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Thyroid dysfunction in patients with suspected or documented supraventricular tachyarrhythmia
International Journal of Arrhythmia volume 20, Article number: 6 (2019)
Background and objectives
The association between thyroid dysfunction and supraventricular tachyarrhythmia (SVT) other than atrial fibrillation (AF) is not well elucidated. We hypothesized that patients with suspected or documented SVT have undetected thyroid dysfunction more frequently than general population.
Subjects and methods
Patients with symptoms suggestive of SVT other than AF who were planned to undergo an EP study at our center were eligible for this study. Patients with known thyroid disease, medications affecting thyroid function test (TFT) or atrial fibrillation were excluded. The primary outcome was prevalence of TFT abnormalities in the study population. The secondary outcome was prevalence of clinically significant arrhythmia during the EP study.
A total of 533 patients were analyzed. Patients were divided into the two groups according to TFT results. Fifty-six (10.5%) patients had abnormal TFT results (thyroid dysfunction group), while 477 (89.5%) had normal thyroid function (euthyroidism group). The overall prevalence of thyroid dysfunction was 10.5%. The thyroid dysfunction group showed a tendency for higher induction of clinically significant SVT than the euthyroidism group. However, thyroid dysfunction was not an independent predictor of clinically significant SVT during EP study.
In this study, patients with suspected SVT who were planned for EP study had a relatively high incidence of thyroid dysfunction. Clinically significant arrhythmia tended to be induced more frequently in the thyroid dysfunction group than in the euthyroidism group. Further investigations are needed to verify the clinical implications of TFT in patients with SVT other than AF.
Many people experience palpitations at some point in their lives. Palpitations, however, are not always due to an arrhythmia, and not all arrhythmias result in palpitations. Furthermore, while some patients are diagnosed by electrocardiogram, others only have symptoms of arrhythmias. Electrophysiology (EP) studies help to elucidate the presence or mechanism of arrhythmia in these patients. Thyroid dysfunction, particularly hyperthyroidism, can cause palpitations, which are one of the common symptoms of thyroid disease . There is a well-established relationship between atrial fibrillation (AF) and thyroid dysfunction. Therefore, a recent guideline recommends the evaluation of thyroid function in AF patients [2,3,4]. Although supraventricular tachyarrhythmias (SVT) other than AF are a common cause of palpitations, the association of non-AF SVTs and thyroid dysfunction has not been well elucidated. The current guidelines recommend ruling out hyperthyroidism in cases of inappropriate sinus tachycardia or premature extra beats [5, 6]. There are a limited number of studies and case reports that investigate the relationship between thyroid dysfunction and SVT other than AF [7,8,9,10]. At our institution, thyroid function test (TFT) has been routinely performed in all patients undergoing EP studies in the work-up of suspected or documented SVT. In this study, we investigated thyroid function abnormality in patients with non-AF SVT to evaluate the clinical value of thyroid function test in this setting.
Materials and methods
Patients with symptoms suggestive of SVT other than AF who were scheduled to undergo an EP study at our institution between January 2014 and May 2017 were eligible for this study. Patients who met any of the following criteria were excluded from the analysis: (1) previous history of thyroidectomy or known thyroid dysfunction, (2) medications that influence TFT, including thyroid hormone, antithyroid drugs, amiodarone, or steroid, (3) no TFT results within 2 months of the EP study, or (4) previous history of AF.
TFT was performed unless patients had undergone TFT within the prior 2 months at our institution. Serum-free T4, total T3, and thyroid stimulating hormone (TSH) were measured using chemiluminescent immunoassay (ADVIA Centaur XP, Siemens). Based on the reference intervals from a recent large nationwide epidemiological study, the normal TFT ranges were defined as 0.62–6.86 mU/L for TSH level and 0.96–1.60 ng/dL for FT4 level . Euthyroidism was defined as TSH and FT4 levels in the normal range. Subclinical hypothyroidism was defined as TSH > 6.86 mU/L with normal FT4 level, and subclinical hyperthyroidism as TSH < 0.62 mU/L with normal FT4 level.
All EP studies were performed after discontinuation of antiarrhythmic drugs. One duodecapolar catheter (or two decapolar catheters) was placed in the high right atrium and coronary sinus. Two quadripolar electrode catheters were placed in the right ventricular apex and His area, respectively. Isoproterenol was infused at a rate of 2–5 mcg/min, unless a significant tachyarrhythmia could be induced by programmed stimulation. If possible, radiofrequency ablation was performed for spontaneous or induced tachyarrhythmia.
A trained study coordinator collected the clinical and laboratory data using a standardized case report form and protocol. The baseline electrocardiograms were reviewed by two EP specialists. The primary outcome was prevalence of TFT abnormality in the study population. The secondary outcome was prevalence of clinically significant arrhythmia during EP study. Two EP specialists determined whether arrhythmias were clinically significant based upon consideration of the following characteristics: (1) sustained arrhythmia during EP study, (2) reproducible induction by programmed stimulation, (3) arrhythmia generating palpitation similar to previous symptoms, or (4) compatible with the previously documented electrocardiogram. The local institutional review board approved the study protocol and waived the requirement for informed consent (IRB No. 2017-10-146).
Continuous variables are presented as median with interquartile range or mean ± standard deviation, whereas categorical variables are presented as number and percentage. Continuous variables were compared between groups using Student’s t-test. Categorical data were compared between groups using Fisher’s exact test or the Chi-square test, as appropriate. A logistic regression model was used to determine the independent predictors of clinically significant arrhythmia during EP study. Variables with a p value < 0.1 on univariate analysis were included in the multivariate analysis. All tests were two-sided, and p values < 0.05 were considered statistically significant. IBM SPSS Statistics software version 23 (IBM Corporation, Armonk, NY, USA) was used for statistical analysis.
Baseline characteristics of the study population
A total of 639 patients with suspected or documented SVT underwent EP study. We excluded patients with history of thyroidectomy or known thyroid disease (n = 33), patients taking medications that affect the TFT (n = 9), patients without TFT results (n = 33), and patients with a previous history of AF (n = 31). Of the final 533 patients, 56 (10.5%) had abnormal TFT results (thyroid dysfunction group), while 477 (89.5%) had normal TFTs (euthyroidism group) (Fig. 1). The types of thyroid dysfunction are shown in Fig. 2. The most common type of thyroid dysfunction was subclinical hyperthyroidism (80.4%). The mean duration between TFT and EP study was 1.3 ± 2.0 days in the thyroid dysfunction group and 1.4 ± 3.2 days in the euthyroidism group (p = 0.97). There was no significant difference in the baseline clinical characteristics between the two TFT groups (Table 1).
EP study results
EP study results are shown in Table 2. Paroxysmal supraventricular tachycardia was the most common SVT, while atrial fibrillation or flutter was the second most commonly induced SVT in both groups. The thyroid dysfunction group showed a tendency for higher induction of clinically significant SVT than the euthyroidism group (94.6% vs. 86.6%, p = 0.09). When patients with previously documented SVT were analyzed separately, clinically significant SVT could be induced in all patients in the thyroid dysfunction group. In contrast, we were unable to induce a significant SVT in 31 (9.2%) patients in the euthyroidism group.
On multivariate logistic regression analysis, a previous documentation of SVT was significantly associated with induction of clinically significant SVT (Table 3).
In the present study, we investigated thyroid function abnormality in patients with suspected or documented SVT undergoing EP study. The major findings of this study were: (1) The prevalence of newly detected thyroid dysfunction in the study population was 10.5%, (2) clinically significant arrhythmia tended to be induced more frequently in the thyroid dysfunction group than the euthyroidism group, while (3) thyroid dysfunction was not an independent predictor of clinically significant arrhythmia during EP study.
Since the relationship between AF and thyroid dysfunction is well established, TFT is recommended in all AF patients [2,3,4]. Recent studies suggest that the risk of AF is not only increased in overt hyperthyroidism, but also in subclinical hyperthyroidism or high normal euthyroid states [3, 12, 13]. Elevated thyroid hormone is believed to play a role in AF through several mechanisms, including an increase in sympathetic tone, ectopic atrial beats, alteration of ionic channels, or a decreased atrial refractory period [14, 15]. However, the current guidelines for management of SVT do not recommend routine evaluation of thyroid function except in the case of inappropriate sinus tachycardia or premature extra beats [5, 6]. This result might be attributable to a lack of relevant data from only a small number of retrospective studies and case reports [7,8,9,10]. Regardless, in our institution, TFT is routinely performed in patients undergoing EP study for suspected or documented SVT. This practice is based on the assumption that thyroid dysfunction may also affect the prevalence of SVT by similar mechanisms that increases the risk of AF. Ectopic beats resulting in conduction delays can initiate re-entrant tachycardia. Increased autonomic tone can also influence the occurrence of tachyarrhythmia associated with enhanced automaticity. Furthermore, in patients with suspected, but not documented SVT, it is difficult to distinguish paroxysmal AF by symptoms alone. More than 600 patients with suspected SVT underwent TFT according to the protocol at our institution. We subsequently analyzed these patients to verify the clinical utility of this routine practice.
The overall prevalence of TFT abnormality in this study was 10.5%. The prevalence of each type of thyroid dysfunction was relatively higher in this study than that of the general Korean population in similar age-groups . In particular, subclinical hyperthyroidism was far more prevalent in our study population than it was in the general population (8.4% vs. 2.9%). This is a simple comparison of numerical values between two different populations. Nevertheless, we believe that it warrants additional analysis, including that with a matching control group. In this study, the thyroid dysfunction group had a tendency for higher induction rate of clinically significant SVT than did the euthyroidism group, irrespective of previous documentation of SVT. Several previous reports have implied that there is an association between thyroid dysfunction and non-AF SVT. Furthermore, some reports have suggested that antithyroid medications or thyroid replacement therapy could alleviate paroxysms of such SVTs [8, 10, 16, 17]. One study even reported that radioactive iodine could be an effective agent to prevent attack of recurrent paroxysmal supraventricular tachycardia in euthyroid patients . However, we are unable to fully explain how thyroid dysfunction affects non-AF SVTs. There are no previous studies that have addressed this mechanism clearly. We suggest it is possible that thyroid dysfunction increases the prevalence of SVT by increasing the frequency of premature beats and altering the autonomic tone, both of which also contribute to the risk of AF. Subclinical hyperthyroidism comprised the majority of thyroid dysfunction in our study (Fig. 2). Therefore, further investigation is needed to determine whether subclinical dysfunction affects arrhythmogenesis. One study suggests that, in euthyroid patients, unusual irritability or sensitivity of the cardiac muscle can result in arrhythmogenesis. Another study found that endogenous subclinical hyperthyroidism can affect intrinsic cardiac morphology and function . However, these hypotheses are unsubstantiated and require further investigation.
In multivariate logistic regression analysis, thyroid dysfunction was not a significant predictor of clinically significant arrhythmia during EP study (p = 0.10). In contrast, documented SVT was significantly associated with clinically significant arrhythmia. We believe that unmeasured variables could have affected the result. For example, patients with overt thyroid dysfunction tend to be symptomatic with weight change, goiter, heat/cold intolerance, or bowel habit change. These patients are more likely to be treated with antithyroid medications or thyroid replacement therapy than they are to be evaluated with an EP study. This reason likely explains why we found subclinical thyroid disease more often than overt thyroid dysfunction in this study. We could not acquire data regarding the detailed reasons for EP study, characteristics, frequency, duration, or severity of the suspected SVT episodes. These data would be meaningful with regard to the homogeneity of the study population. For example, while some patients might have been referred for EP study after only a single episode of palpitations, others may have had recurrent episodes. We may have obtained more significant results if we had performed a subgroup analysis using those data.
To the best of our knowledge, this is the largest study to address the association between thyroid dysfunction and the prevalence of non-AF SVT. We suggest that TFT needs to be considered in patients with suspected or documented supraventricular tachyarrhythmia considering the tendency of higher induction of clinically significant arrhythmia in those with thyroid dysfunction than those without. Although this study cannot provide conclusive evidence regarding whether thyroid dysfunction is associated with SVTs other than AF, we believe that it indicates the need for further discussion about the clinical significance of TFT in patients with suspected SVT.
This study has several limitations. First, this was a cross-sectional single-center study; therefore, the causal relationship between thyroid dysfunction and SVT could not be definitively proven. We were unable to investigate the follow-up outcomes after EP study, and follow-up TFT data were unavailable. Our results are also possibly subject to selection bias, because the study population consisted of patients admitted to a tertiary university hospital for EP study. Patients with symptoms of overt thyroid dysfunction may have been excluded at the outpatient clinic. Similarly, patients with tolerable symptoms could have been medically followed without an EP study. Therefore, our results are not necessarily generalizable to all patients with suspected or documented SVT. Second, the TFT reference ranges used in this study might not apply to other ethnic groups because of differences attributable to genetics and iodine intake. Lastly, an inability to induce SVT during EP study does not equate to an absence of SVT, but rather low arrhythmia inducibility. An SVT could not be induced during the EP studies of 31 patients with previously documented SVT (9.2%).
Availability of data and materials
All data generated or analyzed during this study are included in this published article [and its supplementary information files.
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The Institutional Review Board at Samsung Medical Center approved the study protocol (IRB No. 2017-10-146). Informed consent was waived by the board.
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Gwag, H.B., Jun, J.E., Park, Y. et al. Thyroid dysfunction in patients with suspected or documented supraventricular tachyarrhythmia. Int J Arrhythm 20, 6 (2019). https://doi.org/10.1186/s42444-019-0008-x
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