Raza Shafaat, Osasan Stephen, Sethia Sudiksha, Batool Tayyaba, Bambhroliya Zarna, Sandrugu Joel, Lowe Michael, Okunlola Oluwasemilore, Hamid Pousette
Research, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Neurology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Cureus. 2022 Jun 25;14(6):e26313. doi: 10.7759/cureus.26313. eCollection 2022 Jun.
Sodium-glucose cotransporter 2 (SGLT2) inhibitors have many actions beyond glycemic control. The drug leads to favorable cardiovascular and renal outcomes. In this review, we focused on how SGLT2 inhibitors produce these outcomes and what role it plays in the inhibition of the sympathetic nervous system in diabetic patients. We searched PubMed, Google Scholar, and Biomed Central databases from January 2016 to February 2022. The authors used specific keywords and the Medical Subject Heading (MeSH) strategy. We identified a total of 3,961 records. Strict inclusion-exclusion criteria were followed to gather relevant data. From 3,961 results found through electronic databases, we finally selected 161 studies after the removal of duplicates, excluding irrelevant studies and those that did not fall into inclusion criteria. Forty-one studies underwent an extensive content search and quality appraisal using specific tools. It included a total of 12 best studies to conduct the systematic review supporting data from 17 other studies. Our review found that the SGLT2 inhibitors significantly reduced cardiovascular endpoints, including cardiovascular death, heart failure hospitalization, and all-cause mortality, with varying effects on major adverse cardiovascular (MACE). There were nominal improvements in renal outcomes (decline in renal disease progression, decreased albuminuria, less need for renal replacement therapy [RRT], and stable estimated glomerular filtration rate [eGFR]). Inhibition of the sympathetic nervous system (SNS) is an important and under-studied mechanism of SGLT2 inhibitors. This systematic review explores that SGLT2 inhibitors decrease the time to first cardiovascular event or death, less heart failure hospitalizations (HFH), and reduced MACE. Improvements in renal function preserved eGFR and reduction in RRT. Also, this drug inhibits SNS further by aiding in cardiorenal protection.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂具有许多超出血糖控制的作用。该药物可带来良好的心血管和肾脏结局。在本综述中,我们重点关注SGLT2抑制剂如何产生这些结局,以及它在糖尿病患者交感神经系统抑制中所起的作用。我们检索了2016年1月至2022年2月期间的PubMed、谷歌学术和生物医学中心数据库。作者使用了特定关键词和医学主题词(MeSH)策略。我们共识别出3961条记录。遵循严格的纳入-排除标准来收集相关数据。从通过电子数据库找到的3961个结果中,我们在去除重复项、排除无关研究和不符合纳入标准的研究后,最终选择了161项研究。41项研究使用特定工具进行了广泛的内容检索和质量评估。其中共有12项最佳研究用于进行系统综述,支持来自其他17项研究的数据。我们的综述发现,SGLT2抑制剂显著降低了心血管终点事件,包括心血管死亡、心力衰竭住院和全因死亡率,对主要不良心血管事件(MACE)有不同程度的影响。肾脏结局有一定改善(肾病进展减缓、蛋白尿减少、肾脏替代治疗[RRT]需求降低以及估计肾小球滤过率[eGFR]稳定)。交感神经系统(SNS)的抑制是SGLT2抑制剂一个重要但研究不足的机制。本系统综述探讨了SGLT2抑制剂可减少首次心血管事件或死亡的时间、降低心力衰竭住院率(HFH)并减少MACE。肾功能的改善使eGFR得以保留并减少了RRT。此外,该药物通过辅助心脏肾脏保护进一步抑制SNS。