Otsuka K, Cornélissen G, Halberg F
Department of Medicine, Tokyo Women's Medical College, Daini Hospital, Japan.
Clin Cardiol. 1997 Jul;20(7):631-8. doi: 10.1002/clc.4960200710.
In clinical cardiology, heart rate variability is a putative index of autonomic cardiovascular function. Signs of reduced vagal activity are not only associated with an enhanced risk of sudden cardiac death, but such impaired heart rate variability became a new predictor of sudden cardiac death and other mortality in patients with a variety of diseased states.
It is postulated (1) that the time structure (chronome) of heart rate variability in clinical health includes a circadian rhythm and deterministic chaos, the latter gauged by the correlation dimensions of RR intervals; and (2) that this chronome is altered in patients with coronary artery disease (CAD).
From 24-h Holter records of 11 healthy controls and 10 patients with CAD, 500-s sections around 02:00, 06:00, 10:00, 14:00, 18:00 and 22:00 hours were analyzed for smoothed RR intervals sampled at 4 Hz. Correlation integrals were estimated for embedding dimensions from 1 to 20 with a 1.0-s time lag, using an algorithm modified from Grassberger and Procaccia. The Wilcoxon signed-rank test compares circadian end points assessed by cosinor between the CAD patients and age-matched controls.
A circadian rhythm characterizes the correlation dimension of healthy subjects peaking during the night (p < 0.005). Patients with CAD have a lowered correlation dimension (p < 0.05) and an altered circadian variation which requires the consideration of an approximately 12-h (circasemidian) component.
The results demonstrate the sensitivity of circadian rhythms for the detection of disease. A partial 24- to 12-h (circadian-to-circasemidian) frequency multiplication (or partial variance transposition) in CAD of the correlation dimension, apart from being a potential clue to the etiology of the disease, adds a new feature to a chronocardiology combining, with the fractal scaling, an assessment of circadian and circasemidian components as measures of predictable variability to be tested for use in diagnosis, prognosis, and as putative guides to treatment timing.
在临床心脏病学中,心率变异性是自主心血管功能的一个假定指标。迷走神经活动减弱的迹象不仅与心脏性猝死风险增加有关,而且这种受损的心率变异性成为各种疾病状态患者心脏性猝死和其他死亡率的新预测指标。
假定(1)临床健康状态下心率变异性的时间结构(时间节律)包括昼夜节律和确定性混沌,后者通过RR间期的关联维数来衡量;(2)冠状动脉疾病(CAD)患者的这种时间节律会发生改变。
从11名健康对照者和10名CAD患者的24小时动态心电图记录中,分析凌晨02:00、06:00、10:00、14:00、18:00和22:00左右500秒时间段内以4Hz采样的平滑RR间期。使用从格拉斯贝格尔和普罗卡西亚算法修改而来的算法,对嵌入维数从1到20、时间滞后为1.0秒的相关积分进行估计。采用Wilcoxon符号秩检验比较CAD患者和年龄匹配对照者通过余弦分析法评估的昼夜节律终点。
健康受试者的关联维数具有昼夜节律特征,在夜间达到峰值(p<0.005)。CAD患者的关联维数降低(p<0.05),且昼夜变化改变,需要考虑一个约12小时(近中午)的成分。
结果表明昼夜节律对疾病检测具有敏感性。CAD患者关联维数中部分24至12小时(昼夜至近中午)的频率倍增(或部分方差转置),除了是疾病病因的潜在线索外,还为时间心脏病学增添了一个新特征,该学科结合分形标度,将昼夜和近中午成分的评估作为可预测变异性指标,用于诊断、预后以及作为治疗时机的假定指导进行测试。