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Effect of Beta‐Blockade on Autonomic Modulation of Heart Rate and Neurohormonal Profile in Decompensated Heart Failure
Authors:Doron Aronson  Andrew J Burger
Abstract:Background: One of the putative mechanisms for the salutary effects of beta‐blockers in patients with congestive heart failure (CHF) is their ability to improve autonomic dysfunction. However, patients with profound neurohumoral abnormalities derive little survival benefit from beta‐blockers. The purpose of the current study was to evaluate the effect of beta‐blockers on heart rate variability (HRV) in decompensated CHF. Methods: Time and frequency domain HRV indices were obtained from 24‐hour Holter recordings and compared to assess the role of beta‐blockade in 199 patients (mean age 60 ± 14 years) with decompensated CHF. Neurohormonal differences were assessed by measuring norepinephrine, endothelin‐1, tumor necrosis factor‐a, and interleukin‐6 in a subset of 64 patients. Results: All HRV indices were markedly suppressed but were substantially higher in patients who were on beta‐blockers. Time domain measures of parasympathetic cardiac activity, the percentage of R‐R intervals with > 50 ms variation (4.9 ± 0.6 vs 7.7 ± 1.2%, P = 0.006) and the square root of mean squared differences of successive R‐R intervals (22.7 ± 2.0 vs 31.6 ± 4.1 ms, P = 0.004), were higher in the beta‐blocker group. Spectral analysis revealed that the total power and the ultra‐low frequency power were significantly higher in patients on beta‐blockers (82% and 59%, respectively). The high frequency power, a spectral index of parasympathetic modulation, was 41% higher in the beta‐blocker group (121 ± 25 vs 171 ± 27 ms2, P = 0.02). Norepinephrine and interleukin‐6 levels were substantially lower in patients on beta‐blockers (28% and 61%, respectively). However, these differences did not reach statistical significance. Conclusions: Beta‐blockers improve the impaired cardiac autonomic regulation during high sympathetic stress of decompensated CHF. This effect may play an important role in protecting the myocardium and preventing arrhythmias during transient increases in sympathetic activity. A.N.E. 2001;6(2):98–106
Keywords:heart rate variability  heart failure  beta‐adrenergic blockers  cytokines
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