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Q J Med 2004; 97: 141-151
QJM vol. 97 no. 3 (c) Association of Physicians 2004; all rights reserved.

Patterns of cardiovascular reactivity in disease diagnosis

J.E. Naschitz, I. Rosner1, M. Rozenbaum1, M. Fields, H. Isseroff, J.P. Babich, E. Zuckerman, N. Elias, D. Yeshurun, S. Naschitz and E. Sabo

From the Departments of Internal Medicine A and 1Rheumatology, Bnai Zion Medical Center and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel

Received 29 October 2003 and in revised form 30 December 2003

Background: Aberrations of cardiovascular reactivity (CVR), an expression of autonomic function, occur in a number of clinical conditions, but lack specificity for a particular disorder. Recently, a CVR pattern particular to chronic fatigue syndrome was observed.

Aim: To assess whether specific CVR patterns can be described for other clinical conditions.

Methods: Six groups of patients, matched for age and gender, were evaluated with a shortened head-up tilt test: patients with chronic fatigue syndrome (CFS) (n = 20), non-CFS fatigue (F) (n = 15), neurally-mediated syncope (SY) (n = 21), familial Mediterranean fever (FMF) (n = 17), psoriatic arthritis (PSOR) (n = 19) and healthy subjects (H) (n = 20). A 10-min supine phase was followed by recording 600 cardiac cycles on tilt (5–10 min). Beat-to-beat heart rate (HR) and pulse transit time (PTT) were measured. Results were analysed using conventional statistics, recurrence plot analysis and fractal analysis.

Results: Multivariate analysis evaluated independent predictors of the CVR in each patient group vs. all other groups. Based on these predictors, equations were determined for a linear discriminant score (DS) for each group. The best sensitivities and specificities of the DS, consistent with disease-related phenotypes of CVR, were noted in the following groups: CFS, 90.0% and 60%; SY, 93.3% and 62.5%; FMF, 90.1% and 75.4%, respectively.

Discussion: Pathological disturbances may alter cardiovascular reactivity. Our data support the existence of disease-related CVR phenotypes, with implications for pathogenesis and differential diagnosis.

Address correspondence to Professor J.E. Naschitz, Department of Internal Medicine A, Bnai Zion Medical Center, Haifa 31048, PO Box 4940, Israel. e-mail: naschitz{at}tx.technion.ac.il


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