用一种确定非平稳时间序列数据分形维数的新方法分析无脑胎儿的心率变异性。

H. Shono, M. Shono, T. Iwasaka, H. Sugimori
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引用次数: 1

摘要

人类胎儿心率(HR)的变异分析使用QIS-A,我们设计了一个非平稳时间序列的分形维数确定。通过超声心动图获得15例妊娠23周和3天无脑胎儿和10例妊娠同周正常胎儿的10分钟HR数据。无脑儿保留了脊髓、髓质和部分下丘脑前部。采用Student's t检验比较无脑儿与正常胎儿的分形标度指数。结果表明,每一种情况下的尺度关系都具有以alpha(s)和alpha(l)为特征的交叉模式,分别是交叉点上方和下方的斜率。平均α (s)和平均α (l)在无脑胎儿和正常胎儿之间的差异显著(P < 0.01):平均α (s), 1.0 +/- 0.1 (+/- sd) (1/f波动)和1.6 +/- 0.2 (+/- sem);α(l), 1.6 + / - 0.2(+ / -标准差)和1.4 + / - 0.1(+ /钙)。无脑儿与正常胎儿的平均交叉点有6个显著差异:13.8 +/- 5.7 s (+/- sd)和15.3 +/- 5.6 s (+/- sem)。这些结果揭示了胎儿HR变异的分形结构与中枢神经系统发育之间的关系。特别是,无脑胎儿在1.25 - 13.8 s时间尺度内HR变异性的1/f波动可能与中枢神经系统的缺陷有很强的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of heart rate variability of an anencephalic fetus using a new method to determine a fractal dimension of non-stationary time-serial data.
Human fetal heart rate (HR) variabilities were analyzed using the QIS-A, which we devised to determine a fractal dimension of non-stationary time series. Fifteen 10-min HR data of an anencephalic fetus at 23 weeks and 3 days of gestation and those of 10 normal fetuses at the same weeks of gestation were obtained by ultrasonic cardiography. The anencephalus preserved the spinal cord, medulla and partial anterior hypothalamus. The fractal scaling exponent alpha of the anencephalus was compared with that of each normal fetus by Student's t-test. In results, the scaling relationship in each case had a crossover pattern characterized by alpha(s) and alpha(l), which were slopes above and below a crossover point, respectively. Differences in mean alpha(s) and mean alpha(l) between the anencephalus and each normal fetus were significant (P < 0.01): mean alpha(s), 1.0 +/- 0.1 (+/-SD) (1/f fluctuation) and 1.6 +/- 0.2 (+/-SEM); mean alpha(l), 1.6 +/- 0.2 (+/-SD) and 1.4 +/- 0.1 (+/-SEM). There were six significant differences in mean crossover point between the anencephalus and each normal fetus: 13.8 +/- 5.7 s (+/-SD) and 15.3 +/- 5.6 s (+/-SEM). These results reveal the relationship between fractal structure of fetal HR variability and the developing central nervous system (CNS). In particular, the 1/f fluctuation of HR variability in an anencephalic fetus from the 1.25 to 13.8 s time scale might have a strong relation to the defect of the CNS.
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