SGLT2抑制剂对2型糖尿病患者慢性心力衰竭病程的影响

A. N. Payudis, O. A. Efremova, L. A. Kamyshnikova, Iu. S. Pavlova, O. V. Dudchenko, I. Khamnagadaev, T. Golivets
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摘要

糖尿病(DM)是一组以慢性高血糖为特征的代谢性疾病,是胰岛素分泌或胰岛素作用受损或两者兼而有之的结果。糖尿病的慢性高血糖伴随着各种器官的损伤、功能障碍和衰竭,尤其是眼睛、肾脏、神经、心脏和血管。糖尿病通过其葡萄糖毒性作用、对高脂血症和凝血功能的影响、心脏自主调节功能受损等多种机制,在慢性心力衰竭(CHF)的形成中起着重要作用,是慢性心力衰竭发展的重要危险因素之一。钠-葡萄糖共转运蛋白2型(SGLT2)抑制剂是最近出现的一类抗糖尿病药物,通过抑制葡萄糖在肾脏的重吸收起作用。现有的研究表明,这些药物不仅具有抗糖尿病作用,而且具有明显的器官保护作用,特别是心脏保护作用。今天,人们认为导致这种情况的主要原因是肾脏钠重吸收减少,细胞内钙和钠含量减少,线粒体内钙浓度增加。还考虑了这些药物的生酮作用,它们对氧化应激和心肌炎症和纤维化过程的影响。SGLT2抑制剂最常见的副作用包括尿路和生殖器感染,血糖酮症酸中毒。其他可能的副作用包括下肢截肢、富尼耶坏疽、女性乳腺癌、男性膀胱癌、体位性低血压和急性肾损伤的风险增加以及骨折的可能性增加。在开始使用药物之前,通过充分的患者教育和对危险因素和禁忌症的评估,大多数副作用是可以避免的。尽管SGLT2抑制剂显然需要更多的研究,但它们的广泛使用将对糖尿病患者的健康产生积极影响。
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Effect of SGLT2 inhibitors on the course of chronic heart failure in patients with type 2 diabetes mellitus
Diabetes mellitus (DM) is a group of metabolic diseases characterized by chronic hyperglycemia, which is the result of impaired insulin secretion, insulin action, or both. Chronic hyperglycemia in diabetes is accompanied by damage, dysfunction, and failure of various organs, especially the eyes, kidneys, nerves, heart, and blood vessels. Diabetes mellitus plays a significant role in the formation and is one of the significant risk factors for the development of chronic heart failure (CHF) through its glucose toxic effect, the effect on hyperlipidemia and blood coagulation, impaired autonomic regulation of the heart and a number of other mechanisms. Sodium-glucose cotransporter type 2 (SGLT2) inhibitors are a recently emerging class of antidiabetic drugs that act by inhibiting the reabsorption of glucose in the kidneys. Existing studies of the efficacy and safety of these drugs have shown that they have not only antidiabetic, but also a pronounced organoprotective, especially cardioprotective effect. Today it is believed that the main reason leading to this lies in a decrease in sodium reabsorption in the kidneys, a decrease in the content of intracellular calcium and sodium, and an increase in the concentration of calcium in mitochondria. The role of the ketogenic action of these drugs, their effect on oxidative stress and the processes of inflammation and fibrosis in the myocardium is also considered. The most common side effects of SGLT2 inhibitors include urinary tract and genital infections, euglycemic ketoacidosis. Other possible side effects include an increased risk of lower limb amputations, Fournier gangrene, breast cancer in women, bladder cancer in men, orthostatic hypotension and acute kidney injury, and an increased tendency to fracture. Most side effects can be avoided through adequate patient education and assessment of risk factors and contraindications before starting the use of drugs. Despite the clear need for more research on SGLT2 inhibitors, their widespread use will positively affect the health of the diabetic patient population.
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