Onyali Chike B, Anim-Koranteng Comfort, Shah Hira E, Bhawnani Nitin, Ethirajulu Aarthi, Alkasabera Almothana, Mostafa Jihan A
Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Cureus. 2021 Aug 26;13(8):e17452. doi: 10.7759/cureus.17452. eCollection 2021 Aug.
Chronic kidney disease (CKD) and cardiovascular complications are the leading causes of death in type 2 diabetes mellitus. Apart from the standard therapy, which includes angiotensin-converting enzyme inhibitors (ACEi), angiotensin receptor blockers (ARBs), lipid-lowering medication, and anti-platelet therapy, the new group of drugs termed the 'sodium-glucose co-transporter-2 (SGLT2) inhibitors' have shown promising results in managing complications arising from the cardiovascular and renal systems in diabetics. This article attempts to highlight the role and mechanism of action of this class of drugs. We reviewed 127 articles and analyses of randomized controlled trials using several drugs in the SGLT2 inhibitor family (sotagliflozin, canagliflozin, dapagliflozin, tofogliflozin) over the past five years, out of which 58 met the criteria and aim of the study. These articles were retrieved from PubMed, Google Scholar, and Medline data sources and assessed for quality using the assessment of multiple systematic reviews (AMSTAR) checklist and Cochrane risk-of-bias tool. Results from the review showed significant benefits in reducing progressive renal decline, blood pressure control, heart failure hospitalization, death from renal or cardiovascular complications, myocardial infarction, and stroke. This benefit is also seen in non-diabetic patients, hence postulating that these effects may not be solely due to glycemic control. There are several mechanisms with which it achieves this benefit with the most significant being its role on intraglomerular pressure. Other pathways include blood pressure control, natriuresis, ventricular remodeling, erythropoiesis, lipid metabolism, plasma volume, and electrolyte imbalance. It is clear that the role of SGLT2 inhibitors isn't limited to glycemic control and they can achieve a wide array of functions by affecting different systems. More studies need to be done to completely understand this medication to improve the quality of life in diabetic and non-diabetic patients living with CKD and cardiovascular complications. The pharmacokinetics of this drug could also help set the basis for newer medications.
慢性肾脏病(CKD)和心血管并发症是2型糖尿病患者的主要死因。除了包括血管紧张素转换酶抑制剂(ACEi)、血管紧张素受体阻滞剂(ARB)、降脂药物和抗血小板治疗在内的标准治疗外,一类名为“钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂”的新型药物在控制糖尿病患者心血管和肾脏系统并发症方面已显示出令人鼓舞的结果。本文旨在强调这类药物的作用及作用机制。我们回顾了过去五年中使用SGLT2抑制剂家族中的几种药物(索格列净、卡格列净、达格列净、托格列净)进行的127篇随机对照试验的文章和分析,其中58篇符合研究的标准和目的。这些文章从PubMed、谷歌学术和Medline数据源检索,并使用多重系统评价(AMSTAR)清单和Cochrane偏倚风险工具进行质量评估。综述结果显示,在减少进行性肾脏衰退、控制血压、心力衰竭住院、肾脏或心血管并发症死亡、心肌梗死和中风方面有显著益处。在非糖尿病患者中也观察到了这种益处,因此推测这些作用可能不仅仅归因于血糖控制。它通过多种机制实现这一益处,其中最重要的是其对肾小球内压的作用。其他途径包括控制血压、利钠、心室重塑、红细胞生成、脂质代谢、血容量和电解质失衡。显然,SGLT2抑制剂的作用不限于控制血糖,它们可以通过影响不同系统实现广泛的功能。需要进行更多研究以全面了解这种药物,从而改善患有CKD和心血管并发症的糖尿病和非糖尿病患者的生活质量。这种药物的药代动力学也可为新型药物奠定基础。