Düzen Irfan V, Yavuz Fethi, Vuruskan Ertan, Saracoglu Erhan, Poyraz Fatih, Cekici Yusuf, Alıcı Hayri, Göksülük Hüseyin, Candemir Basar, Sucu Murat, Demiryürek Abdullah T
Department of Cardiology, Faculty of Medicine, University of Gaziantep, Gaziantep 27310, Turkey.
Department of Cardiology, Adana City Hospital, Adana 01060, Turkey.
Exp Ther Med. 2019 Oct;18(4):2777-2782. doi: 10.3892/etm.2019.7929. Epub 2019 Aug 20.
Atrial fibrillation (AF) is an arrhythmia caused by disorganized electrical activity in the atria, and it is an important cause of mortality and morbidity. There is a limited data about Rho/Rho-kinase (ROCK) pathway contribute to AF development. The aim of the present study was to elucidate leukocyte gene expressions in patients with non-valvular AF (NVAF). A total of 37 NVAF patients and 47 age and sex-matched controls were included in this study. mRNA was extracted from leukocytes, and real-time polymerase chain reaction was used for gene expression analysis. A marked increase in and gene expressions in patients with NVAF was observed (P<0.0001). The present study detected significant elevations in and gene expressions (P<0.01). However, there were marked decreases in , and gene expressions in patients with NVAF. No significant modifications were seen in the other Rho GTPase proteins and . To the best of our knowledge, the present study is the first to provide data that gene expression of leukocyte may contribute to the NVAF pathogenesis through activated leukocytes, which promotes the immune or inflammatory cascade.
心房颤动(AF)是一种由心房电活动紊乱引起的心律失常,是死亡率和发病率的重要原因。关于Rho/Rho激酶(ROCK)通路在房颤发生发展中的作用的数据有限。本研究的目的是阐明非瓣膜性房颤(NVAF)患者白细胞的基因表达情况。本研究共纳入37例NVAF患者和47例年龄、性别匹配的对照组。从白细胞中提取mRNA,并采用实时聚合酶链反应进行基因表达分析。观察到NVAF患者和基因表达显著增加(P<0.0001)。本研究检测到和基因表达显著升高(P<0.01)。然而,NVAF患者、和基因表达明显降低。其他Rho GTPase蛋白和未观察到显著变化。据我们所知,本研究首次提供数据表明,白细胞的基因表达可能通过激活白细胞促进免疫或炎症级联反应,从而导致NVAF的发病机制。