Matuszewski Wojciech, Tomaszek Lena, Szklarz Michał, Górny Jan Marek, Kordas Bernard, Rutkowska Joanna, Juranek Judyta
Clinic of Endocrinology, Diabetology and Internal Medicine, School of Medicine, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland.
Department of Pharmacology and Toxicology, School of Medicine, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland.
J Clin Med. 2025 Sep 9;14(18):6348. doi: 10.3390/jcm14186348.
Contemporary diabetes management is progressively moving away from a glucocentric approach, with growing expectations that novel antidiabetic agents offer benefits beyond glycaemic control. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have emerged as a cornerstone in the treatment of type 2 diabetes mellitus (T2DM). In addition to reducing blood glucose levels by promoting renal glucose excretion, these agents contribute significantly to cardio-renal-metabolic protection and are associated with improved cardiovascular outcomes and prolonged survival. Although SGLT2 inhibitors do not exhibit a class effect in all clinical aspects, growing evidence suggests their potential in a variety of additional therapeutic areas. We conducted an in-depth review of current scientific literature and clinical studies regarding this class of drugs. SGLT2 inhibitors demonstrate neuroprotective properties and may provide benefits in neurodegenerative disorders such as Alzheimer's and Parkinson's disease, potentially through the improvement of mitochondrial function and attenuation of inflammatory responses. Their anti-inflammatory and antioxidative effects are closely linked to reductions in cardiac and renal fibrosis. Other observed benefits include weight loss, improved insulin sensitivity, normalization of serum uric acid, and a reduction in hepatic steatosis-each with important metabolic implications. Furthermore, SGLT2 inhibitors have been shown to positively influence iron metabolism and improve erythrocyte indices. Emerging data also indicate beneficial effects in women with polycystic ovary syndrome. Another promising area of investigation involves the modulation of Klotho protein expression and support of vascular homeostasis. In oncology, SGLT2 inhibitors are gaining attention, with encouraging preclinical results observed in malignancies such as pancreatic, thyroid, breast, and lung cancers. Based on a comprehensive evaluation of the existing body of evidence, it is anticipated that the clinical indications for SGLT2 inhibitors will expand beyond the cardio-renal-metabolic axis in the near future.
当代糖尿病管理正逐渐摆脱以血糖为中心的方法,人们越来越期望新型抗糖尿病药物能带来血糖控制之外的益处。钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)已成为2型糖尿病(T2DM)治疗的基石。除了通过促进肾脏葡萄糖排泄来降低血糖水平外,这些药物对心脏-肾脏-代谢具有显著的保护作用,并与改善心血管结局和延长生存期相关。尽管SGLT2抑制剂在所有临床方面并不都表现出类效应,但越来越多的证据表明它们在多种其他治疗领域具有潜力。我们对有关这类药物的当前科学文献和临床研究进行了深入综述。SGLT2抑制剂具有神经保护特性,可能通过改善线粒体功能和减轻炎症反应,在阿尔茨海默病和帕金森病等神经退行性疾病中发挥作用。它们的抗炎和抗氧化作用与心脏和肾脏纤维化的减轻密切相关。其他观察到的益处包括体重减轻、胰岛素敏感性改善、血清尿酸正常化以及肝脂肪变性减轻——每一项都具有重要的代谢意义。此外,SGLT2抑制剂已被证明对铁代谢有积极影响,并能改善红细胞指标。新出现的数据还表明对多囊卵巢综合征女性有有益作用。另一个有前景的研究领域涉及对Klotho蛋白表达的调节和对血管稳态的支持。在肿瘤学领域,SGLT2抑制剂正受到关注,在胰腺癌、甲状腺癌、乳腺癌和肺癌等恶性肿瘤中观察到了令人鼓舞的临床前结果。基于对现有证据的全面评估,预计在不久的将来,SGLT2抑制剂的临床适应证将超出心脏-肾脏-代谢轴的范围。