Fatima Eeshal, Irfan Hamza, Fatima Faiza, Jain Jyoti, Ur Rehman Obaid, Sehar Ayesha, Ahmad Bilal, Kumari Sanjana, Akilimali Aymar
Department of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Department of Internal Medicine, Shaikh Khalifa Bin Zayed Al Nahyan Medical and Dental College, Lahore, Pakistan.
Ann Med Surg (Lond). 2025 May 12;87(6):3700-3706. doi: 10.1097/MS9.0000000000003357. eCollection 2025 Jun.
Heart failure (HF) and diabetes mellitus frequently co-occur, with an incidence of HF among diabetics ranging from 9% to 22%. Clinical research underscores that shared pathophysiological pathways link these conditions, driving advancements in therapeutic strategies that target neuro-hormonal modulation and sodium-glucose co-transporter 2 (SGLT2) inhibition. The SOLOIST-WHF and SCORED trials highlighted the efficacy of sotagliflozin, a dual sodium-glucose co-transporters 1/2 (SGLT1/2) inhibitor, in patients with HF and chronic kidney disease (CKD), demonstrating reductions in cardiovascular mortality and HF-related hospitalizations. Trials with other SGLT2 inhibitors, like dapagliflozin and empagliflozin, in HF, diabetes, and renal disease also showed significant reductions in major adverse cardiovascular events, hospitalizations, and improved kidney function. Furthermore, SGLT2 inhibitors have shown neuroprotective effects, potentially benefiting patients with Alzheimer's and Parkinson's diseases. Dual SGLT1/2 inhibitors, by targeting glucose transport in the renal and intestinal systems, not only reduce blood glucose but also improve insulin sensitivity, weight loss, and cardiovascular health. Sotagliflozin specifically impacts postprandial glucose absorption, mitigating the risks of hypoglycemia and hyperglycemia-related complications. In diabetic CKD, SGLT inhibitors promote renal protection by reducing glucose reabsorption, diuresis, and systemic inflammation. Neuroprotective effects of these agents, including reduced oxidative stress and inflammatory markers, show promise in treating neurodegenerative diseases. While adverse effects like hypoglycemia and ketoacidosis remain concerns, tailored dosing, and monitoring strategies may mitigate these risks. Thus, SGLT inhibitors, especially dual inhibitors like sotagliflozin, offer broad therapeutic benefits in diabetes, HF, CKD, and potentially neurological conditions.
心力衰竭(HF)与糖尿病常常同时出现,糖尿病患者中HF的发病率在9%至22%之间。临床研究强调,共同的病理生理途径将这些病症联系起来,推动了针对神经激素调节和钠-葡萄糖协同转运蛋白2(SGLT2)抑制的治疗策略的进步。SOLOIST-WHF和SCORED试验突出了索格列净(一种双钠-葡萄糖协同转运蛋白1/2(SGLT1/2)抑制剂)在HF和慢性肾脏病(CKD)患者中的疗效,证明其可降低心血管死亡率和与HF相关的住院率。其他SGLT2抑制剂(如达格列净和恩格列净)在HF、糖尿病和肾脏疾病中的试验也显示,主要不良心血管事件、住院率显著降低,肾功能得到改善。此外,SGLT2抑制剂已显示出神经保护作用,可能使阿尔茨海默病和帕金森病患者受益。双SGLT1/2抑制剂通过靶向肾脏和肠道系统中的葡萄糖转运,不仅降低血糖,还改善胰岛素敏感性、减轻体重并促进心血管健康。索格列净特别影响餐后葡萄糖吸收,降低低血糖和高血糖相关并发症的风险。在糖尿病CKD中,SGLT抑制剂通过减少葡萄糖重吸收、利尿和全身炎症来促进肾脏保护。这些药物的神经保护作用,包括降低氧化应激和炎症标志物,在治疗神经退行性疾病方面显示出前景。虽然低血糖和酮症酸中毒等不良反应仍然令人担忧,但量身定制的给药和监测策略可能会降低这些风险。因此,SGLT抑制剂,尤其是像索格列净这样的双抑制剂,在糖尿病、HF、CKD以及潜在的神经系统疾病中具有广泛的治疗益处。