolic diameter of the study group were significantly greater than those of the control group (P< 0.05). DNA sequencing showed that 60 patients carried DSG2 gene variants, among which 18 had missense variant of exon 8. Fifty patients carried TTN gene variants, including 8 in the A-band domain and 3 in the I-band domain. Twenty patients carried 3 variants of the GATA4 gene.

CONCLUSION

Variants of the DSG2, TTN and GATA4 genes in Henan region are correlated with the onset of Brugada syndrome.

摘要

目的

探讨中国河南省DSG2、TTN和GATA4基因与布加综合征之间的相关性。

方法

选取2017年2月至2019年2月期间的100例布加综合征患者作为研究组,100例健康个体作为对照组。进行心电图和超声心动图检查,并采集外周血样本。采用聚合酶链反应(PCR)扩增DSG2、TTN和GATA4基因的编码区并进行测序。将结果与来自GenBank的标准序列进行比较。

结果

心电图显示,研究组所有患者均有心室心律失常,87例(87%)出现室性心动过速(VT),84例(84%)出现T波倒置,51例(51%)出现Epsilon波。超声心动图显示,研究组右心室扩大,右心室内径为(40.0±13.3)mm,右心室呈现不同程度的收缩功能异常。右心房扩大占64%,左心室受累占27%。研究组的右心室直径和左心室舒张直径显著大于对照组(P<0.05)。DNA测序显示,60例患者携带DSG2基因变异,其中18例在外显子8有错义变异。50例患者携带TTN基因变异,其中8例在A带结构域,3例在I带结构域。20例患者携带GATA4基因的3种变异。

结论

河南地区DSG2、TTN和GATA4基因变异与布加综合征的发病相关。

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