High prevalence of altered cardiac repolarization in patients with COPD
© Sievi et al.; licensee BioMed Central Ltd. 2014
Received: 9 August 2013
Accepted: 25 March 2014
Published: 2 April 2014
Altered cardiac repolarization and increased dispersion of repolarization have been identified as risk factors for sudden cardiac death (SCD). The prevalence of and the mechanisms contributing to altered cardiac repolarization are currently unknown in COPD.
In 91 COPD patients, 32 controls matched for age, cardiovascular risk and medication, and 41 healthy subjects, measures of cardiac repolarization and dispersion of repolarization (QTc interval, QT dispersion) were derived from 12-lead electrocardiography (ECG). Prevalence rates of heart rate corrected QT (QTc) >450ms and QT dispersion >60ms were determined to assess the number of subjects at risk for SCD. Univariate and multivariate analyses were used to identify possible factors contributing to altered cardiac repolarization.
QTc was found to be prolonged in 31.9% and QT dispersion in 24.2% of the COPD patients compared to 12.5% in matched controls and 0% in healthy subjects. The QTc interval was longer in COPD patients compared to matched and healthy controls respectively (437.9 ± 29.5 vs. 420.1 ± 25.3 ms, p = 0.001 and vs. 413.4 ± 18.2 ms, p < 0.001). QT dispersion was significantly increased in COPD patients compared to healthy subjects (45.4 (34.8 , 59.5) vs. 39.7 (29.3 , 54.8) ms, p = 0.049). Only oxygen saturation was independently associated with QTc duration in multivariate analysis (β = -0.29, p = 0.015).
One third of a typical COPD population has altered cardiac repolarization and increased dispersion of repolarization, which may be related to hypoxia. Altered cardiac repolarization may expose these patients to an increased risk for malignant ventricular arrhythmias and SCD.
Chronic obstructive pulmonary disease (COPD) is associated with an increased risk of cardiovascular morbidity and mortality [1–3]. Previous population-based studies suggested that patients with COPD have a two to three fold increased risk of sudden cardiac death (SCD) . However, the mechanisms underlying the association between COPD and SCD are currently unclear and predictors of malignant cardiac arrhythmias and SCD in COPD have not been defined.
Alteration of cardiac repolarization is an important mechanism for the development of malignant arrhythmias and the occurrence of SCD [5–7]. Measures derived from the surface electrocardiography (ECG) represent the dispersion of repolarization and the electrical inhomogeneity of the ventricles during repolarization [7, 8]. The findings of previous studies in patients with heart failure , patients with long QT syndrome  and elderly persons  indicated an association between alteration of measures of cardiac repolarization, such as QT interval and QT dispersion with the development of malignant arrhythmia and SCD.
Evidence from longitudinal studies suggests that a low forced expiratory volume in 1 s (FEV1) is associated with an increased risk for ischemic heart and cerebral disease and SCD, even after correcting for conventional cardiovascular risk factors [12, 13]. It has also been suggested that COPD patients may have a higher frequency of cardiac arrhythmias and the severity of airflow obstruction seems to be associated with the occurrence of arrhythmia [14, 15].
Preliminary evidence from a small case-control study suggests that increased maximal QT interval is associated with the development of ventricular arrhythmia in patients with COPD . However, the prevalence of and the mechanisms contributing to altered cardiac repolarization in patients with COPD are currently unknown.
Therefore, the aim of this study was to evaluate the prevalence of and possible factors contributing to altered cardiac repolarization in a group of COPD patients.
157 patients aged between 40 and 75 years with objectively confirmed COPD according to GOLD-guidelines  were assessed for eligibility in the pulmonary outpatient clinic at the University Hospital of Zurich, Switzerland between October 2009 and January 2013. Patients were excluded if they had suffered from a COPD exacerbation within the last 6 weeks or if they suffered from mental or physical disability precluding informed consent or compliance with the protocol.
Matched control subjects
The patient database of the Pulmonary Division of the University Hospital Zurich, Switzerland was screened for control subjects with normal lung function and matched for age, Pocock risk score use of beta blockers and medication affecting QT duration.
Healthy control subjects
Subjects were eligible for the study if they were between 18 and 75 years old and healthy. Exclusion criteria were a previous diagnosis of any lung disease, arterial hypertension, any aortic or cardiac disease.
The study was conducted in accordance with the declaration of Helsinki of the World Medical Association. The Ethics Committee of the Canton of Zurich approved the study (EK-ZH-NR: 1734) and all subjects gave written informed consent to participate when data were obtained for research purposes.
Cardiovascular risk and medication
The Pocock risk score was used to predict the individuals’ 5-year risk of death due to a cardiovascular cause . The Pocock risk score is calculated from 11 known cardiovascular risk factors, including sex, age, smoking status, systolic blood pressure, cholesterol, creatinine, height, diabetes, previous myocardial infarction, stroke and left ventricular hypertrophy.
Patients and control subjects who were included in the study were asked if they used medications affecting the QT interval according to the International Registry of Drug-induced Arrhythmias maintained by the Georgetown University .
All participants underwent standard pulmonary functional testing according to American Thoracic Society guidelines  to measure forced expiratory volume in one second (FEV1) and forced vital capacity (FVC).
Oxygen saturation (SaO2) was measured with a fingertip oximeter PC-60C after the participants rested 5min in supine position.
QTc (QT interval corrected for heart rate) was corrected for heart rate by using the Bazett formula .
Data analysis and statistics
All results are shown as mean values and standard deviation (SD) unless otherwise stated. Statistical analysis was performed with Statistica V6.0 (StatSoft, Tulsa, OK, USA) and STATA 12 (StataCorp, Texas, USA). Differences in QTc interval duration, cardiovascular risk factors, respiratory variables and use of medications between COPD patients, matched controls and healthy control subjects respectively were assessed by one-way ANOVA and χ2 tests. Kruskal Wallis test was used to compare QT dispersion between groups. Post hoc analysis was assessed for variables that showed a p-value of <0.1 across the three groups. For QTc, altered cardiac repolarization was defined as a value of >450ms and for QT dispersion of >60ms [16, 26].
Univariate regression analysis was used to investigate associations between repolarization duration (dependent variable) and cardiovascular risk factors as well as respiratory variables and medications. Multivariate analysis involved regression of variables that showed a univariate regression p-value of <0.1 with adjustment for potential confounders (age). Residual analysis of the model was performed to check the regression assumptions. A two-sided p-value of <0.05 was considered to be statistically significant.
COPD N = 91
Matched controls N = 32
Healthy controls N = 41
Demographics and cardiovascular risk
Current smokers, N (%)
Pack years of smoking, N
Arterial hypertension, N (%)
CAD, N (%)
Arrhythmia, N (%)
Diabetes, N (%)
Pocock risk score, %
Medication affecting QT, N (%)
Beta blockers, N (%)
Antihypertensive medication, N (%)
Anticholinergic medication, N (%)
Combined inhaled long-acting β-adrenergic and steroid, N (%)
Statins, N (%)
Prevalence of altered repolarization measures
The QTc interval was significantly longer in COPD patients compared to matched controls (437.9 ± 29.5 vs. 420.1 ± 25.3 ms, p = 0.001) and compared to healthy subjects (437.9 ± 29.5 vs. 413.4 ± 18.2 ms, p < 0.001). QT dispersion showed a non-significant trend to be increased in COPD patients compared to matched controls (45.4 (34.8, 59.5) vs. 39.7 (29.3, 54.8) ms, p = 0.102). COPD patients showed a significantly increased QT dispersion compared to healthy subjects (45.4 (34.8, 59.5) vs. 40.8 (33.0, 48.8) ms, p = 0.049).
Determinants of altered cardiac repolarization
Univariate regression analysis
Univariate regression analysis of predictors for QTc in all participants
95% confidence interval
Current smoker, N (%)
Pack years of smoking, N
Pocock risk score, %
Medication affecting QT, N (%)
Beta blocker, N (%)
Combined inhaled long-acting β-adrenergic and steroid, N (%)
Statins, N (%)
Multiple regression analysis of predictors for QTc in all participants
95% confidence interval
Pack years of smoking, N
Pocock risk score, %
Combined inhaled long-acting β- adrenergic and steroid, N (%)
Statins, N (%)
This study investigated the prevalence of altered cardiac repolarization in a heterogeneous group of COPD patients and evaluated possible underlying risk factors. The main findings of this study are that approximately one third of a typical COPD population has altered cardiac repolarization and increased dispersion of repolarization, which may be related to hypoxia. Altered cardiac repolarization may expose these patients to an increased risk for malignant ventricular arrhythmias and SCD.
Several pathologies have been reported to increase the risk of SCD including CAD, cardiomyopathies, congenital heart disease and electrophysiological abnormalities including long QT syndrome .
A prolonged QT interval and increased QT dispersion are markers of an increased risk for malignant cardiac arrhythmia and SCD [9, 26]. The QT interval represents the electrocardiographic correlate of ventricular de- and repolarization including the vulnerable period for reentry tachycardia. As such, QTc prolongation to >450 ms has been identified as a risk factor for malignant ventricular arrhythmias and SCD [26, 28]. QT dispersion reflects spatial differences in myocardial recovery time. Previous studies have shown that an increase in QT dispersion >60ms is associated with the development of malignant ventricular arrhythmias  and SCD .
In large population-based studies including elderly subjects, the prevalence of an altered QTc interval has been estimated to be approximately 8% . In contrast, the COPD patients in the current study showed a fourfold higher prevalence of an altered QTc interval compared to the general population. In a case-control study, investigating the risk of SCD in patients with coronary heart disease with and without prolonged QTc interval, the prevalence of prolonged QTc interval was 39% in the group with subsequent SCD . This prevalence of altered QTc in SCD patients is comparable with the findings of the current study in COPD patients.
In a retrospective study including 162 chronic heart disease patients, the prevalence of increased QT dispersion >60 ms was 24% , which is similar to our observations in COPD patients (24%). These findings suggest a comparable prevalence of increased QT dispersion in patients with chronic heart disease and COPD patients.
There are some previous studies examining possible factors leading to an alteration in cardiac repolarization in COPD patients, however, the COPD patients in these studies [16, 31–33] were free from comorbidities. Zulli et al.  found a significant univariate association between QT dispersion with FEV1% pred. and FVC% pred. respectively in COPD patients. However, in the multivariate analysis correcting for covariates, this association did not remain statistically significant. Yildiz et al.  compared 30 COPD patients with and without increased QT dispersion regarding possible factors influencing QT dispersion and found no independently associated factors. Similarly, in our study, only pack years of smoking and use of statins was statistically significantly associated with QT dispersion in the univariate analysis. However, after correcting for age, BMI, SaO2 and use of medication, none of the possible influencing risk factors were independently associated with QT dispersion.
None of the previously described studies [16, 31] examined possible factors leading to an altered QTc interval in COPD patients. In the current study, age, pack years of smoking, Pocock risk score, respiratory variables, use of combined inhaled long-acting β-adrenergic and steroid and consumption of statins were significantly associated with a QTc >450ms in univariate analysis. Only SaO2 remained statistically significantly associated with QTc >450 ms after correction for covariates in the multivariate analysis. Thus, hypoxia may be a risk factor for a prolonged QTc interval. There is some evidence that hypoxia may prolong repolarization duration. In a study by Roche et al. , healthy subjects were exposed to normobaric hypoxic conditions and it was found that hypoxia significantly prolonged the QTc interval. In 12 COPD patients, Tirlapur et al.  observed that patients who had a low mean basal SaO2 (<80%) showed electrocardiographic changes such as a prolonged QTc interval. These findings are somewhat in contrast to the study by Sarubbi et al. , where QTc was measured in 15 hypoxemic/hypercapnic COPD patients before and after oxygen therapy and was not significantly reduced after 24 h of oxygen therapy. Thus it is still a matter of debate whether hypoxia affects cardiac repolarization and the underlying mechanism through which hypoxia may possibly influence cardiac repolarization remains currently unknown.
There is some evidence that autonomic neuropathy may results in prolonged cardiac repolarization in COPD patients. In a case-control study by Stewart et al. , 17 COPD patients with autonomic neuropathy were compared to 17 COPD patients without autonomic neuropathy. QTc was significantly longer in COPD patients with autonomic neuropathy. However, autonomic neuropathy was not measured in our study and thus we cannot directly compare the results of the study by Stewart et al. with our findings.
The current study has some limitations. We performed standard resting 12-lead ECG and not continuous 24-h ECG. Therefore it is not possible to evaluate the prevalence of alteration in cardiac repolarization both during a longer daytime period and during sleep. Furthermore, the cross-sectional study design does not allow to establish a causal relationship between altered cardiac repolarization in COPD patients and malignant ventricular arrhythmias and SCD, respectively. If prolonged cardiac repolarization promotes sudden cardiac death in COPD patients is currently unknown. Further controlled and longitudinal studies are needed to evaluate if prolonged cardiac repolarization promotes malignant ventricular arrhythmia and SCD in COPD patients.
In conclusion, our findings suggest that one third of a typical COPD population has altered cardiac repolarization and increased dispersion of repolarization, which may be related to hypoxia. Altered cardiac repolarization may expose these patients to an increased risk for malignant ventricular arrhythmias and SCD.
This study was supported and funded by "Lunge Zurich" and the Medical Research Foundation of the University of Zurich.
- Anthonisen NR, Connett JE, Enright PL, Manfreda J: Hospitalizations and mortality in the Lung Health Study. Am J Respir Crit Care Med. 2002, 166: 333-339. 10.1164/rccm.2110093.View ArticlePubMedGoogle Scholar
- McGarvey LP, John M, Anderson JA, Zvarich M, Wise RA: Ascertainment of cause-specific mortality in COPD: operations of the TORCH Clinical Endpoint Committee. Thorax. 2007, 62: 411-415. 10.1136/thx.2006.072348.View ArticlePubMedPubMed CentralGoogle Scholar
- Clarenbach CF, Senn O, Sievi NA, Camen G, van Gestel AJ, Rossi VA, Puhan MA, Thurnheer R, Russi EW, Kohler M: Determinants of endothelial function in patients with COPD. Eur Respir J. 2013, 42: 1194-1204. 10.1183/09031936.00144612.View ArticlePubMedGoogle Scholar
- Sin DD, Man SF: Chronic obstructive pulmonary disease as a risk factor for cardiovascular morbidity and mortality. Proc Am Thorac Soc. 2005, 2: 8-11. 10.1513/pats.200404-032MS.View ArticlePubMedGoogle Scholar
- Elming H, Brendorp B, Kober L, Sahebzadah N, Torp-Petersen C: QTc interval in the assessment of cardiac risk. Card Electrophysiol Rev. 2002, 6: 289-294. 10.1023/A:1016345412555.View ArticlePubMedGoogle Scholar
- Straus SM, Kors JA, De Bruin ML, van der Hooft CS, Hofman A, Heeringa J, Deckers JW, Kingma JH, Sturkenboom MC, Stricker BH, Witteman JC: Prolonged QTc interval and risk of sudden cardiac death in a population of older adults. J Am Coll Cardiol. 2006, 47: 362-367. 10.1016/j.jacc.2005.08.067.View ArticlePubMedGoogle Scholar
- Bednar MM, Harrigan EP, Anziano RJ, Camm AJ, Ruskin JN: The QT interval. Prog Cardiovasc Dis. 2001, 43: 1-45.View ArticlePubMedGoogle Scholar
- Antzelevitch C, Shimizu W, Yan GX, Sicouri S: Cellular basis for QT dispersion. J Electrocardiol. 1998, 30 (Suppl): 168-175.View ArticlePubMedGoogle Scholar
- Barr CS, Naas A, Freeman M, Lang CC, Struthers AD: QT dispersion and sudden unexpected death in chronic heart failure. Lancet. 1994, 343: 327-329. 10.1016/S0140-6736(94)91164-9.View ArticlePubMedGoogle Scholar
- Yamaguchi M, Shimizu M, Ino H, Terai H, Uchiyama K, Oe K, Mabuchi T, Konno T, Kaneda T, Mabuchi H: T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity. Clin Sci (Lond). 2003, 105: 671-676. 10.1042/CS20030010.View ArticleGoogle Scholar
- Robbins J, Nelson JC, Rautaharju PM, Gottdiener JS: The association between the length of the QT interval and mortality in the Cardiovascular Health Study. Am J Med. 2003, 115: 689-694. 10.1016/j.amjmed.2003.07.014.View ArticlePubMedGoogle Scholar
- Persson C, Bengtsson C, Lapidus L, Rybo E, Thiringer G, Wedel H: Peak expiratory flow and risk of cardiovascular disease and death. A 12-year follow-up of participants in the population study of women in Gothenburg, Sweden. Am J Epidemiol. 1986, 124: 942-948.PubMedGoogle Scholar
- Schunemann HJ, Dorn J, Grant BJ, Winkelstein W, Trevisan M: Pulmonary function is a long-term predictor of mortality in the general population: 29-year follow-up of the Buffalo Health Study. Chest. 2000, 118: 656-664. 10.1378/chest.118.3.656.View ArticlePubMedGoogle Scholar
- Buch P, Friberg J, Scharling H, Lange P, Prescott E: Reduced lung function and risk of atrial fibrillation in the Copenhagen City Heart Study. Eur Respir J. 2003, 21: 1012-1016. 10.1183/09031936.03.00051502.View ArticlePubMedGoogle Scholar
- Kleiger RE, Senior RM: Longterm electrocardiographic monitoring of ambulatory patients with chronic airway obstruction. Chest. 1974, 65: 483-487. 10.1378/chest.65.5.483.View ArticlePubMedGoogle Scholar
- Yildiz P, Tukek T, Akkaya V, Sozen AB, Yildiz A, Korkut F, Yilmaz V: Ventricular arrhythmias in patients with COPD are associated with QT dispersion. Chest. 2002, 122: 2055-2061. 10.1378/chest.122.6.2055.View ArticlePubMedGoogle Scholar
- Rabe KF, Hurd S, Anzueto A, Barnes PJ, Buist SA, Calverley P, Fukuchi Y, Jenkins C, Rodriguez-Roisin R, van Weel C, Zielinski J: Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease - GOLD executive summary. Am J Respir Crit Care Med. 2007, 176: 532-555. 10.1164/rccm.200703-456SO.View ArticlePubMedGoogle Scholar
- Pocock SJ, McCormack V, Gueyffier F, Boutitie F, Fagard RH, Boissel JP: A score for predicting risk of death from cardiovascular disease in adults with raised blood pressure, based on individual patient data from randomised controlled trials. BMJ. 2001, 323: 75-81. 10.1136/bmj.323.7304.75.View ArticlePubMedPubMed CentralGoogle Scholar
- Drugs that prolong the QTc interval and/or induce Torsade de Pointes. http://www.atforum.com/SiteRoot/pages/addiction_resources/QTDrugs%209-03-02.PDF,
- Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, Crapo R, Enright P, van der Grinten CP, Gustafsson P, Jensen R, Johnson DC, McIntyre N, McKay R, Navajs D, Pedersen OF, Pellegrino R, Viegi G, Wagner J: Standardisation of spirometry. EurRespirJ. 2005, 26: 319-338.Google Scholar
- Rossi VA, Stoewhas AC, Camen G, Steffel J, Bloch KE, Stradling JR, Kohler M: The effects of continuous positive airway pressure therapy withdrawal on cardiac repolarization: data from a randomized controlled trial. Eur Heart J. 2012, 33: 2206-2212. 10.1093/eurheartj/ehs073.View ArticlePubMedGoogle Scholar
- Pickham D, Hasanien AA: Measurement and rate correction of the QT interval. AACN Adv Crit Care. 2013, 24: 90-96. 10.1097/NCI.0b013e318274ba3e.View ArticlePubMedGoogle Scholar
- Erikssen G, Liestol K, Gullestad L, Haugaa KH, Bendz B, Amlie JP: The terminal part of the QT interval (T peak to T end): a predictor of mortality after acute myocardial infarction. Ann Noninvasive Electrocardiol. 2012, 17: 85-94. 10.1111/j.1542-474X.2012.00493.x.View ArticlePubMedGoogle Scholar
- Day CP, McComb JM, Campbell RW: QT dispersion: an indication of arrhythmia risk in patients with long QT intervals. Br Heart J. 1990, 63: 342-344. 10.1136/hrt.63.6.342.View ArticlePubMedPubMed CentralGoogle Scholar
- Bazett HC: The time relations of the blood-pressure changes after excision of the adrenal glands, with some observations on blood volume changes. J Physiol. 1920, 53: 320-339.View ArticlePubMedPubMed CentralGoogle Scholar
- de Bruyne MC, Hoes AW, Kors JA, Hofman A, van Bemmel JH, Grobbee DE: Prolonged QT interval predicts cardiac and all-cause mortality in the elderly. The Rotterdam Study. Eur Heart J. 1999, 20: 278-284. 10.1053/euhj.1998.1276.View ArticlePubMedGoogle Scholar
- Zipes DP, Wellens HJ: Sudden cardiac death. Circulation. 1998, 98: 2334-2351. 10.1161/01.CIR.98.21.2334.View ArticlePubMedGoogle Scholar
- Viskin S: Long QT syndromes and torsade de pointes. Lancet. 1999, 354: 1625-1633. 10.1016/S0140-6736(99)02107-8.View ArticlePubMedGoogle Scholar
- Chugh SS, Reinier K, Singh T, Uy-Evanado A, Socoteanu C, Peters D, Mariani R, Gunson K, Jui J: Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study. Circulation. 2009, 119: 663-670. 10.1161/CIRCULATIONAHA.108.797035.View ArticlePubMedPubMed CentralGoogle Scholar
- Trusz-Gluza M, Wozniak-Skowerska I, Giec L, Szydlo K: Dispersion of the QT interval as a predictor of cardiac death in patients with coronary heart disease. Pacing Clin Electrophysiol. 1996, 19: 1900-1904. 10.1111/j.1540-8159.1996.tb03249.x.View ArticlePubMedGoogle Scholar
- Zulli R, Donati P, Nicosia F, De Vecchi M, Tantucci C, Romanelli G, Grassi V: Increased QT dispersion: a negative prognostic finding in chronic obstructive pulmonary disease. Intern Emerg Med. 2006, 1: 279-286. 10.1007/BF02934761.View ArticlePubMedGoogle Scholar
- Stewart AG, Waterhouse JC, Howard P: The QTc interval, autonomic neuropathy and mortality in hypoxaemic COPD. Respir Med. 1995, 89: 79-84. 10.1016/0954-6111(95)90188-4.View ArticlePubMedGoogle Scholar
- Sarubbi B, Esposito V, Ducceschi V, Meoli I, Grella E, Santangelo L, Iacano A, Caputi M: Effect of blood gas derangement on QTc dispersion in severe chronic obstructive pulmonary disease: evidence of an electropathy?. Int J Cardiol. 1997, 58: 287-292. 10.1016/S0167-5273(96)02876-8.View ArticlePubMedGoogle Scholar
- Roche F, Reynaud C, Pichot V, Duverney D, Costes F, Garet M, Gaspoz JM, Barthelemy JC: Effect of acute hypoxia on QT rate dependence and corrected QT interval in healthy subjects. Am J Cardiol. 2003, 91: 916-919. 10.1016/S0002-9149(03)00040-7.View ArticlePubMedGoogle Scholar
- Tirlapur VG, Mir MA: Nocturnal hypoxemia and associated electrocardiographic changes in patients with chronic obstructive airways disease. N Engl J Med. 1982, 306: 125-130. 10.1056/NEJM198201213060301.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2466/14/55/prepub
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