123
Views
7
CrossRef citations to date
0
Altmetric
Original Research

Impact of chronic obstructive pulmonary diseases on left ventricular diastolic function in hospitalized elderly patients

, , , , , & show all
Pages 81-87 | Published online: 19 Dec 2014

Abstract

Objective

To evaluate the impact of chronic obstructive pulmonary disease (COPD) on left ventricular (LV) diastolic function in hospitalized elderly patients.

Methods

This was a case–control observational study of 148 consecutive hospitalized elderly patients (≥65 years old): 73 subjects without COPD as controls and 75 patients with COPD. Mild-to-moderate COPD was defined as stages 1 and 2, while severe and very severe COPD was defined as stages 3 and 4, according to the Global Initiative for Chronic Obstructive Lung Disease guidelines. Clinical characteristics and echocardiographic parameters were analyzed and compared.

Results

Compared with the control group, patients with COPD had a higher frequency of LV diastolic dysfunction and heart failure with preserved ejection fraction. Smoking frequency, frequency of cerebrovascular diseases and diabetes, and serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels were higher in the COPD group (all P<0.05). COPD patients showed more abnormalities in diastolic function (E/e′: 11.51±2.50 vs 10.42±3.25, P=0.047), but no differences in systolic function and right ventricular function (all P>0.05). Patients with severe/very severe COPD showed no differences in LV diastolic function compared to patients with mild/moderate COPD (P>0.05), but serum NT-proBNP levels were higher in severe/very severe COPD (P<0.05).

Conclusion

Results suggest that early-stage COPD may have an impact on the LV diastolic function. Severe COPD mainly affected right ventricular function. In hospitalized elderly patients with COPD, LV diastolic dysfunction should be taken into account together with right ventricular function.

Introduction

Chronic obstructive pulmonary disease (COPD) is a major cause of morbidity and mortality in the world. COPD causes significant extrapulmonary effects and is associated with comorbidities that could contribute to the severity of the disease and prognosis. The co-existence of COPD and heart failure has been previously described. Population-based studies suggested that COPD increases the risk of cardiovascular morbidity and mortality ~2-fold.Citation1 Another study showed that the risk of developing congestive heart failure was 4.5-fold greater in elderly patients with COPD compared with age-matched controls.Citation2 Left ventricular (LV) diastolic dysfunction (LVDD) has been reported in COPD patients,Citation3 but the relationship between COPD and LVDD or heart failure with preserved ejection fraction (HFpEF) is less well understood.

We hypothesized that COPD has an impact on the frequency of LVDD and HFpEF. The aim of the present study was to evaluate the impact of COPD on LV diastolic function in hospitalized elderly patients.

Methods

Participants

This was a case–control observational study of consecutive patients hospitalized at the Department of Geriatrics and Gerontology between December 2011 and December 2013. Seventy-five patients with COPD were enrolled, as well as 73 subjects without COPD as controls. The diagnosis of COPD was made according to the guidelines of the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria.Citation4 In the COPD group, 49 patients showed mild-to-moderate pulmonary function (GOLD stages 1 and 2) and 26 patients showed severe-to-very severe pulmonary function (GOLD stages 3 and 4).

Exclusion criteria were the following: 1) COPD patients during acute exacerbation period; 2) patients with asthma, hypoxia, or pneumonia; 3) patients with LV systolic dysfunction (LVSD), valvular pathology, or arrhythmia; 4) patients with renal failure; 5) patients with diffuse parenchymal lung diseases, lung carcinoma, or other malignancies; or 6) age <65 years.

The ethics committee of the hospital approved the study protocol. Subjects provided a written informed consent.

Baseline characteristics

A detailed medical history was obtained from each subject. Comorbidities included cardiovascular disease (CVD), hypertension, diabetes mellitus, cerebrovascular diseases, and chronic kidney disease (CKD). Additional demographics data included age, sex, smoking status, height, and weight. Body mass index was calculated as weight (kg)/height (m2).

Pulmonary function tests

Pulmonary function tests (PFTs) were performed using a clinical spirometer (SensoMedics, the Netherlands). Spirom-etry was performed by a trained technician according to the American Thoracic Society/European Respiratory Society guidelines.Citation5 Forced expiratory volume in 1 second (FEV1) and forced vital capacity values were obtained, and the FEV1/forced vital capacity ratio was calculated. PFT results were evaluated according to the guidelines.Citation5 All patients were diagnosed using spirometry.

Echocardiography

Echocardiography was performed using an ultrasound system (Vivid 7; GE Healthcare, Waukesha, WI, USA). Results were analyzed by an echo-cardiologist blinded to all clinical data. Measurements were done at least twice by the same operator. Analyzed images included two-dimensional views from the parasternal long axis and mid-ventricular short axis, and two- and four-chamber views. Left ventricle wall thickness, LV end-diastolic and end-systolic diameters, right ventricle diameter, and left atrium areas were measured. LV ejection fraction (LVEF) was calculated from LV systolic and diastolic volumes using the Simpson’s method using two-dimensional echocardiography. Parameters obtained from Doppler analysis were peak flow velocity of early diastolic filling (E wave), peak flow velocity of late atrial filling (A wave), and septal and lateral annular tissue Doppler velocities (septal and lateral e′). All parameters were measured according to the recommendations of the American Society of Echocardiography.Citation6

HFpEF was diagnosed using the following criteria (2012 ESC Guidelines of Heart Failure Management)Citation7: 1) typical symptoms of heart failure including breathlessness, orthopnea, paroxysmal nocturnal dyspnea, reduced exercise tolerance, fatigue, tiredness, increased time to recover after exercise, and ankle swelling; 2) typical signs of heart failure, such as elevated jugular venous pressure, hepatojugular reflux, third heart sound (gallop rhythm), laterally displaced apical impulse, and cardiac murmur; 3) normal or only mildly reduced LVEF with no evidence of LV dilation; and 4) relevant structural heart disease (LV hypertrophy/left atrial enlargement) and/or diastolic dysfunction.

NT-proBNP

Blood samples were drawn in tubes containing ethylene-diaminetetraacetic acid and were analyzed the same day. After centrifugation, serum and plasma samples were stored at −70°C. N-terminal pro-B-type natriuretic peptide (NT-proBNP) was measured with electrochemiluminescence immunoassay using an Elecsys 2010 system (Roche Diagnostics, Basel, Switzerland). NT-proBNP concentrations are presented as picograms per milliliter.

Statistical analysis

Continuous variables are expressed as mean ± standard deviation, and were compared using the Student’s t-test. Categorical variables are presented as frequency, and were analyzed using the chi-square test. Independent predictors of COPD were analyzed by binary logistic models using backward stepwise regression analysis. Analysis was performed using SPSS 15.0 (SPSS Inc., Chicago, IL, USA). P-values <0.05 were considered statistically significant.

Results

Baseline characteristics

Demographic data are presented in . Most patients were men (n=111, 75%), and the mean age was 80.74±6.75 years. Patients with COPD were older (P=0.027) and included more smokers (P=0.009). There was a higher frequency of cerebrovascular diseases, diabetes mellitus, beta-blockers treatment, and diuretics treatment in the COPD group (all P<0.05). There was no significant difference in terms of body mass index, hypertension, CVD, and CKD between the COPD and control groups.

Table 1 Baseline characteristics of patients in the control and COPD groups

Levels of NT-proBNP were higher in patients with COPD (372.65±651.97 vs 218.76±368.80 pg/mL, P=0.01). Levels of triglycerides, serum albumin, and high-density lipoprotein cholesterol were all lower in the COPD group (all P<0.05) ().

Echocardiographic characteristics

Echocardiographic characteristics are presented in . Compared with the control group, the E/e′ ratio was significantly higher in the COPD group (11.51±2.50 vs 10.42±3.25, P=0.047). No difference was observed in the other echocardiographic parameters (LV structural parameters, right ventricular diastolic diameter, or systolic pulmonary artery pressure of the two groups).

Table 2 Echocardiographic characteristics of patients in the control and in COPD groups

Distribution of COPD stages and frequency of LVDD and HFpEF

In the COPD group, the proportion of patients with stages 1–4 COPD was 6.7%, 58.7%, 30.7%, and 4.0%, respectively. In the present study, 65.4% of patients had mild/moderate COPD and 34.7% had severe/very severe COPD.

In the control group, 28 patients (38.4%) suffered from LVDD and 19 (26.0%) from symptomatic heart failure (NYHA II–IV stage). Among COPD patients, LVDD and symptomatic heart failure were present in 48/75 (64.0%) and 38/75 (50.7%) of patients, respectively (P<0.05).

Differences between mild/moderate and severe/very severe COPD

Patients with severe/very severe COPD had significantly higher levels of NT-proBNP and had a tendency toward a higher frequency of abnormal right ventricular diastolic diameter and systolic pulmonary artery pressure (P=0.078 and P=0.064, respectively). There was no difference in LV diastolic function parameters between patients with different stages of COPD ( and ).

Severity of COPD and cardiovascular function

Binary logistic models showed that age (odds ratio [OR] =1.081, 95% confidence interval [95% CI] =1.000–1.169, P=0.05) and smoking (OR=1.061, 95% CI=1.005–1.121, P=0.03) were independent predictors of COPD ().

Table 3 Multivariate analysis of the predictors of COPD

Discussion

The main finding of the present study was that there was a high frequency of LVDD in elderly patients with COPD, and that LVDD may occur in the early stages of COPD.

Comorbidities of COPD

Several comorbidities are associated with COPD. In an 11-year observational retrospective study (PATHOS) of 21,361 COPD patients (mean age of 68.0 years, 53% females),Citation8 the most common comorbidities were hypertension (33.7%), heart failure (15.2%), ischemic heart disease (15.6%), and diabetes (11.6%). In the present study, the frequency of hypertension, CVD, and diabetes was much higher (69.3%, 38.7%, and 45.4%, respectively). It is well known that the frequency of hypertension, CVD, and diabetes increases substantially with age, and the mean age of the participants of the present study was 80.74±6.75 years, much older than the previous study.Citation8 In addition, the present study was performed in hospitalized patients, which was different from this previous study.

Frequency of LVDD in COPD

The present study observed a high frequency of LVDD in patients with COPD (65.6%), but there was no difference among different stages of COPD. In agreement with these results, Boussuges et al found a high frequency of LVDD in patients with COPD (76%).Citation3 Funk et al also reported a prevalence rate of more than 50%.Citation9 A recent studyCitation10 showed more frequent echocardiographic findings of mild LVDD (88%) in COPD patients, independently of COPD stage. Another studyCitation11 focused on outpatients with severe COPD (FEV1 of 30%–50%), and showed a potentially highest prevalence of LVDD (90%) in patients with severe stable COPD. Therefore, the difference in the frequency of LVDD in patients with COPD between the present and previous studies might be due to different distribution of COPD stages, age, sex, and comorbidities. In addition, a recent studyCitation12 showed diastolic dysfunction in 47.5% of patients with COPD, and only 27.5% of their patients had severe/very severe COPD.

Relationship between COPD and LVDD

There is a well-known association between COPD and heart failure. In the last decade, prior studies mainly focused on the relationship between LVSD right ventricular dysfunction and COPD, but few studies evaluated LVDD and COPD. LVDD can be asymptomatic or associated with heart failure symptoms (eg, HFpEF). The incidence of HFpEF increases with age; hypertension, atrial fibrillation, diabetes mellitus, and female sex are the most common risk factors of HFpEF.Citation7 In the present study, approximately two-thirds of the patients had a diagnosis of hypertension. The left diastolic function changes with aging, and because our study was restricted to elderly patients, we had to consider changes in echocardiographic parameters that are associated with aging,Citation13,Citation14 such as reduced early diastolic filling and increased late diastolic filling.

The potential pathophysiologic mechanism for the association between COPD and LVDD and HFpEF could be systemic inflammation. Inflammation is considered to be one of the systemic manifestations of COPD. Indeed, inflammation can promote atherosclerotic plaque formation, which is associated with myocardial ischemia and LVDD. However, in the present study, leukocyte levels were not different between the control and COPD groups, and there was no correlation with severe stages of COPD. Therefore, these results suggest that there may be some other mechanisms involved in this process.

Furthermore, the presence of cor pulmonale secondary to pulmonary hypertension can lead to interventricular septum deviation toward the left ventricle, which could alter LV structure and delay filling compliance.Citation15 This mechanism could explain why COPD severity was associated with worse diastolic function. In our study, the main significant differences in echocardiographic findings were the left atrium diameter (35.11±3.73 in controls and 37.08±2.82 in COPD) and the E/e′ ratio (10.42±3.25 in controls and 11.51±2.50 in COPD), but there was no difference in systolic pulmonary artery pressure. These results are supported by two previous studies,Citation9,Citation16 implying that even in the absence of right ventricular changes or pulmonary hypertension, LVDD may be already in place.

Besides the two possible mechanisms indicated earlier, LVDD in patients with COPD may be due to abnormal pathophysiological changes in LV preload and/or afterload. Thoracic cavity hyperinflation secondary to emphysema may impair LV filling (preload) and further affect LV diastolic function.Citation17 In the meantime, a relationship between LV diastolic filling and emphysema has also been observed in patients with mild flow obstruction (without hyperinflation).Citation16 This means that the pathogenic causes of impaired LV filling are likely to be multifactorial. The earlier return of reflected arterial wave can increase LV afterload, while the concomitant reduction of aortic diastolic blood pressure may lead to subendocardial ischemia. These effects can act together to affect myocardial relaxation.Citation18

COPD and NT-proBNP

NT-proBNP is an important and helpful indicator in congestive heart failure. Elevated NT-proBNP levels have been found in patients with COPD.Citation19 Moreover, increased NT-proBNP levels can be seen in diseases such as LVDD and right ventricular dysfunction secondary to pulmonary diseases without decreased LVEF.Citation20 Therefore, measurement of NT-proBNP levels can be useful in the diagnosis of impaired right ventricular functions in patients with COPD and HFpEF.

In the present study, we found significant differences between patients with COPD and controls in terms of NT-proBNP values. Serum NT-proBNP values were significantly higher in patients with COPD compared with controls (372.65±651.97 vs 218.76±368.80 pg/mL). These results are supported by previous studies.Citation21,Citation22 Differences in NT-proBNP levels were in accordance with the differences of LVDD and HFpEF between the control and COPD groups. There was no difference in LVDD between the mild/moderate and severe/very severe COPD groups, but NT-proBNP levels remained significantly different. Therefore, results suggest that NT-proBNP levels increase with the severity of COPD and that the mechanisms for these changes may be independent from LVDD.

In the present study, logistic regression analysis showed that age and smoking were independent risk factors for COPD. Previous studies suggested that age and tobacco consumption were associated with COPD.Citation23Citation26 However, further studies are necessary to correctly identify and quantify the risk factors for COPD and LVDD.

Limitations

The present study included a small sample size, which may lead to bias. In addition, patients were not followed up. All patients were hospitalized, which is not representative of the whole population of patients >65 years old. In addition, our database had missing data for some variables. Therefore, additional multicenter prospective studies with a larger number of patients are necessary before being able to generalize our findings.

Conclusion

There is a high frequency of LVDD in hospitalized patients with COPD, and LVDD may occur at the early stages of COPD, prior to changes in right ventricular function and pulmonary hypertension. In hospitalized elderly patients with COPD, LVDD should be taken into account besides right ventricular function. Closer co-operation between pulmonologists and cardiologists is necessary to optimize the management of this large population of patients.

Acknowledgments

This work was supported by the Basic and Clinical Research Cooperation Program of Capital Medical University (grant number 13JL48) and the Beijing Excellent Talents Training Program (grant number 2011D003034000026).

Disclosure

The authors report no conflicts of interest in this work.

References

  • SinDDManSFWhy are patients with chronic obstructive pulmonary disease at increased risk of cardiovascular diseases? The potential role of systemic inflammation in chronic obstructive pulmonary diseaseCirculation2003107111514151912654609
  • CurkendallSMDeLuiseCJonesJKCardiovascular disease in patients with chronic obstructive pulmonary disease, Saskatchewan Canada cardiovascular disease in COPD patientsAnn Epidemiol2006161637016039877
  • BoussugesAPinetCMolenatFLeft atrial and ventricular filling in chronic obstructive pulmonary disease. An echocardiographic and Doppler studyAm J Respir Crit Care Med20001622 pt 167067510934104
  • VestboJHurdSSAgustíAGGlobal strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summaryAm J Respir Crit Care Med2013187434736522878278
  • PellegrinoRViegiGBrusascoVInterpretative strategies for lung function testsEur Respir J200526594896816264058
  • GottdienerJSBednarzJDevereuxRAmerican Society of Echocardiography recommendations for use of echocardiography in clinical trialsJ Am Soc Echocardiogr200417101086111915452478
  • McMurrayJJAdamopoulosSAnkerSDESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESCEur J Heart Fail201214880386922828712
  • StällbergBJansonCJohanssonGManagement, morbidity and mortality of COPD during an 11-year period: an observational retrospective epidemiological register study in Sweden (PATHOS)Prim Care Respir J2014231384524346825
  • FunkGCLangISchenkPValipourAHartlSBurghuberOCLeft ventricular diastolic dysfunction in patients with COPD in the presence and absence of elevated pulmonary arterial pressureChest200813361354135918339780
  • CaramLMFerrariRNavesCRAssociation between left ventricular diastolic dysfunction and severity of chronic obstructive pulmonary diseaseClinics201368677277623778477
  • López-SánchezMMuñoz-EsquerreMHuertasDHigh prevalence of left ventricle diastolic dysfunction in severe COPD associated with a low exercise capacity: a cross-sectional studyPLoS One201386e6803423826360
  • GuptaNKAgrawalRKSrivastavABVedMLEchocardiographic evaluation of heart in chronic obstructive pulmonary disease patient and its co-relation with the severity of diseaseLung India201128210510921712919
  • TigheDAVinchCSHillJCMeyerTEGoldbergRJAurigemmaGPInfluence of age on assessment of diastolic function by Doppler tissue imagingAm J Cardiol200391225425712521648
  • OxenhamHSharpeNCardiovascular aging and heart failureEur J Heart Fail20035442743412921803
  • MinaiOAChaouatAAdnotSPulmonary hypertension in COPD: epidemiology, significance, and management: pulmonary vascular disease: the global perspectiveChest2010137Suppl 639S51S20522579
  • BarrRGBluemkeDAAhmedFSPercent emphysema, airflow obstruction, and impaired left ventricular fillingN Engl J Med2010362321722720089972
  • WatzHWaschkiBMeyerTDecreasing cardiac chamber sizes and associated heart dysfunction in COPD: role of hyperinflationChest20101381323820190002
  • LaurentSCockcroftJVan BortelLEuropean Network for Noninvasive Investigation of Large ArteriesExpert consensus document on arterial stiffness: methodological issues and clinical applicationsEur Heart J200627212588260517000623
  • YapLBMukerjeeDTimmsPMAshrafianHCoghlanJGNatriuretic peptides, respiratory disease, and the right heartChest200412641330133615486400
  • TsaiSHLinYYChuSJHsuCWChengSMInterpretation and use of natriuretic peptides in non-congestive heart failure settingsYonsei Med J201051215116320191004
  • ChiSYKimEYBanHJPlasma N-terminal pro-brain natriuretic peptide: a prognostic marker in patients with chronic obstructive pulmonary diseaseLung2012190327127622246552
  • BozkanatETozkoparanEBaysanODenizOCiftciFYokusogluMThe significance of elevated brain natriuretic peptide levels in chronic obstructive pulmonary diseaseJ Int Med Res200533553754416222887
  • Antonelli-IncalziRImperialeCBelliaVDo GOLD stages of COPD severity really correspond to differences in health status?Eur Respir J200322344444914516133
  • FearyJRRodriguesLCSmithCJHubbardRBGibsonJEPrevalence of major comorbidities in subjects with COPD and incidence of myocardial infarction and stroke: a comprehensive analysis using data from primary careThorax2010651195696220871122
  • LindbergAJonssonACRonmarkELundgrenRLarssonLGLundbackBTen-year cumulative incidence of COPD and risk factors for incident disease in a symptomatic cohortChest200512751544155215888826
  • FukuchiYNishimuraMIchinoseMCOPD in Japan: the Nippon COPD Epidemiology studyRespirology20049445846515612956