Research Article
Cardiovascular manifestations in hyperthyroidism
Department of Medicine, Sri Ramachandra Medical College and Research Institute, Chennai, India
Received: 17 June 2016
Revised: 19 June 2016
Accepted: 22 June 2016
*Correspondence:
Dr. P. Sathyamurthy,
E-mail: drsams30@yahoo.co.in
Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
ABSTRACT
Background: It is well known that thyroid hormone directly affects the heart and peripheral vascular system. In hyperthyroidism, cardiovascular manifestations are frequent findings. Atrial arrhythmias, limitations in exercise tolerance, and congestive heart failure were reported to occur more common in older patients as a result of hyperthyroidism. Cardiovascular signs of hyperthyroidism include tachycardia, widened pulse pressure, marked increase in cardiac output with impaired cardiovascular and respiratory exercise capacity. Most of the cardiac abnormalities return to normal once a euthyroid state has been achieved in a majority of patients. There are very few studies which address the most important cardiovascular manifestations of hyperthyroidism particularly in Indian population. Hence this study is aimed at addressing this area. The aim was to study the prevalence of various cardiac manifestations in overt and subclinical hyperthyroidism.
Methods: 50 patients of hyperthyroidism who visited general medicine department of Sri Ramachandra Medical College, Chennai, India was included in the study. Patients with other co-morbidities which could contribute to cardiovascular manifestations were excluded from the study. All the patients underwent clinical evaluation, basic laboratory tests like CBC, RFT, LFT, serum electrolytes, fasting lipid profile (which included serum triglycerides, LDL, HDL, total cholesterol), FT4, FT3 and TSH and radiological variables were studied in these patients. ECG and 2D ECHO were performed in these patients to analyze the presence of any cardiac manifestations in these patients..
Results: In this study females (60%) were more than males (40%), commonest cardio vascular symptoms were palpitation (78%), followed by dyspnoea (26%) and chest pain (4%). The commonest cardio vascular signs were found to be tachycardia (82%), widened pulse pressure (50%) and pedal edema (12%). The commonest ECG finding was found to be Sinus tachycardia (46%) followed by atrial fibrillation (28%), Non-Specific ST-T changes, left ventricular hypertrophy, RV hypertrophy and RBBB. Systolic dysfunction and chamber enlargement (18%) were the commonest echo findings.
Conclusions: This study shows that cardiovascular manifestations are quite common and varied in hyperthyroidism which are to be looked for in the management.
Keywords: Hyperthyroidism, Cardiovascular manifestations, Atrial fibrillation
INTRODUCTION
Thyroid hormones have a profound effect on numerous metabolic processes, virtually in all tissues and hence every tissue in the body gets affected to a greater or lesser extent in thyroid hormone disturbances, the heart being particularly sensitive to its effect. Thyroid hormone directly affects the heart and peripheral vascular system. The hormone causes increase in heart rate, myocardial ionotrophy and increases the cardiac output by dilating the peripheral arteries.1 In hyperthyroidism, cardiovascular manifestations are frequent findings. Hyperthyroidism can produce changes in blood pressure, myocardial oxygen consumption, cardiac contractility, cardiac output and systemic vascular resistance.2 Atrial arrhythmias, limitations in exercise tolerance, and congestive heart failure were reported to occur more common in older patients as a result of hyperthyroidism.3
Hyperthyroidism results in excessive mortality from increased incidence of circulatory diseases and dysarrhythmias.4 Incidence of cerebral embolism is common in the hyperthyroid patients with atrial fibrillation, especially in the elderly group and anticoagulation was indicated in them. Numerous studies have shown that treatment of hyperthyroidism results in conversion to sinus rhythm in up to two-third of patients. Drugs like beta-blockers help to reduce left ventricular hypertrophy and atrial and ventricular arrhythmias in patients with hyperthyroidism.5
Cardiovascular signs of hyperthyroidism include tachycardia, widened pulse pressure, marked increase in cardiac output with impaired cardiovascular and respiratory exercise capacity.6 In the elderly hyperthyroid patient the symptoms and signs of heart failure or worsening of angina pectoris may dominate the clinical picture and mask the more classical endocrine manifestations of the disease.
Long-term follow-up studies had revealed increase in the mortality in those with a past history of overt hyperthyroidism, as well as those with subclinical hyperthyroidism.7 Supraventricular arrhythmias in particular AF, in elderly patients may account for some of the excess in the cardiovascular and cerebrovascular mortality described, especially because of the AF, which is known to predispose to embolic phenomena.7
Most of the cardiac abnormalities return to normal once a euthyroid state has been achieved in a majority of patients, although AF may persist in a minority group of patients.8 Many studies have been done on the clinical presentation and lab manifestations of hyperthyroidism. However there are very few studies which address the most important cardiovascular manifestations of hyperthyroidism particularly in Indian population. Hence this study is aimed at addressing this area.
METHODS
This study was done in Sri Ramachandra Medical College in the Department of General Medicine with close association with the Department of Cardiology. This observational study included 50 patients with hyperthyroidism based on FT3, FT4 and TSH levels, who fulfilled the inclusion criteria and exclusion criteria. The study protocol was duly approved by the institutional ethics committee of Sri Ramachandra University, Chennai, India. All the patients underwent clinical evaluation, basic laboratory tests like CBC, RFT, LFT, serum electrolytes, fasting lipid profile (which included serum triglycerides, LDL, HDL, total cholesterol), FT4, FT3 and TSH and radiological variables were studied in these patients.
ECG and 2D ECHO were performed in these patients to analyze the presence of any cardiac manifestations.
Inclusion criteria
- • Age >18 years
- • All patients with overt hyperthyroidism of any etiology
- • All patients with subclinical hyperthyroidism of any etiology
Exclusion criteria
- • Patients with hypertension, diabetes mellitus, coronary artery disease, chronic kidney disease on treatment
- • Patients on antiarrhythmic drugs
Statistical analysis
The collected data of the 50 patients was statistically analyzed with SPSS 16.0 version. To describe about the data descriptive statistics frequency analysis, percentage analysis, cross tabulation were used for categorical variables and the mean and SD were used for continuous variables. To find the significance in categorical data Chi-square test was used. In all the above statistical tools the probability value 0.05 is considered as significant.
RESULTS
In this current study 50 patients with hyperthyroidism who consulted Sri Ramachandra Medical College Hospital, Chennai, India during the study period were included. In this study of 50 patients of hyperthyroid, majority of the patients are females of age group between 41-60 years. Similarly majority of incidence in the same age group (Table 1).
In this study out of the total patients, 18% had pallor, 12% had edema, 20% had eye signs and 28% had moist skin. Out of 50 patients 9 had pallor, 6 had edema, 10 had eye signs and 14 had moist skin (Table 2). In this study 66.7% of the female patients and 95% of the male patients had palpitations. In this study 16.7% of the female patients and 40% of the male patients presented with breathlessness. In this study 6.7% of the females presented with chest pain (Table 3).
In this study out of the total patients, 78% presented had palpitations with a highly significant P value; hence these patients might be prone for arrhythmias and tachycardia so they need further cardiac evaluation (Table 3). In this study 26% of patients presented with breathlessness and 4% with chest pain. Out of 50 patients 39 had palpitations, 13 had breathlessness and 2 had chest pain (Table 3). In this study of 50 patients of hyperthyroidism, among the female patients 96.7% and 85% of males, with an average of around 92% of total patients had BMI ranging from 18.5 to 24.99. 3.3% of females and 5% of males, with an average of around 4% of total patients had between 25 to 29.99. And 10% of males, with an average of around 4% of total patients had less than 18.5 (Table 4).
P value-0.603
P value-0.196
P value-0.652
In this study about 18% of the patients had heart rate ranging between 80-100 and about 82% had above 100 (Table 5). In this study about 22% of the patients had SBP of less than 120, 46% had SBP ranging between 120 to 139. 30% had SBP ranging between 140 to 159. And about 2% had above 159 (Table 6).
In this study about 60% of the patients had DBP of less than or equal to 80. 34% had DBP ranging between 80-89 and about 6% had between 90-99 (Table 7).
P Value-0.203
P Value-0.079
P Value-0.537
Among the 50 patients studied 11 patients of which 5 females and 6 males had a pulse pressure ranging from 21-40. 25 patients including 16 females and 9 males had between 41-60. And about 14 patients had above 60 (Table 8). Among the 50 patients 2 males (4%) had loud P2. 3 females and 3 males (12%) had cardiomegaly. 3 females and 11 males (28%) had varying heart sounds with a highly significant P Value suggestive of these patients are more prone for arrhythmia (Table 9).
In this present study the commonest ECG findings were found to be Sinus tachycardia (46%), atrial fibrillation (28%), non-specific ST-T changes (8%), RV hypertrophy (10%), left ventricular hypertrophy (8%) and RBBB (10%) (Table 10). In this study, echocardiographic evaluation showed systolic dysfunction in 18% of patients and chamber enlargement in 18% of patients, followed by diastolic dysfunction in 12%, regurgitant lesion in 6% and pulmonary hypertension in 4% of patients (Table 11).
DISCUSSION
In this current study 50 patients with hyperthyroidism who consulted Sri Ramachandra Medical College Hospital, Chennai, India during the study period were included. The age of the patients in this present study ranged between 19-68 years. In this present study, peak incidence was observed among the age group of 41-60 years (50%), followed by the age group of about 20-40 years (44%).
In this study Females (60%) were more than males (40%). This female preponderance in hyperthyroidism is well known in many other studies as well. In the present study, the commonest symptoms were found to be weight loss, easy fatigue, excessive sweating, tremors, decreased sleep, and increased appetite. In the present study the commonest cardio vascular symptoms were palpitation (78%), followed by dyspnoea (26%) and chest pain (4%). This also goes with the fact that palpitation and dyspnoea are the commonest symptoms of hyperthyroidism patients irrespective of the cause.
Hence in congruent with earlier studies, this study also had majority of patients presenting with palpitation, dyspnoea and chest pain.9,10 In this present study the commonest cardio vascular signs were found to be tachycardia (82%), widened pulse pressure (50%) and pedal edema (12%). Tachycardia was particularly common in the elderly age group. Increased pulse pressure is also seen in these patients. In this study 82% of the patients had tachycardia, as comparable with the Zargar et al.10 In the current study 50% of the patients had widened pulse pressure where as in Klein et al, it is 30%. 12% had pedal edema in present study where as in Klein et al it is 5%.8
In this study sinus tachycardia was found in 46% patients which was 63.5% patients in the study by Zarger et al, however it was mentioned that sinus tachycardia, that is heart rate exceeding 100 beats/min was observed in 40% of patients with hyperthyroidism, occurring more frequently in the younger age group patients, which is comparable with the current study.10 In hyperthyroid patients the prevalence of atrial fibrillation varies between 2% and 20%.1,11 In the study by Barsela S et al 21% of patients had atrial fibrillation, while 8.9% in that of Zarg 28% patients in this study had atrial fibrillation et al and 6% of that of Osman et al.9,10,12 In our study 28% patients in this study had atrial fibrillation which is slightly higher than others.
Intraventricular conduction disturbances like RBBB occur more commonly in about 11% of patients with hyperthyroidism without any associated heart disease of other etiology as mentioned in Zarger et al.10 In comparison, 10% of patients in this study had RBBB. In this present study systolic dysfunction was seen in 18% of the patients, where as in Mercé et al, it was present in 3% of the patients.13
As the current study had more number of patients with atrial fibrillation, it might be the reason for higher systolic dysfunction. In this study pulmonary hypertension was present in about 8.7% of patients however in Sui et al, patients with hyperthyroidism and normal LV systolic function, up to 47% of the patients had PHT.14 Inadequate sample size may be the reason for this difference. The prevalence of diastolic dysfunction increases as the age increased, from 17.9% in patients who are less than 40 years to 100% in those who are all above 60 years.15,16 Present study had diastolic dysfunction in about 12% of patients. Regurgitant lesions were seen in 23% of the patients in the study by Merce et al while in the present study 6% of the patients had the same.13 Over all the cardiovascular manifestations dominated the picture of hyperthyroidism though the frequency is slightly different from the earlier studies. Early identification and management of them is very important since many of them can contribute to serious mortality and morbidity.
Funding: No funding sources
Conflict of interest: None declared
Ethical approval: The study was approved by the Institutional Ethics Committee
REFERENCES
- 1. Klein I, Danzi S. Thyroid disease and heart. Circulation. 2007;116:1725-35.
- 2. Fazio S, Palmieri EA, Lombardi G, Biondi B. Effects of thyroid hormone on the cardiovascular system. Endo Journals Org. 2004;59:31-50.
- 3. Klein I. Thyroid Hormone and the cardiovascular system. Am J Med. 1990;88(6):631-7.
- 4. Tribulova N, Knezl V, Shainberg A, Seki S, Soukup T. Thyroid hormones and cardiac arrhythmias. Vascul Pharmacol. 2010;52(3):102-12.
- 5. Jayaprasad N, Francis J. Atrial Fibrillation and Hyperthyroidism. Indian Pacing Electrophysiol J. 2005;5(4):305-11.
- 6. Symons C. Thyroid heart disease. Br Heart J. 1979;41:257-62.
- 7. Von OK. Cardiac arrhythmias and heart rate in hyperthyroidism. Am J Cardiol. 1989;63:930-3.
- 8. Klein I, Ojamaa K. The cardiovascular system in hyperthyroidism. 8th ed. In: Werner and Ingbar’s The Thyroid: A fundamental and clinical text, Braverman LE, Utiger RD, eds. Philadelphia: Lippincott Williams and Wilkins;2000:777-82.
- 9. Osman F. Cardiovascular manifestations of hyperthyroidism before and after antithyroid therapy: a matched case-control study. J Am Coll Cardiol. 2007;49(1):71-81.
- 10. Zarger. Thyrotoxicosis. Annals of Saudi Medicine. 2000;20(5-6):484-7.
- 11. Parmar MS. Thyrotoxic atrial fibrillation. Med Gen Med. 2005;7(1):74.
- 12. Bar S, Ehrenfeld M, Eliakim M. Arterial embolism in thyrotoxicosis with atrial fibrillation. Arch Intern Med. 1981;141(9):1191-2.
- 13. Mercé J, Ferrás S, Oltra C, Sanz E, Vendrell J, Simón I et al. Cardiovascular abnormalities in hyperthyroidism: a prospective doppler echocardiographic study. Am J Medicine. 2005;118:126-31.
- 14. Siu CW, Zhang XH, Yung C, Kung AW, Lau CP, Tse HF. Hemodynamic changes in hyperthyroidism-related pulmonary hypertension: a prospective echocardiographic study. J Clinic Endocrino Metabo. 2007;92(5):1736-42.
- 15. Roffi M, Cattano F, Topol JE. Thyrotoxicosis and the cardiovascular system: subtle but serious effects. Cleveland Clinic J Med. 2003;7:57-63.
- 16. Yue W. Hyperthyroidism-induced left ventricular diastolic dysfunction: implication in hyperthyroidism-related heart failure. Clinical Endocrinology. 2011;74(5):636-43.
- 17. Fadel BM, Ellahham S, Ringel MD, Lindsay J Jr, Wartofsky L, Burman KD. Hyperthyroid heart disease. Clinical Cardiology. 2000;23:402-8.
- 18. Poliker R. The thyroid and the heart. Circulation. 1993;87:1435-41.
- 19. Boindi B. Effects of subclinical thyroid dysfunction on the heart. Annuals Internal Med. 2002;137:904-14.
- 20. Davis FT, Larsen RP. Thyrotoxicosis. In: William’s Text book of endocrinology, Larsen Melmed, Polonsky, 10th ed. Philadelphia: Saunders. 2003;374-422.
- 21. Davis FT, Larsen RP. Hypothyroidism and thyroiditis. In: William’s text book of endocrinology, Larsen Melmed, Polonsky. 10th ed. Philadelphia: Saunders. 2003;423-55.
- 22. Klein I. Endocrine disorder and cardiovascular diseases. In: Braunwald’s heart disease. 10th ed. Philadelphia: Saunders. 2008;432-49.
- 23. Parry CH. Enlargement of the thyroid gland in connection with enlargement or palpitation of the heart. Collections from the unpublished papers of the late Caleb Hillier Parry.1825;111-25.
- 24. Graves RJ. Newly observed affections of the thyroid gland in females. London Med Surg J. 1835;7:516-7.
- 25. Von BCA. Exophthalmos durch hypertrophie des zellgewebes in der augenho hle. Wschr Ges Heilk. 1840;197-220.
- 26. Zondek H, Leszynsky HE. Pathogenesis of hyperthyroidism. Dual role of iodine in thyroid function. Lancet. 1968;1(7544):671-2.
- 27. Anatomy of the Human Body. Available at http://www.bartleby.com/107/. Accessed on 12 February 2016.
- 28. Nussey S, Whitehead S. Endocrinology: An Integrated Approach. Oxford: BIOS Scientific Publishers. 2001.
- 29. Paul MY. Physiological and molecular basis of thyroid hormone action. Physiological Reviews. 2001;81(3):1097-126.
- 30. Clare BH, Graham RW. The mechanism of thyroid hormone. Thyroid. 2002;12(6):441-6.
- 31. Dillmann WH. Cellular Action of Thyroid Hormone on the Heart. Thyroid. 2002;12(6):447-52.
- 32. Denzi S, Klien I. Thyroid hormone and blood pressure regulation. Current Hypertension Reports. 2003;5:513-52.
- 33. Toft A, Boon N. Thyroid disease and heart. Heart. 2000;84:455-60.
- 34. Dahl P. Thyrotoxic cardiac disease. Current Heart Failure Reports. 2008;5:170-8.
- 35. Gammage MD, Parle JV, Holder RL, Roberts LM, Hobbs FD, Wilson S, et al. Association between serum free thyroxine concentration and atrial fibrillation. Arch Intern Med. 2007;167:928-34.
- 36. Forfar JC, Muir AL, Toft AD. Left ventricular function in hypothyroidism responses to exercise and beta adrenoceptor blockade. Br Heart J. 1982;48:278-84.
- 37. Moolman JA. Thyroid hormone and the heart. Cardiovascular J South Africa. 2002;13(3):159-63.
- 38. Kahaly JG, Dillmann HW. Thyroid hormone action in the heart. Endocrine Reviews. 2005;26:704-28.
- 39. Goland S, Shimoni S, Kracoff O. Dilated cardiomyopathy in thyrotoxicosis. Heart. 1999;81:444-9.
- 40. Ansari SM, Haider S, Awal MA, Khanam N, Siddique AB. Cardiac complications of hyperthyroidism: echocardiographic evaluation of 69 hyperthyroid patients. Transactional Analysis Journal. 2004;17(1):6-9.