Department of Medical Genetics, Afyonkarahisar University of Health Sciences Faculty of Medicine, Zafer Sağlık Külliyesi B Blok, Kat:1, Dörtyol Mah. 2078 Sok. No:3, 03200, Afyonkarahisar, Turkey.
Department of Cardiology, Afyonkarahisar University of Health Sciences Faculty of Medicine, Afyonkarahisar, Turkey.
Mol Biol Rep. 2021 Dec;48(12):7893-7900. doi: 10.1007/s11033-021-06816-w. Epub 2021 Oct 29.
Takotsubo Cardiomyopathy (TC) is a rare disorder that is mostly caused by stress and is often misdiagnosed. We aimed to analyze Takotsubo Syndrome at the molecular level by using the Oxford Nanopore Minion Device and its protocol.
Ten patients who were previously diagnosed with Takotsubo Syndrome (increased after decrease in ejection fraction and without critical stenosis in coronary arteries) and 10 healthy individuals in the control group were included in our project. The mean age was 53 ± 12.2 for the patient group and 52.4 ± 9.9 for the control group, and the left ventricular ejection fraction was 50.3 ± 11.5 for the patient group and 64.2 ± 2.8 for the control group (p < 0.05). Peripheral blood of patients and healthy individuals was taken and their DNA was obtained. By making long reads throughout the genome, the most studied regions responsible for β-adrenergic signaling pathways; The gene expression level of cardiac β-1 ADRB1 (rs1801253-ENST00000369295.4), G > C, (Gly389Arg) and cardiac β-2 ADRB2 (rs1800888-ENSG00000169252), C > T, (Thr165Ile) adrenoceptors was investigated. As a result; no structural variation was detected leading to Takotsubo Cardiomyopathy. The results obtained from the bioinformatics analysis were also checked from the VarSome Tools and similar results were found.
Many publications in TC susceptibility have that may lead to adrenergic pathway dysregulation, most studied adrenergic receptor genes in the similar literatures too. We searched for genetic variants in b1AR and b2AR genes in our study and however we could not find any variants in this study, we think larger numbers of cohort studies are needed.
Takotsubo 心肌病(TC)是一种罕见的疾病,主要由应激引起,且常被误诊。我们旨在通过使用牛津纳米孔 Minion 设备及其方案在分子水平上分析 Takotsubo 综合征。
我们纳入了 10 名先前被诊断为 Takotsubo 综合征(射血分数降低后增加且冠状动脉无严重狭窄)的患者和 10 名健康对照组个体。患者组的平均年龄为 53±12.2 岁,对照组为 52.4±9.9 岁,患者组的左心室射血分数为 50.3±11.5,对照组为 64.2±2.8(p<0.05)。采集患者和健康个体的外周血并获得其 DNA。通过对整个基因组进行长读测序,研究了与β-肾上腺素能信号通路最相关的最受关注的区域;心脏β-1 ADRB1(rs1801253-ENST00000369295.4)基因表达水平,G>G,(甘氨酸 389 突变为精氨酸)和心脏β-2 ADRB2(rs1800888-ENSG00000169252),C>C,(苏氨酸 165 突变为异亮氨酸)肾上腺素能受体。结果:未检测到导致 Takotsubo 心肌病的结构变异。从生物信息学分析中获得的结果也从 VarSome 工具进行了检查,发现了相似的结果。
许多关于 TC 易感性的研究表明,这可能导致肾上腺素能途径失调,在相似的文献中也研究了最受关注的肾上腺素能受体基因。我们在研究中搜索了 b1AR 和 b2AR 基因中的遗传变异,但在这项研究中未发现任何变异,我们认为需要更大规模的队列研究。