Bari Vlasta, Valencia Jose F, Vallverdu Montserrat, Girardengo Giulia, Bassani Tito, Marchi Andrea, Calvillo Laura, Caminal Pere, Cerutti Sergio, Brink Paul A, Crotti Lia, Schwartz Peter J, Porta Alberto
Annu Int Conf IEEE Eng Med Biol Soc. 2013;2013:5554-7. doi: 10.1109/EMBC.2013.6610808.
This study assesses complexity of cardiovascular control in patients affected by type-1 variant of long QT (LQT1) syndrome. Complexity was assessed by refined multiscale entropy of heart period (HP) and QT interval variabilities. HP was taken as the time distance between two consecutive R peaks (RR) and QT interval was approximated as the time distance between the R-peak and T-wave apex (RTa) and between R-peak and T-wave end (RTe). RR, RTa and RTe intervals were automatically extracted from 24h Holter recordings and the daytime period was analyzed (from 02:00 to 06:00 PM). Non mutation carrier (NMC) individuals (n=11), utilized as a control group, were taken from the same family line of the mutation carrier (MC) subjects (n=26). We found that, while NMC and MC groups were indistinguishable based on time domain and complexity analyses of RR dynamics, complexity analysis of RTa and RTe variabilities clearly separates the two populations and suggests an impairment in the cardiac control mechanisms acting on the ventricles.
本研究评估了1型长QT(LQT1)综合征患者心血管控制的复杂性。通过对心动周期(HP)和QT间期变异性的精细多尺度熵来评估复杂性。HP被视为两个连续R波峰之间的时间间隔(RR),QT间期近似为R波峰与T波顶点之间的时间间隔(RTa)以及R波峰与T波终点之间的时间间隔(RTe)。RR、RTa和RTe间期从24小时动态心电图记录中自动提取,并对白天时段(上午02:00至下午06:00)进行分析。作为对照组的非突变携带者(NMC)个体(n = 11)取自与突变携带者(MC)受试者(n = 26)相同的家族系。我们发现,虽然基于RR动态的时域和复杂性分析,NMC组和MC组没有差异,但RTa和RTe变异性的复杂性分析清楚地将这两个人群区分开来,并表明作用于心室的心脏控制机制存在损害。