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Glucose series complexity in hypertensive patients

机译:高血压患者的葡萄糖系列复杂性

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Nonlinear methods have been applied to the analysis of biological signals. Complexity analysis of glucose time series may be a useful tool for the study of the initial phases of glucoregulatory dysfunction. This observational, cross-sectional study was performed in patients with essential hypertension. Glucose complexity was measured with detrended fluctuation analysis (DFA), and glucose variability was measured by the mean amplitudes of glycemic excursion (MAGE). We included 91 patients with a mean age of 59 10 years. We found significant correlations for the number of metabolic syndrome (MS)-defining criteria with DFA (r = 0.233, P =.026) and MAGE (r = 0.396, P <.0001). DFA differed significantly between patients who complied with MS and those who did not (1.44 vs. 1.39, P =.018). The MAGE (f = 5.3, P =.006), diastolic blood pressures (f = 4.1, P =.018), and homeostasis model assessment indices (f = 4.2, P =.018) differed between the DFA tertiles. Multivariate analysis revealed that the only independent determinants of the DFA values were MAGE (beta coefficient = 0.002, 95% confidence interval: 0.001-0.004, P = .001) and abdominal circumference (beta coefficient = 0.002, 95% confidence interval: 0.000015-0.004, P = .048). In our population, DFA was associated with MS and a number of MS criteria. Complexity analysis seemed to be capable of detecting differences in variables that are arguably related to the risk of the development of type 2 diabetes. (C) 2014 American Society of Hypertension. All rights reserved.
机译:非线性方法已经应用于生物信号的分析。葡萄糖时间序列的复杂性分析可能是研究葡萄糖调节功能障碍初始阶段的有用工具。这项观察性横断面研究是针对原发性高血压患者进行的。葡萄糖复杂性通过去趋势波动分析(DFA)进行测量,葡萄糖变异性通过血糖波动的平均幅度(MAGE)进行测量。我们纳入了91位平均年龄为59 10岁的患者。我们发现代谢综合征(MS)定义标准数与DFA(r = 0.233,P = .026)和MAGE(r = 0.396,P <.0001)显着相关。符合MS的患者与不符合MS的患者之间的DFA显着不同(1.44对1.39,P = .018)。 DFA三分位数之间的MAGE(f = 5.3,P = .006),舒张压(f = 4.1,P = .018)和稳态模型评估指标(f = 4.2,P = .018)不同。多变量分析显示,DFA值的唯一独立决定因素是MAGE(β系数= 0.002,95%置信区间:0.001-0.004,P = .001)和腹围(β系数= 0.002,95%置信区间:0.000015- 0.004,P = .048)。在我们的人群中,DFA与MS和许多MS标准相关。复杂性分析似乎能够检测到可能与2型糖尿病发生风险有关的变量差异。 (C)2014年美国高血压学会。版权所有。

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