Analysis of rapid heart rate variability in the assessment of anticholinergic drug effects in humans |
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Authors: | Jani Penttilä Tom Kuusela Harry Scheinin |
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Affiliation: | (1) Department of Pharmacology and Clinical Pharmacology, University of Turku, Turku, Finland;(2) Department of Adolescent Psychiatry, Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland;(3) Department of Physics, University of Turku, Turku, Finland;(4) Turku PET Centre, Turku University Hospital, P.O.B. 52, FIN, 20521 Turku, Finland |
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Abstract: | Anticholinergic agents have widespread therapeutic indications in clinical medicine. In addition, certain other drug groups–such as neuroleptics, antidepressants and antihistamines–possess distinct anticholinergic properties that reduce tolerance and compliance. Especially in patients with heart disease, attention should be paid to cardiac anticholinergic drug effects. The analysis of short-term heart rate variability (HRV) provides a noninvasive tool to estimate vagal cholinergic outflow. In this review article, we present the basic principles of the most relevant techniques to study rapid HRV: the time domain analysis methods RMSSD and pNN50, and the high-frequency (HF) spectral component of HRV. We provide examples of previously reported effects of anticholinergic agents on these measures and also describe how adrenergic drugs may influence them. We have the following recommendations for a clinical pharmacologist investigating anticholinergic agents. (1) If the breathing rate of the study subject can be controlled during the assessment and the electrocardiogram recordings contain good-quality, stationary segments that are at least a few minutes long, then the HF power of HRV should be the method of choice. (2) During uncontrolled conditions, RMSSD should be included in the analyses, because it is less affected by changes in the respiratory pattern and it can be measured from shorter segments of electrocardiogram data. (3) Reduced short-term HRV suggests an anticholinergic, but not necessarily an antimuscarinic drug effect, since the inhibition of cholinergic vagal efferent activity may also originate from central or peripheral adrenergic influences. |
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Keywords: | Cholinergic antagonists Parasympathetic nervous system Heart rate variability |
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