JACC. Cardiovascular imaging

Using Body Weight and Heart Artery Calcium to Guide Semaglutide Treatment in Heart Disease Risk

Updated

Abstract

Among 3,129 participants, 49% had coronary artery calcium (CAC) present, which is linked to significantly higher risks of major adverse cardiovascular events and other health issues.

  • CAC scores indicate a 2.2-fold increased risk for major adverse cardiovascular events in individuals with CAC ≥300 compared to those with CAC = 0.
  • Higher CAC levels are associated with increased risks for heart failure, chronic kidney disease, and all-cause mortality.
  • Five-year number-needed-to-treat calculations reveal considerable differences in risk reduction for those with CAC = 0 versus CAC ≥300 across various health outcomes.
  • The findings suggest that measuring CAC could improve the allocation of semaglutide therapy, potentially enhancing patient care for those without diabetes or established cardiovascular disease.

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Funding

Competing interests

Funding Support and Author Disclosures This research was supported by R01HL071739 and R01HL146666 and MESA was supported by contracts 75N92020D00001, HHSN268201500003I, N01-HC-95159, 75N92020D00005, N01-HC-95160, 75N92020D00002, N01-HC-95161, 75N92020D00003, N01-HC-95162, 75N92020D00006, N01-HC-95163, 75N92020D00004, N01-HC-95164, 75N92020D00007, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, and N01-HC-95169 from the National Heart, Lung, and Blood Institute, and by grants UL1-TR-000040, UL1-TR-001079, and UL1-TR-001420 from the National Center for Advancing Translational Sciences (NCATS). Dr Razavi was supported by the National Heart, Lung, and Blood Institute grant F32HL172499. Dr Razavi was supported by National Heart, Lung, and Blood Institute grants F32HL172499 and L30HL175751. Dr Dzaye has received support from National Institutes of Health grant T32 HL007227. Dr Blaha has received grants from the National Institutes of Health, U.S. Food and Drug Administration, and the American Heart Association; grants and personal fees from Amgen, Bayer, Eli Lilly, and Novo Nordisk; and personal fees from Novartis, Roche, Merck, Boehringer Ingelheim, Vectura, Agepha, and AstraZeneca outside the submitted work. Dr Shapiro has received grants (to institution) from PCORI, DCRI, Amgen, Boehringer Ingelheim, 89Bio, Esperion, Genentech, Novartis, Ionis, Merck, and New Amsterdam; Scientific Advisory Boards with Amgen, Agepha, Ionis, Novartis, Precision BioScience, Novo Nordisk, and New Amsterdam; and has received fees as a consultant with Ionis, Novartis, Regeneron, Aidoc, Shanghai Pharma Biotherapeutics, and Kaneka. Dr Al-Mallah has received grants from Siemens; and consultation fees from Jubulant. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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