Department of Biochemistry, Medical University of Silesia, Sosnowiec, Poland.
Biomed Res Int. 2013;2013:418604. doi: 10.1155/2013/418604. Epub 2013 Jul 2.
Congenital long-QT syndrome is a genetic disorder associated with abnormalities in the function and/or structure of cardiac ion channels. Up to the present, 13 types of the disease have been described (LQTS1-13) which result from the fact that 13 genes of which mutations can have an influence on the occurrence of the disease have been identified. Characteristic symptoms of the disease include the changes in the ECG (QT interval prolonged above 450 ms), "torsade de pointes," fainting, and even sudden cardiac death. The present study has been focused on two types of the disease, namely, LQTS1 and LQTS2. The examination of two appropriate genes expression (KCNQ1; KCNH2) at the transcription level by QRT-PCR in a group of LQTS patients and a healthy control group showed different transcriptional activities of KCNH2 gene in LQTS2 patients compared to the control individuals. KCNQ1 gene expression study did not reveal such differences between both groups. The results indicate that QRT-PCR may serve as a complimentary method to the identification of molecular alterations in genetic determinants of LQTS2 only, but it cannot be used as a sole diagnostic criterion.
先天性长 QT 综合征是一种与心脏离子通道功能和/或结构异常相关的遗传疾病。迄今为止,已经描述了 13 种疾病类型(LQTS1-13),这是因为已经确定了 13 种基因突变可影响疾病发生的基因。该疾病的特征性症状包括心电图(QT 间期延长超过 450ms)改变、“尖端扭转型室性心动过速”、晕厥,甚至心源性猝死。本研究集中于两种疾病类型,即 LQTS1 和 LQTS2。通过 QRT-PCR 在一组 LQTS 患者和健康对照组中检测两个适当的基因表达(KCNQ1;KCNH2),在 LQTS2 患者与对照组相比,KCNH2 基因的转录活性存在差异。KCNQ1 基因表达研究未显示两组之间存在这种差异。结果表明,QRT-PCR 可能是一种补充方法,仅用于鉴定 LQTS2 遗传决定因素中的分子改变,但不能作为唯一的诊断标准。