Why the study?
T2DM is a strong risk factor for HFpEF, but the comparative efficacy of luseogliflozin versus voglibose in these patients required evaluation.
Does luseogliflozin reduce BNP levels compared to voglibose in patients with type 2 diabetes mellitus and heart failure with preserved ejection fraction?
Does luseogliflozin reduce BNP levels compared to voglibose in patients with type 2 diabetes mellitus and heart failure with preserved ejection fraction?
This paper describes the rationale and design of the MUSCAT-HF trial, which evaluates the effect of luseogliflozin versus voglibose on BNP levels in patients with T2DM and HFpEF.
Protocol for MUSCAT-HF leaves open whether luseogliflozin reduces BNP versus voglibose in T2DM-HFpEF; prospective RCT results needed before practice change.
INTRODUCTION: Type 2 diabetes mellitus (T2DM) is a strong risk factor for coronary artery disease and heart failure, particularly heart failure with preserved ejection fraction (HFpEF). The aim of the ongoing MUSCAT-HF (It stands for Prospective Comparison of Luseogliflozin and Alpha-glucosidase on the Management of Diabetic Patients with Chronic Heart Failure and Preserved Ejection Fraction) trial is to evaluate the efficacy of luseogliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, versus voglibose, an alpha-glucosidase inhibitor, using brain natriuretic peptide (BNP) as the index of therapeutic effect in T2DM patients with HFpEF. METHODS AND ANALYSIS: ), use of thiazolidine or not and presence or absence of atrial fibrillation and flutter at screening. After randomisation, participants will receive the study drug for 12 weeks in addition to their background therapy. The primary endpoint is the proportional change in baseline BNP after 12 weeks of treatment. The key secondary endpoints are the change from baseline in the ratio of early mitral inflow velocity to mitral annular early diastolic velocity, body weight and glycaemic control after 12 weeks of treatment. ETHICS AND DISSEMINATION: The study has been approved by the ethics committee and the patients will be included after informed consent. The results will be submitted for publication in peer-reviewed journals. TRIAL REGISTRATION NUMBER: UMIN000018395.
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Ejiri et al. (2019) studied this question.
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