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Effect of propranolol on heart rate variability in hyperthyroidism
BMC Research Notes volume 11, Article number: 151 (2018)
We aimed to determine the effect of propanolol on heart rate variability (HRV) in hyperthyroidism before antithyroid treatment. This was a before and after study, on ten patients presenting overt hyperthyroidism naïve to treatment. In each patient, a resting electrocardiogram was done followed by estimation of cardiac autonomic dysfunction during five maneuvers (Ewing battery tests). Long term HRV measurement was done using 24 h ambulatory electrocardiographic recording. This automatically provided estimation of HRV using SDNN and RMSSD index, LF, HF, and HF/LF ratio. After baseline investigations, 40 mg of propanolol was given twice a day for 3 days and same parameters were measured after 72 h of treatment.
Our patients were aged 40 ± 10 years. Propanolol significantly reduced RR and HR interval (669 ms vs 763 ms and 91 vs 79 bpm; p < 0.01). QT and PR space were significantly extended (360 vs 384 ms and 133 vs 172 ms; p = 0.01). It increases QRS complex and blood pressure response to sustained handgrip but failed to modify previously decreased heart response to deep breathing. HRV parameters such as SDNN, RMSSD, LF, HF and sympathovagal balance estimate by HF/LF ratio remained unchanged. Although a significant reduction in heart excitability, propanolol failed to restore a good sympathovagal balance in hyperthyroidism.
Trial registration NCT03393728 “Retrospectively registered”
Typical clinical signs of hyperthyroidism such as increase in heart rate, cardiac output, systolic blood pressure, myocardial contractility, the presence of tremor suggest a hyper adrenergic state and β-adrenergic blocking agents (β-blockers) have been used in this indication for many years as they rapidly improve signs and symptoms observed in patients with thyrotoxicosis [1,2,3,4]. Propranolol is widely used in hyperthyroidism to relieve cardiac and peripheral manifestations of thyrotoxicosis and is considered as the drug of choice in the treatment of hyperthyroidism [3, 4]. However, it has been suggested that the beneficial effect of propanolol was not related to a reduction in hormone level suggesting that they must be another mechanism of action . On the other hand, thyrotoxicosis is accompanied by a sympathovagal imbalance characterized by a reduced vagal tone and a subsequent increase in sympathetic activity which may contribute to sinus tachycardia generating some cardiac signs of hyperthyroidism including increase in resting heart rate and arrhythmias [6, 7]. Reduced heart rate variability (HRV), a marker of autonomic dysfunction, predicts mortality after acute myocardial infarction and propanolol has been thought to improve recovery of parasympathetic tone in these patients, thereby reducing risk of sudden death . Evidence indicates that the cardiovascular state due to vagal inhibition in patients suffering from thyroid dysfunctions is poor, an attempt should therefore be made to improve vagal tone especially in hyperthyroid subjects to achieve a stable sympathovagal and cardiovascular homeostasis . Although the peripheral effects of propanolol on the metabolism of thyroid hormones such as reducing peripheral conversion of FT4 to FT3 and antagonizing the β-receptor-mediated effects of catecholamines are well known, many questions on its intra-cardiac effect are still unanswered. Whether β blockers, especially propanolol could influence the improvement HRV in hyperthyroidism is unknown and few data are available on the topic . The purpose of this study was to investigate the effect of propranolol on HRV in patients with hyperthyroidism naive to treatment.
Setting and study population
This was a before and after study, which took place at the National Obesity Center of the Yaoundé Central Hospital. The study population was made up of recently diagnosed patients with hyperthyroidism and naïve to antithyroid treatment. All participants fulfilled diagnosis criteria of thyrotoxicosis. Patients having evidence of cardiopulmonary disease or arrhythmia or presenting a contra-indication to beta blockers were excluded. No other medication was taken during the study period.
Procedure and investigations
The study procedure was made of an inclusion visit and three exploratory visits. All patients presenting with signs or symptoms of hyperthyroidism or referred for the management of hyperthyroidism were approached and invited for inclusion.
The study goal and procedure were explained and eligibility assessed. A cardiovascular exam and a resting electrocardiogram were done to every eligible patient in order to exclude those already presenting with findings which may alter HRV analysis such as arrhythmias, bundle branch blocks and myocardial infarction and overt cardiovascular abnormalities.
At the first exploration visit, a resting electrocardiogram was done to every patient. This was followed by the measure of HRV using a continuous electrocardiogram device (heart rate meter Polar RS 800). Electrodes were moisten and placed at the level of the 5th rib on the chest wall in order to pick up waves coming from heart beats and the corresponding watch used to record data attached at the left wrist. This device helped in the evaluation of HRV during a battery of tests and on the following 24 h.
In order to evaluate cardiac autonomic function in our population study, every patient had to performed a battery of five tests according to Ewing battery tests used to assess cardiac autonomic dysfunction . Five minutes after the end of the last maneuver, the patient returned home with the device functioning for the following 24 h. An appointment was given 24 h later and patient went back with the device recording heart rate all day long.
The following day, the device was stopped and each patient received 80 mg of propranolol per day for 03 days administered as 40 mg every 12 h. The next appointment was given 03 days later. The drug was stopped and another resting electrocardiogram was done considering the same measures. HRV was recorded for the second time during the Ewing battery tests and for 24 h using the same procedure.
Data acquisition and analysis were performed using SPSS version 13.0. Continuous variables are expressed as means with standard deviation and categorical variables as count. The Wilcoxon test was used to test differences between before and after treatment measurements. A p < 0.05 was considered as statistically significant.
We enrolled 10 patients presenting overt hyperthyroidism (9 females) with an average age of 40 ± 10 years with extremes ranging from 27 to 60 years. Mean blood pressure of the study population was 115/62 mmHg for a mean heart rate of 98 ± 20 beats/min. The analysis of ECG showed that all ECG parameters were improve after propanolol administration (Table 1).
HRV evaluate by the Ewing battery tests showed abnormal results for the second and the fifth tests at baseline before propanolol administration. Propanolol administration failed to modify heart response to deep breathing but significantly increased blood pressure response to sustained handgrip (− 6.8 vs 1.2; p = 0.04). However, that increase, although significant, remained under normal values set to ≥ 16 (Table 2).
The average value of the R-R interval was significantly increased by propranolol (0.71 vs 0.79; p = 0.028). In contrast, SDNN index, representing the overall HRV but mostly the sympathetic tone remained unchanged after propanolol administration as well as RMSSD, a marker of parasympathetic activity. Otherwise the LF (n.u.), HF (n.u.) and LF/HF ratio were not significantly changed after the administration of propranolol in our population study (Table 3).
This study was carried out in order to determine the effect of propanolol administration on HRV in patients with hyperthyroidism naïve to antithyroid treatment. Our results indicate that 80 mg of propanolol taken for 03 days can significantly slow heart rate and modify parameters of resting ECG. Despite this reduction in cardiac excitability and nerve impulse conduction, it failed to increase parasympathetic tone and overall HRV. It can slightly increase blood pressure response to sustained handgrip though this increase remains under normal set values. A previous study showed that propanolol is effective in the recovery of HRV in patients after 6 weeks of treatment following an acute myocardial infarction . The absence of effect in our study could either be attributed to the short duration of treatment or to an absence of modification specific to HRV in hyperthyroidism. The same beneficial effect of beta-blockers was found in rats, healthy volunteers and patients with ESKD using either lipophilic or hydrophilic beta-blockers which appeared to be effective in increasing the vagal modulation of heart rate [12,13,14,15]. Another reason that could explain the absence of effect in our study is the lipophilicity of propanolol. A comparative evaluation of hydrophilic and lipophilic effects of beta-blockers on HRV suggested that hydrophilic drug achieving peripheral blockade of beta-adrenergic receptors provided greater improvement in HRV than lipophilic drugs and this was associated with a higher HF power and a lower LF/HF ratio during day time activity and stress .
To summarize, the reduction of sinus tachycardia obtained by short term treatment with propanolol in hyperthyroidism may be independent of modification of HRV. This suggests that the reduction of HRV found in hyperthyroidism by many studies is not of great participation in heart rate modification and cardiac signs observed in this condition since propanolol which is one of the most effective drug used in this indication did not significantly modify these parameters despite the clinical effect.
Our study was not a double-blind, placebo-controlled randomized trial what would best evaluate an existing effect.
heart rate variability
root-mean-square of successive differences
standard deviation of all normal R–R intervals
thyroid stimulating hormone
Falcone C, Matrone B, Bozzini S, Guasti L, Falcone R, Benzi A, et al. Time-domain heart rate variability in coronary artery disease patients affected by thyroid dysfunction. Int Heart J. 2014;55(1):33–8.
Tagami T, Yambe Y, Tanaka T, Tanaka T, Ogo A, Yoshizumi H, et al. Short-term effects of β-adrenergic antagonists and methimazole in new-onset thyrotoxicosis caused by Graves’ disease. Intern Med Tokyo Jpn. 2012;51(17):2285–90.
Ramsay I. Adrenergic beta-receptor blockade in hyperthyroidism. Br J Clin Pharmacol. 1975;2(5):385–8.
Peden NR, Isles TE, Stevenson IH, Crooks J. Nadolol in thyrotoxicosis. Br J Clin Pharmacol. 1982;13(6):835–40.
Tanaka T, Yamaguchi T, Kuma K, Hidaka H. Effect of beta-adrenergic blockade on plasma dopamine-beta-hydroxylase activity and triiodothyronine in hyperthyroidism. Endocrinol Jpn. 1980;27(4):447–50.
Petretta M, Bonaduce D, Spinelli L, Vicario ML, Nuzzo V, Marciano F, et al. Cardiovascular haemodynamics and cardiac autonomic control in patients with subclinical and overt hyperthyroidism. Eur J Endocrinol. 2001;145(6):691–6.
Burggraaf J, Tulen JH, Lalezari S, Schoemaker RC, De Meyer PH, Meinders AE, et al. Sympathovagal imbalance in hyperthyroidism. Am J Physiol Endocrinol Metab. 2001;281(1):E190–5.
Lampert R, Ickovics JR, Viscoli CJ, Horwitz RI, Lee FA. Effects of propranolol on recovery of heart rate variability following acute myocardial infarction and relation to outcome in the Beta-Blocker Heart Attack Trial. Am J Cardiol. 2003;91(2):137–42.
Karthik S, Pal GK, Nanda N, Hamide A, Bobby Z, Amudharaj D, et al. Sympathovagal imbalance in thyroid dysfunctions in females: correlation with thyroid profile, heart rate and blood pressure. Indian J Physiol Pharmacol. 2009;53(3):243–52.
Iskandrian AS, Hakki AH, Mattleman S. Cardiac function in hyperthyroidism. Clin Cardiol. 1984;7(3):171–4.
Ewing DJ, Clarke BF. Diagnosis and management of diabetic autonomic neuropathy. Br Med J Clin Res Ed. 1982;285(6346):916–8.
Sal’nikov EV, Fateev MM, Sidorov AV, Fedorov VN, Grigor’eva MV. Effect of beta-adrenoblockers on heart rate variability in awake and narcotized rats. Bull Exp Biol Med. 2007;144(4):494–7.
Lurje L, Wennerblom B, Tygesen H, Karlsson T, Hjalmarson A. Heart rate variability after acute myocardial infarction in patients treated with atenolol and metoprolol. Int J Cardiol. 1997;60(2):157–64.
Tory K, Horváth E, Süveges Z, Fekete A, Sallay P, Berta K, et al. Effect of propranolol on heart rate variability in patients with end-stage renal disease: a double-blind, placebo-controlled, randomized crossover pilot trial. Clin Nephrol. 2004;61(5):316–23.
Vaile JC, Fletcher J, Al-Ani M, Ross HF, Littler WA, Coote JH, et al. Use of opposing reflex stimuli and heart rate variability to examine the effects of lipophilic and hydrophilic beta-blockers on human cardiac vagal control. Clin Sci Lond Engl. 1999;97(5):585–93 (discussion 609–10).
Kardos A, Long V, Bryant J, Singh J, Sleight P, Casadei B. Lipophilic versus hydrophilic beta(1) blockers and the cardiac sympatho-vagal balance during stress and daily activity in patients after acute myocardial infarction. Heart Br Card Soc. 1998;79(2):153–60.
Study conception and design: ATT, EN, MAK, ES and JCM. Data collection: EN, MYD, MAK, ES and JCM. Statistical analysis: ATT, EN, MAK, ES, JCM. Drafting: ATT, CNN, LMK, EN, CM, ES and JCM. Critical discussion and manuscript revision: All authors. All authors read and approved the final manuscript.
We gratefully acknowledge all the patients who have accepted to take part in this study.
The authors declare that they have no competing interests.
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Data will be available from the corresponding author upon request.
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Ethical approval was granted by the Institutional Review Board of the Health Science Foundation, Cameroon, and was performed in accordance with the guidelines of the Helsinki Declaration. Written informed consent was obtained from all the participants.
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Tankeu, A.T., Azabji-Kenfack, M., Nganou, CN. et al. Effect of propranolol on heart rate variability in hyperthyroidism. BMC Res Notes 11, 151 (2018). https://0-doi-org.brum.beds.ac.uk/10.1186/s13104-018-3224-x
- Heart rate variability