Heart Failure With Reduced Ejection Fraction, Type2 Diabetes
Conditions
Brief summary
Diabetic cardiomyopathy is associated with significant morbidity and mortality. It is considered as a cardiac muscle disorder secondary to diabetes mellitus (DM). Certain studies show the clinical benefit of SGLT-s inhibitors on reducing cardiovascular outcomes amongst patients with type II DM that go beyond the correction of hyperglycemic perse. Thus an observational imaging study is proposed to identify mechanistic insights of the drug group over cardiovascular events.
Detailed description
Diabetic cardiomyopathy is defined as ventricular dysfunction in diabetic patients in the absence of coronary artery disease and hypertension. It is considered as a cardiac muscle disorder due to the metabolic consequences of DM characterized by left ventricular hypertrophy, left ventricular diastolic dysfunction (in the early stage), and/or systolic dysfunction. To date, there is no specific treatment proven effective for the condition due to the incomplete understanding of the pathogenesis. Recent studies however prove the efficacy of SGLT-2 inhibitors on reducing the primary composite end point of cardiovascular outcomes including hospitalization for heart failure, cardiovascular death, and all-cause death amongst patients with type II DM. Such clinical benefit is apparently mainly stemmed from the reduction in heart failure related mortality and sudden cardiac death rather than the macro-vascular events such as myocardial infarct and stroke, suggesting addition benefits going beyond the correction of hyperglycemia perse. These studies thus raise the possibility that the drug may have direct effects on the myocardium that conferring the clinical benefit not related the modification of traditional risk factors such as glycemic control, lipid, blood pressure, and obesity. A single-arm, observational cardiac magnetic resonance imaging study is proposed in type II diabetic patients before and 2 months after initiation of dapagliflozin. The aim is to identify mechanistic insights leading to the unexpected clinical benefit of SGLT inhibition.
Interventions
DRUGDapagliflozin
Dapagliflozin, one of the SGLT-2 inhibitors, will be prescribed to DM patients on clinical ground.
Sponsors
The University of Hong Kong
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Single-arm, observational
Eligibility
Sex/Gender
ALL
Age
40 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* type 2 diabetes * 40-90 years old * HbA1c \>= 6.5% * history of heart failure with reduced ejection fraction * indications for SGLT inhibition on clinical ground
Exclusion criteria
* angina pectoris or chest discomfort * prior coronary artery bypass grafts * coronary artery stenting within 6 months of study enrolment * pervious myocardial infarct * any contraindication for stress CMR testing * renal impairment with eGFR \<45ml/min/1.73m2 * limited life expectancy \<5 years, for example due to pulmonary disease, cancer or * significant hepatic failure * contraindication to dapagliflozin or other SGLT2 inhibitors * unable to take dapagliflozin * patients currently on and SGLT2 inhibitor * planned need for concomitant cardiac surgery or coronary intervention * refusal or inability to sign an informed consent * potential for on-compliance towards the requirements in the trial protocol (especially the medical treatment) or follow-up visits
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in myocardial perfusion reserve index | 8-12 weeks | Change in myocardial perfusion reserve index calculated from cardiac MRI |
Countries
Hong Kong
Outcome results
None listed