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Early hemodynamic impact of SGLT2 inhibitors in overweight cardiometabolic heart failure: beyond fluid offloading to vascular adaptation- a preliminary report.

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  • معلومة اضافية
    • المصدر:
      Publisher: BioMed Central Country of Publication: England NLM ID: 101147637 Publication Model: Electronic Cited Medium: Internet ISSN: 1475-2840 (Electronic) Linking ISSN: 14752840 NLM ISO Abbreviation: Cardiovasc Diabetol Subsets: MEDLINE
    • بيانات النشر:
      Original Publication: London : BioMed Central, [2002-
    • الموضوع:
    • نبذة مختصرة :
      Competing Interests: Declarations. Ethics approval and consent to participate: The study was approved by the Local Ethics Committee (Protocol Register No. 170, May 30, 2024). All patients provided written informed consent before participating in the study. Consent for publication: All authors listed above approved the manuscript for publication. Competing interests: The authors declare no competing interests.
      Background: Heart failure (HF) is increasingly recognized as a heterogeneous cardiometabolic disorder, often in the context of overweight/obesity independently from diabetes. Sodium-glucose cotransporter-2 inhibitors (SGLT2i) reduce HF hospitalizations and cardiovascular mortality across ejection fraction (EF) categories, yet their early hemodynamic effects in cardiometabolic HF, and with preserved ejection fraction (HFpEF) in particular, remain underexplored.
      Methods: A prospective, single-center study included 20 consecutive HF patients receiving SGLT2i alongside optimized therapy. Transthoracic echocardiography and non-invasive bioimpedance assessments (NICaS system) were performed at baseline and after 4 weeks.
      Results: The median patient age was 75 years [58-84], with 14 patients (70%) being overweight/obese, and only 4 patients with diabetes. The majority (65%) had HF with preserved EF (HFpEF), 25% with mildly reduced EF (HFmrEF), and 10% with reduced EF (HFrEF). At a median follow-up of 33 days [30-68], significant reductions were observed in body weight (67.65 kg [46-99.20] to 65.50 kg [46.30-97], p = 0.027) and systolic blood pressure (130 mmHg [100-150] to 116.50 mmHg [100-141], p = 0.015). Hemodynamic assessments revealed a significant decrease in total peripheral resistance index (TPRi, 3616.50 dynes·sec·cm3 [1600-5024] to 3098.50 dynes·sec·cm3 [1608-4684], p = 0.002). The left atrial volume index decreased significantly (42.84 ml/m² [27-69.40] to 41.15 ml/m² [26-62.60], p < 0.001); a significant decrease in peak tricuspid regurgitation velocity [2.52 m/Sect. (1.30-3.20]), vs. 2.21 m/Sect. (1.44-2.92), p = 0.023] and in pulmonary artery systolic pressure (PASP) [31.0 mmHg (15.0-40.0) vs. 25.50 mmHg (15.0-38.0-), p = 0.010] was observed. Patients with HFrEF or HFmrEF showed significant reduction in total body water (66.33 [51.45-74.45] vs. 58.68 [55.13-66.50]), while HFpEF patients (overweight/obese, n = 11, 79%) had a significant reduction in TPRi (3681 dynes·sec·cm3 [1600-5024] vs. 3085 dynes·sec·cm3 [1608-4684] p = 0.005).
      Conclusions: Early hemodynamic responses to SGLT2i may differ across HF subtypes. In overweight patients with cardiometabolic HFpEF, our preliminary findings suggest an association with reduced vascular resistance, while in HFrEF/HFmrEF, the primary benefit appears to be volume unloading. However, the vascular effects of SGLT2i remain uncertain, and given the small sample size, these results should be interpreted as hypothesis-generating. Our findings also highlight the potential role of non-invasive hemodynamic monitoring in guiding therapy in HF.
      (© 2025. The Author(s).)
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    • Grant Information:
      PNRR-National Center for Gene Therapy and Drugs based on RNA Technology No. CN00000041 Ministero dell'Università e della Ricerca; PNRR-National Center for Gene Therapy and Drugs based on RNA Technology No. CN00000041 Ministero dell'Università e della Ricerca; PNRR-National Center for Gene Therapy and Drugs based on RNA Technology No. CN00000041 Ministero dell'Università e della Ricerca; POS4 "Cal-Hub-Ria" No. T4-AN-09; PNRRMAD-2022-12376814 Ministero della Salute
    • Contributed Indexing:
      Keywords: Heart failure; Hemodynamics; Non-invasive monitoring; Sodium-glucose cotransporter 2 inhibitors
    • الرقم المعرف:
      0 (Sodium-Glucose Transporter 2 Inhibitors)
    • الموضوع:
      Date Created: 20250327 Date Completed: 20250327 Latest Revision: 20250329
    • الموضوع:
      20250329
    • الرقم المعرف:
      PMC11948974
    • الرقم المعرف:
      10.1186/s12933-025-02699-4
    • الرقم المعرف:
      40140861