{"id":137999,"date":"2023-08-25T11:15:42","date_gmt":"2023-08-25T15:15:42","guid":{"rendered":"https:\/\/cardiologynownews.org\/?p=137999"},"modified":"2023-08-25T11:15:42","modified_gmt":"2023-08-25T15:15:42","slug":"step-hfpef-semaglutide-reduces-heart-failure-symptoms-and-body-weight-in-hfpef-patients-at-one-year","status":"publish","type":"post","link":"https:\/\/cardiologynownews.org\/?p=137999","title":{"rendered":"STEP-HFpEF: Semaglutide reduces heart failure symptoms and body weight in HFpEF patients at one year"},"content":{"rendered":"<p>Key Points:<\/p>\n<ul>\n<li>More than 80% of patients with HFpEF are overweight or obese, but there has not yet been a study examining the use of weight-loss agents in body weight reduction or HF symptomatology in HFpEF.<\/li>\n<li>In the Step-HFpEF study, subcutaneous once-weekly semaglutide was compared with placebo in patients with HFpEF and obesity. The two primary endpoints were change of KCCQ-CCS and body weight from baseline after 52 weeks of treatment.<\/li>\n<li>Semaglutide use resulted in a significant reduction in both heart failure symptomatology and body weight at 52 weeks.<\/li>\n<\/ul>\n<p><!--more--><\/p>\n<p>At least 80% of patients with HFpEF are overweight or obese. Obesity likely contributes not only to ongoing HFpEF pathophysiology, but also to the burden of symptoms in heart failure. GLP-1 receptor agonists have shown great promise in treating obesity, but they have not yet been examined in the setting of HFpEF. In a breaking presentation at the 2023 ESC Congress today, <a href=\"https:\/\/www.georgeclinical.com\/people\/dr-mikhail-kosiborod\">Dr. Kosiborod (Saint Luke\u2019s Health System, Kansas City)<\/a> and his team presented their study: \u201cSTEP HFpEF: once-weekly semaglutide in people with HFpEF and obesity.\u201d This study was simultaneously published in the <em><a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa2306963\">New England Journal of Medicine.<\/a><\/em><\/p>\n<p>The STEP-HFpEF trial (<a href=\"https:\/\/classic.clinicaltrials.gov\/ct2\/show\/NCT04788511\">NCT04788511<\/a>) was a randomized, international, multicenter, double-blind, placebo-controlled trial of HFpEF patients (EF &gt;45%) and obesity (BMI<u>&gt;<\/u>30kg\/m<sup>2<\/sup>) and functional limitation (NYHA score II-IV and Kansas City Cardiomyopathy Questionnaire Clinical Summary Score [KCCQ-CCS] &lt;90). Participants were also required to have at least \u22651 of the following: a) elevated filling pressures on invasive measurement, b) elevated natriuretic peptide (NP) levels with associated echocardiographic abnormalities; or c) HF hospitalization in the previous 12 months with ongoing echocardiographic abnormalities on diuretic requirement. Key exclusion criteria included diabetes (HbA1c &gt;6.5%), prior or planned bariatric surgery, &gt;5kg weight fluctuation within the 90 days prior to randomization, CV event &lt;30 days of randomization, or sBP &gt;160 mm Hg. The two primary endpoints were a) change in KCCQ-CSS score over 52 weeks and b) change in body weight over 52 weeks.<\/p>\n<p>A total of 529 patients were 1:1 randomized to either subcutaneous once-weekly semaglutide (2.4mg) or placebo over 52 weeks. \u00a0The median age was 69, and 56% were women. The median BMI was 37 kg\/m<sup>2<\/sup>. Participants receiving semaglutide had a significantly greater reduction in KCCQ-CSS over 52 weeks compared to placebo (estimated treatment difference [ETD] 7.8 points, 95% CI 4.8-10.9 points, p&lt;0.001). Participants receiving semaglutide also experienced significantly greater reduction in body weight over 52 weeks compared to placebo (ETD 10.7% body weight reduction, 95% CI 9.4%-11.9% reduction, p&lt;0.001). Secondary endpoints included change in 6MWD at 52 weeks from baseline, which was also increased in the semaglutide group (ETD 20.3 meters, 95% CI 8.6-32.1 meters, p&lt;0.001). Semaglutide users also had a higher win-ratio in the hierarchical composite endpoint of clinical benefit, time to death, number of HF events, time to first HF event, change in KCCQ-CSS, and change in 6MWD (stratified win ratio 1.72, 95% CI 1.37-2.15, p&lt;0.001). Semaglutide also resulted in significant reduction in CRP (43.5% reduction, treatment ratio 0.61) and NT-proBNP (20.9% reduction, treatment ratio 0.84) relative to placebo. Semaglutide was generally well-tolerated, with 13.3% of participants experiencing adverse effects leading to discontinuation, of which 9.5% were gastrointestinal. There were fewer adverse events in the semaglutide group relative to placebo (13.3% vs 26.7%, p&lt;0.001).<\/p>\n<p>When discussing the clinical implications of the study at the ESC Congress press conference, Dr. Kosiborod stated: \u201cI think that this study should change the conversation\u2026it is very clear based on these results that in patients with HFpEF, obesity is not just a comorbidity\u2014it appears to be the root cause of heart failure development and progression, and it should be treated as such and should be a target for intervention.\u201d<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Key Points: More than 80% of patients with HFpEF are overweight or obese, but there has not yet been a study examining the use of weight-loss agents in body weight reduction or HF symptomatology in HFpEF. In the Step-HFpEF study, subcutaneous once-weekly semaglutide was compared with placebo in patients with HFpEF and obesity. The two [&hellip;]<\/p>\n","protected":false},"author":40603,"featured_media":137988,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[881,8],"tags":[45,882,47,185],"ppma_author":[1029],"class_list":{"0":"post-137999","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-esc-2023","8":"category-news","9":"tag-conference","10":"tag-esc-2023","11":"tag-featured","12":"tag-news","13":"author-leah-kosyakovsky"},"authors":[{"term_id":1029,"user_id":40603,"is_guest":0,"slug":"leah-kosyakovsky","display_name":"Leah Kosyakovsky","avatar_url":"https:\/\/secure.gravatar.com\/avatar\/864bde69f6f1f80e91e4a97f0a0ba8daa64c2bb702be09ed787444c7dfa045bb?s=96&r=g","0":null,"1":"","2":"","3":"","4":"","5":"","6":"","7":"","8":""}],"_links":{"self":[{"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/posts\/137999","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/users\/40603"}],"replies":[{"embeddable":true,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=137999"}],"version-history":[{"count":1,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/posts\/137999\/revisions"}],"predecessor-version":[{"id":138000,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/posts\/137999\/revisions\/138000"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=\/wp\/v2\/media\/137988"}],"wp:attachment":[{"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=137999"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=137999"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=137999"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/cardiologynownews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fppma_author&post=137999"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}