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钠-葡萄糖共转运蛋白 2 抑制剂改善不同患者群体的心衰结局。

Improving heart failure outcomes with sodium-glucose cotransporter 2 inhibitors in different patient groups.

机构信息

BHF Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.

出版信息

Diabetes Obes Metab. 2023 Jul;25 Suppl 3(Suppl 3):26-32. doi: 10.1111/dom.15171. Epub 2023 Jun 19.

DOI:10.1111/dom.15171
PMID:37334518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10946463/
Abstract

Sodium-glucose cotransporter 2 inhibitors (SGLT-2is) were originally developed for the treatment of hyperglycaemia in type 2 diabetes. Because of regulatory requirements to show the safety of this new class of drugs, a large randomized cardiovascular (CV) outcomes trial was completed but this showed that instead of having a neutral effect on heart failure (HF) outcomes, that these drugs could reduce HF outcomes in this population. Subsequent trials with SGLT-2is have shown that HF hospitalizations are reduced by 30% and CV death or HF hospitalization by 21% in patients with type 2 diabetes. These findings have extended to patients with HF with reduced and mildly reduced or preserved ejection fraction in whom further HF hospitalizations are reduced by 28% and CV death or HF hospitalizations reduced by 23%, and that it is becoming a central therapy for the treatment of HF. Moreover, the benefit in patients with HF is observed regardless of the presence or absence of type 2 diabetes. Similarly, in patients with chronic kidney disease and albuminuria, with and without type 2 diabetes, the benefit of SGLT-2is is clearly seen with a 44% reduction in HF hospitalization and 25% reduction in CV death or HF hospitalization. These trials support the use of SGLT-2is in improving HF outcomes in a broad range of patients, from those with type 2 diabetes, chronic kidney disease and those with pre-existing HF regardless of ejection fraction.

摘要

钠-葡萄糖共转运蛋白 2 抑制剂(SGLT-2is)最初是为治疗 2 型糖尿病的高血糖而开发的。由于监管要求显示这种新药类的安全性,一项大型随机心血管(CV)结局试验已经完成,但该试验表明,这些药物并没有对心力衰竭(HF)结局产生中性影响,反而可以降低该人群的 HF 结局。随后的 SGLT-2is 试验表明,2 型糖尿病患者的 HF 住院率降低了 30%,CV 死亡或 HF 住院率降低了 21%。这些发现已经扩展到射血分数降低、轻度降低或保留的 HF 患者,这些患者的 HF 住院率降低了 28%,CV 死亡或 HF 住院率降低了 23%,并且它正在成为 HF 治疗的核心疗法。此外,无论是否存在 2 型糖尿病,HF 患者都能观察到获益。同样,在伴有或不伴有 2 型糖尿病的慢性肾脏病和白蛋白尿患者中,SGLT-2is 的获益也很明显,HF 住院率降低 44%,CV 死亡或 HF 住院率降低 25%。这些试验支持在广泛的患者中使用 SGLT-2is 来改善 HF 结局,包括 2 型糖尿病、慢性肾脏病和无论射血分数如何都有预先存在的 HF 的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/5fb73fc7b138/DOM-25-26-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/bcf871c23189/DOM-25-26-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/dfd996e97271/DOM-25-26-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/7b22e22277b1/DOM-25-26-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/5fb73fc7b138/DOM-25-26-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/bcf871c23189/DOM-25-26-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/dfd996e97271/DOM-25-26-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10946463/7b22e22277b1/DOM-25-26-g003.jpg
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