SGLT2 Inhibition and Left Ventricular Mass (EMPATROPHY)

Hannover Medical School (MHH)

Status and phase

Terminated

Phase 4

Conditions

Diabetes Mellitus Type 2

Treatments

Drug: Glimepiride

Drug: Empagliflozin

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02728453

CRC-KliPha-001

Details and patient eligibility

About

Patients with type 2 diabetes mellitus are exposed to an excessive heart failure risk secondary to left ventricular hypertrophy and impaired diastolic filling, a condition not addressed by currently available treatments. The abnormality results from obesity-induced volume overload, increased blood pressure, and myocardial fat accumulation. By improving metabolism, body weight, and blood pressure, Empagliflozin addresses the root causes of type 2 diabetes-associated myocardial disease. We will assess left ventricular mass, function, and lipid content in patients with type 2 diabetes mellitus using cardiac magnetic resonance imaging and spectroscopy as well as echocardiography before and after empagliflozin or glimepiride treatment. We expect to observe improvements in left ventricular mass, function, and fat content with empagliflozin. The results of the study will help to position empagliflozin as an antidiabetic agent with the added value of protecting the heart.

Full description

Overview of Medical Indication Type 2 diabetes mellitus is associated with increased heart failure risk. The increased risk results in part from poor glycemic control and obesity, but concomitant arterial hypertension may also contribute. In the Framingham Heart Study, heart failure risk increased by 5% in men and by 7% in women with each 1 kg/m2 increment in body mass index (BMI). Compared with normal weight subjects, obese subjects had a doubling of heart failure risk. Given the rapid increase in the prevalence of obesity and type 2 diabetes mellitus, the number of heart failure patients is likely to increase sharply.

Evidence Heart failure in obesity is explained by increased left ventricular mass and impaired left ventricular diastolic filling rather than systolic dysfunction. Obesity is associated with volume expansion and increased cardiac output. Arterial blood pressure also increases with increasing obesity. In addition, type 2 diabetes mellitus may directly elicit abnormalities in myocardial metabolism and function through intramyocardial triglyceride deposition and lipotoxicity. In a study from our group, obese women with insulin resistance showed increased myocardial lipid accumulation compared with obese insulin-sensitive women, and intramyocardial lipids were reduced by dietary weight loss. Finally, intramyocardial lipids are associated with impaired diastolic function in patients with type 2 diabetes mellitus. Myocardial insulin resistance may also contribute to heart failure, because genetic deletion of cardiac insulin receptors in mice worsens catecholamine-mediated myocardial injury. Heart failure risk may be further exacerbated through obesity-induced neurohumoral activation and systemic inflammation. Inflammatory cytokines are elevated in heart failure and modulate cardiac remodelling through various mechanisms including myocardial hypertrophy, fibrosis, and apoptosis.

Sodium-glucose cotransporter 2 (SGLT2) inhibitors are a new drug class for the treatment of type 2 diabetes mellitus. SGLT2 inhibitors may be particularly suitable in improving cardiac structure and function because they substantially improve systemic glucose metabolism, lower blood pressure, and reduce body weight. These effects reduce sympathetic vasomotor tone, and renin-angiotensin-system activity. Thus, SGLT2 inhibitors including empagliflozin ameliorate metabolic and hemodynamic risk factors tightly linked with left ventricular hypertrophy and heart failure risk. Recently published outcome data suggest a beneficial effect of empagliflozin on heart failure hospitalisation rates and on overall cardiovascular mortality in patients with type 2 diabetes and previously diagnosed cardiovascular disease.

Study Rationale Patients with type 2 diabetes mellitus are exposed to an excessive heart failure risk secondary to left ventricular hypertrophy and impaired diastolic filling, a condition not addressed by currently available treatments. The abnormality results from obesity-induced volume overload, increased blood pressure, and myocardial fat accumulation. By improving metabolism, body weight, and blood pressure, empagliflozin addresses the root causes of myocardial disease associated with type 2 diabetes-. We will assess left ventricular mass, function, and lipid content in patients with type 2 diabetes mellitus before and after 24 weeks treatment with metformin plus empagliflozin or glimepiride. We expect to observe improvements in left ventricular mass, function, and fat content with empagliflozin. The results of the study will help to understand the mechanisms of cardioprotective effects of empagliflozin that have been revealed recently.

Enrollment

7 patients

Sex

All

Ages

40 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

women and men ≥40 and <80 years of age
patients with type 2 diabetes mellitus on stable anti-diabetic treatment for the last 3 months; at screening the following treatment conditions are allowed:
- metformin + sulfonylurea with HbA1c ≥6.5% and ≤9.0%
- metformin monotherapy with HbA1c ≥7.5% and ≤ 9.0%
- metformin + dipeptidylpeptidase-IV inhibitor with ≥6.5% and ≤9.0%
waist circumference ≥80 cm in women or ≥94 cm in men
office blood pressure ≤150/95 mm Hg with a stable dose of a maximum of 4 antihypertensive medications for the last 3 months (24h ambulatory blood pressure measurement (ABPM) is allowed to check accuracy of office values; inclusion with 24h mean blood pressure ≤145/90 mm Hg is possible)
women without childbearing potential defined by:
- at least 6 weeks after surgical sterilization by bilateral tubal ligation or bilateral oophorectomy
- hysterectomy
- ≥ 50 years and in postmenopausal state > 1 year
- < 50 years and in postmenopausal state > 1 year with serum follicle-stimulating Hormone (FSH) > 40 IU/l and serum estrogen < 30 ng/l or a negative estrogen test, both at screening
women of childbearing potential with a negative serum pregnancy test at screening who agree to meet one of the following criteria from the time of screening, during the study and for a period of 4 days following the last administration of study medication:
- correct use of reliable contraception methods. The following are acceptable: hormonal contraceptives (combined oral contraceptives, implants, transdermal patches, hormonal vaginal devices or injections with prolonged release), intrauterine device (IUD/IUS) or a double barrier method, e.g. condom and occlusive cap (diaphragm or cervical/vault caps) with spermicide (foam, gel, film, cream or suppository)
- true abstinence (periodic abstinence and withdrawal are not acceptable methods of contraception)
- sexual relationship only with female partners
- sterile male partners
signed written informed consent and willingness to comply with treatment and follow-up
capability of understanding the investigational nature, potential risks and benefits of the clinical trial

Exclusion criteria

diabetes mellitus type 1
uncontrolled diabetes mellitus type 2 with fasting glucose > 13.3 mmol/l confirmed on a second day
previous treatment with insulin, glucagon-like peptide-1 analogues, or pioglitazone during the last year before screening
previous treatment with empagliflozin
acute illness at screening or randomization according to judgement by the investigator or patient
known or suspected hypersensitivity to empagliflozin, glimepiride or any excipients; known or suspected hypersensitivity to sulfonylureas or sulfonamides
history of multiple severe hypoglycemic episodes
any condition prohibiting MRI studies (e.g. metal implants, claustrophobia, body weight too high) including any suspected reaction after contrast agent application
patient actively attempted to lose weight or experienced unintentional clinically significant weight loss during the last 3 months
bariatric surgery or other gastrointestinal surgery procedures that induce chronic malabsorption
treatment with any weight loss drug in the preceding 6 months
planned significant changes of pre-study physical activity level during study participation
heart failure New York Heart Association (NYHA) III - IV
patients with known severe cardiovascular disease (e.g. myocardial infarction, unstable angina, stable coronary artery disease, stroke or transient ischemic attack)
calculated glomerular filtration rate (eGFR) <60 ml/min/1,73 m2
treatment with loop diuretics
chronic diarrhea, any clinical signs of volume depletion or a haematocrit > 48 % (women) and > 53 % (men)
history of severe volume depletion that required medical therapy
chronic lower urinary tract infections (but not simple asymptomatic bacteriuria)
known acute or chronic liver disease or screening liver enzymes > 3 x upper limit of normal (ULN)
serum potassium < 3.6 or > 5.0 mmol/l
glucose-6-phosphate dehydrogenase deficiency
anemia of unknown origin
pregnancy or lactation period
treatment with systemic glucocorticoids during the last 3 months before screening
chronic treatment with non-steroidal anti-inflammatory drugs (NSAIDs)
changes in thyroid hormone dosage (stable doses of thyroid hormones for the last 3 months are acceptable)
history of drug or alcohol abuse or current abuse
psychosomatic or psychiatric diseases requiring hospitalization during the last 12 months; ongoing treatment with one tricyclic or selective serotonin re-uptake Inhibitor (SSRI) antidepressant drug at a stable dose since the last 3 months is acceptable except for fluoxetine
medical history of cancer except for strictly localized tumors
any medical or surgical intervention planned for the next 7 months after randomization not allowing study participation according to the investigator´s judgment
current participation in any other clinical trial or participation in another clinical trial within 30 days before screening