Department of Physiology, New York Medical College, The Center for Hypotension, 19 Bradhurst Ave., Ste. 1600S, Hawthorne, NY 10532, USA.
Am J Physiol Heart Circ Physiol. 2011 Feb;300(2):H527-40. doi: 10.1152/ajpheart.00257.2010. Epub 2010 Nov 12.
Loss of the cardiovagal baroreflex (CVB), thoracic hypovolemia, and hyperpnea contribute to the nonlinear time-dependent hemodynamic instability of vasovagal syncope. We used a nonlinear phase synchronization index (PhSI) to describe the extent of coupling between cardiorespiratory parameters, systolic blood pressure (SBP) or arterial pressure (AP), RR interval (RR), and ventilation, and a directional index (DI) measuring the direction of coupling. We also examined phase differences directly. We hypothesized that AP-RR interval PhSI would be normal during early upright tilt, indicating intact CVB, but would progressively decrease as faint approached and CVB failed. Continuous measurements of AP, RR interval, respiratory plethysomography, and end-tidal CO2 were recorded supine and during 70-degree head-up tilt in 15 control subjects and 15 fainters. Data were evaluated during five distinct times: baseline, early tilt, late tilt, faint, and recovery. During late tilt to faint, fainters exhibited a biphasic change in SBP-RR interval PhSI. Initially in fainters during late tilt, SBP-RR interval PhSI decreased (fainters, from 0.65±0.04 to 0.24±0.03 vs. control subjects, from 0.51±0.03 to 0.48±0.03; P<0.01) but then increased at the time of faint (fainters=0.80±0.03 vs. control subjects=0.42±0.04; P<0.001) coinciding with a change in phase difference from positive to negative. Starting in late tilt and continuing through faint, fainters exhibited increasing phase coupling between respiration and AP PhSI (fainters=0.54±0.06 vs. control subjects=0.27±0.03; P<0.001) and between respiration and RR interval (fainters=0.54±0.05 vs. control subjects=0.37±0.04; P<0.01). DI indicated respiratory driven AP (fainters=0.84±0.04 vs. control subjects=0.39±0.09; P<0.01) and RR interval (fainters=0.73±0.10 vs. control subjects=0.23±0.11; P<0.001) in fainters. The initial drop in the SBP-RR interval PhSI and directional change of phase difference at late tilt indicates loss of cardiovagal baroreflex. The subsequent increase in SBP-RR interval PhSI is due to a respiratory synchronization and drive on both AP and RR interval. Cardiovagal baroreflex is lost before syncope and supplanted by respiratory reflexes, producing hypotension and bradycardia.
心脏压力反射(CVB)丧失、胸腔血容量减少和过度通气会导致血管迷走性晕厥的血流动力学不稳定呈非线性时变。我们使用非线性相位同步指数(PhSI)来描述心肺参数(收缩压或动脉压(AP)、RR 间隔(RR)和通气)与心搏之间的耦合程度,以及测量耦合方向的方向指数(DI)。我们还直接检查了相位差。我们假设在早期直立倾斜时,AP-RR 间隔 PhSI 正常,表明 CVB 完整,但随着晕厥的临近和 CVB 的失败,AP-RR 间隔 PhSI 会逐渐降低。在 15 名对照者和 15 名晕厥者中,我们在仰卧位和 70 度头高位倾斜时连续记录 AP、RR 间隔、呼吸描记术和呼气末二氧化碳。数据在五个不同的时间点进行评估:基线、早期倾斜、晚期倾斜、晕厥和恢复。在晚期倾斜到晕厥期间,晕厥者的 SBP-RR 间隔 PhSI 表现出双相变化。最初在晚期倾斜期间,晕厥者的 SBP-RR 间隔 PhSI 降低(晕厥者,从 0.65±0.04 降至 0.24±0.03;与对照组,从 0.51±0.03 降至 0.48±0.03;P<0.01),但随后在晕厥时增加(晕厥者=0.80±0.03;与对照组=0.42±0.04;P<0.001),同时相位差从正变为负。从晚期倾斜开始并持续到晕厥期间,晕厥者的呼吸与 AP PhSI(晕厥者=0.54±0.06;与对照组=0.27±0.03;P<0.001)和呼吸与 RR 间隔(晕厥者=0.54±0.05;与对照组=0.37±0.04;P<0.01)之间的相位耦合增加。DI 表明在晕厥者中呼吸驱动 AP(晕厥者=0.84±0.04;与对照组=0.39±0.09;P<0.01)和 RR 间隔(晕厥者=0.73±0.10;与对照组=0.23±0.11;P<0.001)。晚期倾斜时 SBP-RR 间隔 PhSI 的初始下降和相位差的方向性变化表明心脏压力反射丧失。随后 SBP-RR 间隔 PhSI 的增加是由于 AP 和 RR 间隔的呼吸同步和驱动。晕厥前心脏压力反射丧失,被呼吸反射取代,导致低血压和心动过缓。