J Clin Med Res
Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
Journal website http://www.jocmr.org

Original Article

Volume 6, Number 3, June 2014, pages 184-189


Exercise Profile and Diastolic Functions Measured via Tissue Doppler Imaging of Fibromyalgia Patients

Ozlem Balbaloglua, f, Huseyin Edeb, Sadiye Yolcuc, Hakan Akd, Nermin Tanike, Gulacan Tekinb

aDepartment of Physical Medicine and Rehabilitation, Faculty of Medicine, Bozok University, Yozgat, Turkey
bDepartment of Cardiology, Faculty of Medicine, Bozok University, Yozgat, Turkey
cDepartment of Emergency Medicine, Faculty of Medicine, Bozok University, Yozgat, Turkey
dDepartment of Neurosurgery, Faculty of Medicine, Bozok University, Yozgat, Turkey
eDepartment of Neurology, Faculty of Medicine, Bozok University, Yozgat, Turkey
fCorresponding author: Ozlem Balbaloglu, Department of Physical Medicine and Rehabitation, Bozok University, Yozgat, Turkey

Manuscript accepted for publication March 11, 2014
Short title: Cardiovascular Properties of Fibromyalgia Patients
doi: https://doi.org/10.14740/jocmr1799w

Abstract▴Top 

Background: Our aim was to evaluate electrocardiographic and echocardiographic properties and exercise response of patients with fibromyalgia (FM).

Methods: The study included 60 women with primary FM and 30 healthy individuals. Resting electrocardiography, echocardiography and exercise treadmill test were used to compare these two groups. At apical four-chamber window, samples of transmitral diastolic inflow and tissue Doppler imaging of left ventricle lateral wall were obtained. Left ventricle ejection fraction was measured via modified Simpson’s method. Exercise duration, maximal exercise capacity, maximal heart rate (HR) (bpm), maximal HR (%), rate-pressure product at maximal HR (bpm × mmHg), heart rate recovery 1 (bpm), heart rate recovery 2 (bpm) and chronotropic reserve (%) values were calculated.

Results: Resting HR and QTc values were similar in both groups. Echocardiographic measurements in both groups did not reveal statistically significant difference except left ventricle end-diastolic diameter and left atrial diameter. Parameters related to diastolic function of the left ventricle did not differ significantly in both groups. Also, there was not any significant difference between the groups for E/E’ ratio and chronotropic reserve. Exercise treadmill test results were statistically similar for both groups.

Conclusion: Patients with FM presented a normal HR response to exercise and those patients had normal diastolic function similar to their healthy controls.

Keywords: Fibromyalgia; Diastolic function; Electrocardiography; Echocardiography; Exercise treadmill test

Introduction▴Top 

Fibromyalgia (FM) is known as a chronic syndrome characterized by widespread pain and discomfort [1]. In addition to widespread pain present for more than 3 months, patients with FM often report fatigue, nonrestorative sleep, dysfunction mood disturbance, stiffness and cognitive complaints [2-5]. Widespread pain is described as pain above and below the waist and on both sides of the body. Additionally, axial skeletal pain (in the cervical spine, anterior chest, thoracic spine, or lower back) must be seen. According to American College of Rheumatology, a patient must have pain on digital palpation at 11 of 18 predesignated sites, commonly described as tender points, for diagnosis of FM [6]. While the etiology of FM is not fully understood, the data have suggested that FM may result from dysfunction of the autonomic nervous system. This dysfunction has been reported at rest and after a physiological stress such as exercise [7]. However, few studies have searched such relation. Changes in autonomic function have been suggested to increase the risk for cardiovascular events and mortality [8]. In this regard, heart rate (HR) response to a graded exercise test has been largely used for assessing risk and prognosis in patients with overt or subclinical cardiovascular diseases [9, 10]. Similarly QTc and HR variability are other parameters used for assessing autonomic dysfunction at rest. Diastolic dysfuntion is also related to cardiovascular mortality and mortality [11]. There is limited knowledge in the literature about diastolic dysfuntion in FM patients.

In this study, we aimed to compare cardiovascular properties of the patients with FM to those of normal population by using electrocardiographic, echocardiographic and exercise treadmill test findings.

Materials and Methods▴Top 

Sixty female patients diagnosed with FM by Physical Medicine and Rehabilitation Department according to American Collage of Rheumatology criteria and with chest pain at the same time were included in the study between May 2013 and January 2014. All patients were evaluated by Cardiology Department. Resting electrocardiography (ECG), echocardiography and treadmill exercise tests were carried out for all the patients. The results were compared to those of the control group. The study was approved by the ethical committee of our institution and informed consent was obtained from each patient.

Exclusion criteria were: 1) cardiovascular involvement such as arrhythmias, arterial hypertension, heart failure, conduction disturbances, myocarditis and pericarditis; 2) tobacco usage; 3) use of chronotropic and antihypertensive drugs; 4) other chronic rheumatologic diseases such as systemic lupus erythematosus and rheumatoid arthritis; 5) diabetes mellitus; 6) dyslipidemia and 7) chronic kidney disease. At entry, patients and control subjects were not taking any kind of medication.

Resting ECG

Resting ECG of all patients and controls was obtained after the rest of 5 min in the room. Of this ECG, resting HR and QTc interval were measured by using the Bazett formula.

Treadmill exercise test

Modified Bruce treadmill protocol was used to assess the cardiac autonomic modulation in patients with FM in response to exercise. The test was stopped due to either patient’s demand or reaching maximal target HR. HR was continuously recorded at rest, during exercise and at recovery, using a 12-lead electrocardiogram. HR response during exercise was evaluated by the chronotropic reserve measured with the formula (chronotropic reserve = (peak HR - resting HR/220 - age - resting HR) × 100). Chronotropic incompetence was determined when subjects failed to achieve more than 80% of the chronotropic reserve. The recovery period was set at 2 min using the initial workload (1.9 mph). Heart rate recovery (HRR) was defined as the difference between HR at peak exercise and at both first (HRR1) and second (HRR2) minutes after exercise. Maximal HR in percent of target HR, rate-pressure product (HR multiplied with blood pressure at that moment), maximal exercise capacity in the standard metabolic equivalent (MET) and exercise duration were used for analysis.

Echocardiographic examination

In echocardiographic examination, left ventricle end-diastolic diameter (LVEDD), left ventricle end-systolic diameter, posterior wall diastolic thickness, interventricular septum diastolic thickness (IVSd), left atrial size, aortic diameter, left ventricle ejection fractions (LVEF) by using modified Simpson’s method and pulmonary arterial systolic pressure (PASP) were measured in accordance with the rules set by American Echocardiography Society [12]. At apical four-chamber window, by using pulse wave Doppler, mitral E and A waves were measured. E/A ratios of all patients were calculated. All measurements were carried out at the end of expirium. By using pulse wave tissue Doppler imaging, all diastolic myocardial velocities were obtained. In this study, to make the evalution more practical, sample volume at left ventricle lateral wall basal segment was used to obtain E’ and A’ wave velocities at apical four-chamber window. E/E’ ratios were calculated accordingly. All Doppler measurements were carried out for five subsequent cycles and averages of all five measurements were used for statistical analysis.

Statistical analysis

Statistical analysis was carried out by using SPSS 11.5 (Statistical Package for Socia Sciences-SPSS, Inc., Chicago, IL, USA) programme. While categorized variables were expressed as percentage, continuous variables were expressed as arithmetic average ± standard deviation. One-sample Kolmogorov-Smirnov test was applied to check whether continuous variables are distributed normally. All continuous variables of the study were normally distributed. Possible associations between continuous variables were analyzed by using Pearson’s correlation test. Possible statistical difference between group characteristics was analyzed by using Student’s t test. P value < 0.05 was considered statistically significant.

Results▴Top 

Sixty women with primary FM (age: 37.4 ± 7.2 years; BMI: 28.9 ± 4.9 kg/m2) and 30 healthy individuals (age: 39.1 ± 8.5 years; BMI: 30.2 ± 5.3 kg/m2) were included in the study.

Demographic properties of the patients with FM and the control group (CTRL) are shown in Table 1. Both groups were statistically similar in respect to age, weight, height and BMI.

Table 1.
Click to view
Table 1. Demographic Properties of the Patients With Fibromyalgia (FM) and the Control Group
 

Resting HR and QTc values were similar statistically in both groups (P = 0.315 and P = 0.389). Except LVEDD (FM: 44 ± 3 mm vs. CTRL: 46 ± 1 mm, P < 0.05) and LA diameter (FM: 31 ± 5 mm vs. CTRL: 35 ± 2 mm, P < 0.05), all other echocardiographic measurements (LVEF, aort diameter, PASP and IVSd) of both groups were not significantly different. In both groups, parameters related to diastolic function of the left ventricle measured via standard method (mitral flow E/A ratio, P = 0.311) or tissue Doppler imaging (left lateral basal segment E’/A’ ratio, P = 0.917) did not differ significantly. Additionaly, there was not any significant difference between the groups for E/E’ ratio (P = 0.66). The results of electrocardiographic and echocardiographic examinations are introduced in Table 2.

Table 2.
Click to view
Table 2. Electrocardiographic and Echocardiographic Results of the Patients With Fibromyalgia (FM) and the Control Group
 

We did not find any significant correlation for reached maximal HR between FM and the control group (166 ± 11 bpm and 165 ± 9 bpm respectively, P = 0.725). Also rate-pressure product at maximal HR was not siginificantly different in CTRL group compared to FM group (CTRL: 26,542 ± 4,316 bpm × mmHg, FM: 24,163 ± 4,133 bpm × mmHg, P = 0.134). Exercise duration and maximal exercise capacity in MET were similar statistically for both groups (FM: 555 ± 98 sec vs. CTRL: 488 ± 104 sec, P = 0.079 and FM: 9.2 ± 2.2 MET vs. CTRL: 8.3 ± 2.3 MET, P = 0.289). The groups did not differ significantly in respect to chrontropic reserve (FM: 80 ± 12% vs. CTRL: 78 ± 9%, P = 0.620) (Table 3).

Table 3.
Click to view
Table 3. Exercise Test Results of the Patients With Fibromyalgia (FM) and the Control Group
 

HRR values of both groups were similar at the end of first and second minute (Table 3). All subjects enrolled for the sudy had normal HRR1 (value of > 12 bpm) and had normal HRR2 (value of > 24 bpm).

Discussion▴Top 

We aimed to compare cardiovascular properties of the patients with FM to those of normal population by using electrocardiographic, echocardiographic and exercise treadmill test findings.

We found that patients with FM showed similar HR response during and after exercise as volunteer healthy subjects did. We also found that the patients with FM had similar chronotropic reserve as their control group. It has been reported that the patients with FM have autonomic dysfunction which is one of the suspected reason for increased cardiovascular mortality and morbidity [13].

Autonomic dysfunction may be well assessed by evaluating the resting ECG parameters such as QTc interval and HR variability. In this study, we used corrected QT interval. HR-corrected QT interval duration (QTc) has been shown to be related with cardiac autonomic dysfunction in patients with systemic lupus erythematosus, rheumatoid arthritis and chronic inflammatory arthritis [14-16]. In the literature, there is only one study evaluating FM patients [17]. In that study, average corrected QT of patients with FM was significantly longer than patients with chronic fatigue syndrome (417 ± 25 ms vs. 372 ± 22 with P < 0.0001). In our study, we compared corrected QT interval of FM patients with healthy individuals (408 ± 14 ms vs. 404 ± 12 with P = 0.389 respectively). If QTc interval of patients with FM in our study was compared to that of patients with FM in the study by Naschitz et al [17], it would be clearly seen that corrected QT intervals of both FM groups were within normal range defined for general female population, accepted as less than or equal to 470 ms [18]. So it cannot be said easily that the patients with FM had prolonged QTc interval while all the values in concern were within normal range. In this report, the study tried to explain this increased mortality solely via autonomic dysfunction but they never mentioned about any arrhythmic events which are expected to be direct result of autonomic dysfunction [17]. To prove the presence of such relation, long-term follow-up studies should be designed.

Echocardiography is one of the most helpful and frequently used tool in daily cardiology practice to evaluate systolic and diastolic functions of the heart [19]. Diastolic dysfunction, measured by standard mitral flow pattern or tissue Doppler imaging, is a well-known predictor of cardiovascular events and is one of the firstly impaired functions of the heart in concern [20]. In the literature, there is no study evaluating the correlation between autonomic dysfunction and diastolic dysfunction in patients with FM. We did not find any statistically significant difference between FM and control group for diastolic functions. Both groups had similar mitral flow pattern, pulse wave E/A ratio (1.5 ± 0.3 for FM vs. 1.6 ± 0.6 for CTRL, P = 0.311) and left lateral wall basal segment pulse wave TDI values, E’/A’ ratio (1.70 ± 0.55 for FM vs. 1.72 ± 0.65 for CTRL, P = 0.917) and also E/E’ values, very specific parameter for left ventricle filling pressure which is expressed via pulmonary capillary wedge pressure were similar for both groups (6.1 ± 1.6 for FM vs. 5.8 ± 1.2 for CTRL, P = 0.660). E/E’ values of > 12 are accepted as abnormal and none of our patients with FM and control groups had E/E’ value of > 12. In other words, both groups had similar diastolic properties without increased pulmonary capillary wedge pressure.

Exercise ECG test is a very useful method in assessing the cardiac status [21]. Exercise duration, exercise capacity measured in MET, maximal HR expressed as a percentage of target HR, chronotropic reserve and rate-pressure product at maximal HR are some of the parameters used to define the cardiovascular risk of individuals [21]. In our study, all mentioned parameters were similar in both of two groups. Bardal et al [22] reported that patients with FM have similar metabolic and cardiovascular responses to submaximal exercise as in healthy people. Our results were parallel to the findings of Bardal et al [22]. Additionally, we used rate-pressure product to evaluate hemodynamic response to exercise. In this respect, this study was the first study in the literature using the rate-pressure product for comparison of patients with FM and normal population. In our study, we found that average rate-pressure product of FM group was statistically similar to that of control group (24,163 ± 4,133 bpm × mmHg for FM vs. 26,542 ± 4,316 bpm × mmHg for CTRL, P = 0.134). As an index of myocardial oxygen consumption of myocardium, rate-pressure products of both groups were within intermediate range. The importance of such finding needs further investigation.

It is known that markers reflective of autonomic nervous system function can predict major cardiovascular events, total mortality and sudden cardiac death [21]. HRR is one of these markers and decreased HRR, which is HRR1 < 12 bpm and HRR2 < 24 bpm, has been associated with death and cardiac events in a number of populations [21]. In our study, HRR1 (39 ± 12 bpm for FM vs. 36 ± 12 bpm for CTRL, P = 0.438) and HRR2 values (62 ± 11 bpm for FM vs. 58 ± 13 bpm for CTRL, P = 0.372) were similar. In the literature, it had been reported that patients with FM had significantly lower values compared to normal population [13]. When this article was examined in detail, it would be found that all subjects of both groups had clinically normal HRR1 (24.5 ± 3 bpm vs. CTRL: 32.6 ± 2 bpm, P = 0.059) and HRR2 (34.3 ± 4 bpm vs. CTRL: 50.8 ± 3 bpm, P = 0.002) [13]. So comparing categorically two normal populations could not give clinically important difference, although there was statistically difference. So our results did not oppose the literature rather supported.

The other marker reflecting autonomic dysfunction is the chronotropic incompetence, defined as failure of the HR to achieve above 80% of the chronotropic reserve during exercise, independent predictor of all-cause mortality in healthy and diseased subjects [13, 23]. Chronotropic reserves of both groups were similar in our study (80 ± 12 for FM vs. 78 ± 9 for CTRL, P = 0.620). In the literature, there have been few studies searching relation between FM and chronotropic reserve [13]. While Ribeiro et al found average chronotropic reserve value FM when compared with CTRL (72.5 ± 5 vs. 106.1 ± 6, respectively) [13]. Similarly 46.7% of our FM group had CI, while it was 57.1% in the study by Ribeiro et al [13]. In both studies, all factors which could affect chronotropic reserve were excluded, so the difference between the average values of both studies may be due to different treadmill protocols used in the studies (modified Balke vs. modified Bruce) and this needs further investigation.

Conclusions

Patients with FM presented a normal HR response to exercise, suggesting normal cardiac autonomic function. Also we found that patients with FM had normal diastolic function compared to control group. All these findings showed normal cardiac properties rather than properties related to increased risk for cardiac events and mortality. But large scale prospective studies should be designed to clarify in this field.

Acknowledgments

No funding recevied for the study.

Conflict of Interest

None.


References▴Top 
  1. Di Franco, Iannuccelli C, Valesini G. Neuroendocrine immunology of fibromyalgia. Ann N Y Acad Sci. 2010;1193:84-90.
    pubmed
  2. Choy EH, Mease PJ. Key symptom domains to be assessed in fibromyalgia (outcome measures in rheumatoid arthritis clinical trials). Rheum Dis Clin North Am. 2009;35(2):329-337.
    pubmed
  3. Arnold LM, Clauw DJ, McCarberg BH, FibroCollaborative . Improving the recognition and diagnosis of fibromyalgia. Mayo Clin Proc. 2011;86(5):457-464.
    pubmed
  4. Wolfe F, Smythe HA, Yunus MB, Bennett RM, Bombardier C, Goldenberg DL, Tugwell P, et al. The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee. Arthritis Rheum. 1990;33(2):160-172.
    pubmed
  5. Wolfe F, Clauw DJ, Fitzcharles MA, Goldenberg DL, Katz RS, Mease P, Russell AS, et al. The American College of Rheumatology preliminary diagnostic criteria for fibromyalgia and measurement of symptom severity. Arthritis Care Res (Hoboken). 2010;62(5):600-610.
    pubmed
  6. Okifuji A, Turk DC, Sinclair JD, Starz TW, Marcus DA. A standardized manual tender point survey. I. Development and determination of a threshold point for the identification of positive tender points in fibromyalgia syndrome. J Rheumatol. 1997;24(2):377-383.
    pubmed
  7. Kingsley JD. Autonomic dysfunction in women with fibromyalgia. Arthritis Res Ther. 2012;14(1):103.
    pubmed
  8. Tsuji H, Larson MG, Venditti FJ, Jr., Manders ES, Evans JC, Feldman CL, Levy D. Impact of reduced heart rate variability on risk for cardiac events. The Framingham Heart Study. Circulation. 1996;94(11):2850-2855.
    pubmed
  9. Nishime EO, Cole CR, Blackstone EH, Pashkow FJ, Lauer MS. Heart rate recovery and treadmill exercise score as predictors of mortality in patients referred for exercise ECG. JAMA. 2000;284(11):1392-1398.
    pubmed
  10. Sandvik L, Erikssen J, Ellestad M, Erikssen G, Thaulow E, Mundal R, Rodahl K. Heart rate increase and maximal heart rate during exercise as predictors of cardiovascular mortality: a 16-year follow-up study of 1960 healthy men. Coron Artery Dis. 1995;6(8):667-679.
    pubmed
  11. Nosaka K, Nakamura K, Kusano K, Toh N, Tada T, Miyoshi T, Doi M, et al. Serum cystatin C as a biomarker of cardiac diastolic dysfunction in patients with cardiac disease and preserved ejection fraction. Congest Heart Fail. 2013;19(4):E35-39.
    pubmed
  12. Schiller NB, Shah PM, Crawford M, DeMaria A, Devereux R, Feigenbaum H, Gutgesell H, et al. Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms. J Am Soc Echocardiogr. 1989;2(5):358-367.
    pubmed
  13. da Cunha Ribeiro RP, Roschel H, Artioli GG, Dassouki T, Perandini LA, Calich AL, de Sa Pinto Al, et al. Cardiac autonomic impairment and chronotropic incompetence in fibromyalgia. Arthritis Res Ther. 2011;13(6):R190.
    pubmed
  14. Nomura A, Kishimoto M, Takahashi O, Deshpande GA, Yamaguchi K, Okada M. Prolongation of heart rate-corrected QT interval is a predictor of cardiac autonomic dysfunction in patients with systemic lupus erythematosus. Rheumatol Int. 2013;
    pubmed
  15. Lazzerini PE, Acampa M, Capecchi PL, Hammoud M, Maffei S, Bisogno S, Barreca C, et al. Association between high sensitivity C-reactive protein, heart rate variability and corrected QT interval in patients with chronic inflammatory arthritis. Eur J Intern Med. 2013;24(4):368-374.
    pubmed
  16. Panoulas VF, Toms TE, Douglas KM, Sandoo A, Metsios GS, Stavropoulos-Kalinoglou A, Kitas GD. Prolonged QTc interval predicts all-cause mortality in patients with rheumatoid arthritis: an association driven by high inflammatory burden. Rheumatology (Oxford).
    pubmed
  17. Naschitz JE, Slobodin G, Sharif D, Fields M, Isseroff H, Sabo E, Rosner I. Electrocardiographic QT interval and cardiovascular reactivity in fibromyalgia differ from chronic fatigue syndrome. Eur J Intern Med. 2008;19(3):187-191.
    pubmed
  18. Olgin J, Zipes DP. Specific Arrhythmias: Diagnosis and Treatment. In: Braunwald's Heart Disease, A Textbook of Cardiovascular Medicine eds. Bonow RO, Mann DL, Zipes DP, Libby P. Ninth Edition, Elsevier Saunders, Philadelphia, USA, 2012;771-824.
  19. Gibson DG, Brown DJ. Measurement of peak rates of left ventricular wall movement in man. Comparison of echocardiography with angiography. Br Heart J. 1975;37(7):677-683.
    pubmed
  20. Mogelvang R, Sogaard P, Pedersen SA, Olsen NT, Schnohr P, Jensen JS. Tissue Doppler echocardiography in persons with hypertension, diabetes, or ischaemic heart disease: the Copenhagen City Heart Study. Eur Heart J. 2009;30(6):731-739.
    pubmed
  21. Fihn SD, Gardin JM, Abrams J, Berra K, Blankenship JC, Dallas AP, Douglas PS, et al. 2012 ACCF/AHA/ACP/AATS/PCNA/SCAI/STS Guideline for the diagnosis and management of patients with stable ischemic heart disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, and the American College of Physicians, American Association for Thoracic Surgery, Preventive Cardiovascular Nurses Association, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons. J Am Coll Cardiol. 2012;60(24):e44-e164.
    pubmed
  22. Bardal EM, Olsen TV, Ettema G, Mork PJ. Metabolic rate, cardiac response, and aerobic capacity in fibromyalgia: a case-control study. Scand J Rheumatol. 2013;42(5):417-420.
    pubmed
  23. do Prado DL, Gualano B, Miossi R, Sa-Pinto A, Lima F, Roschel H, Borba E, et al. Abnormal chronotropic reserve and heart rate recovery in patients with SLE: a case-control study. Lupus. 2011;20(7):717-720.
    pubmed


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.


Journal of Clinical Medicine 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

 

 
       
 

Journal of Clinical Medicine Research, monthly, ISSN 1918-3003 (print), 1918-3011 (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.jocmr.org   editorial contact: editor@jocmr.org     elmer.editorial2@hotmail.com
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.