Impact of Pheochromocytoma on Left Ventricular Hypertrophy and QTc Prolongation: Comparison with Takotsubo Cardiomyopathy

Pheochromocytoma is a rare catecholamine-producing tumor with a highly variable clinical presentation.1) Pheochromocytoma presentation may include numerous cardiovascular manifestations and is usually identified with prevalent cardiac manifestations or paroxysmal hypertension associated with other signs and symptoms of catecholamine excess.2), 3) Although sinus tachycardia with palpitations is the most prevalent cardiac rhythm abnormality, pheochromocytoma can induce more serious arrhythmias or conduction disturbances, such as prolongation of the QTc interval and ventricular tachycardia followed by cardiac arrest.4)

Although QTc interval prolongation in pheochromocytoma is rare, it has been reported in several cases, and it has been proposed that catecholamine excess may contribute to its development.5), 6), 7) Recently, more attention has been given to the increasing number of cases of Takotsubo cardiomyopathy (TC).8), 9) The relationship between TC and abnormal repolarization has been well-documented, which is probably because systolic dysfunction is associated with both TC and QT-interval prolongation.10) QT interval prolongation and ST-T changes occur during the acute or subacute phase of illness, and these electrocardiography (ECG) changes typically normalize within several weeks of left ventricular (LV) wall motion improvement.10) However, the systolic function and wall motion abnormality are usually normal in pheochromocytoma; therefore, the difference in QTc interval prolongation between pheochromocytoma and TC is not evaluated.

We hypothesized that there would be a difference in left ventricular hypertrophy (LVH) or QTc interval induced by pheochromocytoma, chronic catecholamine excess, TC, and acute transient catecholamine excess. To explore this hypothesis, we reviewed the initial cardiac manifestations of pheochromocytoma prior to diagnosis and compared the results to patients with TC without pheochromocytoma.

The initial cardiac manifestations of pheochromocytoma were labile hypertension (50%), chest pain (20%), syncope (10%), dizziness (10%), and palpitations (10%) (Table 1). The tumor size, serum, and 24-hour urine catecholamine levels of pheochromocytoma are shown in Table 2. All patients had elevated 24-hour urine metanephrine and normetanephrine levels, variable levels of serum epinephrine and urine norepinephrine, and tumor size was correlated with 24-hour urine metanephrine (r=0.792, p<0.001). The precedent stressors for TC patients were surgery, emotional stress, and infection; the stressors were usually accompanied with symptoms, such as chest pain and dyspnea. The majority (90%) of the TC patients showed ST-segment changes (Table 3). Two male patients (10%) with pheochromocytoma showed apical ballooning with LVH, and 15 patients (75%) from the pheochromocytoma group and 19 TC patients (95%) underwent coronary angiography, which revealed that none of the patients had significant stenotic lesions in their coronary arteries. The analysis indicated that the pheochromocytoma group was younger than the TC group, and there were more female TC patients (Table 4). The mean creatinine kinase (CK)-MB elevation, reduced LV EF and ST-segment changes were more prominent in the TC group compared to the pheochromocytoma groups (all p<0.05) (Table 4). The prevalence of QTc prolongation was high in both pheochromocytoma (45%) and TC (55%), and the prevalence was higher in men (pheochromocytoma: male 50%, female 40%; TC: male 100%, female; 31%). There were no correlations between QTc interval and the serum and urine catecholamine levels. However, the TC male patients appeared to have a more prolonged QTc interval (TC: male 499.3±33.3 msec, female 474.5±45.5 msec; pheochromocytoma: male 463.0±45.7, female 461.±71.8 msec).

Table 1
Clinical variables of pheochromocytoma in 20 cases focusing on electrocardiogram and left ventricular hypertrophy

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Table 2
Tumor size, characterization and serum and 24-hour-urine catecholamine levels of 20 pheochromocytoma cases

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Table 3
Clinical variables of stress induced cardiomyopathy in 20 cases focusing on cardiac manifestations

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Table 4
Comparison of clinical, echocardiographic and electrocardiographic parameters between pheochromocytoma and Takotsubo cardiomyopathy (TC)

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Left ventricular mass index (133.3±37.8 vs. 113.3±17.3; p=0.031), RWT (0.55±0.15 vs. 0.47±0.07; p=032), and blood pressure (BP) elevation were more prominent in pheochromocytoma compared to those of TC group. All male with pheochromocytoma exhibited a concentric LVH pattern, whereas female pheochromocytoma patients showed various LVH patterns (normal 40%, concentric remodeling 40%, eccentric hypertrophy 10%, and concentric hypertrophy 10%) (Table 1). The LV geometry was relatively normal in TC patients (males: normal 57%, eccentric hypertrophy 29%, concentric hypertrophy 14%; females: normal 54%, concentric hypertrophy 31%, eccentric hypertrophy 15%) (Table 3).

Although serum epinephrine and norepinephrine levels were not correlated with LVMI, urine epinephrine (r=0.844, p=0.004) and norepinephrine level (r=0.782, p=0.013) were significantly correlated with LVMI. The results indicated that serum epinephrine level was only significantly correlated with RWT (r=0.862, p=0.003) (Table 5).

Table 5
Correlations among the serum and 24-hour-urine catecholamine levels, blood pressure and left ventricular hypertrophy and QTc interval of 20 pheochromocytoma cases

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We estimated the predictors for the QTc prolongation in multivariable linear regression analyses using age, heart rate, gender, LVH, and LV EF as covariates. Male gender {odds ratio (OR); 4.50, 95% confidence interval (CI), 1.17-17.37, p=0.029} and the presence of LVH (OR; 4.89, 95% CI, 1.20-19.94, p=0.027) showed significant associations with the presence of QT prolongation in catecholamine excess state.

This comparative retrospective study demonstrates the prominence of QTc prolongation in patients with catecholamine excess, pheochromocytoma, and TC, regardless of BP and systolic LV function. LVH was more prominent in pheochromocytoma with chronic catecholamine excess; however, acute catecholamine surge might have a role in the electrical remodeling. The independent associations for the QTc prolongation were male gender and the presence of LVH.

Pheochromocytoma is a rare tumor that produces catecholamines and has manifestations that can vary from no significant symptoms to sudden cardiac death (SCD).14) Previous studies showed various initial pheochromocytoma manifestations prior to greater numbers of hypertension diagnoses,15), 16) and reported cardiac complications of pheochromocytoma include hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmia, myocardial ischemia, and SCD.17), 18) Acute complications may contribute to additional cardiac problems, such as LV dysfunction and TC, and several reports have demonstrated that coronary angiography usually reveals no stenosis or obstruction, mimicking TC, in pheochromocytoma patients.8), 9), 19)

Chronic myocardial hypoxia and metabolic myocarditis of hypercatecholaminemia are known causes of pheochromocytoma cardiomyopathy.20) Chronic elevated levels of circulating plasma norepinephrine in pheochromocytoma patients can produce structural and functional LV remodeling, including LVH. Although some authors have shown a positive association between plasma norepinephrine level and LVH,21), 22) other observational studies have demonstrated that the majority of patients with pheochromocytoma have a normal LV mass.23), 24) However, our results showed that there was a predominantly increased LVMI with RWT in male patients with pheochromocytoma, and some patients with TC also exhibited LVH. Systolic and diastolic BP were also higher in male patients with pheochromocytoma with an abnormal LVH pattern, which implies that chronic catecholamine excess produced by an underlying tumor may affect men more than women. Our results, although limited by a small sample size, might suggest that norepinephrine serves as a synergistic partner with arterial hypertension in the pathogenesis of cardiac hypertrophy, even with a transient surge, which might be attenuated by estrogen. Although our results showed no significant association between plasma norepinephrine level and LVMI, the significant positive correlation of urine epinephrine and norepinephrine levels with LVMI suggests that the local delivery of catecholamines to receptors may be more important than their passage through the circulation to induce LVH.

Electrocardiographic abnormalities that include rhythm, conduction and repolarization may occur in patients with pheochormocytoma.25), 26) Several cases have reported that QT interval prolongation could be related to pheochromocytoma,5), 6), 7) and we also experienced a 48-year-old pheochromocytoma woman with marked QT interval prolongation (Fig. 1A) that progressed to torsades de pointes (Fig. 1B), which returned to normal (Fig. 1C) after right adrenal glandectomy. Initially, she was diagnosed with long QT syndrome with torsades de pointes followed by cardiac arrest. However, her 24-hour urinary biochemical analysis showed elevated metanephrine and normetanephrine, and the patient was confirmed as pheochromocytoma. Paroxysmal repolarization mechanisms, such as marked prolongation of the QT interval, remain unclear; however, higher levels of catecholamines may affect cardiac injury and induce longer QTc interval changes.27) QT interval prolongation is also common in the subacute phase of TC and other stress-induced cardiomyopathies,28) and presently there were some differences that could be used to differentiate between these situations. QTc interval prolongation in addition to deep and wide symmetrical T wave inversion, LV systolic dysfunction, and CK-MB elevation were more prominent in the TC group compared to the pheochromocytoma group, which indicated that acute catecholamine release impact on the heart was more dominant in the TC group. This result may also suggest that acute catecholamine surges could cause intracellular calcium overloading and disturb repolarization, which could prolong the QTc interval. Interestingly, our results showed no significant association between catecholamine level and QTc interval, and in some cases of acute catecholamine surges in pheochromocytoma, a much longer QT interval with ST changes occurred independent of catecholamine level or tumor size. Although limited by the retrospective nature of the study, the other interesting finding was that the presence of LVH and male gender were significantly related with the QTc prolongation, indicating that the impact of catecholamine excess on ventricular repolarization might be more pronounced in men. A previous study reported that during metal stress, men react with a more pronounced effect on ventricular electrophysiological properties.29) This difference might be one contributing factor explaining why women are less prone to certain ventricular arrhythmias and SCD than are men. Moreover, similar to our results, a recent study showed that prolonged QTc was independently associated with SCD among subjects with LVH, and merits further evaluation as a predictor of SCD in LVH.30)

Fig. 1
Electrocardiography (ECG) of a patient with prominent QTc prolongation. The patient complained of intermittent palpitation and diaphoresis with syncope for 4 years. A: her ECG on admission showed normal sinus rhythm with a prolonged QTc interval (596 msec). B: two days after admission, a sudden onset of chest pain and syncope with loss of consciousness occurred abruptly, and ECG monitoring indicated torsades de pointes. C: after right adrenal gland removal, her electrocardiography returned to normal.

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The major limitations of this study were the retrospective design and the small sample size. Because pheochromocytoma is a rare disease and the recruited number of patients in this single-center study may have been insufficient, so the differences in manifestations between different sexes or between serum and urine may not represent the general result. There are also significant differences of age, gender proportion, BP as well EF, which could also influence LV geometry and QTc prolongation in both groups. It would be more reasonable to compare the clinical and echocardiographic characteristics of TC to the pheochromocytoma with reduced EF (TC-like cardiomyopathy) or compare the pheochromocytoma to TC with LVH. However, our intention was to compare the difference between chronic catecholamine excess and acute transient catecholamine excess. So, we believe the limitation does not attenuate the clinical meaning of the study. Because our study was a cross-sectional, retrospective study, the causative nature of the LV geometric pattern associations, QTc interval, and catecholamine level or duration could not be established. Moreover, the serum and urine catecholamine assessment was not performed with our TC group. Further studies with a larger patient population and prospective studies that compare pheochromocytoma and TC should be performed to address the limitations of this study.

However, in spite of these limitations, this study demonstrates that cardiac manifestations other than hypertension could be critical initial manifestations of pheochromocytoma, which is important for future diagnoses. Increased LVH with high BP and a prolonged QTc interval, especially in relatively young males with cardiac symptoms and without obvious lesions, could be indicative of underlying pheochromocytoma. Finally, based on the results of this study, unnecessary interventions can be avoided, and cardiac manifestations with an underlying disease can be diagnosed and successfully treated.