Subodh Verma,Mark C. Petrie,Barry A. Borlaug,Javed Butler,Melanie J. Davies,Dalane W. Kitzman,Sanjiv J. Shah,Cecilia Rönnbäck,Steen Zabell Abildstrøm,Karoline Liisberg,Dennis Wolf,Dirk von Lewinski,Małgorzata Lelonek,Vojtěch Melenovský,Michele Senni,Mikhail Kosiborod
Inflammation is thought to be an important mechanism for the development and progression of obesity-related heart failure with preserved ejection fraction (HFpEF). In the STEP-HFpEF Program, once-weekly 2.4 mg semaglutide improved heart failure-related symptoms, physical limitations, and exercise function, reduced the levels of C-reactive protein (CRP), a biomarker of inflammation, and reduced body weight in participants with obesity-related HFpEF. However, neither the prevalence nor the clinical characteristics of patients who have various magnitudes of inflammation in the context of obesity-related HFpEF have been well described. Furthermore, whether the beneficial effects of semaglutide on the various HF efficacy endpoints in the STEP-HFpEF Program are modified by the baseline levels of inflammation has not been fully established. Finally, the relationship between weight reduction and changes in CRP across the STEP-HFpEF Program have not been fully defined.