SGLT-2 inhibitors improve cardiac function in hypertrophic cardiomyopathy: a real-world propensity score-matched

Cong Ding1, Fangchao Lv2, Lin Wang2

  • 1Department of Gastroenterology, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou, Zhejiang, China.

Insights

Sodium-glucose cotransporter 2 inhibitors (SGLT-2i) show promise for hypertrophic cardiomyopathy (HCM). This study found SGLT-2i improved diastolic function and NYHA class in HCM patients without adverse effects.

Area of Science:

  • Cardiology
  • Pharmacology
  • Internal Medicine

Background:

  • Hypertrophic cardiomyopathy (HCM) is a genetic heart condition characterized by left ventricular hypertrophy and diastolic dysfunction.
  • Sodium-glucose cotransporter 2 inhibitors (SGLT-2i) are established treatments for heart failure (HF), but their efficacy in HCM is not well-studied.

Purpose of the Study:

  • To evaluate the clinical effectiveness of SGLT-2i in patients diagnosed with HCM.
  • To assess the impact of SGLT-2i on echocardiographic parameters and functional status in HCM.

Main Methods:

  • A retrospective analysis compared 94 HCM patients treated with SGLT-2i to 94 matched controls.
  • Primary endpoints included changes in echocardiographic measures (septal e', E/e', IVST) and NYHA class at 6 months.
  • Secondary endpoint was heart failure readmission, with a median follow-up of 16.3 months.

Main Results:

  • SGLT-2i treatment led to significant improvements in septal e' (p=0.002), E/e' (p<0.001), IVST (p=0.005), and NYHA class (p=0.031) at 6 months.
  • Multivariate analysis confirmed sustained improvements in septal e', E/e', and NYHA class.
  • No significant difference in heart failure readmission rates was observed between groups (p=0.73).

Conclusions:

  • SGLT-2i administration improved left ventricular diastolic function and NYHA class in HCM patients.
  • Treatment with SGLT-2i did not increase risks of renal dysfunction or hypoglycemia.
  • These findings support the potential therapeutic value of SGLT-2i in managing HCM.
Abstract

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