Impulse response analysis of baroreceptor sensitivity . Panerai, Ronney B., Martin A. James, and John F. Potter. Division of Medical Physics, Faculty of Medicine, University of Leicester, Leicester Royal Infirmary, Leicester LE1 5WW, and Division of Medicine for the Elderly, Faculty of Medicine, University of Leicester, Glenfield Hospital, Leicester LE3 9QP, UK
APStracts 3:0549H, 1996.
The impulse response function (IRF) can express the dynamic relationship between systolic arterial pressure (SAP) and pulse interval (PI) and, consequently, represents an alternative method to assess baroreceptor sensitivity (BRS) in humans. Five normotensive and 13 hypertensive subjects (age 68 +/- 5 years, range 60-74) were studied at rest in the supine position during baseline conditions and following injections of phenylephrine and sodium nitroprusside. SAP and PI signals were derived from multiple 5 min. noninvasive recordings of arterial blood pressure (Finapres) and the ECG. Standard estimates of BRS were obtained by the slopes of transient changes in SAP and PI following the injection of phenylephrineand nitroprusside (BRSPE and BRSSNP) and by spectral analysis ([alpha] index). Impulse responses were obtained by the inverse Fourier transform of the transfer function between PI and SAP. The temporal pattern of the IRF was characterized by a main peak at t = 0, preceded by a 'trough' at t = -1 s. A mathematical model of the baroreflex suggests that the peak value of IRF is linearly related to the BRS. The peak value and its smoothed version were shown to be significantly correlated to [alpha], BRSPE and BRSSNP and significantly reduced in the hypertensive group during the three stages of the protocol. We suggest that IRF might be the ideal method to assess BRS because it does not require any subjective pre -selection of data segments or spectral bands.

Received 20 May 1996; accepted in final form 3 December 1996.
APS Manuscript Number H456-6.
Article publication pending Am. J. Physiol. (Heart Circ. Physiology).
ISSN 1080-4757 Copyright 1996 The American Physiological Society.
Published in APStracts on 31 December 1996