Suppr超能文献

糖尿病和非酒精性脂肪性肝病患者启动SGLT-2抑制剂和GLP-1受体激动剂治疗后的肝脏和肾脏不良结局

Adverse Liver and Renal Outcomes After Initiating SGLT-2i and GLP-1RA Therapy Among Patients With Diabetes and MASLD.

作者信息

Krishnan Arunkumar, Schneider Carolin V, Mukherjee Diptasree, Woreta Tinsay A, Alqahtani Saleh A

机构信息

Department of Medicine, Wake Forest University School of Medicine, Winston Salem, North Carolina, USA.

Department of Supportive Oncology, Atrium Health Levine Cancer, Charlotte, North Carolina, USA.

出版信息

J Diabetes. 2025 Apr;17(4):e70069. doi: 10.1111/1753-0407.70069.

Abstract

CONTEXT

The management of metabolic dysfunction-associated steatotic liver disease (MASLD) and type 2 diabetes mellitus (T2DM) presents a significant clinical challenge, with a focus on preventing progression to liver and renal complications.

OBJECTIVE

To evaluate the liver and renal outcomes among new users of sodium-glucose cotransporter 2 inhibitors (SGLT2i) versus glucagon-like peptide-1 receptor agonists (GLP-1RA), dipeptidyl peptidase-4 inhibitors (DPP4i) and other anti-diabetic medications in patients with MASLD and T2DM.

DESIGN

Retrospective cohort study.

SETTING

Electronic health records.

PARTICIPANTS

A total number of 88 306 patients with MASLD and T2DM were included in a propensity score-matched analysis comparing the effects of anti-diabetic drugs.

INTERVENTION

Patients were categorized into groups based on their initiation of anti-diabetic medications.

MAIN OUTCOME MEASURES

The primary outcomes were the incidence of cirrhosis, hepatic decompensations, and hepatocellular carcinoma. Secondary outcomes were a progression of chronic kidney disease (CKD), severity of CKD stages, and the need for hemodialysis.

RESULTS

In the SGLT2i versus DPP4i, a reduced risk of cirrhosis was observed in the SGLT2i (HR: 0.97), along with fewer hepatic decompensations (HR: 0.84) and a lower incidence of HCC (HR: 0.50). CKD progression, particularly to stages 4-5, was significantly lower in the SGLT2i (HR: 0.53), as was hemodialysis (HR: 0.38). However, SGLT2i exhibited a slightly lower risk of CKD progression (HR: 0.77) and a reduced need for hemodialysis (HR: 0.71) compared to the GLP-1RA, while there was no difference in hepatic outcomes between the GLP-1RA and SGLT2i.

CONCLUSIONS

SGLT2 inhibitors in patients with MASLD and T2DM demonstrated reduced risks of liver complications and a favorable impact on renal outcomes. These findings support the preferential consideration of SGLT2i in managing this patient population, particularly for mitigating the progression of liver and kidney diseases.

摘要

背景

代谢功能障碍相关脂肪性肝病(MASLD)和2型糖尿病(T2DM)的管理面临重大临床挑战,重点在于预防进展为肝脏和肾脏并发症。

目的

评估钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)新使用者与胰高血糖素样肽-1受体激动剂(GLP-1RA)、二肽基肽酶-4抑制剂(DPP4i)及其他抗糖尿病药物在MASLD和T2DM患者中的肝脏和肾脏结局。

设计

回顾性队列研究。

设置

电子健康记录。

参与者

共88306例MASLD和T2DM患者纳入倾向评分匹配分析,比较抗糖尿病药物的效果。

干预

根据患者开始使用抗糖尿病药物的情况进行分组。

主要结局指标

主要结局为肝硬化、肝失代偿和肝细胞癌的发生率。次要结局为慢性肾脏病(CKD)进展、CKD分期严重程度及血液透析需求。

结果

在SGLT2i与DPP4i的比较中,SGLT2i组肝硬化风险降低(HR:0.97),肝失代偿较少(HR:0.84),HCC发生率较低(HR:0.50)。SGLT2i组CKD进展,尤其是进展至4 - 5期的情况显著更低(HR:0.53),血液透析需求也更低(HR:0.38)。然而,与GLP-1RA相比,SGLT2i的CKD进展风险略低(HR:0.77),血液透析需求减少(HR:0.71),而GLP-1RA与SGLT2i在肝脏结局方面无差异。

结论

MASLD和T2DM患者使用SGLT2抑制剂可降低肝脏并发症风险,并对肾脏结局产生有利影响。这些发现支持在管理该患者群体时优先考虑SGLT2i,特别是用于减轻肝脏和肾脏疾病的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f9b/12034490/cdd5918668ae/JDB-17-e70069-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验