Glucagon-like Peptide-1 and Coronary Microvascular Dysfunction in Women With Angina Pectoris and no Coronary Stenosis

NCT ID: NCT02602600

Last Updated: 2018-07-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 33 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-11-19
• Study Completion Date: 2017-04-18

Brief Summary

The aim of the present study is to evaluate the effect of treatment with Liraglutide on the coronary microvasculature and angina symptoms, in overweight patients with microvascular dysfunction and angina pectoris but no coronary artery stenosis.

Detailed Description

Background:

Patients with symptoms and signs of ischemia are referred to coronary angiography (CAG) or CT angiography (CT-CAG). A significant proportion of these patients and especially women appear to have no obstructive coronary stenosis. Patients with angina-like symptoms and no macrovascular coronary stenosis have previously been considered without increased risk of major cardiovascular events, but novel data indicate that this assumption may not be true.

Abnormal coronary flow and metabolic response to stress have been reported, which is consistent with a possible microvascular ethology for the symptoms. Both endothelium- and non-endothelium dependent impaired coronary reactivity may contribute. The endothelium dependent component has been linked to risk factors and pro-inflammatory processes promoting atherosclerosis. The non-endothelium dependent mechanisms may involve vascular smooth muscle cells, undergoing alterations in phenotype in response to physiological and pathophysiological stimuli like hypertension and diabetes.

Both invasive and non-invasive diagnostic methods are available for the assessment of coronary microvascular dysfunction. In the absence of a flow limiting stenosis upstream, indirect measurement is possible by using transthoracic Doppler stress echocardiography (TTDSE). TTDSE provides assessment of coronary blood flow velocity in one of the major coronary vessels that can be used to determine coronary flow velocity reserve (CFR) after hyperemia. This method does primarily assess the non-endothelium dependent component of coronary microvascular dysfunction.

Despite reassurance that no stenosis on major coronary vessels is found, many patients continue to have chest pain resulting in emergency visits, hospitalizations and repeat cardiac catheterizations with adverse effect on quality of life, employment and health care costs.

Treatment options for patients with angina symptoms are lacking when no macrovascular coronary stenosis is found. Standard anti-angina treatments are usually tried, but do not relieve symptoms in many of these patients.

Preclinical studies with Glucagon-like peptide-1 (GLP-1) and GLP-1 receptor (GLP-1R) agonists demonstrate cardioprotective effects. However, the underlying mechanisms are often not well defined. Many studies do not distinguish between direct versus indirect actions of GLP-1R agonists, nor take into account the potential actions of the cleavage product, GLP-1. GLP-1R is found in atrial cardiomyocytes in animal models and in the sinoatrial node in humans. Furthermore endothelial cells and vascular smooth muscle cells seem to be targets for GLP-1 action. In animal models GLP-1 promotes myocardial glucose uptake independent of insulin, increases contractility and coronary flow and improves outcome and survival after myocardial infarction in vivo. Limited data exists on the cardioprotective effect of GLP-1 in humans. A few studies have evaluated the effect of GLP-1 in patients presenting acute myocardial infarction or stenosis of major coronary vessels, whereas no data exists on the effect in patients with stable coronary artery disease. Two randomized studies have investigated the effect of GLP-1 infusion in ST-elevation acute myocardial infarction, and found reduced infarct size at three months follow-up. Several small pilot studies in patients with coronary heart disease have found that GLP-1 infusion or dipeptidyl peptidase-4 inhibitor improves left ventricular ejection fraction. None of the human trials have involved prolonged treatment with GLP-1.

Data from previous work suggest that GLP-1 and weight loss may have beneficial effects on microvascular circulation and cardiovascular risk factors. In a small cross-over study of 20 patients with type2 diabetes but no angina, 10 weeks of GLP1-R agonist treatment (Liraglutide, 1,2 mg/day) led to a small but insignificant improvement in coronary microcirculation, concomitant with a significant decrease in body weight and blood pressure and improvement in glycemic control. Another study included overweight patients with ischemic heart disease and found, that a mean weight loss of 10.6% achieved through a low energy diet improved microvascular function (CFR) and coronary risk factors such as blood pressure, lipid profile, and glycemic control (non-diabetics) as well as symptoms. Thus data on any cardioprotective effect of long-term treatment with GLP-1 in humans is sparse, and it may be speculated that any beneficial effect may be due to the weight lowering effect.

Objective The aim of the present study is to evaluate the effect of treatment with Liraglutide on the coronary microvasculature and angina symptoms, in overweight patients with microvascular dysfunction (CFR≤2,5) and angina pectoris but no coronary artery stenosis.

Hypothesis Liraglutide improves microvascular function and alleviates symptoms in women with angina pectoris and microvascular coronary dysfunction, but no obstructive stenosis of major coronary vessels.

Design An open label trial consisting of a four-weeks control period without intervention, followed by Liraglutide 3 mg once daily for 12 weeks + 2 weeks of weight maintenance diet. Study participants will serve as their own controls during the first four weeks not receiving treatment. Outcome parameters will be measured at baseline and at 4 and 18 weeks. The first two measurements (baseline and four weeks measurements) will in this way serve as documentation of the variance of repeated measurements. Blinding of participants and investigators will not be possible due to the study setup, but investigators will be blinded to pre- and posttreatment measurements when analysing results at the end of the study. Furthermore investigator will be blinded to previous CFR measurements during data collection.

Study drug Liraglutide s a once daily human GLP-1 analogue with 97% linear amino-acid sequence homology to human GLP-1. Liraglutide works by stimulating the release of insulin only when glucose levels become too high and by inhibiting appetite. It lowers blood glucose with the unique advantage that glucose lowering ceases when blood glucose gets into the normal range. Liraglutide is approved in the EU and US for the treatment of type 2 diabetes mellitus at doses up to 1,8 mg administered subcutaneously once daily. Recently the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have approved Liraglutide as obesity treatment. The indication is as an adjunct to lifestyle modifications for chronic weight management in individuals with a body mass index (BMI) of ≥30 kg/m2, or BMI≥27 kg/m2 with at least one weight-related comorbidity such as dysglycaemia (pre-diabetes or type 2 diabetes mellitus), hypertension, dyslipidaemia or obstructive sleep apnoea. The max dose for obesity treatment is 3.0 mg daily.

When prescribed with the aim of weight loss, Liraglutide is administrated subcutaneously and titrated up to the maximally recommended dosage for obesity. By treating participants on the indication overweight interference with other antihyperglycemic medications is avoided. Treatment is initiated with 0.6 mg once daily for one week and increased weekly until the recommended max dose of 3 mg. If it is not possible to reach maximal dosage due to adverse effects, the participants will stay at the highest dose tolerated. Participants will be excluded if they do not tolerate a treatment dose of at least 1.2 mg Liraglutide per day, since a lower dosage is unlikely to result in a weight loss of at least 5% .Treatment duration will be 12 weeks and the last two weeks will consist of a weight maintenance diet before outcome measurements are done. On this dosage and duration a weight loss of at least 5% is expected. Participants will be advised to reduce calorie intake and increase physical activity. Control of compliance will be made at visits by telephone calls (structured open questions interviews) Furthermore participants will note every time the medication is taken in a diary.

Participants Study participants will be recruited from an ongoing multicenter study of women with symptoms and signs of angina pectoris, 'Improving diagnosis and treatment of women with angina pectoris and microvascular disease (iPower)'. Before inclusion in the iPower study, participants have undergone CAG or CT-CAG with no significant stenosis of major coronary vessels. As part of the iPower study the coronary flow reserve is measured by transthoracic doppler stress echocardiography with dipyridamole induces stress.

Diagnostic methods Fasting blood samples will be collected. Some of the blood samples will be stored in a biobank. Blood samples will be stored until the end of the study (last patient, last visit) plus five years, and the blood samples will be destroyed thereafter.

Angina symptoms will be assess by the Seattle Angina Questionnaire (SAQ) which is a 19-item health-related quality-of-life measure for patients with coronary artery disease.

A score change of 10 points is clinically perceptible to patients and is considered a clinically relevant difference, while a substantial change is considered to be a change of 20 points.

Echocardiographic measurements of CFR, systolic and diastolic function including strain will be done both at rest and during dipyridamole induced stress. CFR is calculated as the ratio between coronary flow velocity during hyperemia and rest. Coronary microvascular dysfunction is defined as CFR<2.5.

Endothelial function will be measured by flow mediated dilation (FMD). Peripheral endothelial function correlates well with coronary endothelial function.

A whole body dual X-ray absorptiometry (DEXA) scan will be performed at baseline and after 18 weeks to estimate body composition.

Statistics There are two main outcomes: Microvascular function assessed by CFR and symptom burden assessed by SAQ.

CFR is a continuous response variable. A difference in repeated measurements within each subject is found to be normally distributed with a standard deviation 0.35. If the mean change in CFR post treatment is 0.23, the investigators will need to study 27 subjects to be able to reject the null hypothesis that there will be no change in the mean CFR with probability (power) 0.9. The Type I error probability associated with this test of the null hypothesis is 0.05. At least 33 participants will be included in anticipation of around 20% drop-out.

SAQ has four subscales each with a score from 1-100. According to previous studies a change in SAQ score of 10 points is perceptible by the patients and therefore clinically meaningful. The investigators have not found data on within-study subject variation on SAQ. However, previous trials have obtained changes in SAQ of 10-20 points after an intervention. Based on these findings the investigators expect to see a change in SAQ score of at least 10 point. By estimating a SD of 15, it is calculated that 26 study subjects is sufficient to attain a statistical power of >90% to detect a significant difference of 10 points post treatment in any SAQ item.

For the remaining secondary outcomes, if the response is normally distributed, the investigators will be able to detect a true difference in the mean response of participants of 0.66 x the SD of the within group change with a probability (power) 0.9. The Type I error probability associated with this test of the null hypothesis, that the population mean is unchanged after the intervention, is 0.05.

Monitoring:

The study will be monitored by the unit for Good Clinical Practice (GCP-unit) at the University of Copenhagen. Quality checks of data, data registry procedures and source data verification will be performed by the GCP-unit.

Conditions

Microvascular Angina

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Liraglutide

Liraglutide up to 3.0 mg daily injected subcutaneously (minimum 1.2 mg daily) for 12 weeks followed by 2 weeks of weight maintenance diet. Before initiating treatment participants will serve as their own controls for 4 weeks.

Group Type: EXPERIMENTAL

Liraglutide

Intervention Type: DRUG

• Liraglutide up to 3 mg daily injected subcutaneously (minimum 1.2 mg daily) for 12 weeks.
• Weight maintenance diet for 2 weeks

Interventions

Liraglutide

• Liraglutide up to 3 mg daily injected subcutaneously (minimum 1.2 mg daily) for 12 weeks.
• Weight maintenance diet for 2 weeks

Intervention Type: DRUG

Other Intervention Names

Victoza

Eligibility Criteria

Inclusion Criteria

• Women aged 40-75 with angina-like symptoms assessed by the Seattle Angina Questionnaire (SAQ).
• Women aged 40-75 with angina-like symptoms assessed by the Seattle Angina Questionnaire (SAQ).
• Referred for ischemic heart disease (IHD) assessment with no significant coronary stenosis (>50%) at coronary angiography or CT-angiography
• Impaired CFR assessed by echo Doppler flow (defined ratio≤2,5).
• BMI≥25kg/m2

Exclusion Criteria

• Allergy to dipyridamole, theophyllamine or liraglutide
• Previous myocardial infarction or revascularization
• No episodes of chest pain within 6 months before inclusion
• Diabetes (reported, noted in journal or patient on antidiabetic medication)
• Other causes of chest discomfort deemed highly likely
• Left ventricular ejection fraction <45
• Significant valvular disease
• Congenital heart disease
• severe co-morbidity with limited life-expectancy< 1 year
• Severe asthma
• Severe chronic obstructive pulmonary disease
• Pregnancy (pregnancy test will be done at inclusion)
• No use of contraception although in child-bearing age. A woman is regarded fertile, following menarche and until becoming post-menopausal unless permanently sterile. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. The birth control methods considered safe and effective includes combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal), progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable), intrauterine device (IUD) and intrauterine hormone-releasing system ( IUS). Women in child-bearing age will have to use one of the above mentioned contraceptive methods from inclusion in the study until the end of study participation.
• physical or mental disability
• active cancer
• significant renal (eGRF<30) or hepatic co-morbidity
• chronic alcohol abuse
• atrial fibrillation
• Atrio-ventricular block>1st degree
• chronic or previous acute pancreatitis
• inflammatory bowel disease
• history of thyroid carcinoma
• participation in other clinical trial if relevant for the present study.
• Language- or other barrier to giving informed consent
• No signed informed consent

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Eva Prescott

OTHER

Sponsor Role: lead

Responsible Party

Eva Prescott

MD, DMSc

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Eva IB Prescott, MD, DMSc

Role: PRINCIPAL_INVESTIGATOR

Bispebjerg Hospital

Locations

Bispebjerg University Hospital

Copenhagen, Copenhagen Northwest, Denmark

Countries

Denmark

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Other Identifiers

GAP

Identifier Type: -

Identifier Source: org_study_id