Naschitz Jochanan E, Rozenbaum Michael, Fields Madeline, Isseroff Hillel, Enis Sean, Babich Jay P, Peck Shannon, Peck Elisabeth Rubin, Gaitini Louis, Naschitz Shaul, Sabo Edmond, Rosner Itzhak
Department of Internal Medicine A, Bnai Zion Medical Center and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Clin Sci (Lond). 2005 Jan;108(1):37-46. doi: 10.1042/CS20040092.
Aberrations of CVR (cardiovascular reactivity), an expression of autonomic function, lack specificity for a particular disorder. Recently, a CVR pattern particular to chronic fatigue syndrome has been observed. In the present study, we aimed to develop methodologies for assessing disease-specific CVR patterns. As a prototype, a population of 50 consecutive patients with FMF (familial Mediterranean fever) was studied and compared with control populations. A 10 min supine/30 min head-up tilt test with recording of the heart rate and blood pressure or the pulse transit time was performed. Five studies were conducted applying different methods. In each study, statistical analysis identified independent predictors of CVR in FMF. Based on regression coefficients of these predictors, a linear DS (discriminant score) was computed for every subject. Each study established an equation to assess CVR, calculate DS for FMF and determine the sensitivity and specificity of the DS cut-off. In each of the five studies, abnormal CVR was observed in FMF patients. The best accuracy (88% sensitivity and 90.1% specificity for FMF) was obtained by a method based on beat-to-beat heart rate and pulse transit time recordings. Data was processed by fractal and recurrence quantitative analysis with recordings in FMF patients compared with a mixed control population. Identification of disease-specific CVR patterns was possible with the methodologies described in the present study. In FMF, disease-specific CVR may be explained by the interplay between neuroendocrine loops specific to FMF with cardiovascular homoeostatic mechanisms. Recognition of disease-specific CVR patterns may advance the understanding of homoeostatic mechanisms and have implications in clinical practice.
心血管反应性(CVR)异常是自主神经功能的一种表现,对特定疾病缺乏特异性。最近,观察到一种慢性疲劳综合征特有的CVR模式。在本研究中,我们旨在开发评估疾病特异性CVR模式的方法。作为一个原型,对连续50例家族性地中海热(FMF)患者进行了研究,并与对照组进行了比较。进行了一项10分钟仰卧/30分钟头高位倾斜试验,记录心率、血压或脉搏传输时间。采用不同方法进行了五项研究。在每项研究中,统计分析确定了FMF中CVR的独立预测因素。根据这些预测因素的回归系数,为每个受试者计算了一个线性判别分数(DS)。每项研究都建立了一个评估CVR的方程,计算FMF的DS,并确定DS临界值的敏感性和特异性。在五项研究中的每一项中,FMF患者均观察到异常CVR。基于逐搏心率和脉搏传输时间记录的方法获得了最佳准确性(FMF的敏感性为88%,特异性为90.1%)。通过分形分析和递归定量分析对数据进行处理,将FMF患者的记录与混合对照组进行比较。使用本研究中描述的方法可以识别疾病特异性CVR模式。在FMF中,疾病特异性CVR可能由FMF特有的神经内分泌环路与心血管稳态机制之间的相互作用来解释。识别疾病特异性CVR模式可能会增进对稳态机制的理解,并对临床实践产生影响。