Cardiol Res
Cardiology Research, ISSN 1923-2829 print, 1923-2837 online, Open Access
Article copyright, the authors; Journal compilation copyright, Cardiol Res and Elmer Press Inc
Journal website http://www.cardiologyres.org

Original Article

Volume 6, Number 6, December 2015, pages 346-351


The Evaluation of Type 2 Diabetes Mellitus Related Changes in Diastolic Dysfunction During Exercise Using Conventional and Tissue Doppler Echocardiography

Hakan Ozkana, d, Sedat Akdemirb, Selma Tiryakiogluc, Hasan Arib, Tahsin Bozatb

aBahcesehir University, Faculty of Medicine, Department of Cardiology, Istanbul, Turkey
bBursa Yuksek Ihtisas Hospital, Department of Cardiology, Bursa, Turkey
cBursa State Hospital, Department of Cardiology, Bursa, Turkey
dCorresponding Author: Hakan Ozkan, Ciragan Caddesi, Osmanpasa Mektebi Sokak No: 4 - 6, 34353 Besiktas, Istanbul, Turkey

Manuscript accepted for publication November 06, 2015
Short title: Diastolic Dysfunction in T2DM
doi: http://dx.doi.org/10.14740/cr439w

Abstract▴Top 

Background: The aim of this study was to evaluate the relationship between changes in diastolic functions during exercise and the exercising capacity in diabetic patients with diastolic dysfunction and to compare them with healthy individuals and diabetic patients without diastolic dysfunction.

Methods: Totally 70 patients prospectively were included in the study and three groups were formed. Forty-six diabetic patients were divided into two groups: those with (group 1) and without (group 2) diastolic dysfunction. The control group (group 3) consisted of 24 patients. All patients were subjected to treadmill exercising test. Echocardiographical assessment was made before exercise and immediately after peak exercise.

Results: Exercising time was dramatically decreased in group 1 compared to the other groups (group 1: 396 ± 125 second, group 2: 487 ± 66 second and group 3: 519 ± 102 second). In group 1, the diastolic mitral flow pattern at rest was transformed into pseudo-normal pattern at peak exercise from abnormal relaxation pattern (E/A ratio 0.70 ± 0.11 during rest, 1.02 ± 0.16; P < 0.0001 during peak exercise). Deceleration time (DT) and iso-volumetric relaxation time (IVRT) turned to normal values (DT 238.86 ± 39.48 millisecond during rest and 199.5 ± 23.57 millisecond during peak exercise; P = 0.001, IVRT 102.83 ± 16.22 millisecond during rest and 74.36 ± 8.67 millisecond during peak exercise; P = 0.001). In groups 2 and 3, the mitral flow pattern, DT and IVRT remained within normal limits during rest and exercise. E/Em ratio, which is one of the parameters of tissue Doppler, increased during peak exercise in the diabetic group with diastolic dysfunction (E/Em ratio 7.85 ± 3.31 during rest and 11.14 ± 3.40 after peak exercise; P < 0.0001).

Conclusions: Diabetic patients with diastolic dysfunction demonstrated a reduced exercise capacity, which may be due to aggravation of pre-existing left ventricular dysfunction.

Keywords: Diastolic dysfunction; Type 2 diabetes mellitus; Impaired exercise capacity; Tissue Doppler

Introduction▴Top 

Diastolic functions during exercise may be used as an early sign of this diabetic heart disease preceding the systolic damage due to its independent association with exercise capacity. To evaluate the relationship between changes in diastolic functions during exercise and the exercising capacity in diabetic patients with diastolic dysfunction who have not a previous history of cardiovascular disease may reveal early sings of diabetic cardiac disease. Mitral annulus pulse-wave tissue Doppler (PWTD) imaging is the relatively new approach for the assessment of left ventricular diastolic functions.

Material and Methods▴Top 

A total of 70 subjects (51 men, 19 women, mean age 52.8 ± 4.2 years) are composed of type 2 diabetes mellitus patients and normal individuals who applied to the cardiology department. Diabetic patients suffering from exercitional dyspnea referred from internal medicine policlinic for further evaluation were prospectively enrolled in the study. Those who have a previous history of coronary artery disease, hypertension, peripheral artery disease, cerebrovascular disease, echocardiographically diagnosed heart valve disease, left ventricle hypertrophy and/or a segmental contractility defect, any ST-T change in ECG, chest pain and/or ischemia detected by treadmill exercise test were not included in the study.

Diabetic patients were divided into two groups according to echocardiographic evidence of diastolic dysfunction. Group 1 consisted of 30 diabetic patients with diastolic dysfunction and group 2 included 16 diabetic patients without diastolic dysfunction. The control group (group 3) consisted of 24 healthy volunteers. Assessment was made between three groups. The following criteria were used for the diagnosis of diastolic dysfunction: 1) E/A ratio < 1 or > 2; 2) deceleration time (DT) < 150 or > 220 ms; 3) iso-volumetric relaxation time (IVRT) < 60 or > 100 ms; 4) annular tissue Doppler velocity in any section < 8 cm/s. All patients in group 1 met E/A ratio < 1, DT > 220 and IVRT > 100 criteria for diagnosis of stage 1 diastolic dysfunction.

All patients underwent physical examinations after taking detailed anamnesis. Their body mass indices (kg/m2) were calculated. Using the venous blood samples of diabetic patients, fasting blood glucose levels and HbA1c levels were checked. M-mode and Doppler echocardiographical parameters were assessed at rest in all patients. All patients underwent exercising test using Bruce protocol. Exercise capacity was assessed by both exercise duration and metabolic equivalent (MET). Immediately after cessation of maximal exercise, left ventricular diastolic functions were reassessed by Doppler echocardiography.

Transthoracic echocardiographies of subjects were made using 3.5 - 4.5 MHz probe with Doppler echocardiography device (Vivid 7 Pro GE) in left lateral decubitus position. Echocardiographical parameters were measured from at least three consecutive cardiac cycles during expirium and the mean values were calculated. M-mode tracings from the parasternal long-axis view were used to measure left atrium size, left ventricular wall thickness and diameters, ejection fraction and fractional shortening as the systolic function indicators. Furthermore left ventricular mass (LVM) was calculated by using the formula: LVM = 0.8 × 1.04((Left ventricular end-diastolic diameter + septum thickness + posterior wall thickness)3 - (Left ventricular end-diastolic diameter)3) + 0.6) [1].

Pulsed-wave (PW) Doppler is performed in the apical four-chamber view at the level of mitral valve leaflet tips to measure early diastolic flow peak velocity (E), late diastolic flow peak velocity (A), early and late diastolic flow peak velocity ratio (E/A), E wave DT (the interval from the peak of E to the point where the deceleration curve lowers to the baseline) and IVRT (the period between when blood flow through the aortic valve ceases and when it begins through the mitral valve) respectively. Pulmonary vein flow velocities were assessed from apical four-chamber view by placing PW sample volume 0.5 - 1 cm upstream in the right upper pulmonary vein. Pulmonary vein systolic flow peak velocity (S), pulmonary vein diastolic flow peak velocity (D), pulmonary vein reverse flow velocity (Ap) and S/D ratio were measured. PWTD sampling was performed at the level of the lateral mitral annulus. A PW Doppler sample volume at 1 cm within the lateral MV insertions of MV leaflets over an A4C view. All Doppler signals were recorded with a chart recorder set at 100 mm/s. The average of three end-expiratory cycles was used. Parallel to the long axis of the left ventricular wall early diastolic wave peak velocity (Em), late diastolic wave peak velocity (Am), the ratio of early and late diastolic wave peak velocities (Em/Am), and ratio of early mitral diastolic flow peak velocity to early mitral annular diastolic flow peak velocities (E/Em) were calculated respectively.

Patients with suspected coronary artery disease and those with insufficient exercise capacity underwent Tc-99m MIBI SPECT myocardial perfusion scintigraphy. Patients with myocardial perfusion defect were excluded from the study. Informed consent was given to all participants.

Statistical analysis of collected data was conducted using SPSS 8.0 Windows statistic package program. All hemodynamic and left ventricular diastolic function parameters were assessed within and among the groups at rest and after peak exercise. Parametric data were assessed using Student’s t-test and non-parametrical data were analyzed with Chi-square test. The distribution of the groups in terms of basic features was assessed using Kruskal-Wallis test. A value of P < 0.05 was considered statistically significant.

Results▴Top 

The mean age of 51 female and 19 male patients who participated in the study was 52.8 ± 4.2 years (range 35 - 60 years). Baseline characteristics of the three groups are shown in Table 1.

Table 1.
Click to view
Table 1. Baseline Characteristics of the Patients
 

There were not any significant differences among groups in M-mode transthoracic echocardiographic measurements (Table 2).

Table 2.
Click to view
Table 2. M-Mode Echocardiographical Measurements of the Groups
 

In diabetic patients with diastolic dysfunction (group 1), significant increases in heart rates, systolic and diastolic blood pressures were detected at peak exercise when compared to the resting values. Peak early diastolic mitral flow velocity (E) was detected significantly increased, the peak late diastolic flow velocity (A) velocity was also increased but this increase was not statistically significant (E wave velocity 0.66 ± 0.14 m/s at rest, 0.99 ± 0.16 m/s after peak exercise; P < 0.0001, A wave velocity 0.93 ± 0.15 m/s at rest, 0.98 ± 0.21 m/s after peak exercise; P = 0.068). For that reason, the E/A ratio changed significantly and showed pseudo-normalization after peak exercise (E/A ratio 0.70 ± 0.11 in relaxation and 1.02 ± 0.16; P < 0.0001 after peak exercise). Comparison of group 1 hemodynamic and diastolic function parameters at rest and after peak exercise is summarized in Table 3, data of group 2 are summarized in Table 4 and data of group 3 are shown in Table 5. E/A ratio before and after exercise significantly changed however still remained > 1. Therefore it was not significant for diastolic dysfunction in group 2. Tissue Doppler findings showing diastolic functions parameters were not statistically significant.

Table 3.
Click to view
Table 3. Comparison of Resting and Post-Exercise Hemodynamic and Diastolic Function Parameters in Group 1
 

Table 4.
Click to view
Table 4. Comparison of Resting and Post-Exercise Hemodynamic and Diastolic Function Parameters in Group 2
 

Table 5.
Click to view
Table 5. Comparison of Resting and Post-Exercise Hemodynamic and Diastolic Function Parameters in Group 3
 

No significant difference was observed among groups at rest in terms of heart rate (group 1: 87.43 ± 9.42, group 2: 82.87 ± 3.63, group 3: 81.37 ± 8.77; P value 1-2 = 0.38, P value 1-3 = 0.27, P value 2-3 = 0.98), systolic (group 1: 116.66 ± 8.33, group 2: 113.12 ± 9.28, group 3: 114.37 ± 10.35; P value 1-2 = 0.89, P value 1-3 = 0.71, P value 2-3 = 0.88) and diastolic blood pressures (group 1: 75.93 ± 8.02, group 2: 73.75 ± 5.91, group 3: 78.16 ± 6.53; P value 1-2 = 0.69, P value 1-3 = 0.57, P value 2-3 = 0.31). In both diabetic patient groups, the rate of E wave was lower (E wave velocity group 1: 0.66 ± 0.14 m/s, group 2: 0.89 ± 0.13 m/s, group 3: 0.93 ± 0.14 m/s), and the velocity of A wave was higher than control group (group 1: 0.93 ± 0.15 m/s, group 2: 0.77 ± 0.11 m/s, group 3: 0.70 ± 0.11 m/s). In group 1, E/A ratio was < 1 and DT and IVRT were longer than normal. In other two groups, these values were within normal limits. Assessment of pulmonary vein recordings showed significantly higher Ap wave velocity in group 1 than other groups (group 1: 0.35 ± 0.005 m/s, group 2: 0.28 ± 0.02 m/s, group 3: 0.26 ± 0.038 m/s). The lowest S/D ratio was also detected in group 1 but the difference was not statistically significant. Comparing the lateral mitral annulus measurements Em velocity (group 1: 0.09 ± 0.025 m/s, group 2: 0.12 ± 0.01 m/s, group 3: 0.14 ± 0.02 m/s) and Em/Am ratios (group 1: 0.79 ± 0.40; group 2: 1.0 ± 0.41; group 3: 1.45 ± 0.53 m/s) were detected significantly lower in group 1 than other groups. Immediately after the peak exercise in group 1 E/A ratio, DT and IVRT turned to normal ranges when S and D wave velocity and the S/D ratio were detected lower than that observed by two other groups. However, S/D ratio was not statistically significant between three groups (Table 6).

Table 6.
Click to view
Table 6. Comparison of Post-Exercise Hemodynamic and Echocardiographical Doppler Parameters Among the Groups
 

Ap wave velocity was higher in group 1 than the other two groups and the calculated value was over the normal limits. In group 1 lateral mitral annulus Em wave velocity and Em/Am ratio were lower than the other groups, while the E/Em ratio was detected significantly highest. The data of Doppler echocardiographical assessments and hemodynamic parameters after peak exercise among the groups are shown in Table 6. According to the findings, the exercise time and METs values were significantly low in group 1 when compared with groups 2 and 3 (7.61 ± 1.53 in group 1, 9.28 ± 1.86 in group 2 and 9.87 ± 1.92 in group 3, P value for group 1-2 = 0.001, group 1-3 = 0.001). Diastolic parameters in group 1 were changed and pseudo-normal pattern was seen after exercise; however, we could not find the similar changes in group 2 or 3. Similarly, Em/Am was significantly lower and E/E’ ratio was significantly increased in group 1.

Discussion▴Top 

Diastolic dysfunction, whose importance and the role in the pathophysiology of heart failure are being increasingly understood, has a high morbidity despite its low mortality rate [2, 3]. In a study conducted in patients admitted to hospital with a primary diagnosis of congestive heart failure, it was reported that 30-50% of all patients had preserved left ventricular systolic functions and the heart failure was caused by diastolic dysfunction [4]. The increased frequency of heart failure in patients with diabetes mellitus was demonstrated in both clinical and epidemiological studies [5]. Diastolic dysfunction is one of the first findings of this disease. In a study conducted in 206 patients by Bajraktari et al, diastolic dysfunction prevalence was found as high as 68% in the diabetic patients [6].

Doppler echocardiography is the most commonly used method for assessment of left ventricular diastolic function. Mitral and pulmonary vein Doppler analyses are being used for this purpose. Mitral annulus PWTD imaging is the relatively new approach for the assessment of left ventricular diastolic functions [7]. The data obtained from tissue Doppler imaging give more information about left ventricular filling pressures and survey.

In studies made on diastolic dysfunction, it was reported that this disorder was related to the decrease in the exercise performance [8-11]. In the study conducted by Poirier et al in 19 normotensive type 2 diabetic patients, they have revealed that patients with diastolic dysfunction have lower exercise performance than patients who have normal diastolic function [12]. Similarly in our study, exercise capacity was found lower in diabetic patients with diastolic dysfunction than similar patients in terms of age and sex whose diastolic functions were normal and than control individuals (exercise duration group 1: 396 ± 125 s, group 2: 487 ± 66 s, group 3: 519 ± 102 s).

In this study after peak exercise, a statistically significant increase in A wave velocity and a decrease in E/A ratio are detected in those with normal diastolic function and in those with diastolic dysfunction both E and A wave velocities are found increased. Furthermore, the increase in E wave velocity is statistically significant other than A wave increase. In patient with diastolic dysfunction E/A ratio increased and reached the normal value (E/A > 1). Impaired DT and IVRT decreased to normal limits.

Comparison of two diabetic groups revealed that patients with diastolic dysfunction showed significant D, S and Ap wave velocities after peak exercise while in patients without diastolic dysfunction, only the D wave velocity increased significantly. In the group with diastolic dysfunction, the increase in pulmonary vein reverse A wave velocity is significant and this value exceeded 0.35 m/s (Ap 0.35 ± 0.005 during relaxation, 0.45 ± 0.08 m/s; P = 0.002 during peak exercise).

Different from the other case studies which investigate the changes in diastolic function parameters after exercise in diabetic patients, our study reports mitral annular tissue Doppler velocities, as well. The tissue Doppler views of the all patients were taken before and after peak exercise. In the individuals with diabetic diastolic dysfunction, after peak exercise non-significant increases were observed in Em/Am ratio, in Em and Am wave velocities, while E/Em ratio increase was statistically significant. In diabetic patients whose diastolic functions were normal while there were significant increases in Em and Am velocities after exercise, Em/Am and E/Em ratios were similar to the rest values. In the control group, following the exercise while meaningful increases were observed in Em velocity and E/Em ratio was significantly changed. This finding may be explained by the limited amount of the study population.

E/Em ratio is one of the best echocardiographical parameters demonstrating the decrease in exercise capacities. In a study conducted by Skaluba et al in 121 patients, the relationship between left ventricular diastolic function parameters and duration of exercise was assessed and it was reported that the parameter showing the best correlation with the exercise capacity was E/Em ratio, decreased exercise tolerance was shown in patients with high E/Em ratios [13]. Similarly, in our study after peak exercise, the group with diabetic diastolic dysfunction showed lower exercise capacity and significantly higher E/Em ratio than the other groups. And this supports the relation between exercise capacity and E/Em ratio. The decrease of exercitional capacity suggests as a result of worsening diastolic functions with exercise when the increase in E/Em ratio is associated with high left ventricular filling pressure. This decrease in the duration of exercise is related to the worsening of diastolic functions during exercise. This worsening of diastolic functions arising from exercise has been demonstrated with the transformation of diastolic functions from abnormal relaxation pattern to peak at rest and to pseudo-normal left ventricular diastolic filling pattern after peak exercise.

Pseudo-normalization was demonstrated not only with the reversal of mitral E/A wave velocity ratio, but also with normalization of IVRT and pulmonary venous reverse flow velocity increase up to 0.35 m/s after peak exercise. Both this worsening in the left ventricular filling pattern and the increase in the E/Em ratio indicates that there are increases in left ventricular diastolic pressure and decrease in left ventricular relaxation rate after exercise. Depending on these, there would be increase in left atrium pressure as well. Due to worsening of abnormal left ventricular filling pattern, further increase in left atrium pressure may lead to increase in pulmonary vascular pressure and decrease in exercise tolerance. As a result of these changes, the duration of exercise would decrease. In a study conducted by Nair et al in 30 patients with hypertensive diastolic dysfunction, worsening in diastolic functions after exercise was found related to decrease in exercise performance [9].

The normal ventricle response to exercise is accelerated relaxation and associated with increased elastical relaxation. It is shown that both E and A velocities are increased with exercise. Relaxation disorder of myocardium during rest may not increase own relaxation under the hemodynamical stress of exercise and increased cardiac flow and may cause an increase in ventricular filling pressure. As a result, asymptomatic patients at rest may be symptomatic with a decrease in exercise duration [14]. Consequently, our study once more revealed that in patients with diabetic diastolic dysfunction exercise capacity decreases due to worsening of the existing diastolic dysfunction. Furthermore, this finding was supported by tissue Doppler echocardiographical inspection. We consider that further studies need to evaluate the efficacy of diastolic dysfunction treatment on the exercise capacity in diabetic patients with diastolic dysfunction.

The main limitation of the study is the amount of the study population. These findings might be academically stronger when the study consists of larger amount of patients. The re-evolution of the echocardiographic examination and exercise capacity after the treatment of diastolic dysfunction is another limitation of the study.

Conclusion

Diabetic patients with diastolic dysfunction demonstrated a reduced exercise capacity, which may be due to aggravation of pre-existing left ventricular dysfunction.

Conflict of Interest

None.

Abbreviations

A: late diastolic flow peak rate (with pulsed Doppler); Am: late diastolic wave peak rate (with tissue Doppler); Ap: pulmonary vein inverse flow rate; D: pulmonary vein diastolic flow peak rate; DT: deceleration time; E: early diastolic flow peak rate (pulsed Doppler); Em: early diastolic wave peak rate (with tissue Doppler); IVRT: isovolumetric relaxation time; PWTD: pulse wave tissue Doppler; S: pulmonary vein systolic flow peak rate; SPSS: Statistical Package for the Social Sciences; LVM: left ventricular mass; METs: metabolic equivalent


References▴Top 
  1. Guidelines from the Canadian Cardiovascular Society and the Canadian Hypertension Society on the echocardiographic determination of left ventricular mass. Task Force of the Echocardiography Section. Can J Cardiol. 1995;11(5):391-395.
    pubmed
  2. Vasan RS, Benjamin EJ, Levy D. Prevelence, clinical features of cardiac failure. Br Heart J. 1994;72:53-59.
  3. Vasan RS, Benjamin EJ, Levy D. Congestive heart failure with normal left ventricular systolic function. Clinical approaches to the diagnosis and treatment of diastolic heart failure. Arch Intern Med. 1996;156(2):146-157.
    doi pubmed
  4. Cregler LL, Georgiou D, Sosa I. Left ventricular diastolic dysfunction in patients with congestive heart failure. J Natl Med Assoc. 1991;83(1):49-52.
    pubmed
  5. Garcia MJ, Ares MA, Asher C, Rodriguez L, Vandervoort P, Thomas JD. An index of early left ventricular filling that combined with pulsed Doppler peak E velocity may estimate capillary wedge pressure. J Am Coll Cardiol. 1997;29(2):448-454.
    doi
  6. Bajraktari G, Qirko S, Bakalli A, Rexhepaj N, Elizi S. Reduced left ventricular diastolic function in asymptomatic patients with non-insulin-dependent diabetes mellitus. Med Arh. 2004;58(6):339-341.
    pubmed
  7. Nagueh SF, Middleton KJ, Kopelen HA, Zoghbi WA, Quinones MA. Doppler tissue imaging: a noninvasive technique for evaluation of left ventricular relaxation and estimation of filling pressures. J Am Coll Cardiol. 1997;30(6):1527-1533.
    doi
  8. Stoddard MF, Johnstone J, Dillon S, Kupersmith J. The effect of exercise-induced myocardial ischemia on postischemic left ventricular diastolic filling. Clin Cardiol. 1992;15(4):265-273.
    doi pubmed
  9. Nair VM, Tekin UN, Khan IA, Rahmatullah SI, Arora P, Mahankali BD, Sacchi TJ, et al. Worsening of left ventricular diastolic dysfunction during exercise causes decreased exercise tolerance in hypertension. Clin Cardiol. 2000;23(9):660-664.
    doi pubmed
  10. Lapu-Bula R, Robert A, De Kock M, D'Hondt AM, Detry JM, Melin JA, Vanoverschelde JL. Relation of exercise capacity to left ventricular systolic function and diastolic filling in idiopathic or ischemic dilated cardiomyopathy. Am J Cardiol. 1999;83(5):728-734.
    doi
  11. Poirier P, Garneau C, Bogaty P, Nadeau A, Marois L, Brochu C, Gingras C, et al. Impact of left ventricular diastolic dysfunction on maximal treadmill performance in normotensive subjects with well-controlled type 2 diabetes mellitus. Am J Cardiol. 2000;85(4):473-477.
    doi
  12. Poirier P, Bogaty P, Garneau C, Marois L, Dumesnil JG. Diastolic dysfunction in normotensive men with well-controlled type 2 diabetes: importance of maneuvers in echocardiographic screening for preclinical diabetic cardiomyopathy. Diabetes Care. 2001;24(1):5-10.
    doi pubmed
  13. Skaluba SJ, Litwin SE. Mechanisms of exercise intolerance: insights from tissue Doppler imaging. Circulation. 2004;109(8):972-977.
    doi pubmed
  14. Okmen AS, Yildirim A, Soylu O et al. The effect of exercise on a bicycle ergometer on diastolic filling parameters in patients with diastolic dysfunction. Arch Turk Soc Cardiol. 2005;33:268-275.


This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Cardiology Research is published by Elmer Press Inc.

 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Cardiology Research, bimonthly, ISSN 1923-2829 (print), 1923-2837 (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.

This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.cardiologyres.org   editorial contact: editor@cardiologyres.org
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.