The Syndrome X-ercise Study SYNDEX (SYNDEX)

Effect of Aerobic High-intensity Exercise Training on Coronary Flow Reserve and Endothelial Function in Individuals With Chest Pain and Normal Coronary Angiogram

This pilot study evaluates the effect of exercise training on CFR, functional capacity, heart rate variability, endothelial function and quality of life in patients with no obstructive coronary artery disease and angina.

Study Overview

• Status: Unknown
• Conditions: Angina
• Intervention / Treatment: Other: Exercise training

Detailed Description

Impaired coronary flow reserve (CFR) is associated with increased mortality in patients with chest pain despite normal coronary arteries (chest pain and normal coronary angiograms (CPNCA)) , . Furthermore, impaired CFR without any concomitant impairment of regional or global left ventricular function have additional prognostic significance . In patients with hypertension both microvascular dysfunction and increased left ventricular mass (LVM) are described sequels . LVM has also been associated with endothelial dysfunction and coronary artery remodelling . In addition, patients with hypertrophic obstructive cardiomyopathy (HOCM) and an impaired micro vascular cardiac circulation assessed with PET, have been documented to have a poor prognosis . Also diastolic dysfunction as measured by Em/Am ratio during stress dobutamine echocardiography is related to CFR . Patients with Diabetes Mellitus have an impaired prognosis and longstanding disease influence microvascular physiology . Several methods have been utilized to assess micro vascular function including intracoronary Doppler measurements. CRF can now be assessed with transthoracic Doppler registration .

Several patients with angina and normal coronary arteries show persistence and even worsening of angina symptoms over time. . These patients constitute a therapeutic problem with considerable residual morbidity associated with functional limitation and reduced quality of life . The primary end point in the treatment of these patients is symptom control .

Reduced physical activity is one of the major avoidance behaviours in patients with coronary heart disease . On the other hand several studies have documented the positive effect of ET in this population . Psychological morbidity with great impact on daily living is well known in both patients with cardiovascular disease and in patients with chest pain with no obvious physical disease. This includes patients with CPNCA. These patients constitute a relatively large proportion of patients taken care of by the health authority system indicating that this issue has economic consequences for the society that is not neglectable2.

Exercise training (ET) has been shown to improve endothelial function in patients with coronary artery disease (CAD) and to reduce LVM in hypertension.. ET also improves endothelial dysfunction and reverse inflammation in CAD. It is also associated with improved outcome in the general population and in patients with CAD and heart failure. It has been documented that hs-CRP correlates with symptoms and ECG markers of myocardial ischemia in CPNCA patients . Whether hs-CRP is related to the pathogenesis of angina in these patients deserves further investigation. Whether ET may influence on pathological reduced CFR is currently not known.

Interventions proposed in CPNCA patients are directed at either improving microvascular function or decreasing chest pain perception, in an attempt to counteract the accepted pathophysiological mechanisms of the syndrome. A multidisciplinary approach and a genuine, sympathetic appreciation by the health staff of the devastating effect of cardiac syndrome X on the patients' quality of life usually have a positive therapeutic impact . Unfortunately, most treatments have been evaluated in small numbers of patients and/or in uncontrolled trials, thus making it difficult to establish their real degree of effectiveness. Tynni Lee 11 investigated the effects of physical training and relaxation therapy on exercise capacity and quality of life in patients with syndrome X. It is the first trial reported to assess the effect of physiotherapy intervention in terms of quality of life in patients with coronary syndrome X. Female patients with this syndrome benefit from physical training in terms of exercise capacity and quality of life, and from relaxation therapy in terms of quality of life. However a limitation is the small sample size and therefore non-significant findings may be due to an inability to detect a difference among groups. Further studies with larger number of patients are recommended. Different modes of physiotherapy could have the potential to break the vicious circle of effort-induced chest pain, functional limitations and poor quality of life in the patients with coronary syndrome.

• Study Type: Interventional
• Enrollment (Anticipated): 30
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Alf Inge Larsen, Md, PhD; Phone Number: 004795889896; Email: laai@sus.no

Study Locations

• Norway
  • Stavanger, Norway, 4068
    • Recruiting
    • Stavanger University Hospital
    • Contact: Alf Inge Larsen, MD, PhD; Phone Number: +4751513201; Email: laai@sus.no

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: ADULT; OLDER_ADULT; CHILD
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• outpatients and patients admitted to the hospital with a history of repeated episodes of exercise induced chest pain.
• normal or near normal coronary angiogram or negative CT coronary angiogram
• age > 18 years
• being able to participate in training groups 3 times a week.

Exclusion Criteria:- Prior myocardial infarction

• serious valve disease
• cancer
• previous radiation or drug therapy for cancer
• musculoskeletal problems making ET impossible
• ongoing serious inflammatory disease
• intracardiac devices
• presumed insufficient acoustic windows because of severe emphysema or gross overweight
• atrial fibrillation
• participation in other ongoing studies.
• contrast allergy
• contraindication to adenosine infusion
• vasospasm angina

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: NON_RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Exercise training; High intensity aerobic exercise training	Other: Exercise training; high intensity aerobic interval training
NO_INTERVENTION: No training; No exercise training, only ordinary daily life activities.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Coronary flow reserve	Changes of Cornary flow reserve following 3 months of exercise training	3 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Endothelial function	Arterial diameter after occlusion at baseline and at 3 months follow up	3 months
Functional capacity	Changes in cardiopulmonary exercise testing following 3 months of exercise training	3 months

Collaborators and Investigators

• Sponsor: Helse Stavanger HF
• Collaborators: University of Bergen; University of Stavanger
• Investigators: Principal Investigator: Alf Inge Larsen, MD, PhD, Helse Stavanger HF

Study record dates

Study Major Dates

• Study Start: January 1, 2014
• Primary Completion (ANTICIPATED): December 1, 2017
• Study Completion (ANTICIPATED): February 1, 2018

Study Registration Dates

• First Submitted: August 24, 2016
• First Submitted That Met QC Criteria: September 13, 2016
• First Posted (ESTIMATE): September 19, 2016

Study Record Updates

• Last Update Posted (ESTIMATE): September 19, 2016
• Last Update Submitted That Met QC Criteria: September 13, 2016
• Last Verified: September 1, 2016

More Information

Terms related to this study

• Keywords: angina; coronary flow reserve; exercise training
• Other Study ID Numbers: 362Syndex

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO